A Re-Evaluation of Random-Effects Meta-Analysis
Open accessAbstract
Summary: Meta-analysis in the presence of unexplained heterogeneity is frequently undertaken by using a random-effects model, in which the effects underlying different studies are assumed to be drawn from a normal distribution. Here we discuss the justification and interpretation of such models, by addressing in turn the aims of estimation, prediction and hypothesis testing. A particular issue that we consider is the distinction between inference on the mean of the random-effects distribution and inference on the whole distribution. We suggest that random-effects meta-analyses as currently conducted often fail to provide the key results, and we investigate the extent to which distribution-free, classical and Bayesian approaches can provide satisfactory methods. We conclude that the Bayesian approach has the advantage of naturally allowing for full uncertainty, especially for prediction. However, it is not without problems, including computational intensity and sensitivity to a priori judgements. We propose a simple prediction interval for classical meta-analysis and offer extensions to standard practice of Bayesian meta-analysis, making use of an example of studies of ‘set shifting’ ability in people with eating disorders.
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Written from the paper’s full text.
TL;DR
This paper re-evaluates random-effects meta-analysis, arguing that inference should address the whole distribution of effects—especially prediction—rather than only the mean effect. It proposes a simple classical prediction interval and illustrates the issues with 14 studies of set-shifting ability in eating disorders.
Key findings
- Focusing only on the mean of the random-effects distribution is insufficient: two meta-analytic data sets can produce identical mean estimates and standard errors while differing greatly in heterogeneity, so τ² and the whole distribution matter.
- Distribution-free classical methods can estimate μ and τ² but cannot satisfactorily address prediction; the paper proposes an approximate prediction interval using a t-distribution with k−2 degrees of freedom.
- In the 14-study set-shifting example, heterogeneity was Q=16.73, df=13, P=0.02, I²=22%, and τ²=0.022; the classical random-effects interval was 0.19–0.53, while the approximate prediction interval for a new study ranged from −0.01 to 0.74.
- Bayesian normal random-effects analysis gave μ median 0.36 (95% credible interval 0.18–0.55), θ_new median 0.36 (−0.12–0.84), P(θ_new<0)=0.950, and τ² median 0.023 (0.000024–0.196); Bayesian credible intervals were wider because uncertainty in τ² was properly accounted for.
Methods
- The paper is a methodological re-evaluation structured around estimation, prediction, and hypothesis testing, comparing distribution-free, classical parametric, Bayesian, and non-normal/flexible random-effects approaches.
- The example uses 14 comparative studies of set-shifting ability in people with eating disorders versus healthy controls, taken from Roberts et al. (2007), with effect sizes as standardized differences in means and their standard errors.
- Analyses include classical inverse-variance random-effects meta-analysis with a moment estimate of between-study variance, and Bayesian normal random-effects meta-analysis via MCMC in WinBUGS with a uniform prior for τ (>0) and a vague N(0,10³) prior for μ; sensitivity analyses used a t-distribution with 4 degrees of freedom, an inverse gamma prior, and a shrinkage prior.
Limitations
- Stated: the Bayesian approach has problems including computational intensity and sensitivity to a priori judgements; prior choice can substantially affect results; model uncertainty is not accounted for; the normal random-effects assumption is strong and usually made without convincing evidence; few studies make τ² and μ imprecise; separating diversity from bias is difficult; and caution is warranted with funnel plot asymmetry.
- Stated: the example data were available only as effect sizes and confidence intervals, from which standard errors were calculated; more detailed data should be explicitly modelled when available.
- Evident: the example has only 14 studies and some large within-study standard errors; the paper notes that meta-analyses with very small numbers of studies (2–4) pose particular problems, and prediction intervals depend on the number of studies and within-study standard errors.
Model-written summary. Check it against the paper before relying on it.
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Claims the paper makes
0 of 31 cited sources checked · 0 supported · 0 flagged
- Findingreasoning
In the 14-study set shifting meta-analysis, the approximate prediction interval for the true effect in a new study ranges from −0.01 to 0.74.
“The approximate prediction interval (12) for the true effect in a new study, however, ranges from −0.01 to 0.74, which is slightly less convincing.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
- Findingcitation
Using an inverse gamma distribution for τ2 with parameters 0.001 and 0.001 produces a prediction interval from −0.008 to 0.73 (P(θnew<0)=0.973).
“Alternatively using an inverse gamma distribution for τ2 with parameters 0.001 and 0.001 (Smith et al., 1995) produces a prediction interval from −0.008 to 0.73 (P(θnew<0)=0.973)”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Smith et al., 1995 source
Not checked in the free run.
- Findingown data
In the Bayesian normal random-effects meta-analysis of the set shifting data, the posterior median for τ2 is 0.023 with 95% credible interval (0.000024, 0.196).
“| τ2 | 0.023 | (0.000024, 0.196) | — |”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
- Findingcitation
In the 14-study set shifting meta-analysis, there is some heterogeneity between effect sizes, accounting for 22% of the variation in point estimates by using I2.
“There is some heterogeneity between the effect sizes, accounting for 22% of the variation in point estimates by using the statistic I2 (Higgins and Thompson, 2002).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Higgins and Thompson, 2002
Not checked in the free run.
- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
- Findingreasoning
In the 14-study set shifting meta-analysis, a random-effects meta-analysis reveals a statistically significant benefit on average.
“A random-effects meta-analysis reveals a statistically significant benefit on average, based on the inference in equation (13) regarding μ alone.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
- Findingown data
In the 14-study set shifting meta-analysis, the majority of trials indicate greater set shifting deficiency in people with eating disorders.
“It is evident from Table 1, as well as from the estimated effect sizes, plotted with 95% confidence intervals in Fig. 2, that the majority of trials indicate greater set shifting deficiency in people with eating disorders.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
- Findingcitation
In the 14-study set shifting meta-analysis, the test for qualitative interaction produces a statistically non-significant test statistic Q*=2.56, compared with a critical value of 14.15 for a significance level of 5%.
“Correspondingly, the test for qualitative interaction (9) produces a statistically non-significant test statistic Q*=2.56, compared with a critical value of 14.15 for a significance level of 5% (Gail and Simon, 1985).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Gail and Simon, 1985 source
Not checked in the free run.
- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
- Interpretationreasoning
In biomedical and social sciences, an assumption of homogeneity of effects across studies can seldom be made.
“However, such an assumption of homogeneity can seldom be made for studies in the biomedical and social sciences.”
Quote in the paperNot a substantial claim - Interpretationreasoning
The conventional test from a random-effects meta-analysis shares the property of not rejecting hypothesis (1) when effects are variable and centred on 0.
“This property is shared with the conventional test from a random-effects meta-analysis, i.e. of hypothesis (2) against”
Quote in the paperSubstantial claim - Interpretationreasoning
Estimation of the heterogeneity variance τ2 is just as important as estimation of the mean effect μ.
“Estimation of τ2 is just as important.”
Quote in the paperNot a substantial claim - Interpretationreasoning
A sole focus on estimating the mean of a random-effects distribution may be misleading.
“A sole focus on estimating the mean of a random-effects distribution may be misleading, as demonstrated in Fig. 1, and emphasis should be placed on the whole distribution of underlying effects.”
Quote in the paperSubstantial claim - Interpretationnone given
A major benefit of a random-effects model over a common effect model is that inferences can be made for studies not included in the meta-analysis.
“A major benefit of a random-effects model over the common effect model is that inferences can be made for studies that are not included in the meta-analysis, say for θnew drawn from f(Φ).”
Quote in the paperSubstantial claim - Interpretationreasoning
Neither the conventional common-effect test nor the conventional random-effects test can distinguish between null hypotheses (1) and (2).
“More specifically, neither test can distinguish between the null hypotheses (1) and (2).”
Quote in the paperSubstantial claim - Interpretationreasoning
Unless there is a genuine lack of effect underlying every study, assuming a common parameter is untenable.
“Unless there is a genuine lack of effect underlying every study, to assume the existence of a common parameter would seem to be untenable.”
Quote in the paperNot a substantial claim - Interpretationnone given
In the absence of a specific distributional assumption for the random effects, point estimation of μ and τ2 poses no problem.
“In the absence of a specific distributional assumption for f(Φ), we can address some, but not all, of our important objectives. Point estimation of μ and τ2 poses no problem, although confidence intervals rely on approximating distributions, sometimes based on the central limit theorem, which may not be realistic when there are few studies.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The available effect estimates are unbiased for the study-specific effects θi.
- The authors state this as an assumption: The estimated variances may be used in place of the true variances.
- Interpretationreasoning
The naive presentation of inference only on the mean of the random-effects distribution is highly misleading.
“The naive presentation of inference only on the mean of the random-effects distribution is highly misleading.”
Quote in the paperNot a substantial claim - Interpretationnone given
The particular form assumed for the random-effects distribution can impact on the conclusions of the meta-analysis.
“The particular form that is assumed for the distribution can impact on the conclusions of the meta-analysis.”
Quote in the paperSubstantial claim - Interpretationreasoning
To account for uncertainty in τ2, a t-distribution should provide a better basis than a normal distribution.
“To account for uncertainty in τ2, a t-distribution should provide a better basis than a normal distribution.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The random-effects distribution is normal.
- Interpretationreasoning
Because exchangeability is a judgement of similarity, the Bayesian approach requires no sampling mechanism for the generation of the θi.
“Since exchangeability, and hence the random-effects distribution for the treatment effects, is a judgement of similarity, the Bayesian approach requires no sampling mechanism for the generation of the θi.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The underlying effects are exchangeable.
- Interpretationreasoning
Empirical Bayes methods arise naturally from the classical normal random-effects model.
“Empirical Bayes methods arise quite naturally from the classical normal random-effects model.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The random-effects distribution is normal.
- Interpretationnone given
The key difficulty with NPML is that realistic predictions are unlikely to follow from the discrete distribution for the random effects, especially when the studies include one or more outliers.
“Furthermore, the key difficulty with NPML with regard to our important objectives is that realistic predictions are unlikely to follow from the discrete distribution for the random effects, especially when the studies include one or more outliers.”
Quote in the paperSubstantial claim - Interpretationreasoning
In the presence of potential biases, results from a random-effects model are challenging to interpret.
“In the presence of potential biases, therefore, results from a random-effects model are challenging to interpret.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The true (unbiased) effects Φi follow a normal distribution across studies.
- The authors state this as an assumption: The study-specific bias components βi follow a normal distribution.
- The authors state this as an assumption: The diversity and bias components are uncorrelated.
- The authors state this as an assumption: The effect being evaluated in the ith study is the sum of the true effect and bias: θi=Φi+βi.
- Interpretationcitation
Interpreting the random-effects assumption as random sampling of studies is inappropriate because studies are individually designed dependent on previous results and the evolutionary process of scientific research.
“This implies that the types of participants, natures of exposures, design aspects, and so on, are randomly selected from a distribution of possibilities, which is an inappropriate interpretation because studies are individually designed dependent on the results of previous studies (Peto, 1987) and the evolutionary process of scientific research (Colditz et al., 1995).”
Quote in the paperSubstantial claim0 of 2 sources checked - Interpretationnone given
With the additional assumption of normality for the random effects, the confidence interval for the random-effects mean in expression (8) relies only on the assumption that τ2 is estimated without uncertainty.
“With the additional assumption of normality for the random effects, the confidence interval for the random-effects mean in expression (8) relies only on the assumption that τ2 (in addition to the ) is estimated without uncertainty.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The random-effects distribution is normal.
- Premisecitation
Standard random-effects meta-analysis methods assume a normal distribution for the random effects.
“Standard random-effects meta-analysis methods make this assumption (Whitehead, 2002), and we now discuss the extent to which classical and Bayesian approaches with a normal distribution for the random effects allow the important questions to be addressed.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Whitehead, 2002 source
Not checked in the free run.
- The authors state this as an assumption: The random-effects distribution is normal.
- Premisecitation
The choice of prior distribution can have substantial effects on the results of a Bayesian meta-analysis.
“The choice of prior distribution, even among those that are intended to be non-informative, can have substantial effects on the results of the analysis (Lambert et al., 2005).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Lambert et al., 2005 source
Not checked in the free run.
- Premisecitation
If the underlying effects are deemed exchangeable, then under broad conditions the θi are independent and identically distributed conditional on f(Φ).
“If the underlying effects are deemed to be exchangeable then, under broad conditions, it follows that the θi are independent and identically distributed conditional on f(Φ) (Bernardo and Smith, 1994; O'Hagan, 1994).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Bernardo and Smith, 1994 source
Not checked in the free run.
- cites O'Hagan, 1994
Not checked in the free run.
- The authors state this as an assumption: The underlying effects are exchangeable.
- Interpretationnone given
In the absence of a specific distributional assumption for the random effects, prediction cannot satisfactorily be addressed.
“The objective that we consider to be most important, however, that of prediction, cannot satisfactorily be addressed.”
Quote in the paperSubstantial claim - Premisecitation
A common misinterpretation of the random-effects assumption is that the studies themselves are sampled from a population of studies.
“A common misinterpretation of the random-effects assumption is that the studies themselves are sampled from a population of studies (Hedges, 1987; Anello and Fleiss, 1995; Colditz et al., 1995).”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisenone given
Using MCMC methods in a Bayesian framework, parametric distributions for the random effects offer the same opportunities for inference as a normal distribution.
“Using MCMC methods in a Bayesian framework, parametric distributions for the random effects offer the same opportunities for inference as a normal distribution.”
Quote in the paperNot a substantial claim - Premisecitation
The deviance information criterion provides an alternative criterion that does not require proper prior distributions.
“The deviance information criterion provides an alternative criterion, which is analogous to Akaike's criterion, which does not require proper prior distributions (Spiegelhalter et al., 2002).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Spiegelhalter et al., 2002 source
Not checked in the free run.
- Premisenone given
Some parametric distributions may not have parameters that naturally describe an overall mean or the heterogeneity across studies.
“However, some parametric distributions may not have parameters that naturally describe an overall mean, or the heterogeneity across studies.”
Quote in the paperSubstantial claim - Interpretationnone given
Meta-analyses with very small numbers of studies (say 2-4) pose particular problems in a classical framework since the estimation of τ2, and hence of μ, is highly imprecise.
“Meta-analyses with very small numbers of studies (say 2–4) pose particular problems in a classical framework since the estimation of τ2, and hence of μ, is highly imprecise.”
Quote in the paperSubstantial claim - Premisecitation
A relationship between treatment effect and study size (or study precision) induces an asymmetric funnel plot.
“A relationship between treatment effect and study size (or study precision) induces an asymmetric funnel plot.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Egger et al., 1997 source
Not checked in the free run.
- Interpretationreasoning
An effective number of degrees of freedom for such a t-distribution is difficult to determine because it depends on the extent of heterogeneity, the sizes of within-study standard errors, and the number of studies.
“An effective number of degrees of freedom for such a t-distribution is difficult to determine, since it depends on the extent of the heterogeneity and the sizes of the within-study standard errors as well as the number of studies in the meta-analysis.”
Quote in the paperSubstantial claim - Interpretationreasoning
With the addition of a normal distribution assumption, a classical hypothesis test of whether the mean of the random-effects distribution is non-zero is available.
“With the addition of a normal distribution assumption, a classical hypothesis test of whether the mean of the random-effects distribution is non-zero is available.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The random-effects distribution is normal.
- Interpretationnone given
If study-level covariates summarizing risk of bias are centred at a value indicating freedom from bias, then the intercept and residual heterogeneity from a random-effects metaregression suitably estimate μΦ and the heterogeneity of true effects.
“Providing that these are centred at a value indicating freedom from bias, then the intercept and residual heterogeneity from this analysis suitably estimate μΦ and respectively.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The true (unbiased) effects Φi follow a normal distribution across studies.
- The authors state this as an assumption: The study-specific bias components βi follow a normal distribution.
- The authors state this as an assumption: The diversity and bias components are uncorrelated.
- The authors state this as an assumption: The effect being evaluated in the ith study is the sum of the true effect and bias: θi=Φi+βi.
- Interpretationreasoning
An advantage of a Bayesian approach to random-effects meta-analysis over a classical implementation of the same model is the allowance for all uncertainties, particularly in obtaining a predictive distribution for the true effect in a new study.
“An advantage of a Bayesian approach to random-effects meta-analysis over a classical implementation of the same model is the allowance for all uncertainties, particularly in obtaining a predictive distribution for the true effect in a new study.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The random-effects distribution is normal.
- Interpretationreasoning
The Bayesian allowance for uncertainty may be important when there are few studies in the meta-analysis.
“This may be important when there are few studies in the meta-analysis.”
Quote in the paperSubstantial claim - Interpretationnone given
In a typical meta-analysis, the small or moderate number of studies would carry little information about the Dirichlet process parameter α.
“We can in principle use the observed data to learn about α, although the small or moderate number of studies in a typical meta-analysis would carry little information.”
Quote in the paperNot a substantial claim - Premisecitation
In a classical framework, the major limitation in applying non-normal parametric random-effects distributions is the computational complexity in performing the inference.
“In a classical framework, the major limitation in applying non-normal parametric random-effects distributions is the computational complexity in performing the inference (Aitkin, 1999a).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Aitkin, 1999a
Not checked in the free run.
- Premisenone given
The usual random-effects model makes a strong assumption that the distributions of the study-specific biases βi are identical across studies.
“The usual random-effects model (10) makes a strong assumption that the distributions of the study-specific biases βi are identical across studies, thus giving μ =μΦ+μβ and .”
Quote in the paperSubstantial claim - Interpretationnone given
If there are no studies falling into the 'best' category for any item, then the intercept in the metaregression analysis cannot be estimated.
“Furthermore, if there are no studies falling into the ‘best’ category for any item, then the intercept in the metaregression analysis cannot be estimated.”
Quote in the paperNot a substantial claim - Interpretationnone given
Implementing a common effect model produces confidence intervals that do not allow for variation in underlying effects.
“implementing a common effect model produces confidence intervals that do not allow for variation in underlying effects and should be avoided”
Quote in the paperSubstantial claim - Interpretationreasoning
Focusing on the mean of a random-effects distribution is insufficient.
“focusing on the mean of a random-effects distribution is insufficient.”
Quote in the paperSubstantial claim - Interpretationown data
The confidence interval for the underlying mean in a random-effects meta-analysis does not incorporate a measure of the extent of heterogeneity.
“It may be a common misconception that the confidence interval for the underlying mean in a random-effects meta-analysis, because it is typically wider than for a common effect meta-analysis, incorporates a measure of the extent of heterogeneity. However, as we demonstrate in Fig. 1 this is not so”
Quote in the paperSubstantial claim
- May combine two claims. 25
- Classified as probably not a substantial claim. 29
May combine two claims.
Findingown dataVarious sensitivity analyses have small effects on the results and do not materially affect the conclusions from the Bayesian meta-analysis.
“Various sensitivity analyses have small effects on the results, though they do not materially affect the conclusions from the Bayesian meta-analysis.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
FindingcitationUsing the shrinkage prior advocated by DuMouchel and Normand (2000) produces a prediction interval from −0.009 to 0.72 (P(θnew<0)=0.973).
“using the shrinkage prior that was advocated by DuMouchel and Normand (2000) produces a prediction interval from −0.009 to 0.72 (P(θnew<0)=0.973)”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites DuMouchel and Normand (2000)
Not checked in the free run.
May combine two claims.
Findingown dataIn the 14-study set shifting meta-analysis, the estimate of the heterogeneity variance is 0.022 and the test for heterogeneity is statistically significant at conventional levels.
“The estimate of the heterogeneity variance is 0.022 and the test for heterogeneity is statistically significant at conventional levels of significance.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
May combine two claims.
Findingnone givenUsing a t-distribution with 4 degrees of freedom for the random effects yields a prediction interval from −0.16 to 0.89 (P(θnew<0)=0.947).
“Using a t-distribution with 4 degrees of freedom for the random effects yields a prediction interval from −0.16 to 0.89 (P(θnew<0)=0.947).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn the Bayesian normal random-effects meta-analysis of the set shifting data, results for μ and θnew are comparable with the classical results, with credible intervals being wider because the Bayesian analyses account for uncertainty in the estimation of τ2.
“Results for μ and θnew are comparable with the classical results, with credible intervals being wider because the Bayesian analyses properly account for uncertainty in the estimation of τ2.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
May combine two claims.
Findingown dataIn the Bayesian normal random-effects meta-analysis of the set shifting data, the posterior median for μ is 0.36 with 95% credible interval (0.18, 0.55) and P(μ>0)=0.999.
“| μ | 0.36 | (0.18, 0.55) | 0.999 |”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
May combine two claims.
Findingown dataIn the Bayesian normal random-effects meta-analysis of the set shifting data, the posterior median for θnew is 0.36 with 95% credible interval (−0.12, 0.84) and P(θnew>0)=0.950.
“| θnew | 0.36 | (−0.12, 0.84) | 0.950 |”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The random effects in the meta-analysis are normally distributed.
Classified as probably not a substantial claim. May combine two claims.
PremisecitationSelection of covariates to explain heterogeneity can be difficult both practically and theoretically.
“Although sources of heterogeneity should ideally be investigated (Thompson, 1994), selection of covariates to explain heterogeneity can be difficult, both practically (Higgins et al., 2002) and theoretically (Thompson and Higgins, 2002).”
Quote in the paperSubstantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningRealistic interpretation of predictions from a random-effects model can be difficult.
“Realistic interpretation of predictions from a random-effects model can, however, be difficult.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Interpretationnone givenThe heterogeneity variance τ2 describes the extent of heterogeneity and has a crucial role in assessing the degree of consistency of effects across studies.
“This variance explicitly describes the extent of the heterogeneity and has a crucial role in assessing the degree of consistency of effects across studies, which is an element of random-effects meta-analysis that often receives too little attention.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationcitationA single parameter cannot adequately summarize heterogeneous effects, so focusing on the mean effect alone is usually insufficient.
“However, a single parameter cannot adequately summarize heterogeneous effects (Raudenbush and Bryk, 1985) and so focusing on μ alone is usually insufficient.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Raudenbush and Bryk, 1985 source
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May combine two claims.
InterpretationreasoningThe conventional test from a common effect meta-analysis may be misleading if there is heterogeneity and will not reject hypothesis (1) if effects are variable and centred on 0.
“Although often useful, the test may be misleading if there is heterogeneity and in particular will not reject hypothesis (1) if effects are variable and centred on 0.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationMeta-analyses are often built on an assumption that directions of effect are consistent across studies, yet formal tests of this supposition are not routinely undertaken.
“Meta-analyses are often built on an assumption that directions of effect are consistent across studies (Peto, 1987), yet formal tests of this important supposition are not routinely undertaken.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Peto, 1987 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenAn important rationale for meta-analyses is the possibility of increased power compared with individual studies to detect moderate effects.
“An important rationale for meta-analyses is the possibility of increased power, compared with the individual studies, to detect moderate effects.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable). May combine two claims.
InterpretationcitationThe usual null hypothesis that all effects are equal is typically untenable, and homogeneity tests should be discouraged in favour of quantifying the extent of heterogeneity.
“We have argued that such a null hypothesis is typically untenable and have discouraged the use of homogeneity tests in favour of quantifying the extent of heterogeneity (Higgins and Thompson, 2002).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Higgins and Thompson, 2002
Not checked in the free run.
May combine two claims.
Interpretationnone givenIn the absence of a specific distributional assumption for the random effects, confidence intervals rely on approximating distributions, sometimes based on the central limit theorem, which may not be realistic when there are few studies.
“Point estimation of μ and τ2 poses no problem, although confidence intervals rely on approximating distributions, sometimes based on the central limit theorem, which may not be realistic when there are few studies.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The available effect estimates are unbiased for the study-specific effects θi.
- The authors state this as an assumption: The estimated variances may be used in place of the true variances.
May combine two claims.
PremisecitationNPML has been noted to be unstable and has not been widely adopted.
“However, NPML has been noted to be unstable (Van Houwelingen et al., 1993) and has not been widely adopted.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Van Houwelingen et al., 1993 source
Not checked in the free run.
Classified as probably not a substantial claim.
PremisecitationNPML procedures provide a discrete distribution based on a finite number of mass points.
“NPML procedures provide a discrete distribution that is based on a finite number of mass points (Laird, 1978; Böhning, 2005).”
Quote in the paperSubstantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S4 (based).
Interpretationnone givenThe assumption of a normal distribution for the random-effects distribution allows the calculation of confidence intervals and prediction intervals.
“The assumption of a normal distribution for the random-effects distribution allows the calculation of confidence intervals and prediction intervals.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The random-effects distribution is normal.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Interpretationnone givenA second potential advantage of a Bayesian approach is the intuitive interpretation of posterior distributions in terms of probability, including the ready availability of probabilities that effects exceed specified levels.
“A second potential advantage of a Bayesian approach is the intuitive interpretation of posterior distributions in terms of probability, including the ready availability of probabilities that effects exceed specified levels.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenA particular advantage of the NPML approach is its ability to detect and incorporate outliers.
“A particular advantage of the NPML approach is its ability to detect and incorporate outliers.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
InterpretationreasoningBayesian probabilities can address a variety of questions more readily than classical hypothesis tests.
“Bayesian probabilities can address a variety of questions more readily than classical hypothesis tests.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningAn asymmetric funnel plot leads necessarily to a difference in point estimates between common effect and random-effects meta-analyses (using standard inverse variance methods), because random-effects methods give relatively more weight to less precise studies.
“Whatever the reason for it, an asymmetric funnel plot leads necessarily to a difference in point estimates between common effect and random-effects meta-analyses (using standard inverse variance methods), because random-effects methods give relatively more weight to less precise studies.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based).
Interpretationnone givenMeta-analyses of a large number of large studies lend themselves to relatively complex models, since there may be strong evidence against a normal distribution assumption for the random effect.
“Meta-analyses of a large number of large studies lend themselves to relatively complex models, since there may be strong evidence against a normal distribution assumption for the random effect.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenThe posterior distribution for the underlying mean μ is readily available from a Bayesian meta-analysis.
“The posterior distribution for the underlying mean μ is readily available from a Bayesian meta-analysis.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningIn practice, it can be difficult to separate diversity from bias, and this lack of identifiability often necessitates the use of the conventional random-effects model.
“In practice, it can be difficult to separate diversity from bias, and it is partly this lack of identifiability that often necessitates the use of the conventional random-effects model.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The true (unbiased) effects Φi follow a normal distribution across studies.
- The authors state this as an assumption: The study-specific bias components βi follow a normal distribution.
- The authors state this as an assumption: The diversity and bias components are uncorrelated.
- The authors state this as an assumption: The effect being evaluated in the ith study is the sum of the true effect and bias: θi=Φi+βi.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Interpretationnone givenThe posterior distributions for the study-specific effects θi are readily available from a Bayesian analysis and provide fully Bayesian shrunken estimates.
“The posterior distributions for the study-specific effects θi are readily available from a Bayesian analysis. These provide fully Bayesian shrunken estimates, in which inference for each particular study is performed by ‘borrowing strength’ from the other studies.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
PremisecitationAn important distinction when considering heterogeneity of effect sizes is between the effects of diversity and bias.
“An important distinction to make when considering heterogeneity of effect sizes is between the effects of diversity (variation in populations, interventions, exposures, outcome measures etc.) and bias (variation in the quality of the design and conduct of the studies) (Glasziou and Sanders, 2002; Greenland and O'Rourke, 2001).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Glasziou and Sanders, 2002
Not checked in the free run.
- cites Greenland and O'Rourke, 2001
Not checked in the free run.
Probably not a substantial claim: may not pass S2 (checkable), S4 (based).
Interpretationnone givenNo model for the random-effects distribution will be true.
“No model for the random-effects distribution will be ‘true’, and we might seek a parsimonious model that adequately fits the observed data.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningBayesian uncertainty does not extend to the choice of model for the random effects, which is more difficult to defend empirically when there are few studies.
“However, this uncertainty does not extend to the choice of model for the random effects, which is more difficult to defend empirically when there are few studies.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The random-effects distribution is normal.
May combine two claims.
Premisenone givenTests for heterogeneity have low power when there are few studies, and heterogeneity may be just as likely for small numbers of studies as it is for large numbers of studies.
“Tests for heterogeneity have low power when there are few studies, and heterogeneity may be just as likely for small numbers of studies as it is for large numbers of studies.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationWhen 2×2 contingency tables are available for binary outcomes, meta-analyses are appropriately performed by using binomial likelihoods.
“For example, when 2×2 contingency tables are available for binary outcomes, meta-analyses are appropriately performed by using binomial likelihoods (Smith et al., 1995; Warn et al., 2002).”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S4 (based).
Interpretationnone givenBayesian posterior probabilities can depend heavily on the distribution of the assumed likelihood and prior specification.
“Bayesian posterior probabilities in particular can depend heavily on the distribution of the assumed likelihood and prior specification.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The prior distributions of μ and τ2 are independent.
Probably not a substantial claim: may not pass S4 (based).
Premisenone givenThe derivation of predictive distributions for the effect θnew in a future study has received little methodological attention in a frequentist context.
“The derivation of the predictive distributions for the effect θnew in a future study has received little methodological attention in a frequentist context.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationIt is unclear how prior distributions should be specified, and Bayes factors can be very sensitive to them.
“However, it is unclear how prior distributions should be specified, which is an important limitation since Bayes factors can be very sensitive to them (Kass and Raftery, 1995).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Kass and Raftery, 1995 source
Not checked in the free run.
Probably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing). May combine two claims.
InterpretationreasoningSuch an infinite population does not in reality exist, although the construct allows inference about treatment effects to be extended to a broader population than the studies at hand.
“Such an infinite population does not in reality exist, although the construct does allow inference about treatment effects to be extended to a broader population than the studies at hand.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based).
Interpretationnone givenThe true predictive distribution is a complex function of the degree of heterogeneity, the number of studies, and the within-study standard errors.
“The true predictive distribution is a complex function of the degree of heterogeneity, the number of studies and the within-study standard errors.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenBayes factors may be used to provide evidence specifically in favour of a null hypothesis.
“A particular advantage is that they may be used to provide evidence specifically in favour of a null hypothesis.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Premisenone givenFrom a classical point of view, parametric random-effects meta-analysis is formally interpreted in the context of an imaginary universe or population of similar effects from which the effects in observed studies are independently and identically sampled.
“From a classical point of view, interpretation of parametric random-effects meta-analysis is formally in the context of an imaginary ‘universe’, or ‘population’ of similar effects from which the effects in the observed studies are independently and identically sampled.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningA realistic predictive distribution must recognize that τ2 is estimated, usually from a small number of studies, and that imprecision in τ2 affects both terms in the variance of θnew.
“A realistic predictive distribution must recognize, however, that τ2 is estimated, usually from a small number of studies, and imprecision in affects both terms in the variance of θnew.”
Quote in the paperSubstantial claim- The authors state this as an assumption: Approximately, the predictive distribution of θnew follows a t-distribution with k−2 degrees of freedom.
Classified as probably not a substantial claim.
InterpretationreasoningThe most parsimonious choice for the random-effects distribution is the normal distribution, requiring only two parameters for full specification.
“Requiring only two parameters for its full specification, the most parsimonious choice is also the conventional choice, where f(Φ) is chosen to be a normal distribution: (10)”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenIt remains difficult to implement non-normal distributions outside an MCMC approach to the analysis.
“Flexible distributions such as Bayesian semiparametric models are available, although it remains difficult to implement non-normal distributions outside an MCMC approach to the analysis.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing), S4 (based). May combine two claims.
Interpretationnone givenA Bayesian approach has the additional advantages of flexibility, allowing incorporation of full uncertainty in all parameters (but not uncertainty in the model) and of yielding more readily interpretable inferences.
“A Bayesian approach has the additional advantages of flexibility, allowing incorporation of full uncertainty in all parameters (but not uncertainty in the model) and of yielding more readily interpretable inferences.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningIn many situations, the usual normal distribution assumption for random effects is the most feasible assumption given the limited number of studies and the lack of strong evidence for or against the assumption.
“In many situations this is the most feasible assumption given the limited number of studies and the lack of strong evidence for or against the assumption.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
InterpretationreasoningThe rationale is not strong for opting for a common effect model when there are very few studies.
“Thus the rationale is not strong for opting for a common effect model in this situation.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
InterpretationreasoningMeta-analyses of very few studies need not default to a common effect model, since informative prior distributions for the extent of heterogeneity can be incorporated in a simple Bayesian approach.
“Meta-analyses of very few studies need not ‘default’ to a common effect model, since informative prior distributions for the extent of heterogeneity can be incorporated in a simple Bayesian approach.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationCertain common effect approaches have practical advantages over random-effects methods, such as being easier to implement, and the one-step 'Peto' method has desirable properties when binary events are rare.
“Furthermore, certain common effect approaches have practical advantages over random-effects methods. For example, they are easier to implement, and the one-step ‘Peto’ method has been observed to have desirable properties when binary events are rare (Bradburn et al., 2006).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Bradburn et al., 2006 source
Not checked in the free run.
The authors state this as an assumption.
If an effect exists then heterogeneity exists, although it may be negligible.
“We assume a priori that if an effect exists then heterogeneity exists, although it may be negligible.”
The authors state this as an assumption.
The available effect estimates are unbiased for the study-specific effects θi.
“For generality, the situation that we address assumes only the availability of effect estimates that are unbiased for θi (i =1,…,k), with sampling variance (i.e. squared standard error) .”
The authors state this as an assumption.
The estimated variances may be used in place of the true variances.
“We shall follow the conventional assumption that estimates (which are independent of ) may be used in place of the true variances, and we use the two interchangeably.”
The authors state this as an assumption.
The effect estimates from each study are normally distributed.
“We are willing to assume normality of the effect estimates from each study, so(6)”
The authors state this as an assumption.
The prior distributions of μ and τ2 are independent.
“It is standard to assume prior independence of μ and τ2.”
The authors state this as an assumption.
Approximately, the predictive distribution of θnew follows a t-distribution with k−2 degrees of freedom.
“Again taking a t-distribution with k−2 degrees of freedom, we assume that, approximately, (11)”
The authors state this as an assumption.
The between-study variance is common to each study.
“The assumption of a common between-study variance for each study is a strong one that we return to in Section 8.1.”
The authors state this as an assumption.
The underlying effects are exchangeable.
“Fundamental to a Bayesian approach to random-effects meta-analysis is the concept of exchangeability. Exchangeability represents a judgement that the treatment effects may be non-identical but their magnitudes cannot be differentiated a priori (Skene and Wakefield, 1990; Gelman et al., 1995).”
The authors state this as an assumption.
The random-effects distribution is normal.
“Requiring only two parameters for its full specification, the most parsimonious choice is also the conventional choice, where f(Φ) is chosen to be a normal distribution: (10)”
The authors state this as an assumption.
The random effects in the meta-analysis are normally distributed.
“by assuming a normal distribution for the random effects”
“Using a normal distribution for the underlying effects in different studies is a strong assumption”
The authors state this as an assumption.
The true (unbiased) effects Φi follow a normal distribution across studies.
“we represent this by using a normal distribution across the ‘true’ (unbiased) effects”
The authors state this as an assumption.
The study-specific bias components βi follow a normal distribution.
“Suppose that the study-specific bias components follow a normal distribution such that .”
The authors state this as an assumption.
The diversity and bias components are uncorrelated.
“assuming that the diversity and bias components are uncorrelated”
The authors state this as an assumption.
The effect being evaluated in the ith study is the sum of the true effect and bias: θi=Φi+βi.
“The effect being evaluated in the ith study, θi, is the sum of the true effect and bias: θi=Φi+βi.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
A 95% prediction interval was calculated to reflect the expected dispersion of true effects in future clinical settings.
“In addition to the pooled 95% CI, a 95% prediction interval (PI) was calculated to reflect the expected dispersion of true effects in future clinical settings (20,21).”
From Comparison of point‑of‑care HbA1c devices with laboratory HPLC methods: A systematic review and meta‑analysis (2026) · cites this paper as [21]
The 95% prediction interval reflects the expected dispersion of true effects in future clinical settings.
“a 95% prediction interval (PI) was calculated to reflect the expected dispersion of true effects in future clinical settings (20,21).”
From Comparison of point‑of‑care HbA1c devices with laboratory HPLC methods: A systematic review and meta‑analysis (2026) · cites this paper as [21]
Bayesian methods are particularly relevant when confronting sparse data, multiple comparisons, collinearity, or non-identification, and for deriving PI.
“This is particularly relevant when confronting sparse data, multiple comparisons, collinearity, or non-identification, and for deriving PI.51”
From A framework for meta-analysis of prediction model studies with binary and time-to-event outcomes (2019) · cites this paper as [51]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Probability of a negative predicted effect has the wrong direction
MinorThe text says the probability that θnew is below zero is 0.950, but Table 2 assigns 0.950 to the probability that it is above zero. The same sentence describes the cumulative probability at zero as approximately 5%, supporting the table's direction.
“Note that P(θnew<0)=0.950 in Table 2 corresponds to the point at which the full curve in Fig. 3(b) crosses the vertical axis (at approximately 5% probability)”
“| Parameter | Median | 95% credible interval | P(parameter > 0) | | --- | --- | --- | --- | | μ | 0.36 | (0.18, 0.55) | 0.999 | | θnew | 0.36 | (−0.12, 0.84) | 0.950 |”
Classical interval is labelled a credible interval
MinorTable 1 labels the reported classical random-effects interval a credible interval, whereas the text identifies the results as a classical analysis, for which it elsewhere uses confidence-interval terminology.
“Random-effects meta-analysis: standardized mean difference (95% credible interval 0.19–0.53); U*=4.23 (P =2×10−5); .”
“Classical normal random-effects meta-analysis results as traditionally presented appear at the bottom of Table 1.”
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“Heterogeneity Several estimators of the heterogeneity variance 72 are available that are based on normal likelihoods, including iterative maximum likelihood and restricted maximum likelihood estimates (DerSimonian and Laird, 1986; DerSimonian and Kacker, 2007).”
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MethodInfluentialIncorporating variations in the quality of individual randomized trials into meta-analysis
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MethodBayesian approaches to random-effects meta-analysis: a comparative study
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BackgroundMethodInfluentialBORROWING STRENGTH FROM EXTERNAL TRIALS IN A META-ANALYSIS
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MethodEncyclopedia of statistical sciences
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A LIKELIHOOD APPROACH TO META-ANALYSIS WITH RANDOM EFFECTS
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“The choice of prior distribution, even among those that are intended to be non-informative, can have substantial effects on the results of the analysis (Lambert et al., 2005).”
BackgroundA systematic review and meta-analysis of set-shifting ability in eating disorders
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MethodMultiple-bias modelling for analysis of observational data
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“Alternative approaches to dealing with specific sources of bias are available (Eddy et al., 1992; Greenland, 2005).”
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“…aspects, and so on, are randomly selected from a distribution of possibilities, which is an inappropriate interpretation because studies are individually designed dependent on the results of previous studies (Peto, 1987) and the evolutionary process of scientific research (Colditz et al., 1995).”
BackgroundResultConfidence intervals for the amount of heterogeneity in meta‐analysis
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MethodA General Maximum Likelihood Analysis of Variance Components in Generalized Linear Models
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BackgroundA bivariate approach to meta-analysis
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“However, NPML has been noted to be unstable (Van Houwelingen et al., 1993) and has not been widely adopted.”
BackgroundBias Modelling in Evidence Synthesis
Turner, R., Spiegelhalter, D. J., Smith, G. C. S., & Thompson, S. G. (2008) · Journal of the Royal Statistical Society Series A (Statistics in Society) · doi:10.1111/j.1467-985x.2008.00547.x · Cited by 315 · see citing works
Self-citationEmpirical bayes meta-analysis.
Raudenbush, S. W., & Bryk, A. S. (1985) · Journal of Educational Statistics · doi:10.3102/10769986010002075 · Cited by 299 · cited 2× · see citing works
“Metaanalytic implementations have made use of the EM algorithm and bootstrapping (Raudenbush and Bryk, 1985; Laird and Louis, 1989).”
BackgroundMethodWarn, D. E., Thompson, S. G., & Spiegelhalter, D. J. (2002) · Statistics in Medicine · doi:10.1002/sim.1189 · Cited by 277 · cited 1× · see citing works
“For example, when 2×2 contingency tables are available for binary outcomes, metaanalyses are appropriately performed by using binomial likelihoods (Smith et al., 1995; Warn et al., 2002).”
MethodSelf-citationHeterogeneity in Meta-analysis of Data from Epidemiologic Studies: A Commentary
Colditz, G. A., Burdick, E., & Mosteller, F. (1995) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a117644 · Cited by 245 · cited 2× · see citing works
“A common misinterpretation of the random-effects assumption is that the studies themselves are sampled from a population of studies (Hedges, 1987; Anello and Fleiss, 1995; Colditz et al., 1995).”
BackgroundResultSpiegelhalter, D. J., & Best, N. G. (2003) · Statistics in Medicine · doi:10.1002/sim.1586 · Cited by 236 · cited 1× · see citing works
“The following approach, which was described by Spiegelhalter and Best (2003), might help to separate heterogeneity due to biases from heterogeneity due to diversity.”
MethodSelf-citationComputer-Assisted Analysis of Mixtures and Applications: Meta-Analysis, Disease Mapping, and Others
Böhning, D. (1999) · Medical Entomology and Zoology · Cited by 220 · see citing works
Meta-Analysis in Medicine and Health Policy
Stangl, D. K. (2000) · CRC Press eBooks · doi:10.1201/9780203909935 · Cited by 213 · see citing works
Investigating causes of heterogeneity in systematic reviews
Glasziou, P., & Sanders, S. (2002) · Statistics in Medicine · doi:10.1002/sim.1183 · Cited by 213 · cited 2× · see citing works
“) and bias (variation in the quality of the design and conduct of the studies) (Glasziou and Sanders, 2002; Greenland and O’Rourke, 2001).”
BackgroundSome Thoughts on Empirical Bayes Estimation
Robbins, H. E. (1983) · The Annals of Statistics · doi:10.1214/aos/1176346239 · Cited by 182 · cited 1× · see citing works
“In particular, for the case of all estimates having the same (known) sampling error (σ21 = . . . =σ2k =σ2, say), and with τ2 known, then the linear function of yi that minimizes the expected mean-squared error is (Robbins, 1983) θ̃i =λμ̂+ .1−λ/θ̂i, where λ=σ2=.σ2 + τ2/.”
Ohlssen, D. I., Sharples, L. D., & Spiegelhalter, D. J. (2006) · Statistics in Medicine · doi:10.1002/sim.2666 · Cited by 164 · see citing works
Self-citationA comparison of the power of two tests for qualitative interactions
Piantadosi, S., & Gail, M. H. (1993) · Statistics in Medicine · doi:10.1002/sim.4780121305 · Cited by 153 · cited 2× · see citing works
“Such tests have been developed (Gail and Simon, 1985; Piantadosi and Gail, 1993; Pan and Wolfe, 1997), addressing a null hypothesis: H0 :{θi < 0 ∀i} or {θi > 0 ∀i}: Gail and Simon (1985) described the use of a test statistic QÅ =min{∑ θ̂2i σ̂−2i I+i , ∑ θ̂2i σ̂−2i I−i }, .9/ where I+i =1 if θ̂i >0…”
BackgroundBayesian Measures of Model Complexity and Fit
Spiegelhalter, D. J., Best, N. G., Carlin, B. P., & Van Der Linde, A. (2002) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/1467-9868.00353 · Cited by 151 · cited 1× · see citing works
“The deviance information criterion provides an alternative criterion, which is analogous to Akaike’s criterion, which does not require proper prior distributions (Spiegelhalter et al., 2002).”
MethodFlexible parametric models for random‐effects distributions
Lee, K. J., & Thompson, S. G. (2007) · Statistics in Medicine · doi:10.1002/sim.2897 · Cited by 148 · cited 1× · see citing works
“For example, a t-distribution or skewed distribution might be used to reduce the effect of outlying studies (Smith et al., 1995; Lee and Thompson, 2007), and mixture distributions have been advocated to account for studies belonging to unknown groupings (Bdhning, 2000).”
BackgroundSelf-citationModels for Potentially Biased Evidence in Meta-Analysis using Empirically Based Priors
Welton, N. J., Ades, A. E., Carlin, J. B., Altman, D. G., & Sterne, J. A. C. (2008) · Journal of the Royal Statistical Society Series A (Statistics in Society) · doi:10.1111/j.1467-985x.2008.00548.x · Cited by 147 · see citing works
Meta-analysis by the confidence profile method
Eddy, D. M. (1992) · Cited by 144 · see citing works
Computer-Assisted Analysis of Mixtures and Applications
Böhning, D. (2000) · Technometrics · doi:10.1080/00401706.2000.10485740 · Cited by 130 · cited 1× · see citing works
“For example, a t-distribution or skewed distribution might be used to reduce the effect of outlying studies (Smith et al., 1995; Lee and Thompson, 2007), and mixture distributions have been advocated to account for studies belonging to unknown groupings (Böhning, 2000).”
BackgroundValid Inference in Random Effects Meta‐Analysis
Follmann, D. A., & Proschan, M. A. (1999) · Biometrics · doi:10.1111/j.0006-341x.1999.00732.x · Cited by 127 · cited 1× · see citing works
“…researchers have investigated the distribution of the Wald statistic T = μ̂=ŜE.μ̂/, with suggestions to use tk−4 (Berkey et al., 1995), tk−2 (Raghunathan and Ii, 1993) or tk−1 (Follmann and Proschan, 1999), or to use a modified Wald statistic with a tk−1-distribution (Hartung and Knapp, 2001a, b).”
MethodInter‐study differences: How should they influence the interpretation and analysis of results?
Bailey, K. R. (1987) · Statistics in Medicine · doi:10.1002/sim.4780060327 · Cited by 108 · cited 1× · see citing works
“Extensive discussions of meta-analytic tests, particularly relating to common effect analyses, appear elsewhere (Hedges and Olkin, 1985; Bailey, 1987; Thompson, 1998).”
BackgroundKendall's advanced theory of statistics. Vol.2B: Bayesian inference
O’Hagan, A., & Forster, J. J. (2004) · Cited by 99 · see citing works
Exploratory or analytic meta-analysis: Should we distinguish between them?
Anello, C., & Fleiss, J. L. (1995) · Journal of Clinical Epidemiology · doi:10.1016/0895-4356(94)00084-4 · Cited by 95 · cited 1× · see citing works
“A common misinterpretation of the random-effects assumption is that the studies themselves are sampled from a population of studies (Hedges, 1987; Anello and Fleiss, 1995; Colditz et al., 1995).”
BackgroundKendall's Advanced Theory of Statistics, Vol. 2B: Bayesian Inference
Ankerst, D. P. (2005) · Journal of the American Statistical Association · doi:10.1198/jasa.2005.s62 · Cited by 91 · see citing works
Assessing the Amount of Heterogeneity in Random‐Effects Meta‐Analysis
Knapp, G., Biggerstaff, B. J., & Hartung, J. G. (2006) · Biometrical Journal · doi:10.1002/bimj.200510175 · Cited by 84 · cited 1× · see citing works
“…of uncertainty in the estimate, including a full likelihood approach to the meta-analysis (Hardy and Thompson, 1996), and a method based on a χ2-distribution for a random-effects version of the Q-statistic (Viechtbauer, 2007; Knapp et al., 2006); Viechtbauer (2007) reviewed several methods.”
MethodStatistical Methodology in the Pharmaceutical Sciences
Ziegel, E. R. (1991) · Technometrics · doi:10.1080/00401706.1991.10484820 · Cited by 81 · see citing works
A Bayesian Semiparametric Model for Random-Effects Meta-Analysis
Burr, D. L., & Doss, H. (2005) · Journal of the American Statistical Association · doi:10.1198/016214504000001024 · Cited by 78 · cited 1× · see citing works
“Bayesian semiparametric random-effects distributions have been proposed (Burr et al., 2003; Burr and Doss, 2005; Ohlssen et al., 2007) based on Dirichlet process priors.”
MethodLee, W. (1997) · Statistics in Medicine · doi:10.1002/(sici)1097-0258(19970415)16:7 · Cited by 74 · see citing works
Burr, D. L., Doss, H., Cooke, G. E., & Goldschmidt‐Clermont, P. J. (2003) · Statistics in Medicine · doi:10.1002/sim.1375 · Cited by 70 · cited 1× · see citing works
“Bayesian semiparametric random-effects distributions have been proposed (Burr et al., 2003; Burr and Doss, 2005; Ohlssen et al., 2007) based on Dirichlet process priors.”
MethodVangel, M. G., & Rukhin, A. L. (1999) · Biometrics · doi:10.1111/j.0006-341x.1999.00129.x · Cited by 67 · cited 1× · see citing works
“Better, likelihood-based approaches may be used that incorporate uncertainty in the estimation of τ2 (Hardy and Thompson, 1996; Vangel and Rukhin, 1999).”
MethodHierarchical models for multicentre binary response studies
Skene, A. M., & Wakefield, J. C. (1990) · Statistics in Medicine · doi:10.1002/sim.4780090808 · Cited by 66 · cited 1× · see citing works
“Exchangeability represents a judgement that the treatment effects may be nonidentical but their magnitudes cannot be differentiated a priori (Skene and Wakefield, 1990; Gelman et al., 1995).”
BackgroundKendall's Advanced Theory of Statistics: Vol. 2B, Bayesian Inference.
Dickey, J., & O’Hagan, A. (1996) · Journal of the American Statistical Association · doi:10.2307/2291686 · Cited by 63 · see citing works
Using empirical bayes methods in biopharmaceutical research
Louis, T. A. (1991) · Statistics in Medicine · doi:10.1002/sim.4780100604 · Cited by 54 · cited 2× · see citing works
“These expressions can be improved on to account for uncertainty in 2 and #2 (Louis, 1991; Morris and Normand, 1992).”
BackgroundMeta‐Analysis of Clinical Trials
Thompson, S. G. (2005) · Encyclopedia of Biostatistics · doi:10.1002/0470011815.b2a01034 · Cited by 52 · see citing works
Self-citationWelton, N. J., Ades, A. E., Caldwell, D. M., & Peters, T. J. (2008) · Journal of the Royal Statistical Society Series A (Statistics in Society) · doi:10.1111/j.1467-985x.2008.00558.x · Cited by 51 · cited 1× · see citing works
“The parameters underlying the bias distributions could also, in principle, be either subjectively assessed (Turner et al., 2008) or estimated by using analyses of multiple meta-analyses (Welton et al., 2008).”
MethodApproximate Bayesian inference for random effects meta-analysis
Abrams, K. R., & Sansó, B. (1998) · Statistics in Medicine · doi:10.1002/(sici)1097-0258(19980130)17:2 · Cited by 50 · see citing works
Accumulating evidence from independent studies: What we can win and what we can lose
Light, R. J. (1987) · Statistics in Medicine · doi:10.1002/sim.4780060304 · Cited by 49 · cited 2× · see citing works
“These expressions can be improved on to account for uncertainty in 2 and #2 (Louis, 1991; Morris and Normand, 1992). The problem was tackled in particular by Morris (1983). Metaanalytic implementations have made use of the EM algorithm and bootstrapping (Raudenbush and Bryk, 1985; Laird and Louis, 1989).”
BackgroundNonlinear Regression, Quasi Likelihood, and Overdispersion in Generalized Linear Models
Tjur, T. (1998) · The American Statistician · doi:10.1080/00031305.1998.10480567 · Cited by 41 · cited 2× · see citing works
“For example, for Poisson and logistic models the standard error may be multiplied by j/{ Q/(k - 1)} (Tjur, 1998) which approximates the ratio of standard errors from usual random-effects analysis and common effect analyses (Higgins and Thompson, 2002).”
MethodComputer-modeling and Graphical Strategies for Meta-analysis
DuMouchel, W., & Normand, S. T. (2000) · Chapman & Hall/CRC biostatistics series · doi:10.1201/9780203909935.ch6 · Cited by 38 · cited 2× · see citing works
“973), and using the shrinkage prior that was advocated by DuMouchel and Normand (2000) produces a prediction interval from -0.”
MethodInfluentialAnalysis of binary data from a multicentre clinical trial
Raghunathan, T. E., & Yoichi (1993) · Biometrika · doi:10.1093/biomet/80.1.127 · Cited by 30 · see citing works
Empirical Bayes Confidence Intervals for a Series of Related Experiments
Laird, N. M., & Louis, T. A. (1989) · Biometrics · doi:10.2307/2531491 · Cited by 29 · cited 1× · see citing works
“Metaanalytic implementations have made use of the EM algorithm and bootstrapping (Raudenbush and Bryk, 1985; Laird and Louis, 1989).”
MethodEmpirical Bayes Methods in Clinical Trials Meta‐Analysis
Stijnen, T., & van Houwelingen, H. C. (1990) · Biometrical Journal · doi:10.1002/bimj.4710320316 · Cited by 26 · see citing works
Böhning, D. (2005) · PubMed · Cited by 20 · see citing works
Hedges, L. V. (1987) · Statistics in Medicine · doi:10.1002/sim.4780060333 · Cited by 16 · see citing works
Cox, D., & Keogh, R. H. (2015) · Wiley StatsRef: Statistics Reference Online · doi:10.1002/9781118445112.stat00415.pub2 · Cited by 14 · see citing works
Böhning, D. (2005) · Methods of Information in Medicine · doi:10.1055/s-0038-1633931 · Cited by 14 · cited 1× · see citing works
“NPML procedures provide a discrete distribution that is based on a finite number of mass points (Laird, 1978; Böhning, 2005).”
BackgroundCommentary on pooling the results of clinical trials
Hedges, L. V. (1987) · Statistics in Medicine · Cited by 10 · see citing works
Modeling and Implementation Issues in Bayesian Meta-Analysis
Pauler, D. K., & Wakefield, J. (2000) · doi:10.1201/9780203909935-16 · Cited by 8 · see citing works
Facilitated analysis of data on drug regimen compliance
de Klerk, E., van der Linden, S., van der Heijde, D. M. F. M., & Urquhart, J. (1997) · Statistics in Medicine · doi:10.1002/(sici)1097-0258(19970730)16:14 · Cited by 2 · see citing works
Rose effect and the Euro: The magic is gone
Havránek, T. (2009) · Econstor (Econstor) · Cited by 1 · see citing works
Detecting and describing heterogeneity in meta-analysis
Hardy, R. J., & Thompson, S. G. (1998) · Statistics in Medicine · doi:10.1002/(sici)1097-0258(19980430)17:8
Self-citation
Flagged first, then by citations
6 of the 100 references couldn’t be matched to a known paper.
Research works printed but not linked: 3
- DuMouchel, 1994, Hierarchical Bayes linear models for meta-analysis
- Morris, 1992, Hierachical models for combining information and for meta-analysis, Bayes. Statist., 4, 321
- Stein, 1956, Proc. 3rd Berkeley Symp, 197
Cited by
Sorted by citations
How to perform a meta-analysis with R: a practical tutorial
Balduzzi, S., Rücker, G., & Schwarzer, G. (2019) · Evidence Based Mental Health · doi:10.1136/ebmental-2019-300117 · Cited by 5,827 · see citing works
Salanti, G., Ades, A. E., & Ioannidis, J. P. A. (2011) · Journal of Clinical Epidemiology · doi:10.1016/j.jclinepi.2010.03.016 · Cited by 3,766 · see citing works
“Predictive intervals Predictive intervals address the uncertainty in the treatment effect that may be expected in a new study comparing a specific pair of treatments [18].”
BackgroundInterpretation of random effects meta-analyses
Riley, R. D., Higgins, J. P. T., & Deeks, J. J. (2011) · BMJ · doi:10.1136/bmj.d549 · Cited by 2,884 · see citing works
Self-citationWhat Is the Male-to-Female Ratio in Autism Spectrum Disorder? A Systematic Review and Meta-Analysis
Loomes, R., Hull, L., & Mandy, W. P. L. (2017) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2017.03.013 · Cited by 2,804 · see citing works
Chapter 9: Analysing Data and Undertaking Meta-Analyses
Deeks, J. J., Higgins, J. P. T., & Altman, D. G. (2008) · Cited by 2,782 · see citing works
Self-citationGraphical tools for network meta-analysis in STATA
Chaimani, A., Higgins, J. P. T., Mavridis, D., Spyridonos, P., & Salanti, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076654 · Cited by 2,473 · see citing works
“and predictive ranking probabilities (the probability that each treatment will be placed in each rank in a future study [39,40]) can be estimated with the suboption predict.”
BackgroundSelf-citationPlea for routinely presenting prediction intervals in meta-analysis.
IntHout, J., Ioannidis, J. P. A., Rovers, M. M., & Goeman, J. J. (2016) · BMJ Open · doi:10.1136/bmjopen-2015-010247 · Cited by 2,264 · see citing works
“effects are to be expected for 95% of similar (exchangeable) studies that might be conducted in the future.(4) Therefore, it is well suited to evaluate the variability of the effect of an intervention over different settings.”
BackgroundAnalysing data and undertaking meta‐analyses
Deeks, J. J., Higgins, J. P., Altman, D. G., & on behalf of the Cochrane Statistical Methods Group (2019) · Cochrane Handbook for Systematic Reviews of Interventions · doi:10.1002/9781119536604.ch10 · Cited by 2,672 · see citing works
Self-citationBasics of meta‐analysis: <i>I</i> <sup>2</sup> is not an absolute measure of heterogeneity
Borenstein, M., Higgins, J. P. T., Hedges, L. V., & Rothstein, H. R. (2017) · Research Synthesis Methods · doi:10.1002/jrsm.1230 · Cited by 1,848 · see citing works
“In any real analysis, these values are estimated with error, and if we want to take account of that error, the appropriate formula (Higgins et al., 2009; Riley et al., 2011) is”
BackgroundInfluentialSelf-citationAnalysing Data and Undertaking Meta‐Analyses
Deeks, J. J., Higgins, J. P., & Altman, D. G. (2008) · Cochrane Handbook for Systematic Reviews of Interventions · doi:10.1002/9780470712184.ch9 · Cited by 1,800 · see citing works
Self-citationWilmot, E. G., Edwardson, C. L., Achana, F. A., Davies, M. J., Gorely, T., Gray, L. J., Khunti, K., Yates, T., & Biddle, S. J. H. (2012) · Diabetologia · doi:10.1007/s00125-012-2677-z · Cited by 1,789 · see citing works
Meta-analysis of individual participant data: rationale, conduct, and reporting
Riley, R. D., Lambert, P. C., & Abo-Zaid, G. (2010) · BMJ · doi:10.1136/bmj.c221 · Cited by 1,701 · see citing works
“The one step and two step individual participant data meta-analyses gave identical results. The pooled treatment effect was estimated at -10.16 (95% CI -12.27 to -8.06), indicating that hypertension treatment reduced systolic blood pressure by, on average, 10.16 mm Hg compared with controls. There was also, however, a…”
ResultInfluentialSalanti, G. (2012) · Research Synthesis Methods · doi:10.1002/jrsm.1037 · Cited by 1,729 · see citing works
“Presentation of the results using predictive intervals (Higgins et al., 2009), although infrequent, best conveys the uncertainty due to heterogeneity (Salanti et al., 2010a).”
BackgroundMethodInfluentialRapsomaniki, E., Timmis, A., George, J., Pujades-Rodriguez, M., Shah, A. D., Denaxas, S., White, I. R., Caulfield, M. J., Deanfield, J. E., Smeeth, L., et al. (2014) · The Lancet · doi:10.1016/s0140-6736(14)60685-1 · Cited by 1,643 · see citing works
Meta‐analysis and Mendelian randomization: A review
Bowden, J., & Holmes, M. V. (2019) · Research Synthesis Methods · doi:10.1002/jrsm.1346 · Cited by 1,670 · see citing works
Evaluating the quality of evidence from a network meta-analysis
Salanti, G., Del Giovane, C., Chaimani, A., Caldwell, D. M., & Higgins, J. P. T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0099682 · Cited by 1,402 · see citing works
“A particularly convenient way to do this is to look at predictive intervals for the effect in a new study of each comparison [14;25;26].”
BackgroundSelf-citationDobbins, M., Husson, H., DeCorby, K., & LaRocca, R. L. (2013) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd007651.pub2 · Cited by 1,358 · see citing works
The heterogeneity statistic I2 can be biased in small meta-analyses
von Hippel, P. T. (2015) · BMC Medical Research Methodology · doi:10.1186/s12874-015-0024-z · Cited by 1,229 · see citing works
“Under a random-effects model, by contrast, we assume that the true effects βk in the meta-analysis were drawn at random from a larger population of effects, and we seek to make inferences about that larger population [16].”
MethodA meta-analysis of sex differences in human brain structure
Ruigrok, A. N. V., Salimi-Khorshidi, G., Lai, M.-C., Baron-Cohen, S., Lombardo, M. V., Tait, R. J., & Suckling, J. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.12.004 · Cited by 1,192 · see citing works
Effect of lower sodium intake on health: systematic review and meta-analyses
Aburto, N. J., Ziolkovska, A., Hooper, L., Elliott, P., Cappuccio, F. P., & Meerpohl, J. J. (2013) · BMJ · doi:10.1136/bmj.f1326 · Cited by 1,242 · see citing works
“31 32 We used funnel plots to assess whether there was small study bias.”
BackgroundMethodInfluentialDias, S., Sutton, A. J., Ades, A. E., & Welton, N. J. (2013) · Medical Decision Making · doi:10.1177/0272989x12458724 · Cited by 1,207 · see citing works
Trial Sequential Analysis in systematic reviews with meta-analysis
Wetterslev, J., Jakobsen, J. C., & Gluud, C. N. (2017) · BMC Medical Research Methodology · doi:10.1186/s12874-017-0315-7 · Cited by 1,207 · see citing works
White, I. R., Barrett, J. K., Jackson, D., & Higgins, J. P. T. (2012) · Research Synthesis Methods · doi:10.1002/jrsm.1045 · Cited by 1,114 · see citing works
“d+bdi, can be compared by instead drawing d b from N d;Vþ Σ̂ (Higgins et al., 2009; Riley et al., 2011).”
BackgroundMethodSelf-citationMethodological issues and advances in biological meta-analysis
Nakagawa, S., & Santos, E. S. A. (2012) · Evolutionary Ecology · doi:10.1007/s10682-012-9555-5 · Cited by 1,032 · see citing works
Conceptual and technical challenges in network meta-analysis
Cipriani, A., Higgins, J. P. T., Geddes, J. R., & Salanti, G. (2013) · Annals of Internal Medicine · doi:10.7326/0003-4819-159-2-201307160-00008 · Cited by 1,072 · see citing works
“Random-effects meta-analysis can be applied (33, 34).”
Self-citationImpact of Intraoperative Stimulation Brain Mapping on Glioma Surgery Outcome: A Meta-Analysis
Hamer, P. C. D. W., Robles, S. G., Zwinderman, A. H., Duffau, H., & Berger, M. S. (2012) · Journal of Clinical Oncology · doi:10.1200/jco.2011.38.4818 · Cited by 1,046 · see citing works
Is psychology suffering from a replication crisis? What does “failure to replicate” really mean?
Maxwell, S. E., Lau, M. Y., & Howard, G. S. (2015) · American Psychologist · doi:10.1037/a0039400 · Cited by 1,018 · see citing works
Commentary: Heterogeneity in meta-analysis should be expected and appropriately quantified
Higgins, J. P. T. (2008) · International Journal of Epidemiology · doi:10.1093/ije/dyn204 · Cited by 995 · see citing works
Self-citationKatsanos, K. H., Spiliοpoulos, S., Kitrou, P. M., Krokidis, M. E., & Karnabatidis, D. (2018) · Journal of the American Heart Association · doi:10.1161/jaha.118.011245 · Cited by 1,031 · see citing works
“Hence, a different, but similar treatment effect was assumed as the basis for the random effects modeling.(58) In addition, different methods of analyses (with or without continuity correction and Bayesian methods) were employed to interrogate potential bias and uncertainty arising from meta-analysis of low event rate…”
MethodPopulation Incidence of Guillain-Barré Syndrome: A Systematic Review and Meta-Analysis
Sejvar, J. J., Baughman, A. L., Wise, M. P., & Morgan, O. W. (2011) · Neuroepidemiology · doi:10.1159/000324710 · Cited by 959 · see citing works
Aburto, N., Hanson, S., Gutiérrez, H., Hooper, L., Elliott, P., & Cappuccio, F. P. (2013) · BMJ · doi:10.1136/bmj.f1378 · Cited by 958 · see citing works
Lane, M. M., Gamage, E., Du, S., Ashtree, D. N., McGuinness, A. J., Gauci, S., Baker, P., Lawrence, M. A., Rebholz, C. M., Srour, B., et al. (2024) · BMJ · doi:10.1136/bmj-2023-077310 · Cited by 1,057 · see citing works
“31 In an umbrella review, if the 95% prediction intervals exclude the null, it indicates a statistically significant range of effect estimates.”
Suurmond, R., van Rhee, H., & Hak, T. (2017) · Research Synthesis Methods · doi:10.1002/jrsm.1260 · Cited by 881 · see citing works
“139 If we assume that all studies provide estimates of different true effects, we must also assume that no single overall effect size can express these different true effects' best.(39) Therefore, the prediction interval accurately embraces the notion of heterogeneity and the dispersion of true effects.”
BackgroundHarbord, R. M., & Higgins, J. P. T. (2008) · The Stata Journal: Promoting communications on statistics and Stata · doi:10.1177/1536867x0800800403 · Cited by 897 · see citing works
Self-citationTurner, R. M., Davey, J., Clarke, M. J., Thompson, S. G., & Higgins, J. P. (2012) · International Journal of Epidemiology · doi:10.1093/ije/dys041 · Cited by 837 · see citing works
Self-citationBarnett, D. W., Barnett, A. H., Nathan, A., Cauwenberg, J. V., & Cerin, E. (2017) · International Journal of Behavioral Nutrition and Physical Activity · doi:10.1186/s12966-017-0558-z · Cited by 848 · see citing works
Hadfield, J. D., & Nakagawa, S. (2010) · Journal of Evolutionary Biology · doi:10.1111/j.1420-9101.2009.01915.x · Cited by 813 · see citing works
“This type of assumption has been criticized even in the context of controlled clinical trials (Higgins et al., 2009), and would seem untenable when the data are associated with different species (West & Sheldon, 2002).”
MethodLevin, A. T., Hanage, W. P., Owusu-Boaitey, N., Cochran, K. B., Walsh, S. P., & Meyerowitz-Katz, G. (2020) · European Journal of Epidemiology · doi:10.1007/s10654-020-00698-1 · Cited by 844 · see citing works
Multivariate meta-analysis for non-linear and other multi-parameter associations
Gasparrini, A., Armstrong, B., & Kenward, M. G. (2012) · Statistics in Medicine · doi:10.1002/sim.5471 · Cited by 772 · see citing works
“The theoretical arguments that underpin the definition of this modelling framework closely follow the simple univariate model, recently re-evaluated in detail [26].”
White, I. R. (2015) · The Stata Journal Promoting communications on statistics and Stata · doi:10.1177/1536867x1501500403 · Cited by 778 · see citing works
“…ranks. cumulative makes the bar or line graph show cumulative ranks. predict ranks the true effects in a future study with the same covariates, thus allowing for heterogeneity as well as parameter uncertainty, as in the calculation of prediction intervals (Higgins, Thompson, and Spiegelhalter 2009).”
Jakobsen, J. C., Wetterslev, J., Winkel, P., Lange, T., & Gluud, C. (2014) · BMC Medical Research Methodology · doi:10.1186/1471-2288-14-120 · Cited by 704 · see citing works
“However, this use would imply integration of complicated models and software for analysing the review results [24,40,41] and would entail the need for specifying multiple prior distributions, which has its own problems [12,24,40,41].”
BackgroundMethodA guide to systematic review and meta-analysis of prognostic factor studies
Riley, R. D., Moons, K. G. M., Snell, K. I. E., Ensor, J., Hooft, L., Altman, D. G., Hayden, J. A., Collins, P. G. S., & Debray, T. P. A. (2019) · BMJ · doi:10.1136/bmj.k4597 · Cited by 754 · see citing works
Barker, T. H., Migliavaca, C. B., Stein, C., Colpani, V., Falavigna, M., Aromataris, E., & Munn, Z. (2021) · BMC Medical Research Methodology · doi:10.1186/s12874-021-01381-z · Cited by 738 · see citing works
Risk factors for type 2 diabetes mellitus: An exposure-wide umbrella review of meta-analyses
Bellou, V., Belbasis, L., Tzoulaki, I., & Evangelou, E. (2018) · PLOS ONE · doi:10.1371/journal.pone.0194127 · Cited by 713 · see citing works
Han, B., & Eskin, E. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2011.04.014 · Cited by 680 · see citing works
Belbasis, L., Bellou, V., Εvangelou, Ε., Ioannidis, J. P. A., & Tzoulaki, I. (2015) · The Lancet Neurology · doi:10.1016/s1474-4422(14)70267-4 · Cited by 669 · see citing works
Moja, L., Piatti, A., Pecoraro, V. L., Ricci, C., Virgili, G., Salanti, G., Germagnoli, L., Liberati, A., & Banfi, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046175 · Cited by 658 · see citing works
Cerin, E., Nathan, A., Cauwenberg, J. V., Barnett, D. W., & Barnett, A. H. (2017) · International Journal of Behavioral Nutrition and Physical Activity · doi:10.1186/s12966-017-0471-5 · Cited by 645 · see citing works
“In line with methodological recommendations for meta-analyses [44], specific combinations of environmental attributes and AT outcomes examined less than five times were considered to be insufficiently studied.”
BackgroundCrocker, J. C., Ricci‐Cabello, I., Parker, A., Hirst, J. A., Chant, A., Petit-Zeman, S., Evans, D., & Rees, S. (2018) · BMJ · doi:10.1136/bmj.k4738 · Cited by 627 · see citing works
Selenium for preventing cancer
Vinceti, M., Filippini, T., Del Giovane, C., Dennert, G., Zwahlen, M., Brinkman, M., Zeegers, M. P., Horneber, M., D'Amico, R., & Crespi, C. M. (2018) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd005195.pub4 · Cited by 649 · see citing works
Quraishi, M. N., Widlak, M., Bhala, N., Moore, D., Price, M., Sharma, N., & Iqbal, T. H. (2017) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.14201 · Cited by 617 · see citing works
Power analysis for random-effects meta-analysis
Jackson, D., & Turner, R. (2017) · Research Synthesis Methods · doi:10.1002/jrsm.1240 · Cited by 619 · see citing works
Quantifying the impact of between-study heterogeneity in multivariate meta-analyses
Jackson, D., White, I. R., & Riley, R. D. (2012) · Statistics in Medicine · doi:10.1002/sim.5453 · Cited by 577 · see citing works
Dray, J., Bowman, J., Campbell, E., Freund, M., Wolfenden, L., Hodder, R. K., McElwaine, K., Tremain, D., Bartlem, K., Bailey, J., et al. (2017) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2017.07.780 · Cited by 566 · see citing works
“Research suggests that the inclusion of 4 or fewer studies in random effects meta-analysis may result in imprecise estimations of between-study variance.(105) Therefore, results in the present review of meta-analyses based on minimal numbers of trials, such as for the outcomes of conduct problems, internalizing proble…”
ResultDoi, S. A. R., Barendregt, J. J., Khan, S., Thalib, L., & Williams, G. M. (2015) · Contemporary Clinical Trials · doi:10.1016/j.cct.2015.05.009 · Cited by 585 · see citing works
“A greater diversity that leads to dissimilarity of effects would not bemeta-analyzed [17].”
BackgroundJuhl, C. B., Christensen, R., Roos, E. M., Zhang, W., & Lund, H. (2013) · Arthritis & Rheumatology · doi:10.1002/art.38290 · Cited by 580 · see citing works
“Prediction intervals encompassing the effect of a future study with 95% certainty were estimated in order to evaluate the quantitative impact of inconsistency according to the method of Higgins et al using the between-study variance 2 and the standard error (14).”
MethodA Nondegenerate Penalized Likelihood Estimator for Variance Parameters in Multilevel Models
Chung, Y., Rabe‐Hesketh, S., Dorie, V., Gelman, A., & Liu, J. (2013) · Psychometrika · doi:10.1007/s11336-013-9328-2 · Cited by 566 · see citing works
What causes psychosis? An umbrella review of risk and protective factors
Radua, J., Ramella‐Cravaro, V., Ioannidis, J. P. A., Reichenberg, A., Phiphopthatsanee, N., Amir, T., Yenn Thoo, H., Oliver, D., Davies, C., Morgan, C., et al. (2018) · World Psychiatry · doi:10.1002/wps.20490 · Cited by 553 · see citing works
Classroom management self-efficacy and burnout: A multivariate meta-analysis
Aloe, A. M., Amo, L. C., & Shanahan, M. E. (2014) · Educational Psychology Review · doi:10.1007/s10648-013-9244-0 · Cited by 560 · see citing works
Burke, D. L., Ensor, J., & Riley, R. D. (2017) · Statistics in Medicine · doi:10.1002/sim.7141 · Cited by 538 · see citing works
Bowden, J., Tierney, J. F., Copas, A. J., & Burdett, S. (2011) · BMC Medical Research Methodology · doi:10.1186/1471-2288-11-41 · Cited by 551 · see citing works
“We note that this does not reflect the state-of-the-art in what can estimated via a random effects meta-analysis; one can for instance also estimate trial level effect parameters (θ + ui), predict the likely effects of future studies and test hypotheses relating to these additional parameters [19].”
BackgroundMethodDietary fiber and health outcomes: an umbrella review of systematic reviews and meta-analyses
Veronese, N., Solmi, M., Caruso, M. G., Giannelli, G., Osella, A. R., Evangelou, E., Maggi, S., Fontana, L., Stubbs, B., & Tzoulaki, I. (2018) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqx082 · Cited by 536 · see citing works
Multivariate meta‐analysis: Potential and promise
Jackson, D., Riley, R., & White, I. R. (2011) · Statistics in Medicine · doi:10.1002/sim.4172 · Cited by 530 · see citing works
“Similarly, it allows a joint prediction region [63] for the true sensitivity and specificity in an individual study setting.”
BackgroundUmer, A., Kelley, G. A., Cottrell, L., Giacobbi, P. R., Innes, K. E., & Lilly, C. L. (2017) · BMC Public Health · doi:10.1186/s12889-017-4691-z · Cited by 520 · see citing works
Meta‐analysis and traditional systematic literature reviews—What, why, when, where, and how?
Paul, J., & Barari, M. M. (2022) · Psychology and Marketing · doi:10.1002/mar.21657 · Cited by 579 · see citing works
NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity
Moriyama, T., Nishii, R., Pérez-Andreu, V., Yang, W., Antillón‐Klussmann, F., Zhao, X., Lin, T.-N., Hoshitsuki, K., Nersting, J., Kihira, K., et al. (2016) · Nature Genetics · doi:10.1038/ng.3508 · Cited by 478 · see citing works
Malin, G. L., Morris, R. K., & Khan, K. S. (2010) · BMJ · doi:10.1136/bmj.c1471 · Cited by 461 · see citing works
“As the focus of this review was to establish the association between cord pH and adverse outcome rather than the value of cord pH as a prognostic test, we did not calculate other summary statistics (including sensitivity, specificity, and likelihood ratios). We calculated the estimated predictive interval for each met…”
The Association between Time Spent Outdoors and Myopia in Children and Adolescents
Sherwin, J. C., Reacher, M. H., Keogh, R. H., Khawaja, A. P., Mackey, D. A., & Foster, P. J. (2012) · Ophthalmology · doi:10.1016/j.ophtha.2012.04.020 · Cited by 483 · see citing works
Evidence Synthesis for Decision Making 3
Dias, S., Sutton, A. J., Welton, N. J., & Ades, A. E. (2013) · Medical Decision Making · doi:10.1177/0272989x13485157 · Cited by 468 · see citing works
Al-Khudairy, L., Loveman, E., Colquitt, J. L., Mead, E., Johnson, R. E., Fraser, H., Olajide, J., Murphy, M., Velho, R., O’Malley, C. L., et al. (2017) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd012691 · Cited by 459 · see citing works
Random-Effects Meta-analysis of Inconsistent Effects: A Time for Change
Cornell, J. E., Mulrow, C. D., Localio, R., Stack, C. B., Meibohm, A. R., Guallar, E., & Goodman, S. N. (2014) · Annals of Internal Medicine · doi:10.7326/m13-2886 · Cited by 453 · see citing works
Corporate governance and environmental social governance disclosure: A meta‐analytical review
Lagasio, V., & Cucari, N. (2019) · Corporate Social Responsibility and Environmental Management · doi:10.1002/csr.1716 · Cited by 452 · see citing works
Meta-analysis of multiple outcomes: a multilevel approach
Van den Noortgate, W., López-López, J. A., Marín-Martínez, F., & Sánchez-Meca, J. (2015) · Behavior Research Methods · doi:10.3758/s13428-014-0527-2 · Cited by 450 · see citing works
Active versus expectant management for women in the third stage of labour
Begley, C., Gyte, G. M., Devane, D., McGuire, W. L., & Weeks, A. D. (2015) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd007412.pub4 · Cited by 448 · see citing works
Sleep problems and work injuries: A systematic review and meta-analysis
Uehli, K., Mehta, A. J., Miedinger, D., Hug, K., Schindler, C., Holsboer‐Trachsler, E., Leuppi, J. D., & Künzli, N. (2013) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2013.01.004 · Cited by 448 · see citing works
Neil‐Sztramko, S., Caldwell, H. A. T., & Dobbins, M. (2021) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd007651.pub3 · Cited by 494 · see citing works
Fetal and umbilical Doppler ultrasound in high-risk pregnancies
Alfirević, Ž., Stampalija, T., & Gyte, G. M. (2013) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd007529.pub3 · Cited by 440 · see citing works
Environmental risk factors and Parkinson's disease: An umbrella review of meta-analyses
Bellou, V., Belbasis, L., Tzoulaki, I., Εvangelou, Ε., & Ioannidis, J. P. A. (2015) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2015.12.008 · Cited by 429 · see citing works
Association of Endometrial Cancer Risk With Postmenopausal Bleeding in Women
Clarke, M. A., Long, B. J., Del Mar Morillo, A., Arbyn, M., Bakkum-Gamez, J. N., & Wentzensen, N. (2018) · JAMA Internal Medicine · doi:10.1001/jamainternmed.2018.2820 · Cited by 426 · see citing works
Guidance on the use of the weight of evidence approach in scientific assessments
Hardy, A., Benford, D., Halldorsson, T. I., Jeger, M. J., Knutsen, H. K., More, S. J., Naegeli, H., Noteborn, H. P. J. M., Ockleford, C., Ricci, A., et al. (2017) · EFSA Journal · doi:10.2903/j.efsa.2017.4971 · Cited by 419 · see citing works
“Linkov et al. (2015) consider that multicriteria decision analysis can be used as a proxy for the Bayesian approach to weight of evidence assessment when model formulation is restricted by data limitations.”
MethodMultivariate Random-effects Meta-regression: Updates to Mvmeta
White, I. R. (2011) · The Stata Journal: Promoting communications on statistics and Stata · doi:10.1177/1536867x1101100206 · Cited by 400 · see citing works
Turner, R. M., Jackson, D., Wei, Y., Thompson, S. G., & Higgins, J. P. T. (2015) · Statistics in Medicine · doi:10.1002/sim.6381 · Cited by 410 · see citing works
“A Bayesian random-effects meta-analysis is advantageous in allowing researchers to incorporate external evidence on the likely extent of between-study heterogeneity in a particular research setting, to reduce the imprecision [3, 4], as well as facilitating prediction of effects in future studies and flexibility in mod…”
BackgroundSelf-citationDavey, J., Turner, R. M., Clarke, M. J., & Higgins, J. P. (2011) · BMC Medical Research Methodology · doi:10.1186/1471-2288-11-160 · Cited by 404 · see citing works
Self-citationRhodes, K. M., Turner, R., & Higgins, J. P. T. (2014) · Journal of Clinical Epidemiology · doi:10.1016/j.jclinepi.2014.08.012 · Cited by 398 · see citing works
“Alternatively, we can allow for heterogeneity in a random-effects metaanalysis, estimating the summary effect and the betweenstudy variance [2].”
BackgroundSelf-citationSummarizing historical information on controls in clinical trials
Neuenschwander, B. E., Capkun-Niggli, G., Branson, M., & Spiegelhalter, D. J. (2010) · Clinical Trials · doi:10.1177/1740774509356002 · Cited by 398 · see citing works
Self-citationWorkplace interventions for reducing sitting at work
Shrestha, N., Kukkonen-Harjula, K. T., Verbeek, J. H. A. M., Ijaz, S., Hermans, V., & Bhaumik, S. (2016) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd010912.pub3 · Cited by 385 · see citing works
Li, X., Meng, X., Timofeeva, M. N., Tzoulaki, I., Tsilidis, K. K., Ioannidis, J. P. A., Campbell, H. J., & Τheodoratou, E. (2017) · BMJ · doi:10.1136/bmj.j2376 · Cited by 402 · see citing works
Barbui, C., Purgato, M., Abdulmalik, J., Acarturk, C., Eaton, J., Gastaldon, C., Gureje, O., Hanlon, C., Jordans, M., Lund, C., et al. (2020) · The Lancet Psychiatry · doi:10.1016/s2215-0366(19)30511-5 · Cited by 349 · see citing works
“21 Prediction intervals further account for heterogeneity between studies and specify the uncertainty for the effect that would be expected in a new study examining that same research question.”
A comparison of treatment effectiveness between clear aligner and fixed appliance therapies
Ke, Y., Zhu, Y., & Zhu, M. (2019) · BMC Oral Health · doi:10.1186/s12903-018-0695-z · Cited by 347 · see citing works
Comprehensive Meta‐Analysis Software
Borenstein, M. (2022) · Wiley eBooks · doi:10.1002/9781119099369.ch27 · Cited by 383 · see citing works
Lawry, S., Samii, C., Hall, R., Leopold, A., Hornby, D., & Mtero, F. (2016) · Journal of Development Effectiveness · doi:10.1080/19439342.2016.1160947 · Cited by 354 · see citing works
Prevalence and outcomes of incidental imaging findings: umbrella review
O’Sullivan, J. W., Muntinga, T., Grigg, S. E., & Ioannidis, J. P. A. (2018) · BMJ · doi:10.1136/bmj.k2387 · Cited by 341 · see citing works
Veroniki, A. A., Cogo, E., Rios, P., Straus, S. E., Finkelstein, Y., Kealey, R., Reynen, E., Soobiah, C., Thavorn, K., Hutton, B., et al. (2017) · BMC Medicine · doi:10.1186/s12916-017-0845-1 · Cited by 339 · see citing works
“For the NMA effect estimates, a 95% predictive interval (PrI) was also presented, capturing the magnitude of τ(2) and presenting the interval within which we would expect the treatment effect of a future study to lie [40, 41].”
Teughels, W., Feres, M., Oud, V., Martín, C., Matesanz, P., & Herrera, D. (2020) · Journal Of Clinical Periodontology · doi:10.1111/jcpe.13264 · Cited by 342 · see citing works
Prevalence of Autism Spectrum Disorder in Preterm Infants: A Meta-analysis
Agrawal, S., Rao, S. C., Bulsara, M. K., & Patole, S. (2018) · PEDIATRICS · doi:10.1542/peds.2018-0134 · Cited by 332 · see citing works
Synthesising quantitative evidence in systematic reviews of complex health interventions
Higgins, J. P. T., López-López, J. A., Becker, B. J., Davies, S. R., Dawson, S., Grimshaw, J. M., McGuinness, L. A., Moore, T. H. M., Rehfuess, E. A., Thomas, J., et al. (2019) · BMJ Global Health · doi:10.1136/bmjgh-2018-000858 · Cited by 322 · see citing works
Self-citationKunutsor, S. K., Whitehouse, M. R., Lenguerrand, E., Blom, A. W., Beswick, A. D., & INFORM Team (2016) · PLoS ONE · doi:10.1371/journal.pone.0151537 · Cited by 331 · see citing works
“We also estimated 95% prediction intervals which are used to determine the degree of heterogeneity, as they provide a region in which about 95% of the true study effects are expected to be found [18, 19].”
MethodMortality in Parkinson's disease: A systematic review and meta‐analysis
Macleod, A. D., Taylor, K. S. M., & Counsell, C. E. (2014) · Movement Disorders · doi:10.1002/mds.25898 · Cited by 328 · see citing works
An extended mixed‐effects framework for meta‐analysis
Sera, F., Armstrong, B., Blangiardo, M., & Gasparrini, A. (2019) · Statistics in Medicine · doi:10.1002/sim.8362 · Cited by 334 · see citing works
“26 The pooled estimate can be derived under fixed-effects or random-effects assumptions, 27,28 with random-effects models incorporating the underlying between-study variation into the weights.”
Visualizing Assumptions and Results in Network Meta-analysis: The Network Graphs Package
Chaimani, A., & Salanti, G. (2015) · The Stata Journal Promoting communications on statistics and Stata · doi:10.1177/1536867x1501500402 · Cited by 323 · see citing works
“The extent of uncertainty in the estimated treatment effects in meta-analysis is re-flected not only by the confidence intervals but also by the predictive intervals that incorporate the extent of heterogeneity (Higgins, Thompson, and Spiegelhalter 2009; Riley, Higgins, and Deeks 2011).”
Background
- Authors
- Higgins, J. P. T., Thompson, S. G., & Spiegelhalter, D. J.
- Affiliations
- MRC Biostatistics Unit (GB)
- Corresponding author
- Higgins, Julian P. T.
- Venue
- Journal of the Royal Statistical Society Series A: Statistics in Society
- Publisher
- Oxford University Press (OUP)
- Published
- 2008-07-24
- Volume
- 172
- Issue
- 1
- Pages
- 137-159
- ISSN
- 0964-1998 (ISSN-L)
- 1467-985X
- PMC
- PMC2667312
- OpenAlex
- W2108116635
- Semantic Scholar
- b42717775886e436d97964fca187c3248684112e
- Cited by
- 2,569
- References
- 100
- Citations by year
- 2026: 222 · 2025: 197 · 2024: 219 · 2023: 186 · 2022: 208 · 2021: 246 · 2020: 224 · 2019: 160 · 2018: 153 · 2017: 124 · 2016: 128 · 2015: 117 · 2014: 93 · 2013: 96 · 2012: 89
- FWCI
- 38.18
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Journal of the Royal Statistical Society Series A (Statistics in Society) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Explore Bristol Research (publishedVersion)
- Bristol Research (University of Bristol) (submittedVersion)
- Funders
- UK Medical Research Council (U.1052.00.011, U.1052.00.001, U.1052.00.005)
- Topics
- Social Sciences › Decision Sciences › Statistics, Probability and Uncertainty › Meta-analysis and systematic reviews
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods and Bayesian Inference
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Epidemiology
- Keywords
- random-effects meta-analysis, heterogeneity, Bayesian meta-analysis, prediction intervals, nonparametric inference, hypothesis testing, set-shifting, eating disorders, prior sensitivity
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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