Diabetes mellitus in people with schizophrenia, bipolar disorder and major depressive disorder: a systematic review and large scale meta‐analysis
Open accessAbstract
Type 2 diabetes mellitus (T2DM) is highly predictive of cardiovascular diseases and can have particularly deleterious health impacts in people with severe mental illness (SMI), i.e. schizophrenia, bipolar disorder or major depressive disorder. This meta‐analysis aimed: a) to describe pooled frequencies of T2DM in people with SMI; b) to analyze the influence of demographic, illness and treatment variables as well as T2DM assessment methods; and c) to describe T2DM prevalence in studies directly comparing persons with each specific SMI diagnosis to general population samples. The trim and fill adjusted pooled T2DM prevalence among 438,245 people with SMI was 11.3% (95% CI: 10.0%‐12.6%). In antipsychotic‐naïve participants, the prevalence of T2DM was 2.9% (95% CI: 1.7%‐4.8%). There were no significant diagnostic subgroup differences. A comparative meta‐analysis established that multi‐episode persons with SMI (N=133,470) were significantly more likely to have T2DM than matched controls (N=5,622,664): relative risk, RR=1.85, 95% CI: 1.45‐2.37, p<0.001. The T2DM prevalence was consistently elevated in each of the three major diagnostic subgroups compared to matched controls. Higher T2DM prevalences were observed in women with SMI compared to men (RR=1.43, 95% CI: 1.20‐1.69, p<0.001). Multi‐episode (versus first‐episode) status was the only significant predictor for T2DM in a multivariable meta‐regression analysis (r 2=0.52, p<0.001). The T2DM prevalence was higher in patients prescribed antipsychotics, except for aripriprazole and amisulpride. Routine screening and multidisciplinary management of T2DM is needed. T2DM risks of individual antipsychotic medications should be considered when making treatment choices.
AI snapshot
Written from the paper’s full text.
TL;DR
This systematic review and meta-analysis found that approximately 11.3% of people with severe mental illness had type 2 diabetes, with multi-episode SMI patients about 1.85 times more likely to have T2DM than matched general population controls. T2DM prevalence did not differ significantly across schizophrenia, bipolar disorder, and major depressive disorder diagnostic subgroups.
Key findings
- Trim-and-fill adjusted pooled T2DM prevalence among 438,245 people with SMI was 11.3% (95% CI 10.0–12.6); in antipsychotic-naïve participants it was 2.9% (95% CI 1.7–4.8).
- Multi-episode SMI (N=133,470) had significantly higher T2DM than matched controls (N=5,622,664): RR=1.85, 95% CI 1.45–2.37, p<0.001; diagnostic subgroup RRs vs controls were 2.04 for schizophrenia/related psychoses, 1.89 for bipolar disorder, and 1.43 for MDD.
- Women with SMI had higher T2DM prevalence than men (RR=1.43, 95% CI 1.20–1.69, p<0.001); multi-episode vs first-episode status was the only significant predictor in multivariable meta-regression (r²=0.52, p<0.001).
- Except for aripiprazole and amisulpride, all individual antipsychotics had significantly higher T2DM risk than antipsychotic-naïve participants; North America had higher prevalence (12.5%) than Europe (7.7%, p<0.001).
Methods
- Systematic review/meta-analysis following MOOSE and PRISMA; searched Medline, PsycARTICLES, Embase, and CINAHL from inception to August 1, 2015, without language restrictions.
- Included observational studies and RCTs in adults with DSM-IV-TR/ICD-10 schizophrenia or related psychotic disorders, bipolar disorder, or MDD that reported study-defined T2DM prevalences; 118 publications with 135 T2DM prevalences were included.
- Random-effects meta-analysis; relative risks for direct within-study comparisons; subgroup analyses and meta-regressions for demographic, illness, treatment, assessment, and geographic moderators; publication bias assessed with Egger/Begg tests and trim-and-fill.
Limitations
- Stated: few studies used oral glucose tolerance testing as the gold standard; chart reviews carry selection bias and diagnostic reliability/validity concerns; mostly cross-sectional data prevent certainty about directionality of the medication–T2DM association; clinical subtypes of MDD/bipolar disorder were not controlled; publication bias and heterogeneity were encountered, though trim-and-fill adjusted for bias and the multivariable model explained over half of between-study heterogeneity; inadequate lifestyle behavior data.
- Stated: only a minority of studies provided mean age by sex, so women with schizophrenia may have been older, potentially confounding the higher T2DM risk in women.
- Evident from text (not listed among stated limitations): many analyses relied on self-report or chart review rather than blood testing, and antipsychotic risk comparisons may be affected by order effects, such as switching from higher-risk agents.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 37 cited sources checked · 0 supported · 0 flagged
- Findingown data
There were no significant diagnostic subgroup differences in T2DM prevalence.
“There were no significant diagnostic subgroup differences.”
- Also stated in: § DISCUSSION · plain
“comparative meta-analyses found no significant differences across schizophrenia, schizophrenia spectrum disorders, bipolar disorder and MDD.”
Quote in the paperSubstantial claim - Also stated in: § DISCUSSION · plain
- Findingown data
T2DM prevalence was consistently elevated in each of the three major diagnostic subgroups compared to matched controls.
“The T2DM prevalence was consistently elevated in each of the three major diagnostic subgroups compared to matched controls.”
- Also stated in: § DISCUSSION · plain
“T2DM prevalences were consistently elevated for each of the three diagnostic subgroups compared to the general population”
Quote in the paperSubstantial claim - Also stated in: § DISCUSSION · plain
- Findingown data
The trim and fill adjusted pooled T2DM prevalence among 438,245 people with SMI was 11.3% (95% CI 10.0%-12.6%).
“The trim and fill adjusted pooled T2DM prevalence among 438,245 people with SMI was 11.3% (95% CI: 10.0%-12.6%).”
- Also stated in: § T2DM prevalence · plain
“Applying the trim and fill method, adjusting for 13 studies, the prevalence of T2DM was 11.3% (95% CI: 10.0%-12.6%).”
- Also stated in: § DISCUSSION · plain
“Approximately one in 10 individuals with SMI (11.3%; 95% CI: 10.0%-12.6%)had T2DM”
Quote in the paperSubstantial claim - Also stated in: § T2DM prevalence · plain
- Findingown data
In antipsychotic-naive participants, the prevalence of T2DM was 2.9% (95% CI 1.7%-4.8%).
“In antipsychotic-na€ ıve participants, the prevalence of T2DM was 2.9% (95% CI: 1.7%-4.8%).”
- Also stated in: § Medication use · plain
“The prevalence of T2DM was lowest in antipsychotic-na€ ıve participants (2.9%, 95% CI: 1.7%-4.8%).”
Quote in the paperSubstantial claim - Also stated in: § Medication use · plain
- Findingown data
Multi-episode (versus first-episode) status was the only significant predictor for T2DM in a multivariable meta-regression analysis (r2=0.52, p<0.001).
“Multi-episode (versus first-episode) status was the only significant predictor for T2DM in a multivariable meta-regression analysis (r 2 50.52, p<0.001).”
Quote in the paperSubstantial claim
- Findingown data
Multi-episode persons with SMI (N=133,470) were significantly more likely to have T2DM than matched controls (N=5,622,664): RR=1.85, 95% CI 1.45-2.37, p<0.001.
“multi-episode persons with SMI (N5133,470) were significantly more likely to have T2DM than matched controls (N55,622,664): relative risk, RR51.85, 95% CI: 1.45-2.37,p<0.001.”
- Also stated in: § Relative risk (RR) of T2DM in diagnostic subgroups compared with general population controls · plain
“multi-episode persons with SMI (N5133,470; 12.2%, 95% CI: 9.7-15.2%;Q56166, p<0.01) had significantly increased risk of T2DM (RR51.85,95% CI: 1.45-2.37,p<0.001;Q51302.0,p<0.001; 38 studies).”
- Also stated in: § DISCUSSION · plain
“the relative risk for T2DM in multi-episode persons with SMI was almost double (RR51.85,95% CI: 1.45-2.37)that found in matched general population comparison samples.”
Quote in the paperSubstantial claim - Also stated in: § Relative risk (RR) of T2DM in diagnostic subgroups compared with general population controls · plain
- Findingown data
Higher T2DM prevalences were observed in women with SMI compared to men (RR=1.43, 95% CI 1.20-1.69, p<0.001).
“Higher T2DM prevalences were observed in women with SMI compared to men (RR51.43,95% CI: 1.20-1.69,p<0.001).”
- Also stated in: § Demographic variables · plain
“A relative risk meta-analysis across 29 studies (including 32 comparisons) directly comparing T2DM frequencies in men (N535,400) versus women (N533,283) with SMI found a higher T2DM prevalence in women (RR51.43;95% CI: 1.20-1.69,p<0.001).”
- Also stated in: § DISCUSSION · plain
“we found that women with SMI had a higher risk for developing T2DM than men.”
Quote in the paperSubstantial claim - Also stated in: § Demographic variables · plain
- Findingown data
There was no significant difference in T2DM between schizophrenia and MDD (OR=1.27, 95% CI 0.96-1.68, p=0.10).
“and of schizophrenia (13.7%, 95% CI: 11.6%-16.1%;Q50.3, p50.58;N5893) versus MDD (11.1%, 95% CI: 9.2%-13.3%;N5911) (two studies; OR51.27, 95% CI: 0.96-1.68,z51.66, p50.10;Q56.0, p50.80,I 2 50).”
Quote in the paperNot a substantial claim - Findingown data
Higher T2DM prevalence was observed in studies relying upon clinical data from file and chart reviews versus self-report studies.
“In contrast, a higher T2DM prevalence was observed in studies relying upon clinical data gleaned from file and chart reviews versus self-report studies.”
Quote in the paperNot a substantial claim - Findingown data
Compared to healthy controls, the relative risk of T2DM was 1.43 in patients with MDD (N=10,895; 95% CI 0.88-2.25, p=0.029; three studies).
“and 1.43 in patients with MDD (N510,895; 95% CI: 0.88-2.25,p50.029;Q52.15, p50.34; three studies).”
Quote in the paperSubstantial claim - Findingreasoning
There was a trend for retrospective studies to be associated with higher T2DM prevalences than prospective ones.
“In line with this interpretation, there was a trend for retrospective studies to be associated with higher T2DM prevalences than prospective ones.”
Quote in the paperNot a substantial claim - Findingown data
The estimated weighted mean prevalence of T2DM among 438,245 people with SMI was 10.2% (95% CI 9.1%-11.4%; Q=14228.7, p<0.001).
“The estimated weighted mean prevalence of T2DM among 438,245 people with SMI was 10.2% (95% CI: 9.1%-11.4%;Q514228.7,p<0.001).”
Quote in the paperSubstantial claim - Findingown data
T2DM prevalence was significantly higher in North America (12.5%, 95% CI 10.9%-14.3%; 58 studies) than in Europe (7.7%, 95% CI 6.3%-9.3%; 32 studies) (p<0.001).
“The T2DM prevalence was significantly higher in North America (12.5%, 95% CI: 10.9%-14.3%;58 studies) than in Europe (7.7%, 95% CI: 6.3%-9.3%;32 studies) (p<0.001).”
Quote in the paperNot a substantial claim - Findingown data
Compared to healthy controls, the relative risk of T2DM was 2.04 in patients with schizophrenia or related psychotic disorders (N=115,538; 95% CI 1.69-2.49, p<0.001; 29 studies).
“Compared to healthy controls, the relative risk of T2DM was 2.04 in patients with schizophrenia or related psychotic disorders (N5115,538; 95% CI: 1.69-2.49,p<0.001;Q51302.0,p<0.001,I 2 597.8; 29 studies)”
Quote in the paperSubstantial claim - Findingown data
There were insufficient studies directly comparing T2DM prevalence in patients with bipolar disorder versus MDD.
“There were insufficient studies directly comparing T2DM prevalence in patients with bipolar disorder versus MDD.”
Quote in the paperNot a substantial claim - Findingown data
The meta-analysis found geographical differences in T2DM prevalence among people with SMI.
“Our meta-analysis highlighted geographical differences in T2DM, mirroring the different prevalences in the general population”
Quote in the paperSubstantial claim - Findingown data
T2DM risk in people treated with clozapine tended (p=0.05) to be higher than the risk in those treated with olanzapine.
“The T2DM risk in people treated with clozapine tended (p50.05) to be higher than the risk in those treated with olanzapine.”
Quote in the paperNot a substantial claim - Findingcitation
Psychotropic medication use, including antidepressants, lithium and antipsychotic medications, is associated with higher T2DM prevalence.
“Our data confirm prior evidence that psychotropic medication use, including that of antidepressants, lithium and antipsychotic medications 26 , is associated with higher T2DM prevalence.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [26] source
Not checked in the free run.
- Findingown data
First-episode schizophrenia patients had a significantly lower T2DM prevalence than multi-episode schizophrenia patients (4.0% vs 13.1%, z=23.89, p<0.001).
“Comparing T2DM in first-versus multi-episode patients within the different diagnostic subgroups (see Table 1) demonstrated that first-episode schizophrenia patients (4.0%, 95% CI: 2.5%-6.2%)had a significantly lower T2DM prevalence than multi-episode schizophrenia patients (13.1%, 95% CI: 11.7%-14.8%,z523.89,p<0.001).”
Quote in the paperNot a substantial claim - Findingown data
There was no difference in T2DM prevalence between population based and non-population based studies.
“There was also no difference in T2DM prevalence between population based and non-population based studies.”
Quote in the paperNot a substantial claim - Findingown data
General population controls had a T2DM prevalence of 6.2% (95% CI 4.8%-8.0%).
“compared with general population controls (N55,622,664; 6.2%, 95% CI: 4.8%-8.0%;Q518,592, p<0.01)”
Quote in the paperSubstantial claim - Findingown data
There was no significant difference in T2DM in first-episode patients (4.4%, 95% CI 2.5%-7.6%) versus controls (0.9%, 95% CI 0.03%-2.4%) (RR=4.64, 95% CI 0.73-29.3, p=0.10; three studies).
“There was no significant difference in T2DM in first-episode patients (4.4%, 95% CI: 2.5%-7.6%;Q52, p50.4) versus controls (0.9%, 95% CI: 0.03%-2.4%;Q53, p50.3) (RR54.64,95% CI: 0.73-29.3,p50.10;Q51302.0,p50.23; three studies).”
Quote in the paperNot a substantial claim - Findingown data
There was no significant difference in T2DM between schizophrenia and bipolar disorder (OR=1.22, 95% CI 0.84-1.77, p=0.28).
“The same was true for the comparison of schizophrenia (13.7%, 95% CI: 8.2%-22.1%;Q5131, p<0.01;N56,005) versus bipolar disorder (13.7%, 95% CI: 9.2%-20.0%;Q546, p<0.01;N53,138) (six studies; OR51.22,95% CI: 0.84-1.77,z51.08, p50.28;Q517.1, p50.004,I 2 570.8)”
Quote in the paperSubstantial claim - Findingown data
Compared to healthy controls, the relative risk of T2DM was 1.89 in patients with bipolar disorder (N=4,688; 95% CI 1.29-2.77, p<0.001; six studies).
“1.89 in patients with bipolar disorder (N54,688; 95% CI: 1.29-2.77,p<0.001;Q52.2, p50.34,I 2 57.3; six studies)”
Quote in the paperSubstantial claim - Findingown data
The final sample comprised 438,245 unique persons with SMI and 5,622,664 matched controls.
“The final sample comprised 438,245 unique persons with SMI and 5,622,664 matched controls.”
Quote in the paperSubstantial claim - Findingown data
No other significant geographical differences were observed.
“No other significant geographical differences were observed.”
Quote in the paperNot a substantial claim - Premisecitation
Major risk factors for CVD in SMI include antipsychotic medication use and an unhealthy lifestyle.
“Major risk factors include antipsychotic medication use and an unhealthy lifestyle 7”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] source
Not checked in the free run.
- Premisecitation
Recent meta-analyses demonstrated that all diagnostic SMI subgroups have a higher risk for developing T2DM than the general population.
“Recent meta-analyses [17][18][19][20] demonstrated that all diagnostic SMI subgroups have a higher risk for developing T2DM than the general population.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [17][18][19][20]
Not checked in the free run.
- Premisecitation
The most important cause for this shortened life expectancy is cardiovascular disease (CVD).
“The most important cause for this shortened life expectancy is cardiovascular disease (CVD) 6 .”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [6] source
Not checked in the free run.
- Interpretationreasoning
Lifestyle and other environmental factors, with or without genetic risk differences, may influence T2DM prevalence in people with SMI.
“indicating the possible influence of lifestyle and other environmental factors with or without genetic risk differences.”
Quote in the paperSubstantial claim - Premisecitation
The glucose screening rate in people with SMI is 44.3% (95% CI: 36.3%-52.4%).
“The low glucose screening rates (44.3%;95% CI: 36.3%-52.4%)12”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [12] source
Not checked in the free run.
- Study design and conductown data
Publication bias was indicated by the Begg-Mazumdar (Kendall's tau=0.15, p=0.009) and Egger test (bias=25.39, 95% CI 27.33 to 23.45, p<0.001).
“The Begg-Mazumdar (Kendall's tau50.15,p50.009) and Egger test (bias525.39,95% CI: 27.33 to 23.45, p<0.001) indicated presence of publication bias.”
Quote in the paperSubstantial claim - Interpretationown data
The geographical differences in T2DM prevalence among people with SMI mirror the different prevalences in the general population.
“Our meta-analysis highlighted geographical differences in T2DM, mirroring the different prevalences in the general population”
Quote in the paperSubstantial claim - Interpretationcitation
The significantly increased prevalence of T2DM in North America versus Europe suggests a combined impact of genetic, lifestyle and/or environmental risk factors.
“We also observed a significantly increased prevalence of T2DM in North America versus Europe, in keeping with the overall population prevalences 30 , which suggests a combined impact of genetic, lifestyle and/or environmental risk factors.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [30]
Not checked in the free run.
- Interpretationown data
First-episode diagnosis is a unique predictor of lower T2DM prevalence independent of mean age.
“The current meta-analysis adds to the evidence that a first-episode diagnosis is a unique predictor of lower T2DM prevalence independent of mean age, a finding that was also apparent in a recent analysis of metabolic syndrome prevalences across patients with the same three main SMIs 33 .”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [33] source
Not checked in the free run.
- Interpretationreasoning
This finding is likely due to the fact that, in chart review studies, patients were followed back a longer time, extending the detection period.
“This finding is likely due to the fact that, in chart review studies, patients were followed back a longer time, extending the detection period.”
Quote in the paperNot a substantial claim - Study design and conductown data
The authors were able to explain over half of the between-study heterogeneity in multivariable metaregression analysis.
“were able to explain over half of the between-study heterogeneity in our multivariable metaregression analysis.”
Quote in the paperNot a substantial claim - Study design and conductnone given
Variables such as clinical subtypes of major depressive disorder (MDD) and bipolar disorder were not reported and controlled for.
“Third, variables such as clinical subtypes of MDD and bipolar disorder were not reported and controlled for.”
Quote in the paperNot a substantial claim - Study design and conductown data
The study findings were mainly based on cross-sectional rather than longitudinal data.
“because our study findings were mainly based on cross-sectional rather than longitudinal data”
Quote in the paperSubstantial claim - Premisecitation
Many people with mental ill health are not offered timely treatment even after an established diagnosis of T2DM is made.
“Even after an established diagnosis of T2DM is made, many of those with mental ill health are not offered timely treatment 42”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [42] source
Not checked in the free run.
- Study design and conductown data
There were inadequate data on lifestyle behaviors, precluding meta-analytic assessment of these factors as moderating or mediating variables.
“Fifth, there were inadequate data on lifestyle behaviors, precluding meta-analytic assessment of these factors as moderating or mediating variables.”
Quote in the paperNot a substantial claim - Study design and conductnone given
Only a limited number of studies assessed T2DM using an oral glucose tolerance test as the gold standard.
“First, only a limited number of studies assessed T2DM using an oral glucose tolerance test as the gold standard.”
Quote in the paperNot a substantial claim - Study design and conductreasoning
Directionality of the association between medication use and observed T2DM risk cannot be deduced with certainty from cross-sectional data.
“directionality of the association between medication use and observed T2DM risk cannot be deduced with certainty”
Quote in the paperSubstantial claim - Study design and conductown data
The authors adjusted for publication bias using trim and fill analysis.
“we adjusted for publication bias using the trim and fill analysis”
Quote in the paperNot a substantial claim
- May combine two claims. 30
- Classified as probably not a substantial claim. 29
May combine two claims.
Findingown dataT2DM prevalence was higher in patients prescribed antipsychotics, except for aripiprazole and amisulpride.
“The T2DM prevalence was higher in patients prescribed antipsychotics, except for aripriprazole and amisulpride.”
- Also stated in: § Medication use · plain
“Except for aripiprazole and amisulpride, all individual antipsychotics had significantly (p<0.05)higher T2DM risk compared to antipsychotic-na€ ıve participants”
Quote in the paperSubstantial claim- Also stated in: § Medication use · plain
Probably not a substantial claim: may not pass S4 (based).
Findingnone givenThere are differences in T2DM prevalences across assessment methods.
“As there are differences in T2DM prevalences across assessment methods”
Quote in the paperNot a substantial claimMay combine two claims.
FindingreasoningPatient self-report yielded numerically the lowest T2DM prevalences; the T2DM prevalence was significantly lower compared with chart review data.
“Finally, as expected, patient self-report yielded numerically the lowest T2DM prevalences; the T2DM prevalence was significantly lower compared with chart review data.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Findingown dataTwenty papers, including 64 analyses, reported on antipsychotics (monotherapy) and T2DM frequencies.
“Twenty papers, including 64 analyses, reported on antipsychotics (monotherapy) and T2DM frequencies.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown data44.5% (95% CI 29.2%-60.4%) of included participants smoked.
“Thirty-one studies (N577,028) reported smoking frequencies, and 44.5% (95% CI: 29.2%-60.4%) of the included participants smoked.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThere were no data in first-episode bipolar disorder or MDD patients, precluding a comparison with multi-episode patients.
“There were no data in firstepisode bipolar disorder or MDD patients, precluding a comparison with multi-episode patients.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataSeparate meta-regression analyses revealed that higher T2DM frequencies were moderated by older age, longer illness duration, and first-episode versus multi-episode status, but not by gender, ethnicity, and smoking status.
“Separate meta-regression analyses (see Table 2) revealed that higher T2DM frequencies were moderated by older age, longer illness duration, and first-episode versus multiepisode status, but not by gender, ethnicity, and smoking status.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataThe search yielded 323 publications, of which 118 (including 135 T2DM prevalences) met inclusion criteria.
“After excluding duplicates and irrevelant hits, our search yielded 323 publications, of which 118 (including 135 T2DM prevalences) met inclusion criteria (Figure 1).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown data56.8% of participants with SMI were male (range 0-100).
“56.8% were male (range 0-100)”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown data69% of participants with SMI were Caucasian (range 0-100; 37 studies).
“69% were Caucasian (range 0-100; 37 studies)”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn the current meta-analysis, quetiapine (and a trend for clozapine) was associated with an even higher T2DM risk than olanzapine use.
“In the current meta-analysis, quetiapine (and a trend for clozapine) was associated with an even higher T2DM risk than olanzapine use.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataMean illness duration was 16.1 years (range 0-35 years; 29 studies).
“Mean illness duration was 16.1 years (range 0-35 years; 29 studies).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataTreatment duration, percentage of antidepressant use and percentage of lithium use, but not percentage of other mood stabilizers use, were significant mediators of T2DM prevalence.
“Separate meta-regression analyses (see Table 2) showed that treatment duration, percentage of antidepressant use and percentage of lithium use, but not percentage of other mood stabilizers use, were significant mediators of T2DM prevalence.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThirty-four studies provided data on T2DM prevalences comparing multi-episode patients with healthy control subjects, and three studies compared first-episode schizophrenia patients with controls.
“Thirty-four studies provided data on T2DM prevalences comparing multi-episode patients with healthy control subjects, and three studies compared first-episode schizophrenia patients with controls.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataA trend for higher T2DM was found in retrospective studies versus cross-sectional (p=0.054) and versus prospective (p=0.053) studies.
“A trend for higher T2DM was found in retrospective studies versus cross-sectional (p50.054) and versus prospective (p50.053)studies.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataExcept for a higher risk for quetiapine versus olanzapine (p=0.04), no differences in risk profile between individual medications were found.
“Except for a higher risk for quetiapine versus olanzapine (p50.04),we did not find any differences in risk profile between individual medications.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThere were no significant differences between various treatment settings, and data collection before versus after the year 2000.
“There were no significant differences between the various treatment settings, and data collection before versus after the year 2000.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThe mean age of participants with SMI was 44.3 years (range 23.1-77.6 years).
“The mean age of participants with SMI was 44.3 years (range 23.1-77.6 years)”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataTwo independent reviewers searched databases and screened titles/abstracts, with a third reviewer available for mediation.
“Two independent reviewers (DV, BS) searched Medline, Psyc-ARTICLES, Embase and CINAHL from database inception to August 1, 2015, without language restrictions.”
- Also stated in: § Search criteria, study selection and critical appraisal · plain
“After the removal of duplicates, the reviewers screened the titles and abstracts of all potentially eligible articles.They both applied the eligibility criteria, and a list of full text articles was developed through consensus.”
- Also stated in: § Search criteria, study selection and critical appraisal · plain
“A third reviewer (CC) was available for mediation throughout this process.”
Quote in the paperNot a substantial claim- Also stated in: § Search criteria, study selection and critical appraisal · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationT2DM is a major risk factor for CVD.
“Type 2 diabetes mellitus (T2DM) is a major risk factor for CVD.”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationT2DM confers about a two-fold excess risk for coronary heart disease, major stroke subtypes, and deaths attributed to other vascular causes.
“It confers about a two-fold excess risk for coronary heart disease, major stroke subtypes, and deaths attributed to other vascular causes 13,14 .”
Quote in the paperNot a substantial claim0 of 2 sources checkedClassified as probably not a substantial claim.
Study design and conductnone givenMethodological appraisal included evaluation of bias (confounding, overlapping data, publication bias).
“Methodological appraisal included evaluation of bias (confounding, overlapping data, publication bias).”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe mortality gap translates to a 10-20 year shortened life expectancy.
“This mortality gap translates to a 10-20 year shortened life expectancy 3,4”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductcitationPublication bias was tested using Egger's regression method and Begg-Mazumdar test.
“Publication bias was tested using the Egger's regression method 23 and Begg-Mazumdar test 24 , with a p-value <0.05 suggesting the presence of bias.”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductcitationThe systematic review was conducted in accordance with MOOSE guidelines and PRISMA standard.
“This systematic review was conducted in accordance with the Meta-analysis of Observational Studies in Epidemiology (MOOSE) guidelines 21 and in line with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) standard 22 .”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPeople with SMI have a two to three times higher risk for premature death than the general population.
“People with severe mental illness (SMI) -defined as schizophrenia, bipolar disorder or major depressive disorder (MDD)have a two to three times higher risk for premature death than the general population 1,2 .”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationWhen publication bias was encountered, a trim and fill adjusted analysis was conducted.
“When we encountered publication bias, we conducted a trim and fill adjusted analysis 25 to remove the most extreme small studies from the positive side of the funnel plot, and recalculated the effect size iteratively, until the funnel plot was symmetrical around the (new) effect size.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [25] source
Not checked in the free run.
May combine two claims.
PremisecitationVariations in the risk for glucose abnormalities are evident in the literature, with the highest risk being associated with clozapine, olanzapine and quetiapine in carefully designed studies.
“Variations in the risk for glucose abnormalities are evident in the literature, with the highest risk being associated with clozapine, olanzapine and quetiapine in carefully designed studies 25,34,35 .”
Quote in the paperNot a substantial claim0 of 3 sources checkedClassified as probably not a substantial claim.
Study design and conductreasoningOnly comparisons of specific SMI groups or SMI with matched general population performed within the same study were included to minimize variability.
“In both analyses, only comparisons of specific SMI groups or a SMI group with a matched general population group were included that had been performed within the same study, in order to minimize variability of T2DM frequencies due to different sampling and assessment procedures.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductreasoningDiagnostic and gender differences were not calculated across studies; only data of studies comparing these differences on a patient level were pooled.
“In order to reduce heterogeneity, we did not calculate diagnostic and gender differences across studies, but pooled only data of studies that compared these differences on a patient level.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationScreening for T2DM and cardiovascular disease (CVD) risk factors is still suboptimal, with only slight improvement over the last decade.
“screening for T2DM and CVD risk factors is still suboptimal, with only slight improvement over the last decade 12”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [12] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationcitationThe higher risk for T2DM in women with SMI than men may be related to a greater propensity to obesity and central obesity in women with SMI compared to men, since central obesity is a significant risk factor for hyperglycaemia.
“This finding warrants further investigation, but may be related to a greater propensity to obesity and central obesity in women with SMI compared to men 32 , since central obesity is a significant risk factor for hyperglycaemia.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [32] source
Not checked in the free run.
May combine two claims.
PremisecitationProfessional barriers to screening within mental health settings reflect lack of clarity about clinical responsibility, lack of understanding about what should be measured and when, uncertainty about how to interpret results, lack of access to necessary equipment, and incomplete communication between primary and secondary care.
“Professional barriers to screening within mental health settings may in their turn reflect lack of clarity about whose clinical responsibility the screening is, lack of understanding about what should be measured and when, uncertainity about how to interpret results, and lack of access to necessary equipment 41 , as well as incomplete communication between primary and secondary care.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [41] source
Not checked in the free run.
May combine two claims.
InterpretationreasoningOther diagnostic-independent factors likely influence T2DM frequency, including hyperglycaemia following psychotropic medication use and long-term exposure to unhealthy lifestyle behaviors, as well as potential genetic factors linking psychiatric and medical risk.
“Thus, other diagnosticindependent factors likely influence T2DM frequency, including hyperglycaemia following psychotropic medication use 26 and long-term exposure to unhealthy lifestyle behaviors 27,28 , as well as potential genetic factors linking psychiatric and medical risk 29 .”
Quote in the paperSubstantial claim0 of 4 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenOnly a minority of analyzed studies provided information about the mean age in women and men, and it is possible that women with schizophrenia were older, which could have confounded the results.
“On the other hand, only a minority of analyzed studies did provide information about the mean age in women and men, and it is possible that women with schizophrenia were older, which could have confounded the results.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductreasoningThis finding should be interpreted with caution, as order effects cannot be excluded, in that patients who acquired marked T2DM risk or developed even frank T2DM on a higher-risk agent, such as olanzapine, could have been switched to another antipsychotic, including quetiapine, potentially leading to risk misattribution.
“However, this finding should be interpreted with caution, as order effects cannot be excluded, in that patients who acquired marked T2DM risk or developed even frank T2DM on a higher-risk agent, such as olanzapine, could have been switched to another antipsychotic, including quetiapine, potentially leading to risk misattribution.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationOther antidepressants, including tricyclic antidepressants, may exacerbate glycaemic dysfunction or have little effect on glucose homeostasis.
“whereas others, including tricyclic antidepressants, may exacerbate glycaemic dysfunction or have little effect on glucose homeostasis 46,47”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationSome antidepressants may, in some circumstances, reduce hyperglycaemia, normalize glucose homeostasis and increase insulin sensitivity.
“previous studies 45 found that some antidepressants may, in some circumstances, reduce hyperglycaemia, normalize glucose homeostasis and also increase insulin sensitivity”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationEmerging evidence suggests that SMI and T2DM share some pathophysiological features, including hypothalamic-pituitary-adrenal and mitochondrial dysfunction, neuro-inflammation, common genetic links and epigenetic interactions.
“Emerging evidence 48 suggests that SMI and T2DM share some pathophysiological features, including hypothalamic-pituitary-adrenal and mitochondrial dysfunction, neuro-inflammation, common genetic links and epigenetic interactions.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [48] source
Not checked in the free run.
Probably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningWithout systematic screening following detailed recommendations and using acceptable and accurate diagnostic tests, the true prevalence of T2DM in patients with SMI will remain unknown and underestimated.
“Without systematic screening following detailed recommendations and using acceptable and accurate diagnostic tests, the true prevalence of T2DM in patients with SMI will remain unknown and underestimated.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Interpretationnone givenWhen T2DM is detected, people with SMI are likely to require additional pharmacological management, but this is unlikely to be significantly different from the general population.
“When T2DM is detected, people with SMI are likely to require additional pharmacological management, but this is unlikely to be significantly different from the general population.”
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 givenAny deterioration in mental health may result in compromised management of T2DM, and comprehensive management may require an adjustment to the diabetes care plan.
“However, clinicians should be aware that any deterioration in mental health may result in compromised management of T2DM, and comprehensive management may require an adjustment to the diabetes care plan.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationAntipsychotic medications are increasingly used as first line treatments for bipolar disorder and MDD.
“Since antipsychotic medications are increasingly used as first line treatments for bipolar disorder 43 and MDD 44”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [43] source
Not checked in the free run.
- cites [44]
Not checked in the free run.
May combine two claims.
Study design and conductown dataThe meta-analysis encountered publication bias and heterogeneity in most analyses.
“a threat to the validity of any meta-analysis is publication bias and heterogeneity, which we encountered in most of our analyses.”
Quote in the paperNot a substantial claim
The paper relies on this without support.
Meta-analytic data comparing T2DM risks across different psychiatric diagnoses are currently lacking.
“However, meta-analytic data comparing T2DM risks across different psychiatric diagnoses are currently lacking.”
The paper relies on this without support.
There are no meta-analytic data that combine all major diagnostic SMI subgroups.
“Furthermore, there are no meta-analytic data that combine all major diagnostic SMI subgroups”
The paper relies on this without support.
Information on the prevalence of T2DM among people with SMI prescribed different antipsychotic medication classes is insufficient.
“and information on the prevalence of T2DM among people with SMI prescribed different antipsychotic medication classes is insufficient.”
The paper relies on this without support.
Using chart reviews has inherent problems with selection bias and the reliability and validity of T2DM diagnosis.
“There are inherent problems with using chart reviews in relation to se-lection bias and the reliability and validity of the T2DM diagnosis.”
The paper relies on this without support.
The pathophysiology underlying the association between SMI and T2DM is complex and not well understood.
“the pathophysiology underlying the association between SMI and T2DM is complex and not well understood, requiring further investigation.”
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?
People with severe mental illness have higher levels of somatic comorbidities and premature mortality than the general population.
“People with severe mental illness (schizophrenia, bipolar disorder or major depressive disorder) have higher levels of somatic comorbidities and premature mortality than the general population 1-3 .”
From Sedentary behavior and physical activity levels in people with schizophrenia, bipolar disorder and major depressive disorder: a global systematic review and meta-analysis (2017) · cites this paper as [3]
The Abstract states that people with severe mental illness have a two- to threefold higher risk of premature death than the general population. The Discussion finds elevated type 2 diabetes prevalence in the three diagnostic groups, supporting a higher level of one somatic comorbidity, but the paper does not establish the broader claim about somatic comorbidities generally. (LLM, conf=0.84)
Experimental — accuracy not yet measured
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.
MDD relative-risk confidence interval conflicts with its p-value
MajorThe reported 95% confidence interval for the MDD relative risk includes 1, but the reported p-value of 0.029 indicates significance at the 0.05 level.
Reported 0.029 · recomputed -1.37
“1.43 in patients with MDD (N510,895; 95% CI: 0.88-2.25,p50.029;Q52.15, p50.34; three studies).”
Conflicting numbers of studies comparing multi-episode patients with controls
MinorThe section says 34 studies compared multi-episode patients with controls, but describes the pooled multi-episode comparison as comprising 38 studies.
“Thirty-four studies provided data on T2DM prevalences comparing multi-episode patients with healthy control subjects”
“multi-episode persons with SMI (N5133,470; 12.2%, 95% CI: 9.7-15.2%;Q56166, p<0.01) had significantly increased risk of T2DM (RR51.85,95% CI: 1.45-2.37,p<0.001;Q51302.0,p<0.001; 38 studies).”
Cites
Preferred Reporting Items for Systematic Reviews and Meta-Analyses: the PRISMA statement
Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G., & for the PRISMA Group (2009) · BMJ · doi:10.1136/bmj.b2535 · Cited by 83,823 · see citing works
Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement
Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G., & The PRISMA Group (2009) · PLoS Medicine · doi:10.1371/journal.pmed.1000097 · Cited by 64,042 · see citing works
Bias in meta-analysis detected by a simple, graphical test
Egger, M., Smith, G. D., Schneider, M., & Minder, C. (1997) · BMJ · doi:10.1136/bmj.315.7109.629 · Cited by 56,722 · see citing works
Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement
Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G., & the PRISMA Group* (2009) · Annals of Internal Medicine · doi:10.7326/0003-4819-151-4-200908180-00135 · Cited by 37,554 · see citing works
Dermyshi, E., Wang, Y., Yan, C., Hong, W., Qiu, G., Gong, X., & Zhang, T. (2017) · Neonatology · doi:10.1159/000454668 · Cited by 24,577 · see citing works
Stroup, D. F. (2000) · JAMA · doi:10.1001/jama.283.15.2008 · Cited by 20,623 · see citing works
Wang, G., Ma, R., Qiao, G., Wada, K., Aizawa, Y., & Satoh, T. (2015) · Integrative Medicine International · doi:10.1159/000368408 · Cited by 18,759 · see citing works
Operating characteristics of a rank correlation test for publication bias
Begg, C. B., & Mazumdar, M. (1994) · Biometrics · doi:10.2307/2533446 · Cited by 16,955 · see citing works
International Diabetes Federation 2017
Carracher, A. M., Marathe, P. H., & Close, K. L. (2018) · Journal of Diabetes · doi:10.1111/1753-0407.12644 · Cited by 13,369 · see citing works
Murray, C. J. L., Vos, T., Lozano, R., Naghavi, M., Flaxman, A. D., Michaud, C., Ezzati, M., Shibuya, K., Salomon, J. A., Abdalla, S., et al. (2012) · The Lancet · doi:10.1016/s0140-6736(12)61689-4 · Cited by 8,888 · see citing works
The Emerging Risk Factors Collaboration (2010) · The Lancet · doi:10.1016/s0140-6736(10)60484-9 · Cited by 5,125 · see citing works
A Nonparametric “Trim and Fill” Method of Accounting for Publication Bias in Meta-Analysis
Duval, S., & Tweedie, R. (2000) · Journal of the American Statistical Association · doi:10.1080/01621459.2000.10473905 · Cited by 2,955 · see citing works
Grundy, S. M., Benjamin, I. J., Burke, G. L., Chait, A., Eckel, R. H., Howard, B. V., Mitch, W., Smith, S. C., & Sowers, J. R. (1999) · Circulation · doi:10.1161/01.cir.100.10.1134 · Cited by 2,698 · see citing works
DE HERT, M., CORRELL, C. U., BOBES, J., CETKOVICH‐BAKMAS, M., COHEN, D., ASAI, I., DETRAUX, J., GAUTAM, S., MÖLLER, H., NDETEI, D. M., et al. (2011) · World Psychiatry · doi:10.1002/j.2051-5545.2011.tb00014.x · Cited by 2,488 · see citing works
Self-citationRisks of all-cause and suicide mortality in mental disorders: a meta-review
Chesney, E., Goodwin, G. M., & Fazel, S. (2014) · World Psychiatry · doi:10.1002/wps.20128 · Cited by 2,115 · see citing works
Saha, S., Chant, D., & McGrath, J. (2007) · Archives of General Psychiatry · doi:10.1001/archpsyc.64.10.1123 · Cited by 2,065 · see citing works
Vancampfort, D., Stubbs, B., Mitchell, A. J., De Hert, M., Wampers, M., Ward, P. B., Rosenbaum, S., & Correll, C. U. (2015) · World Psychiatry · doi:10.1002/wps.20252 · Cited by 1,271 · see citing works
Self-citationMetabolic and cardiovascular adverse effects associated with antipsychotic drugs.
De Hert, M., Detraux, J., van Winkel, R., Yu, W., & Correll, C. U. (2012) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2011.156 · Cited by 1,145 · see citing works
De Hert, M., Dekker, J. M., Wood, D., Kahl, K. G., Holt, R. I. G., & Möller, H.-J. (2009) · European Psychiatry · doi:10.1016/j.eurpsy.2009.01.005 · Cited by 951 · see citing works
DE HERT, M., COHEN, D., BOBES, J., CETKOVICH‐BAKMAS, M., LEUCHT, S., NDETEI, D. M., NEWCOMER, J. W., UWAKWE, R., ASAI, I., MÖLLER, H., et al. (2011) · World Psychiatry · doi:10.1002/j.2051-5545.2011.tb00036.x · Cited by 870 · see citing works
Self-citationCorrell, C. U., Detraux, J., De Lepeleire, J., & De Hert, M. (2015) · World Psychiatry · doi:10.1002/wps.20204 · Cited by 820 · see citing works
Self-citationLawrence, D., Hancock, K. J., & Kisely, S. (2013) · BMJ · doi:10.1136/bmj.f2539 · Cited by 819 · see citing works
Chang, C.-K., Hayes, R. D., Perera, G., Broadbent, M. T. M., Fernandes, A. C., Lee, W. E., Hotopf, M., & Stewart, R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019590 · Cited by 714 · see citing works
Lamers, F., Vogelzangs, N., Merikangas, K. R., de Jonge, P., Beekman, A. T. F., & Penninx, B. W. J. H. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.144 · Cited by 691 · see citing works
Mitchell, A. J., Malone, D., & Carney, C. P. (2009) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.107.045732 · Cited by 359 · see citing works
Major Depressive Disorder Treatment Guidelines in America and Europe
Davidson, J. R. T. (2010) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.9058se1c.04gry · Cited by 344 · see citing works
Mitchell, A. J., Delaffon, V., Vancampfort, D., Correll, C. U., & De Hert, M. (2012) · Psychological Medicine · doi:10.1017/s003329171100105x · Cited by 332 · see citing works
Self-citationVancampfort, D., Wampers, M., Mitchell, A. J., Correll, C. U., Herdt, A. D., Probst, M., & Binder, M. D. (2013) · World Psychiatry · doi:10.1002/wps.20069 · Cited by 320 · see citing works
Self-citationStubbs, B., Vancampfort, D., Hert, M. D., & Mitchell, A. (2015) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12439 · Cited by 232 · see citing works
Self-citationHert, M. A. F. D., Vancampfort, D., Correll, C. U., Mercken, V., Peuskens, J., Sweers, K., van Winkel, R., & Mitchell, A. J. (2011) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.110.084665 · Cited by 216 · see citing works
Self-citationNielsen, J., Skadhede, S., & Correll, C. U. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.78 · Cited by 207 · see citing works
Self-citationRamasubbu, R., Taylor, V. H., Samaan, Z., Sockalingham, S., Li, M., Patten, S., Rodin, G., Schaffer, A., Beaulieu, S., & McIntyre, R. S. (2012) · Annals of Clinical Psychiatry · doi:10.1177/104012371202400110 · Cited by 206 · see citing works
Vancampfort, D., Mitchell, A. J., De Hert, M., Sienaert, P., Probst, M., Buys, R., & Stubbs, B. (2015) · Depression and Anxiety · doi:10.1002/da.22387 · Cited by 171 · see citing works
Self-citationMortality in Schizophrenia and Other Psychoses: A 10-Year Follow-up of the ӔSOP First-Episode Cohort
Reininghaus, U., Dutta, R., Dazzan, P., Doody, G. A., Fearon, P., Lappin, J., Heslin, M., Onyejiaka, A., Donoghue, K., Lomas, B., et al. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbu138 · Cited by 156 · see citing works
Treatment with antipsychotics and the risk of diabetes in clinical practice
Kessing, L. V., Thomsen, A. F., Mogensen, U. B., & Andersen, P. K. (2010) · British Journal of Psychiatry · doi:10.1192/bjp.bp.109.076935 · Cited by 152 · see citing works
Associations between sedentary behaviour and metabolic parameters in patients with schizophrenia
Vancampfort, D., Probst, M., Knapen, J., Carraro, A., & De Hert, M. (2012) · Psychiatry Research · doi:10.1016/j.psychres.2012.03.046 · Cited by 149 · see citing works
Self-citationGardner-Sood, P., Lally, J., Smith, S., Atakan, Z., Ismail, K., Greenwood, K. E., Keen, A., O'Brien, C., Onagbesan, O., Fung, C., et al. (2015) · Psychological Medicine · doi:10.1017/s0033291715000562 · Cited by 140 · see citing works
Self-citationMitchell, A. J., Lord, O., & Malone, D. (2012) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.111.094532 · Cited by 136 · see citing works
Vancampfort, D., De Hert, M., Skjerven, L. H., Gyllensten, A. L., Parker, A., Mulders, N., Nyboe, L., Spencer, F., & Probst, M. (2012) · Disability and Rehabilitation · doi:10.3109/09638288.2011.587090 · Cited by 127 · see citing works
Self-citationPrevalence and Predictors of Type 2 Diabetes Mellitus in People With Bipolar Disorder
Vancampfort, D., Mitchell, A. J., Binder, M. D., Sienaert, P. A., Probst, M., Buys, R., & Stubbs, B. (2015) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.14r09635 · Cited by 115 · see citing works
Self-citationAvoidable mortality in people with schizophrenia or bipolar disorder in <scp>E</scp>ngland
Hoang, U., Goldacre, M. J., & Stewart, R. (2013) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12045 · Cited by 109 · see citing works
Mitchell, A. J., & Lord, O. (2010) · Journal of Psychopharmacology · doi:10.1177/1359786810382056 · Cited by 108 · see citing works
Correll, C. U., Joffe, B. I., Rosen, L. M., Sullivan, T. B., & Joffe, R. T. (2015) · World Psychiatry · doi:10.1002/wps.20187 · Cited by 102 · see citing works
Self-citationEllingrod, V. L., Taylor, S. F., Dalack, G., Grove, T. B., Bly, M. J., Brook, R. D., Zöllner, S. K., & Pop-Busui, R. (2012) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0b013e3182485888 · Cited by 84 · see citing works
Antipsychotics and Diabetes: An Age-Related Association
Hammerman, A., Dreiher, J., Klang, S. H., Munitz, H., Cohen, A. D., & Goldfracht, M. (2008) · Annals of Pharmacotherapy · doi:10.1345/aph.1l015 · Cited by 75 · see citing works
Glucose Metabolism and Antidepressant Medication
M. Hennings, J., Schaaf, L., & Fulda, S. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212803523662 · Cited by 64 · cited 1× · see citing works
“For example, previous studies (45) found that some antidepressants may, in some circumstances, reduce hyperglycaemia, normalize glucose homeostasis and also increase insulin sensitivity, whereas”
ResultMarkers of inflammation in schizophrenia: association vs. causation
Manu, P., Correll, C. U., Wampers, M., Mitchell, A. J., Probst, M., Vancampfort, D., & De Hert, M. (2014) · World Psychiatry · doi:10.1002/wps.20117 · Cited by 59 · see citing works
Self-citationGierisch, J. M., Nieuwsma, J. A., Bradford, D. W., Wilder, C. M., Mann-Wrobel, M. C., McBroom, A. J., Hasselblad, V., & Williams, J. W. (2014) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.13r08558 · Cited by 59 · see citing works
Pillarella, J., Higashi, A., Alexander, G. C., & Conti, R. (2012) · Psychiatric Services · doi:10.1176/appi.ps.201100092 · Cited by 53 · see citing works
McIntyre, R. S., Alsuwaidan, M., Goldstein, B. I., Taylor, V. H., Schaffer, A., Beaulieu, S., & Kemp, D. E. (2012) · Annals of Clinical Psychiatry · doi:10.1177/104012371202400108 · Cited by 45 · cited 1× · see citing works
“Thus, considering the observed increased T2DM risks, screening for and trying to minimize risk factors (including adverse lifestyle factors and specific antipsychotic medication choice) should be a key priority in the multidisciplinary treatment of people with SMI (36-39).”
BackgroundThe prevention of diabetes and cardiovascular disease in people with schizophrenia
Holt, R. I. G. (2015) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12443 · Cited by 37 · see citing works
Diabetes, physical activity participation and exercise capacity in patients with schizophrenia
Vancampfort, D., De Hert, M., Sweers, K., De Herdt, A., Detraux, J., & Probst, M. (2013) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12077 · Cited by 34 · see citing works
Self-citationAntidepressant use and glycemic control
Mojtabai, R. (2013) · Psychopharmacology · doi:10.1007/s00213-013-2972-5 · Cited by 24 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- World Health Organization, 1999, Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus
- International Diabetes Federation. IDF diabetes atlas. Sixth edition update. Brussels: International Diabetes Federation 2014.
Cited by
Sorted by citations
Physical Activity and Incident Depression: A Meta-Analysis of Prospective Cohort Studies
Schuch, F. B., Vancampfort, D., Firth, J., Rosenbaum, S., Ward, P. B., Silva, E. S., Hallgren, M., Ponce De Leon, A., Dunn, A. L., Deslandes, A. C., et al. (2018) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2018.17111194 · Cited by 1,763 · see citing works
Self-citationGlobal trends in diabetes complications: a review of current evidence
Harding, J. L., Pavkov, M. E., Magliano, D. J., Shaw, J. E., & Gregg, E. W. (2018) · Diabetologia · doi:10.1007/s00125-018-4711-2 · Cited by 1,674 · see citing works
Firth, J., Siddiqi, N., Koyanagi, A., Siskind, D., Rosenbaum, S., Galletly, C., Allan, S., Caneo, C., Carney, R., Carvalho, A. F., et al. (2019) · The Lancet Psychiatry · doi:10.1016/s2215-0366(19)30132-4 · Cited by 1,531 · see citing works
Self-citationVancampfort, D., Firth, J., Schuch, F. B., Rosenbaum, S., Mugisha, J., Hallgren, M., Probst, M., Ward, P. B., Gaughran, F., De Hert, M., et al. (2017) · World Psychiatry · doi:10.1002/wps.20458 · Cited by 957 · see citing works
Self-citationVieta, E., Berk, M., Schulze, T. G., Carvalho, A. F., Suppes, T., Calabrese, J. R., Gao, K., Miskowiak, K. W., & Grande, I. (2018) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2018.8 · Cited by 891 · see citing works
Correll, C. U., Solmi, M., Croatto, G., Schneider, L. K., Rohani-Montez, S. C., Fairley, L., Smith, N., Bitter, I., Gorwood, P. A. P. M., Taipale, H. T., et al. (2022) · World Psychiatry · doi:10.1002/wps.20994 · Cited by 717 · see citing works
Self-citationStubbs, B., Vancampfort, D., Hallgren, M., Firth, J., Veronese, N., Solmi, M., Brand, S., Cordes, J., Malchow, B., Gerber, M., et al. (2018) · European Psychiatry · doi:10.1016/j.eurpsy.2018.07.004 · Cited by 697 · see citing works
Self-citationSchuch, F., Vancampfort, D., Firth, J., Rosenbaum, S., Ward, P., Reichert, T., Bagatini, N. C., Bgeginski, R., & Stubbs, B. (2017) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.10.050 · Cited by 663 · see citing works
Self-citationSolmi, M., Seitidis, G., Mavridis, D., Correll, C. U., Dragioti, E., Guimond, S., Tuominen, L. J., Dargél, A., Carvalho, A. F., Fornaro, M., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02138-4 · Cited by 605 · see citing works
Self-citationCarvalho, A. F., Firth, J., & Vieta, E. (2020) · New England Journal of Medicine · doi:10.1056/nejmra1906193 · Cited by 562 · see citing works
Impaired Glucose Homeostasis in First-Episode Schizophrenia
Pillinger, T., Beck, K., Gobjila, C., Donocik, J. G., Jauhar, S., & Howes, O. D. (2017) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2016.3803 · Cited by 464 · see citing works
2. Diagnosis and Classification of Diabetes: Standards of Care in Diabetes—2026
American Diabetes Association Professional Practice Committee for Diabetes*, Bajaj, M., McCoy, R. G., Balapattabi, K., Bannuru, R. R., Bellini, N. J., Bennett, A. K., Beverly, E. A., Briggs Early, K., ChallaSivaKanaka, S., et al. (2026) · Diabetes Care · doi:10.2337/dc26-s002 · Cited by 473 · see citing works
Ashdown-Franks, G., Firth, J., Carney, R., Carvalho, A. F., Hallgren, M., Koyanagi, A., Rosenbaum, S., Schuch, F. B., Smith, L., Solmi, M., et al. (2020) · Sports Medicine · doi:10.1007/s40279-019-01187-6 · Cited by 446 · see citing works
Self-citationSolmi, M., Murru, A., Pacchiarotti, I., Undurraga, J., Veronese, N., Fornaro, M., Stubbs, B., Monaco, F., Vieta, E., Seeman, M., et al. (2017) · Therapeutics and Clinical Risk Management · doi:10.2147/tcrm.s117321 · Cited by 438 · see citing works
Self-citationCardiovascular disease in patients with severe mental illness
Nielsen, R. E., Banner, J., & Jensen, S. E. (2021) · Nature Reviews Cardiology · doi:10.1038/s41569-020-00463-7 · Cited by 389 · see citing works
Taipale, H., Tanskanen, A., Mehtälä, J., Vattulainen, P., Correll, C. U., & Tiihonen, J. (2020) · World Psychiatry · doi:10.1002/wps.20699 · Cited by 415 · see citing works
Self-citationWhat is the risk‐benefit ratio of long‐term antipsychotic treatment in people with schizophrenia?
Correll, C. U., Rubio, J. M., & Kane, J. M. (2018) · World Psychiatry · doi:10.1002/wps.20516 · Cited by 324 · see citing works
Self-citationMasuda, T., Misawa, F., Takase, M., Kane, J. M., & Correll, C. U. (2019) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2019.1702 · Cited by 321 · see citing works
Self-citationEfficacy and Safety of Lumateperone for Treatment of Schizophrenia
Correll, C. U., Davis, R. E., Weingart, M., Saillard, J., O’Gorman, C., Kane, J. M., Lieberman, J. A., Tamminga, C. A., Mates, S. L., & Vanover, K. E. (2020) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2019.4379 · Cited by 289 · see citing works
Self-citationMaj, M., van Os, J., De Hert, M., Gaebel, W., Galderisi, S., Green, M. F., Guloksuz, S., Harvey, P. D., Jones, P. B., Malaspina, D., et al. (2021) · World Psychiatry · doi:10.1002/wps.20809 · Cited by 285 · see citing works
The Role of Exercise in Preventing and Treating Depression
Schuch, F. B., & Stubbs, B. (2019) · Current Sports Medicine Reports · doi:10.1249/jsr.0000000000000620 · Cited by 272 · see citing works
Self-citationPhysical activity, exercise, and mental disorders: it is time to move on
Schuch, F. B., & Vancampfort, D. (2021) · Trends in Psychiatry and Psychotherapy · doi:10.47626/2237-6089-2021-0237 · Cited by 251 · see citing works
Self-citationIntegrating mental health with other non-communicable diseases
Stein, D. J., Benjet, C., Gureje, O., Lund, C., Scott, K. M., Poznyak, V., & van Ommeren, M. (2019) · BMJ · doi:10.1136/bmj.l295 · Cited by 245 · see citing works
Solmi, M., Firth, J., Miola, A., Fornaro, M., Frison, E., Fusar‐Poli, P., Dragioti, E., Shin, J. I., Carvalho, A. F., Stubbs, B., et al. (2019) · The Lancet Psychiatry · doi:10.1016/s2215-0366(19)30414-6 · Cited by 243 · see citing works
Self-citationVancampfort, D., Firth, J., Correll, C. U., Solmi, M., Siskind, D., De Hert, M., Carney, R., Koyanagi, A., Carvalho, A. F., Gaughran, F., et al. (2019) · World Psychiatry · doi:10.1002/wps.20614 · Cited by 227 · see citing works
Self-citationMazereel, V., Detraux, J., Vancampfort, D., van Winkel, R., & Binder, M. D. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.573479 · Cited by 205 · see citing works
Self-citationWu, Y., Wang, L., Tao, M., Cao, H., Yuan, H., Ye, M., Chen, X., Wang, K., & Zhu, C. (2023) · Epidemiology and Psychiatric Sciences · doi:10.1017/s2045796023000756 · Cited by 217 · see citing works
Solmi, M., Sharma, M. S., Osimo, E. F., Fornaro, M., Bortolato, B., Croatto, G., Miola, A., Vieta, E., Pariante, C. M., Smith, L., et al. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.07.014 · Cited by 198 · see citing works
Tiihonen, J., Tanskanen, A., & Taipale, H. (2018) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2018.17091001 · Cited by 196 · see citing works
Wang, R., Chen, Z., Zhou, Y., Shen, L., Zhang, Z., & Wu, X. L. (2019) · Social Science & Medicine · doi:10.1016/j.socscimed.2019.112518 · Cited by 197 · see citing works
Bueno, H., Deaton, C., Farrero, M., Forsyth, F., Braunschweig, F., Buccheri, S., Dragan, S. R., Gevaert, S., Held, C., Kurpas, D., et al. (2025) · European Heart Journal · doi:10.1093/eurheartj/ehaf191 · Cited by 209 · see citing works
Second-Generation Antipsychotics and Dysregulation of Glucose Metabolism: Beyond Weight Gain
Grajales, D., Ferreira, V., & Valverde, Á. M. (2019) · Cells · doi:10.3390/cells8111336 · Cited by 181 · see citing works
Stubbs, B., Vancampfort, D., Veronese, N., Kahl, K. G., Mitchell, A. J., Lin, P.-Y., Tseng, P.-T., Mugisha, J., Solmi, M., Carvalho, A. F., et al. (2017) · Psychological Medicine · doi:10.1017/s0033291717000551 · Cited by 167 · see citing works
Self-citationAssociation between antipsychotic medication use and diabetes
Holt, R. I. G. (2019) · Current Diabetes Reports · doi:10.1007/s11892-019-1220-8 · Cited by 162 · see citing works
Bottaccioli, A. G., Bottaccioli, F., & Minelli, A. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13728 · Cited by 92 · see citing works
Stubbs, B., Koyanagi, A., Veronese, N., Vancampfort, D., Solmi, M., Gaughran, F., Carvalho, A. F., Lally, J., Mitchell, A. J., Mugisha, J., et al. (2016) · BMC Medicine · doi:10.1186/s12916-016-0734-z · Cited by 151 · see citing works
Self-citationClinical risk factors for the development of tardive dyskinesia
Solmi, M., Pigato, G., Kane, J. M., & Correll, C. U. (2018) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2018.02.012 · Cited by 152 · see citing works
Self-citationFirth, J., Stubbs, B., Teasdale, S. B., Ward, P. B., Veronese, N., Shivappa, N., Hebert, J. R., Berk, M., Yung, A. R., & Sarris, J. (2018) · World Psychiatry · doi:10.1002/wps.20571 · Cited by 145 · see citing works
Self-citationSolmi, M., Fiedorowicz, J. G., Poddighe, L., Delogu, M., Miola, A., Høye, A., Heiberg, I. H., Stubbs, B., Smith, L., Larsson, H., et al. (2021) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2021.21010031 · Cited by 146 · see citing works
Self-citationQuality of life in schizophrenia: a meta-analysis of comparative studies.
Dong, M., Lu, L., Zhang, L., Zhang, Y.-S., Ng, C. H., Ungvari, G. S., Li, G., Meng, X., Wang, G., & Xiang, Y.-T. (2019) · Psychiatric Quarterly · doi:10.1007/s11126-019-09633-4 · Cited by 142 · see citing works
Stubbs, B., Vancampfort, D., Firth, J., Schuch, F. B., Hallgren, M., Smith, L., Gardner, B., Kahl, K. G., Veronese, N., Solmi, M., et al. (2018) · Journal of Affective Disorders · doi:10.1016/j.jad.2017.12.104 · Cited by 138 · see citing works
Self-citationTreatment-resistant schizophrenia: current insights on the pharmacogenomics of antipsychotics
Lally, J., Gaughran, F., Timms, P. W., & Curran, S. R. (2016) · Pharmacogenomics and Personalized Medicine · doi:10.2147/pgpm.s115741 · Cited by 131 · see citing works
Self-citationStubbs, B., Koyanagi, A., Schuch, F. B., Firth, J., Rosenbaum, S., Veronese, N., Solmi, M., Mugisha, J., & Vancampfort, D. (2016) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12654 · Cited by 128 · see citing works
Self-citationDragioti, E., Radua, J., Solmi, M., Gosling, C. J., Oliver, D., Lascialfari, F., Ahmed, M., Cortese, S., Estradé, A., Arrondo, G., et al. (2023) · World Psychiatry · doi:10.1002/wps.21068 · Cited by 130 · see citing works
Self-citationO’Connor, R. C., Worthman, C. M., Abanga, M. A., Athanassopoulou, N., Boyce, N., Chan, L. F., Christensen, H. M., Das‐Munshi, J., Downs, J. L., Koenen, K. C., et al. (2023) · The Lancet Psychiatry · doi:10.1016/s2215-0366(23)00058-5 · Cited by 128 · see citing works
Blood-brain barrier imaging as a potential biomarker for bipolar disorder progression
Kamintsky, L., Cairns, K., Veksler, R., Bowen, C., Beyea, S., Friedman, A., & Calkin, C. (2019) · NeuroImage: Clinical · doi:10.1016/j.nicl.2019.102049 · Cited by 108 · see citing works
Correll, C. U., Newcomer, J. W., Silverman, B. L., DiPetrillo, L., Graham, C. E., Jiang, Y., Du, Y., Simmons, A., Hopkinson, C., McDonnell, D., et al. (2020) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2020.19121279 · Cited by 120 · see citing works
Self-citationLindekilde, N., Scheuer, S. H., Rutters, F., Knudsen, L., Lasgaard, M., Rubin, K. H., Henriksen, J. E., Kivimäki, M., Andersen, G. S., & Pouwer, F. (2022) · Diabetologia · doi:10.1007/s00125-021-05609-x · Cited by 119 · see citing works
Speyer, H., Jakobsen, A. S., Westergaard, C., Nørgaard, H. C. B., Pisinger, C., Krogh, J., Hjorthøj, C., Nordentoft, M., Gluud, C., Correll, C. U., et al. (2019) · Psychotherapy and Psychosomatics · doi:10.1159/000502293 · Cited by 116 · see citing works
Self-citationBiazus, T. B., Beraldi, G. H., Tokeshi, L., Rotenberg, L. D. S., Dragioti, E., Carvalho, A. F., Solmi, M., & Lafer, B. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02109-9 · Cited by 121 · see citing works
Krogmann, A., Peters, L., von Hardenberg, L., Bödeker, K., Nöhles, V. B., & Correll, C. U. (2019) · CNS Spectrums · doi:10.1017/s109285291900124x · Cited by 116 · see citing works
Self-citationThe pharmacological management of metabolic syndrome
Larsen, J. R., Dima, L., Correll, C. U., & Manu, P. (2018) · Expert Review of Clinical Pharmacology · doi:10.1080/17512433.2018.1429910 · Cited by 117 · see citing works
Self-citationGenetic contributions to bipolar disorder: current status and future directions
O’Connell, K. S., & Coombes, B. J. (2021) · Psychological Medicine · doi:10.1017/s0033291721001252 · Cited by 115 · see citing works
Goldstein, B. I., Baune, B. T., Bond, D. J., Chen, P., Eyler, L. T., Fagiolini, A. M., Gomes, F. A., Hájek, T., Hatch, J. K., McElroy, S. L., et al. (2020) · Bipolar Disorders · doi:10.1111/bdi.12921 · Cited by 112 · see citing works
Calabrese, J. R., Durgam, S., Satlin, A., Vanover, K. E., Davis, R. E., Chen, R., Kozauer, S. G., Mates, S. L., & Sachs, G. S. (2021) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2021.20091339 · Cited by 113 · see citing works
Lomholt, L. H., Andersen, D. V., Sejrsgaard-Jacobsen, C., Øzdemir, C. M., Graff, C., Schjerning, O., Jensen, S. E., Straszek, S. P. V., Licht, R. W., Grøntved, S., et al. (2019) · International Journal of Bipolar Disorders · doi:10.1186/s40345-018-0140-x · Cited by 106 · see citing works
Vancampfort, D., Firth, J., Stubbs, B., Schuch, F. B., Rosenbaum, S., Hallgren, M. Å., Deenik, J., Ward, P. B., Mugisha, J., Damme, T. V., et al. (2025) · World Psychiatry · doi:10.1002/wps.21314 · Cited by 117 · see citing works
Self-citationSkonieczna‐Żydecka, K., Łoniewski, I., Misera, A., Stachowska, E., Maciejewska, D., Marlicz, W. M., & Galling, B. (2018) · Psychopharmacology · doi:10.1007/s00213-018-5102-6 · Cited by 101 · see citing works
Self-citationCzosnek, L., Lederman, O., Cormie, P., Zopf, E., Stubbs, B., & Rosenbaum, S. (2019) · Mental Health and Physical Activity · doi:10.1016/j.mhpa.2018.11.001 · Cited by 94 · see citing works
Self-citationFirth, J., Veronese, N., Cotter, J., Shivappa, N., Hébert, J. R., Ee, C., Smith, L., Stubbs, B., Jackson, S. E., & Sarris, J. J. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00350 · Cited by 97 · see citing works
Self-citationCorrell, C. U., Sikich, L., Reeves, G. M., Johnson, J. L., Keeton, C. P., Spanos, M., Kapoor, S., Bussell, K., Miller, L., Chandrasekhar, T., et al. (2020) · World Psychiatry · doi:10.1002/wps.20714 · Cited by 97 · see citing works
Self-citationAshdown‐Franks, G., Stubbs, B., Koyanagi, A., Schuch, F. B., Firth, J., Veronese, N., & Vancampfort, D. (2018) · Journal of Affective Disorders · doi:10.1016/j.jad.2018.09.036 · Cited by 97 · see citing works
Self-citationAssociation of Schizophrenia With the Risk of Breast Cancer Incidence
Zhuo, C., & Triplett, P. T. (2018) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2017.4748 · Cited by 96 · see citing works
Obesity: pathophysiology and therapeutic interventions
Kong, Y., Yang, H., Nie, R., Zhang, X., Zuo, F., Zhang, H., & Nian, X. (2025) · Molecular Biomedicine · doi:10.1186/s43556-025-00264-9 · Cited by 89 · see citing works
Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia
Hackinger, S., Prins, B. P., Mamakou, V., Zengini, E., Marouli, E., Brčić, L., Serafetinidis, I., Lamnissou, K., Kontaxakis, V. P., Dedoussis, G. V., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0304-6 · Cited by 86 · see citing works
Antioxidant Properties of Second-Generation Antipsychotics: Focus on Microglia
Caruso, G., Grasso, M., Fidilio, A., Tascedda, F., Drago, F., & Caraci, F. (2020) · Pharmaceuticals · doi:10.3390/ph13120457 · Cited by 88 · see citing works
Ashdown‐Franks, G., Williams, J., Vancampfort, D., Firth, J., Schuch, F. B., Hubbard, K., Craig, T., Gaughran, F., & Stubbs, B. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.06.058 · Cited by 87 · see citing works
Self-citationRossom, R. C., Hooker, S. A., O’Connor, P. J., Crain, A. L., & Sperl‐Hillen, J. M. (2022) · Journal of the American Heart Association · doi:10.1161/jaha.121.021444 · Cited by 86 · see citing works
Krivoy, A., Onn, R., Vilner, Y., Hochman, E., Weizman, S., Paz, A., Hess, S., Sagy, R., Kamhi-Nesher, S., Kalter, E., et al. (2017) · EBioMedicine · doi:10.1016/j.ebiom.2017.11.027 · Cited by 86 · see citing works
Gómez‐Revuelta, M., Pelayo‐Terán, J. M., Juncal‐Ruíz, M., Vázquez-Bourgón, J., Suárez‐Pinilla, P., Romero-Jiménez, R., Setién‐Suero, E., Ayesa‐Arriola, R., & Crespo‐Facorro, B. (2020) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyaa004 · Cited by 90 · see citing works
Atypical antipsychotics, insulin resistance and weight; a meta-analysis of healthy volunteer studies
Burghardt, K. J., Seyoum, B., Mallisho, A., Burghardt, P. R., Kowluru, R. A., & Yi, Z. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.01.004 · Cited by 82 · see citing works
Solmi, M., Tiihonen, J., Lähteenvuo, M., Tanskanen, A. J., Correll, C. U., & Taipale, H. T. (2021) · Schizophrenia Bulletin · doi:10.1093/schbul/sbab087 · Cited by 82 · see citing works
Self-citationLi, N., Zhou, T. G., & Fei, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158281 · Cited by 83 · see citing works
The Role of Physical Exercise in Chronic Musculoskeletal Pain: Best Medicine—A Narrative Review
la Corte‐Rodríguez, H. D., Román-Belmonte, J. M., Luis, C. R., Madrid-Gonzalez, J., & Rodriguez-Merchan, E. C. (2024) · Healthcare · doi:10.3390/healthcare12020242 · Cited by 86 · see citing works
Hansen, P. S., Laursen, M. F., Grøntved, S., Straszek, S. P. V., Licht, R. W., & Nielsen, R. E. (2018) · Bipolar Disorders · doi:10.1111/bdi.12684 · Cited by 79 · see citing works
Brain age in bipolar disorders: Effects of lithium treatment
Gestel, H. V., Franke, K., Petite, J., Slaney, C., Garnham, J. S., Helmick, C. A., Johnson, K., Uher, R., Alda, M., & Hájek, T. (2019) · Australian & New Zealand Journal of Psychiatry · doi:10.1177/0004867419857814 · Cited by 79 · see citing works
Correll, C. U., Ng‐Mak, D., Stafkey-Mailey, D., Farrelly, E., Rajagopalan, K., & Loebel, A. D. (2017) · Annals of General Psychiatry · doi:10.1186/s12991-017-0133-7 · Cited by 78 · see citing works
Self-citationVeronese, N., Stubbs, B., Solmi, M., Ajnakina, O., Carvalho, A. F., & Maggi, S. (2017) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000537 · Cited by 77 · see citing works
Self-citationMarques, A., Gómez‐Baya, D., Peralta, M., Frasquilho, D., Santos, T., Martins, J., Ferrari, G., & de Matos, M. G. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17165674 · Cited by 77 · see citing works
Hassan, L., Peek, N. B., Lovell, K., Carvalho, A. F., Solmi, M., Stubbs, B., & Firth, J. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01344-2 · Cited by 75 · see citing works
Self-citationRobinson, D. J., Hanson, K., Jain, A. B., Kichler, J. C., Mehta, G., Melamed, O. C., Vallis, M., Bajaj, H. S., Barnes, T., Gilbert, J., et al. (2023) · Canadian Journal of Diabetes · doi:10.1016/j.jcjd.2023.04.009 · Cited by 73 · see citing works
Stubbs, B., Koyanagi, A., Schuch, F. B., Firth, J., Rosenbaum, S., Gaughran, F., Mugisha, J., & Vancampfort, D. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbw111 · Cited by 72 · see citing works
Self-citationTrends in utilization and dosing of antipsychotic drugs in Scandinavia: Comparison of 2006 and 2016
Højlund, M., Pottegård, A., Johnsen, E., Kroken, R. A., Reutfors, J., Munk‐Jørgensen, P., & Correll, C. U. (2019) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.13945 · Cited by 68 · see citing works
Self-citationIlyas, A., Chesney, E., & Patel, R. (2017) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.117.203240 · Cited by 71 · see citing works
Harding, J. L., Weber, M. B., & Shaw, J. E. (2024) · Wiley eBooks · doi:10.1002/9781119697473.ch3 · Cited by 78 · see citing works
Rosa, C. D., Sampogna, G., Luciano, M., Vecchio, V. D., Pocai, B., Borriello, G., Giallonardo, V., Savorani, M., Pinna, F., Pompili, M., et al. (2017) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2017.1325321 · Cited by 68 · see citing works
Ayerbe, L., Forgnone, I., Foguet-Boreu, Q., González, E., Addo, J., & Ayis, S. (2018) · Psychological Medicine · doi:10.1017/s0033291718000302 · Cited by 57 · see citing works
Gomes‐da‐Costa, S., Marx, W., Corponi, F., Anmella, G., Murru, A., Pons-Cabrera, M. T., Giménez‐Palomo, A., Gutiérrez-Arango, F., Llach, C.-D., Fico, G., et al. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.07.011 · Cited by 67 · see citing works
Li, S., Yang, D., Zhou, C., Chen, L., Liu, L., Lin, R., Li, X., Liu, Y., Qiu, H., Cao, H., et al. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14497 · Cited by 71 · see citing works
Svensson, C. K., Larsen, J. R., Vedtofte, L., Jakobsen, M. S. L., Jespersen, H. R., Jakobsen, M. I., Koyuncu, K., Schjerning, O., Nielsen, J., Ekstrøm, C. T., et al. (2019) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12982 · Cited by 66 · see citing works
Self-citationSemaglutide Treatment of Antipsychotic-Treated Patients With Schizophrenia, Prediabetes, and Obesity
Ganeshalingam, A. A., Uhrenholt, N. G., Arnfred, S., Gæde, P., Düring, S. W., Stenager, E. N., Bünger, N., Pedersen, A. K., Bilenberg, N., & Frystyk, J. (2025) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2025.2332 · Cited by 68 · see citing works
Neurobiological effects of aerobic exercise, with a focus on patients with schizophrenia
Maurus, I., Hasan, A., Röh, A., Takahashi, S., Rauchmann, B., Keeser, D., Malchow, B., Schmitt, A., & Falkai, P. (2019) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-019-01025-w · Cited by 62 · see citing works
Croatto, G., Vancampfort, D., Miola, A., Olivola, M., Fiedorowicz, J. G., Firth, J., Alexinschi, O., Gaina, M. A., Makkai, V., Soares, F. C., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-022-01770-w · Cited by 66 · see citing works
Self-citationThe evidence for physical activity in the management of major mental illnesses
Ashdown‐Franks, G., Sabiston, C. M., & Stubbs, B. (2019) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000526 · Cited by 64 · see citing works
Self-citationRomain, A. J., Marleau, J. D., & Baillot, A. (2017) · Journal of Affective Disorders · doi:10.1016/j.jad.2017.08.065 · Cited by 63 · see citing works
The Gut Microbiome in Schizophrenia and the Potential Benefits of Prebiotic and Probiotic Treatment
Liu, J. C. W., Gorbovskaya, I., Hahn, M., & Müller, D. J. (2021) · Nutrients · doi:10.3390/nu13041152 · Cited by 65 · see citing works
Possidente, C., Fanelli, G., Serretti, A., & Fabbri, C. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105298 · Cited by 60 · see citing works
New Advances in the Pharmacology and Toxicology of Lithium: A Neurobiologically Oriented Overview
Bortolozzi, A. A., Fico, G., Berk, M., Solmi, M., Fornaro, M., Quevedo, J., Zarate, C. A., Kessing, L. V., Vieta, E., & Carvalho, A. F. (2024) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000007 · Cited by 63 · see citing works
Pełka-Wysiecka, J., Kaczmarczyk, M., Bąba-Kubiś, A., Liśkiewicz, P., Wroński, M., Skonieczna-Żydecka, K., Marlicz, W., Misiak, B., Starzyńska, T., Kucharska-Mazur, J., et al. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8101605 · Cited by 59 · see citing works
Wang, R., Bishwajit, G., Zhou, Y., Wu, X. L., Feng, D., Tang, S., Chen, Z., SHAW, I. F., Wu, T., Song, H., et al. (2019) · PLoS ONE · doi:10.1371/journal.pone.0221430 · Cited by 60 · see citing works
- Authors
- Vancampfort, D., Correll, C. U., Galling, B., Probst, M., De Hert, M., Ward, P. B., Rosenbaum, S., Gaughran, F., Lally, J., & Stubbs, B.
- Affiliations
- KU Leuven (BE)
- Hofstra University (US)
- Zucker Hillside Hospital (US)
- KU Leuven ‐ University of Leuven, Z.org KU Leuven Kortenberg Belgium
- UNSW Sydney (AU)
- King's College London (GB)
- ORCID
- Venue
- World Psychiatry
- Publisher
- Wiley
- Published
- 2016-06
- Volume
- 15
- Issue
- 2
- Pages
- 166-174
- ISSN
- 1723-8617 (ISSN-L)
- 2051-5545
- PMC
- PMC4911762
- OpenAlex
- W2414864695
- Semantic Scholar
- ed66999de667844601bb084a362cd63d6d85944f
- Cited by
- 659
- References
- 53
- Citations by year
- 2026: 52 · 2025: 55 · 2024: 42 · 2023: 70 · 2022: 54 · 2021: 92 · 2020: 71 · 2019: 75 · 2018: 73 · 2017: 57 · 2016: 17
- FWCI
- 10.63
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- World Psychiatry (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Research Portal (King's College London) (submittedVersion, other-oa)
- Lirias (submittedVersion, other-oa)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
- Keywords
- type 2 diabetes, severe mental illness, schizophrenia, bipolar disorder, major depressive disorder, antipsychotic drugs, diabetes prevalence, sex differences, aripiprazole, amisulpride, diabetes screening, cardiovascular risk
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.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-10.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-10.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review