Cited by 321Diabetes, Cardiovascular Risks, and LipoproteinsDiabetes Management and ResearchStatistical Methods in Epidemiology

Prediction models for risk of developing type 2 diabetes: systematic literature search and independent external validation study

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Abbasi, A., Peelen, L. M., Corpeleijn, E., van der Schouw, Y. T., Stolk, R. P., Spijkerman, A. M. W., van der A, D. L., Moons, K. G. M. +3 more·2012·BMJ

Abstract

OBJECTIVE: To identify existing prediction models for the risk of development of type 2 diabetes and to externally validate them in a large independent cohort. DATA SOURCES: Systematic search of English, German, and Dutch literature in PubMed until February 2011 to identify prediction models for diabetes. DESIGN: Performance of the models was assessed in terms of discrimination (C statistic) and calibration (calibration plots and Hosmer-Lemeshow test).The validation study was a prospective cohort study, with a case cohort study in a random subcohort. SETTING: Models were applied to the Dutch cohort of the European Prospective Investigation into Cancer and Nutrition cohort study (EPIC-NL). PARTICIPANTS: 38,379 people aged 20-70 with no diabetes at baseline, 2506 of whom made up the random subcohort. OUTCOME MEASURE: Incident type 2 diabetes. RESULTS: The review identified 16 studies containing 25 prediction models. We considered 12 models as basic because they were based on variables that can be assessed non-invasively and 13 models as extended because they additionally included conventional biomarkers such as glucose concentration. During a median follow-up of 10.2 years there were 924 cases in the full EPIC-NL cohort and 79 in the random subcohort. The C statistic for the basic models ranged from 0.74 (95% confidence interval 0.73 to 0.75) to 0.84 (0.82 to 0.85) for risk at 7.5 years. For prediction models including biomarkers the C statistic ranged from 0.81 (0.80 to 0.83) to 0.93 (0.92 to 0.94). Most prediction models overestimated the observed risk of diabetes, particularly at higher observed risks. After adjustment for differences in incidence of diabetes, calibration improved considerably. CONCLUSIONS: Most basic prediction models can identify people at high risk of developing diabetes in a time frame of five to 10 years. Models including biomarkers classified cases slightly better than basic ones. Most models overestimated the actual risk of diabetes. Existing prediction models therefore perform well to identify those at high risk, but cannot sufficiently quantify actual risk of future diabetes.

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  • Most professional organizations recommended a two-stage strategy, starting with first-stage selection of people at higher risk by a questionnaire or risk score and followed by second-stage testing for conventional biomarkers such as FPG, HbA1c, or OGTT.

    “Most of them recommended a two-stage strategy, starting with the first-stage of selection of people at higher risk by a questionnaire or risk score and followed by the second-stage of testing for conventional biomarkers such as FPG, HbA1c, or OGTT [12,39].”

    From A Novel Testing Model for Opportunistic Screening of Pre-Diabetes and Diabetes among U.S. Adults (2015) · cites this paper as [39]

    The Introduction (page not supplied) says European guidelines and the International Diabetes Federation recommend a questionnaire or risk score to identify people at high risk; it describes a different screening recommendation from the American Diabetes Association. The paper discusses models incorporating biomarkers, but our copy does not say that most professional organizations recommend the claimed two-stage sequence or subsequent FPG, HbA1c, or OGTT testing. (LLM, conf=0.85)

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Authors
Abbasi, A., Peelen, L. M., Corpeleijn, E., van der Schouw, Y. T., Stolk, R. P., Spijkerman, A. M. W., van der A, D. L., Moons, K. G. M., Navis, G., Bakker, S. J. L., & Beulens, J. W. J.
Affiliations
  • University Medical Center Groningen (NL)
  • University Medical Center Utrecht (NL)
  • National Institute for Public Health and the Environment (NL)
Corresponding author
Abbasi, A.
Venue
BMJ
Publisher
BMJ
Published
2012-09-18
Volume
345
Issue
sep18 2
Pages
e5900-e5900
ISSN
1756-1833 (ISSN-L)
OpenAlex
W2133466960
Cited by
321
References
10
Citations by year
2026: 15 · 2025: 11 · 2024: 13 · 2023: 13 · 2022: 19 · 2021: 29 · 2020: 42 · 2019: 26 · 2018: 18 · 2017: 34 · 2016: 28 · 2015: 27 · 2014: 21 · 2013: 24 · 2012: 1
FWCI
18.73
Type
journal article
Language
en
Open access
Licence
cc-by-nc
Locations
  • BMJ (publishedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
  • Pure Amsterdam UMC (publishedVersion, other-oa)
  • Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion, other-oa)
  • University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, other-oa)
  • Rivm (National Institute for Public Health and the Environment) (submittedVersion)
  • Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
Funders
  • Nierstichting
  • Diabetes Fonds
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
  • Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Epidemiology
Keywords
type 2 diabetes, diabetes risk prediction models, external validation, discrimination (statistics), calibration, biomarkers, glucose concentration, EPIC-NL cohort, new-onset diabetes, risk overestimation
MeSH terms
Adult, Aged, Blood Glucose, Data Interpretation, Statistical, Diabetes Mellitus, Type 2, Europe, Female, Humans, Male, Middle Aged, Risk Factors, Reproducibility of Results, Models, Statistical, Cohort Studies, Biomarkers, Incidence, Confidence Intervals, MEDLINE, Risk Assessment

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