Evidence map›Paper›PMID 41221791›Full record

ArticleDiabetes, obesity & metabolism2026

Estimating the risk of cardiovascular outcomes and all-cause mortality in individuals with type 2 diabetes: Validation of the UKPDS outcomes model using TECOS and EXSCEL data.

Ruth L Coleman, Amanda I Adler, Philip M Clarke, Darren K McGuire, Rury R Holman

Abstract readValidation Study
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Article in Diabetes, obesity & metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ruth L ColemanDiabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.ORCID 0000-0002-5194-8550
Amanda I AdlerDiabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Philip M ClarkeHealth Economics Research Centre, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Darren K McGuireDivision of Cardiology, Department of Medicine, University of Texas Southwestern Medical Center and Parkland Health and Hospital System, Dallas, Texas, USA.
Rury R HolmanDiabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

Funding

Amylin PharmaceuticalsMerck Sharp and Dohme USNational Institute for Health Research Oxford Biomedical Research Centre
6 · The paper itself

Abstract

aimsTo evaluate United Kingdom Prospective Diabetes Study Outcomes Model version 2 (UKPDS-OM2) cardiovascular risk estimates for people with type 2 diabetes using TECOS and EXSCEL data. MATERIALS AND

methodsWe compared model-simulated and TECOS and EXSCEL observed event rates for the composite outcome of cardiovascular death, myocardial infarction (MI) or stroke, each component, and all-cause mortality. Risk factors analysed were age, sex, race/ethnicity, height, diabetes duration, atrial fibrillation, albuminuria, and baseline plus annual measures of smoking, HDL-cholesterol, LDL-cholesterol, weight, systolic blood pressure, HbA

resultsMedian follow-up was 3.0 and 3.2 years for the 14 671 TECOS and 14 752 EXSCEL participants, respectively. The primary outcome occurred in TECOS for 839 (11.4%) and 851 (11.6%) sitagliptin and placebo group participants, respectively (hazard ratio [HR] 0.98, 95%CI 0.89-1.08), compared with UKPDS-OM2 simulated events of 776 (10.6%) and 778 (10.6%), respectively (relative risk 1.00). The primary outcome occurred in EXSCEL for 839 (11.4%) and 905 (12.2%) once-weekly exenatide and placebo group participants, respectively (HR 0.92, 95%CI 0.84-1.01), compared with UKPDS-OM2-simulated events of 579 (7.9%) and 593 (8.0%), respectively (relative risk 0.98).

conclusionsUKPDS-OM2 accurately simulated relative risks between randomized groups in both trials. The proportion of participants with the primary outcome was accurately estimated in both TECOS arms but underestimated by around one-third in both EXSCEL arms.

Indexed as

Cardiovascular DiseasesDiabetes Mellitus, Type 2Diabetic AngiopathiesAgedCause of DeathFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedProspective StudiesRisk AssessmentRisk FactorsUnited Kingdomcardiovascular risk estimatesmortalitymyocardial infarctiontype 2 diabetesUKPDS outcomes model

Identifiers

PMID41221791
PMCPMC12803570

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.