Evidence map›Paper›PMID 40417914›Full record

ArticleBiometrics2025

A semicompeting risks model with an application to UK Biobank data to identify risk factors for diabetes onset and progression.

Md Tuhin Sheikh, Hongyu Zhao

Abstract read
In one paragraph

Article in Biometrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Md Tuhin SheikhDepartment of Biostatistics, Yale University, New Haven, CT 06510, United States.
Hongyu ZhaoDepartment of Biostatistics, Yale University, New Haven, CT 06510, United States.

Funding

Statistical Methods for Genetic Risk Predictions across Diverse PopulationsR01HG012735 · NHGRI · YALE UNIVERSITY · PI ZHAO, HONGYU · 2022 to 2025
$2.4M
NHGRI NIH HHS R01 HG012735NIH HHS R01 HG012735
6 · The paper itself

Abstract

Type 2 diabetes (T2D) is a major health concern worldwide with multiple disease stages, including onset, progression to complications, and death. Understanding the roles of genetic and nongenetic factors at different disease stages is crucial for gaining insights into disease etiology, possible prevention, and treatment strategies. The UK Biobank (UKB) is a valuable resource for studying complex diseases, including T2D, with comprehensive data from half a million volunteer participants. However, the UKB data present some unique challenges due to their semicompeting risks structure, involving 2 nonterminal events (T2D and complications) and one terminal event (death). In this paper, we propose a new shared gamma frailty-based semicompeting risks model within the Bayesian framework to account for subsequent nonterminal and terminal events and enable appropriate analysis. We further propose incorporating prevalent cases, that is, individuals with diabetes at enrollment, to gain more insights into the progression to complications and complications to death. To integrate prevalent cases, we introduce a power prior approach that leads to improved model fit and more efficient estimates. Simulation results demonstrate the efficacy of our modeling framework. We apply our method to identify the impacts of various risk factors at different stages of T2D development.

Indexed as

Biological Specimen BanksDiabetes Mellitus, Type 2Models, StatisticalBayes TheoremComputer SimulationDisease ProgressionFemaleHumansMaleRisk AssessmentRisk FactorsUK BiobankUnited KingdomBayesian survival analysisgamma frailty modelpower priorprevalent datatype 2 diabetes

Identifiers

PMID40417914
PMCPMC12104815

What OpenQuestion holds

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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.