Evidence map›Paper›PMID 40326431›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2025

Development and Validation of Mortality Prediction Models among Frail Participants in the UK Biobank Study.

Chenkai Wu, Yanxin Wang, Junhan Tang, Jianhong Xu, Jonathan K L Mak, Qian-Li Xue

Abstract readValidation Study
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Chenkai WuGlobal Health Research Center, Duke Kunshan University, Kunshan, Jiangsu, China.ORCID 0000-0002-2256-0653
Yanxin WangGlobal Health Research Center, Duke Kunshan University, Kunshan, Jiangsu, China.
Junhan TangGlobal Health Research Center, Duke Kunshan University, Kunshan, Jiangsu, China.
Jianhong XuGlobal Health Research Center, Duke Kunshan University, Kunshan, Jiangsu, China.
Jonathan K L MakDepartment of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.ORCID 0000-0003-4454-8580
Qian-Li XueDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.ORCID 0000-0001-8818-7444

Funding

Technological Assessment and Solutions Core - RC4P30AG021334 · NIA · JOHNS HOPKINS UNIVERSITY · PI Jeremy D Walston · 2003 to 2026
$33.2M
NIA NIH HHS P30 AG021334
6 · The paper itself

Abstract

backgroundIdentifying effective risk assessment strategies and prediction models for frail populations is crucial for precise mortality risk identification and improved patient management. This study aimed to evaluate whether prediction models incorporating survey data combined with biomarkers, physical measurements, or both could enhance mortality risk prediction in frail individuals than survey-only models.

methods15 754 frail participants aged 40-72 from the UK Biobank were included. We used Cox models to assess all-cause mortality risk and Light Gradient Boosting Machines for variable selection by sex. Performance was evaluated through discrimination, calibration, and reclassification.

resultsIn the survey-only models, we selected 24 predictors for males and 19 for females; age and number of treatments were the top predictors for both sexes. In the biomarker models, we selected 15 predictors for males and 24 for females. In the physical measurement models, we retained 24 predictors for males and 23 for females. The base models showed good discrimination: C-statistic was 0.73 (95% CI, 0.72-0.75) for males and 0.74 (95% CI, 0.72-0.76) for females in development, and 0.70 (95% CI, 0.65-0.75) for males and 0.78 (95% CI, 0.73-0.83) for females in validation. Although incorporating additional predictors led to some improvement in model performance, the overall enhancement was not substantial.

conclusionsSurvey-based models predicted mortality in frail individuals effectively, with only minor improvements from adding biomarkers or physical measurements. These findings highlighted the value of surveys in forecasting outcomes and informed personalized management strategies to improve health for the frail.

Indexed as

Frail ElderlyFrailtyMortalityAdultAgedBiological Specimen BanksFemaleGeriatric AssessmentHumansMaleMiddle AgedProportional Hazards ModelsRisk AssessmentUK BiobankUnited KingdomBiomarkerPhysical measurementSurvey data

Identifiers

PMID40326431
PMCPMC13376669

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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.