Evidence map›Paper›PMID 40415079›Full record

ArticleAging clinical and experimental research2025

Heterogeneity in mortality risk prediction: a study of vulnerable adults in the Canadian longitudinal study on aging.

Mame Fana Ndiaye, Mark R Keezer, Quoc Dinh Nguyen

Abstract read
In one paragraph

Article in Aging clinical and experimental research, 2025. 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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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Mame Fana NdiayeResearch Centre of the Centre Hospitalier de l'Université de Montréal (CRCHUM), Montreal, Canada.
Mark R KeezerResearch Centre of the Centre Hospitalier de l'Université de Montréal (CRCHUM), Montreal, Canada.
Quoc Dinh NguyenResearch Centre of the Centre Hospitalier de l'Université de Montréal (CRCHUM), Montreal, Canada. quoc.dinh.nguyen@umontreal.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMortality prediction models are essential for clinical decision-making, but their performance may vary across patient subgroups. This study aimed to evaluate how a general mortality prediction model performs across subgroups defined by vulnerability factors and to test whether model improvements could improve prediction accuracy.

methodsWe analyzed data from 49,266 participants in the Canadian Longitudinal Study on Aging. A general mortality prediction model (Model A) was developed using Cox proportional hazard regression with LASSO, incorporating variables spanning sociodemographic factors, lifestyle habits, comorbidities, and physical/cognitive function measures. Performance was evaluated across subgroups defined by age, frailty, multimorbidity, cognitive function, and functional impairment using discrimination (c-index), calibration, and Brier scores. We tested two additional strategies: incorporating subgroup-specific variables (Model B) and developing tailored models for different mortality risk categories (Models C1, C2, C3).

resultsOver a median 6-year follow-up, 7.5% (3672) participants died. The general model performed well overall (c-index: 0.82, 95% CI 0.80-0.84; Brier: 0.036, 95% CI 0.032-0.040), but performance varied across subgroups. It was lower in frail individuals (c-index: 0.73, 95% CI 0.71-0.75; Brier: 0.12, 95% CI 0.11-0.13) and those with multiple chronic conditions (c-index: 0.76, 95% CI 0.75-0.78; Brier: 0.08, 95% CI 0.07-0.08), with risk underestimated in these groups. Neither incorporating subgroup variables nor developing risk-stratified models significantly improved performance.

conclusionImportant variability in performance, particularly in vulnerable groups, highlights the limitations of a one-size-fits-all and underscores the need for more granular predictive models that account for subpopulation-specific characteristics to enhance mortality risk prediction.

Indexed as

AgingMortalityAgedAged, 80 and overCanadaFemaleFrailtyHumansLongitudinal StudiesMaleMiddle AgedProportional Hazards ModelsRisk AssessmentRisk FactorsAging populationCLSAHealth outcomesMortality predictionPersonalized medicine

Identifiers

PMID40415079
PMCPMC12104110

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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.