Evidence map›Paper›PMID 40680237›Full record

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

Using machine-learning to identify differences in the association between blood-based biomarkers and later life health across race and ethnicity.

Mateo P Farina, Eric T Klopack, Eileen M Crimmins

Abstract read
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. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Mateo P FarinaDepartment of Human Development and Family Science and the Population Research Center, University of Texas at Austin, Austin, Texas, United States.ORCID 0000-0002-0765-6550
Eric T KlopackDavis School of Gerontology, University of Southern California Los Angeles California, United States.ORCID 0000-0002-0019-1332
Eileen M CrimminsDavis School of Gerontology, University of Southern California Los Angeles California, United States.

Funding

USC/UCLA Center on Biodemography &Population HealthP30AG017265 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JENNIFER A AILSHIRE · 1999 to 2026
$17.9M
Scientific & Technical CoreP2CHD042849 · NICHD · UNIVERSITY OF TEXAS AT AUSTIN · PI MARK D. HAYWARD · 2017 to 2026
$5.2M
Biological Underpinnings of Socioeconomic Differentials in Health and MortalityR01AG060110 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CRIMMINS, EILEEN M · 2018 to 2022
$2.6M
Epigenetic Mechanisms Linking Lifetime Social and Environmental Exposures to Cognitive AgingR00AG076964 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI FARINA, MATTHEW · 2024 to 2024
$249k
Austin by the Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentHealth and Retirement StudyNIA NIH HHS NIA U01AG009740NIA NIH HHS P30 AG017265NIA NIH HHS R00 AG076964NIA NIH HHS R01 AG060110NICHD NIH HHS P2C HD042849NIH HHSNIH HHS P2CHD042849NIH HHS P30AG017265NIH HHS R00AG076964NIH HHS R01AG060110Population Research CenterThe University of TexasUniversity of Michigan
6 · The paper itself

Abstract

Increasingly, biomarkers are used to understand health and health inequalities among older adults. Combined with advancements in machine-learning approaches, researchers are using predictive algorithms of later life health to identify biomarkers of interest and create biological risk scores. However, these algorithms may select biomarkers that are most important for the majority populations, which, in most population-based samples, would reflect the health and aging of White older adults. Understanding how biomarker selection varies across race/ethnicity across different types of health outcomes is paramount to advancing GeroScience research. We used the 2016 Venous Blood Substudy (VBS) of the Health and Retirement Study. We fit race-stratified boosted decision tree models to predict all-cause mortality, multimorbidity, diabetes, and heart conditions from 54 biomarkers in the 2016 VBS that covered 11 biological systems. We, then, graphed biomarkers that had feature values above .01 for each algorithm to show racial/ethnic differences in biomarker selection. We found more variation in biomarker selection across racial/ethnic groups for all-cause mortality. We found little variation in biomarker selection for heart conditions and diabetes. There was some variation for multimorbidity but with substantial overlap across racial/ethnic groups. Although machine-learning approaches for developing biological risk scores and identifying biomarkers linked to later life health will yield additional insight into aging processes in human populations, researchers must consider how these approaches may differ across race/ethnicity for different types of health conditions and its potential implications for GeroScience research.

Indexed as

BiomarkersEthnicityMachine LearningRacial GroupsAgedAged, 80 and overAgingDiabetes MellitusFemaleHumansMaleMiddle AgedUnited StatesBiomarkersbiodemographybiomarkersmachine learningracial/ethnic groups

Identifiers

PMID40680237
PMCPMC12360776

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.