Evidence map›Paper›PMID 40580468›Full record

ArticleThe journals of gerontology. Series B, Psychological sciences and social sciences2025

Does the southern health disadvantage extend to accelerated biological aging: evidence from the health and retirement study.

Addam Reynolds, Mateo P Farina, Eileen Crimmins

Abstract read
In one paragraph

Article in The journals of gerontology. Series B, Psychological sciences and social sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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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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

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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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Addam ReynoldsAndrus Gerontology Center, Los Angeles, California, United States.
Mateo P FarinaDepartment of Human Development, University of Texas, Austin, Texas, United States.ORCID 0000-0002-0765-6550
Eileen CrimminsLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, United States.

Funding

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
NIA NIH HHS R00AG076964NIA NIH HHS R01 AG060110
6 · The paper itself

Abstract

objectivesRecent studies have shown worse health across various conditions (i.e., morbidity, disability, and mortality) among residents in the U.S. South compared to other regions. Accelerated aging may be a pathway underlying part of this disadvantage; however, few studies have examined this. To address this gap in the literature, this study examines whether accelerated aging measures are associated with residence in the U.S. South in childhood and older adulthood.

methodsUsing the 2016 Venous Blood Study (VBS) of the Health and Retirement Study, we use linear regression models to examine the association between Southern residential history in childhood and adulthood and biological aging (i.e., PhenoAge, GrimAge, DunedinPACE, Expanded Biological Age, and an Epigenetic Factor Score). We also evaluate the sensitivity of these patterns, adjusting for demographic composition and health behaviors, such as age, gender/sex, parental education, educational attainment, race/ethnicity, having a higher BMI, smoking status, health insurance coverage, and preventative healthcare uptake.

resultsHaving been born and currently residing in the U.S. South is positively associated with accelerated aging measured by PhenoAge, GrimAge, DunedinPACE, our Epigenetic Factor, and Expanded Biological Age. These associations were attenuated after adjusting for demographic composition and health behaviors; only DunedinPACE, our Epigenetic Factor, and Expanded Biological Age had significant associations after the adjustment for demographic composition and health behaviors. DISCUSSION: Accelerated aging among those with residential Southern histories in childhood and adulthood may partially account for the Southern health disadvantage.

Indexed as

AgingAging, PrematureHealth Status DisparitiesAgedAged, 80 and overFemaleHumansLongitudinal StudiesMaleMiddle AgedUnited Statesaging accelerationepigenetic agingGeroScienceregionality

Identifiers

PMID40580468
PMCPMC12409411

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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.