Evidence map›Paper›PMID 38807566›Full record

ArticleBiodemography and social biology

Racial/Ethnic differences in inflammation levels among older adults 56+: an examination of sociodemographic differences across inflammation measure.

K J Davidson-Turner, Mateo P Farina, Mark D Hayward

Abstract read
In one paragraph

Article in Biodemography and social biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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

8 citing papers in PubMed.

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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.

K J Davidson-TurnerDepartment of Sociology, University of Texas at Austin, Austin, Texas, USA.ORCID 0009-0007-9828-7829
Mateo P FarinaDepartment of Human Development and Family Sciences, University of Texas at Austin, Austin, Texas, USA.
Mark D HaywardDepartment of Sociology, University of Texas at Austin, Austin, Texas, USA.

Funding

HRS Yrs29-34: Y33 SSA CoFundingU01AG009740 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jessica Faul, KENNETH M LANGA · 1990 to 2026
$555.8M
RESEARCH TRAINING IN GERONTOLOGYT32AG000037 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JENNIFER A AILSHIRE, EILEEN M CRIMMINS · 1985 to 2026
$13.2M
Program Development and Pilot CoreP30AG066614 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI KAREN L FINGERMAN · 2020 to 2026
$5.2M
Scientific & Technical CoreP2CHD042849 · NICHD · UNIVERSITY OF TEXAS AT AUSTIN · PI Catherine A Calder · 2017 to 2026
$5.2M
Education, Early Life Conditions, and Trends in DementiaR56AG057778 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI HAYWARD, MARK D. · 2018 to 2018
$411k
Epigenetic Mechanisms Linking Lifetime Social and Environmental Exposures to Cognitive AgingR00AG076964 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI FARINA, MATTHEW · 2024 to 2024
$249k
Epigenetic Mechanisms Linking Lifetime Social and Environmental Exposures to Cognitive AgingK99AG076964 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI FARINA, MATTHEW · 2022 to 2023
$200k
NIA NIH HHS K99 AG076964NIA NIH HHS P30 AG066614NIA NIH HHS R00 AG076964NIA NIH HHS R56 AG057778NIA NIH HHS T32 AG000037NIA NIH HHS U01 AG009740NICHD NIH HHS P2C HD042849
6 · The paper itself

Abstract

objectiveChronic inflammation is a key biological risk factor for many widespread adult health conditions. This study examines racial/ethnic differences in inflammation across several inflammatory markers, including selected cytokines that are identified as important for aging and age-related health outcomes.

methodsData came from the 2016 Venous Blood Collection Subsample of the Health and Retirement Study. Using logistic regression models, we compared high-risk categories of C-reactive protein and cytokine markers (IL-6, IL-10, IL-1RA, TNFR1, and TGF-Beta), across race/ethnicity and whether these differences persisted among men and women.

resultsThe findings provided evidence of significant race/ethnic differences in inflammatory measures, but the patterns differed across marker types.

conclusionsThese findings emphasize that race/ethnic differences are not consistently captured across markers of inflammation and that researchers should proceed with caution when using individual markers of inflammation in an effort to not overlook potential racial/ethnic differences in biological risk.

Indexed as

BiomarkersEthnicityInflammationAgedAged, 80 and overC-Reactive ProteinCytokinesFemaleHumansLogistic ModelsMaleMiddle AgedRacial GroupsRisk FactorsSociodemographic FactorsUnited StatesBiomarkersC-Reactive ProteinCytokines

Identifiers

PMID38807566
PMCPMC11257156

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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.