Evidence map›Paper›PMID 37343002›Full record

ArticlePloS one2023

Biological expressions of early life trauma in the immune system of older adults.

Grace A Noppert, Kate A Duchowny, Rebecca Stebbins, Allison E Aiello, Jennifer B Dowd, Philippa Clarke

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 7% of its field
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

6 authors at 5 institutions in 2 countries.

Grace A NoppertInstitute for Social Research, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0002-2040-960X
Kate A DuchownyInstitute for Social Research, University of Michigan, Ann Arbor, Michigan.
Rebecca StebbinsSocial, Genetic, & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology, and Neuroscience, King's College London, London, United Kingdom.
Allison E AielloCarolina Population Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Jennifer B DowdLeverhulme Centre for Demographic Science, University of Oxford, Oxford, United Kingdom.
Philippa ClarkeInstitute for Social Research, University of Michigan, Ann Arbor, Michigan.
University of Michigan · USKing's College London · GBLeverhulme Trust · GBUniversity of California, San Francisco · USUniversity of North Carolina at Chapel Hill · US

Funding

Research Education CoreP30AG024824 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Neil Alexander · 2004 to 2026
$29.2M
From Biological to Social Processes: Interdisciplinary Training in Life Course ResearchT32HD091058 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ROBERT A HUMMER, Amanda L Thompson · 2017 to 2026
$4.3M
Immunosenescence, socioeconomic disadvantage and dementia in the US aging populationR01AG075719 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Allison E Aiello, Grace A Noppert · 2022 to 2026
$3.6M
Social Disadvantage and Its Impact on Pathogen Burden and Immune Dysfunction Across the Life CourseR00AG062749 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NOPPERT, GRACE A · 2021 to 2023
$747k
Examining the role of the neighborhood environment on muscle function in older adultsR00AG066846 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DUCHOWNY, CATHERINE · 2023 to 2025
$742k
Examining the role of the neighborhood environment on muscle function in older adultsK99AG066846 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DUCHOWNY, CATHERINE · 2021 to 2022
$250k
NIA NIH HHS K99 AG066846NIA NIH HHS P30 AG024824NIA NIH HHS R00 AG062749NIA NIH HHS R00 AG066846NIA NIH HHS R01 AG075719NICHD NIH HHS T32 HD091058
6 · The paper itself

Abstract

backgroundPoor immune function is associated with increased risk for a number of age-related diseases, however, little is known about the impact of early life trauma on immune function in late-life.

methodsUsing nationally representative data from the Health and Retirement Study (n = 5,823), we examined the association between experiencing parental/caregiver death or separation before age 16 and four indicators of immune function in late-life: C-reactive Protein (CRP), Interleukin-6 (IL-6), soluble Tumor Necrosis Factor (sTNFR), and Immunoglobulin G (IgG) response to cytomegalovirus (CMV). We also examined racial/ethnic differences.

findingsIndividuals that identified as racial/ethnic minorities were more likely to experience parental/caregiver loss and parental separation in early life compared to Non-Hispanic Whites, and had poorer immune function in late-life. We found consistent associations between experiencing parental/caregiver loss and separation and poor immune function measured by CMV IgG levels and IL-6 across all racial/ethnic subgroups. For example, among Non-Hispanic Blacks, those that experienced parental/caregiver death before age 16 had a 26% increase in CMV IgG antibodies in late-life (β = 1.26; 95% CI: 1.17, 1.34) compared to a 3% increase in CMV antibodies among Non-Hispanic Whites (β = 1.03; 95% CI: 0.99, 1.07) controlling for age, gender, and parental education.

interpretationOur results suggest a durable association between experiencing early life trauma and immune health in late-life, and that structural forces may shape the ways in which these relationships unfold over the life course.

Indexed as

Cytomegalovirus InfectionsInterleukin-6AdolescentAgedHumansImmune SystemImmunoglobulin GUnited StatesWhiteImmunoglobulin GInterleukin-6

Identifiers

PMID37343002
PMCPMC10284407
OpenAlexW4381486650

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.