Evidence map›Paper›PMID 34282132›Full record

ArticleTranslational psychiatry2021

Adversity in early life and pregnancy are immunologically distinct from total life adversity: macrophage-associated phenotypes in women exposed to interpersonal violence.

Kirstin Aschbacher, Melissa Hagan, Iris M Steine, Luisa Rivera, Steve Cole, Alyssa Baccarella, Elissa S Epel, Alicia Lieberman, Nicole R Bush

Abstract read
In one paragraph

Article in Translational psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 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

9 authors.

Kirstin AschbacherDepartment of Psychiatry, Weill Institute for Neurosciences, University of California, San Francisco, USA. Kirstin.Aschbacher@ucsf.edu.ORCID http://orcid.org/0000-0001-6191-6432
Melissa HaganDepartment of Psychiatry, Weill Institute for Neurosciences, University of California, San Francisco, USA.
Iris M SteineDepartment of Psychology, University of California, Berkeley, USA.
Luisa RiveraDepartment of Anthropology, Emory University, Atlanta, Georgia.
Steve ColeDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, USA.
Alyssa BaccarellaDepartment of Pediatrics, Columbia University, New York, USA.
Elissa S EpelDepartment of Psychiatry, Weill Institute for Neurosciences, University of California, San Francisco, USA.
Alicia LiebermanDepartment of Psychiatry, Weill Institute for Neurosciences, University of California, San Francisco, USA.
Nicole R BushDepartment of Psychiatry, Weill Institute for Neurosciences, University of California, San Francisco, USA.ORCID http://orcid.org/0000-0003-0217-9975

Funding

Engaging University of California Stakeholders for Biorespository ResearchUL1TR000004 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRANDIS, JENNIFER RUBIN · 2012 to 2015
$78.0M
JPB Foundation JPB Network on Toxic StressJPB Foundation N/ANCATS NIH HHS UL1 TR000004Robert Wood Johnson Foundation (RWJF) N/AU.S. Department of Health & Human Services | SAMHSA | Center for Mental Health Services (CMHS) 5U79SM080030
6 · The paper itself

Abstract

Early childhood and pregnancy are two sensitive periods of heightened immune plasticity, when exposure to adversity may disproportionately increase health risks. However, we need deeper phenotyping to disentangle the impact of adversity during sensitive periods from that across the total lifespan. This study examined whether retrospective reports of adversity during childhood or pregnancy were associated with inflammatory imbalance, in an ethnically diverse cohort of 53 low-income women seeking family-based trauma treatment following exposure to interpersonal violence. Structured interviews assessed early life adversity (trauma exposure ≤ age 5), pregnancy adversity, and total lifetime adversity. Blood serum was assayed for pro-inflammatory (TNF-a, IL-1ß, IL-6, and CRP) and anti-inflammatory (IL-1RA, IL-4, and IL-10) cytokines. CD14+ monocytes were isolated in a subsample (n = 42) and gene expression assayed by RNA sequencing (Illumina HiSeq 4000; TruSeq cDNA library). The primary outcome was a macrophage-associated M1/M2 gene expression phenotype. To evaluate sensitivity and specificity, we contrasted M1/M2 gene expression with a second, clinically-validated macrophage-associated immunosuppressive phenotype (endotoxin tolerance) and with pro-inflammatory and anti-inflammatory cytokine levels. Adjusting for demographics, socioeconomic status, and psychopathology, higher adversity in early life (ß = .337, p = 0.029) and pregnancy (ß = .332, p = 0.032) were each associated with higher M1/M2 gene expression, whereas higher lifetime adversity (ß = -.341, p = 0.031) was associated with lower immunosuppressive gene expression. Adversity during sensitive periods was uniquely associated with M1/M2 imbalance, among low-income women with interpersonal violence exposure. Given that M1/M2 imbalance is found in sepsis, severe COVID-19 and myriad chronic diseases, these findings implicate novel immune mechanisms underlying the impact of adversity on health.

Indexed as

COVID-19Child, PreschoolCytokinesFemaleHumansMacrophagesPhenotypePregnancyRetrospective StudiesSARS-CoV-2ViolenceCytokines

Identifiers

PMID34282132
PMCPMC8289995

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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.