Evidence map›Paper›PMID 32422015›Full record

ReviewCritical reviews in immunology2019

Defining Early Life Stress as a Precursor for Autoimmune Disease.

Jamie Y Choe, Maya Nair, Riyaz Basha, Byung-Jin Kim, Harlan P Jones

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Adverse childhood experiences in patients with psoriasis.Trends in psychiatry and psychotherapy · 2022
    Article
  3. Article
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

5 authors at 3 institutions in 1 country.

Jamie Y ChoeDepartment of Microbiology, Immunology and Genetics, Graduate School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, Texas 76107; Texas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, Texas 76107.
Maya NairDepartment of Microbiology, Immunology and Genetics, Graduate School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, Texas 76107.
Riyaz BashaTexas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, Texas 76107.
Byung-Jin KimDepartment of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Harlan P JonesDepartment of Microbiology, Immunology and Genetics, Graduate School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, Texas 76107.
University of North Texas · USJohns Hopkins Medicine · USTexas College · US

Funding

Texas Center for Minority Health, Education, Research and OutreachU54MD006882 · NIMHD · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI VISHWANATHA, JAMBOOR K. · 2017 to 2022
$6.0M
Promoting Diversity in Research Training for Health ProfessionalsR25HL125447 · NHLBI · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI RANJAN, AMALENDU PRAKASH · 2016 to 2020
$1.0M
2/2 Pilot Project 2: Langston University-UNTHSC Partnership for Cancer Research and EducationP20CA233355 · NCI · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI BASHA, RIYAZ · 2018 to 2021
$1.0M
NCI NIH HHS P20 CA233355NHLBI NIH HHS R25 HL125447NIMHD NIH HHS U54 MD006882
6 · The paper itself

Abstract

Childhood exposure to traumatic events, termed early life stress (ELS), is now widely recognized for causing long-term negative health effects that may not manifest until adulthood. Allostatic load (AL) describes the cumulative "wear-and-tear" effects of chronic stress on the body that may adversely affect human health by accelerating other disease processes. Recent epidemiological studies have reported higher stress levels in industrialized countries and trends of increasing prevalence in autoimmune diseases during recent decades. To elucidate mechanisms of stress-related immune dysregulation, most animal studies up to now have focused on AL and stress-triggered events occurring in adults but have not explored ELS in the context of autoimmune disorders. We have identified a current gap in understanding the impact of ELS on immune system ontogeny and its potential for priming genetically susceptible individuals who are at increased risk for autoimmune diseases later in life, through mechanisms involving neuroendocrine-immune cross talk. In this review, we highlight the intersection between stress and immune function, with a focus on ELS as consequential for increased autoimmune disorder risks later in life.

Indexed as

AdultAnimalsAutoimmune DiseasesChildGene-Environment InteractionGenetic Predisposition to DiseaseHumansPrevalenceStress, Psychological

Identifiers

PMID32422015
PMCPMC11102636
OpenAlexW2998890012

What OpenQuestion holds

Textmetadata
LicenceTDM
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.