Evidence map›Paper›PMID 25422961›Full record

ArticleDevelopment and psychopathology2014

Interleukin 1B gene (IL1B) variation and internalizing symptoms in maltreated preschoolers.

Kathryn K Ridout, Stephanie H Parade, Ronald Seifer, Lawrence H Price, Joel Gelernter, Paloma Feliz, Audrey R Tyrka

Open access · greenAbstract read
In one paragraph

Article in Development and psychopathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Genetic Contributions of Inflammation to Depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Pooled it
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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

7 authors at 4 institutions in 1 country.

Kathryn K RidoutButler Hospital Mood Disorders Research Program and Laboratory for Clinical and Translational Neuroscience.
Stephanie H ParadeAlpert Medical School of Brown University.
Ronald SeiferAlpert Medical School of Brown University.
Lawrence H PriceButler Hospital Mood Disorders Research Program and Laboratory for Clinical and Translational Neuroscience.
Joel GelernterYale University School of Medicine and VA CT Healthcare Center.
Paloma FelizE. P. Bradley Hospital Bradley/Hasbro Children's Research Center.
Audrey R TyrkaButler Hospital Mood Disorders Research Program and Laboratory for Clinical and Translational Neuroscience.
Brown University · USBradley Hospital · USButler Hospital · USVA Connecticut Healthcare System · US

Funding

Promoting Research Training During Psychiatry ResidencyR25MH101076 · NIMH · BROWN UNIVERSITY · PI AUDREY TYRKA · 2013 to 2026
$2.8M
Childhood Maltreatment:Biomarkers of Risk and ResilienceR01MH083704 · NIMH · BUTLER HOSPITAL (PROVIDENCE, RI) · PI TYRKA, AUDREY · 2010 to 2014
$2.6M
NIMH NIH HHS R01 MH083704NIMH NIH HHS R25 MH101076
6 · The paper itself

Abstract

Evidence now implicates inflammatory proteins in the neurobiology of internalizing disorders. Genetic factors may influence individual responses to maltreatment; however, little work has examined inflammatory genetic variants in adults and none in children. The present study examined the role of an interleukin 1B gene (IL1B) variant in preschoolers exposed to maltreatment and other forms of adversity in internalizing symptom development. One hundred ninety-eight families were enrolled, with one child (age 3-5 years) from each family. Adversity measures included child protective service documentation of moderate-severe maltreatment in the last 6 months and interview-assessed contextual stressors. Internalizing symptoms were measured using the Child Behavior Checklist and the Diagnostic Infant and Preschool Assessment. Maltreated children had higher major depressive disorder (MDD) and posttraumatic stress disorder symptoms and marginally higher internalizing symptoms on the Child Behavior Checklist. Controlling for age, sex, and race, IL1B genotype was associated with MDD symptoms (p = .002). Contextual stressors were significantly associated with MDD and posttraumatic stress disorder and marginally with internalizing symptoms. The IL1B genotype interacted with contextual stress such that children homozygous for the minor allele had more MDD symptoms (p = .045). These results suggest that genetic variants of IL1B may modulate the development of internalizing symptoms in the face of childhood adversity.

Indexed as

DepressionGene-Environment InteractionLife Change EventsMajor Depressive DisorderStress Disorders, Post-TraumaticChild AbuseChild, PreschoolFemaleHumansInterleukin-1betaMaleIL1B protein, humanInterleukin-1beta

Identifiers

PMID25422961
PMCPMC4459595
OpenAlexW2313508942

What OpenQuestion holds

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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.