Evidence map›Paper›PMID 25837715›Full record

ArticleJournal of affective disorders2015

Genetic and childhood trauma interaction effect on age of onset in bipolar disorder: An exploratory analysis.

Amit Anand, Daniel L Koller, William B Lawson, Elliot S Gershon, John I Nurnberger, BiGS Collaborative

Open access · greenAbstract read
In one paragraph

Article in Journal of affective disorders, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 55 citations in OpenAlex.

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  12. Childhood Maltreatment in Bipolar Disorders.Current topics in behavioral neurosciences · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Data Resources for Human Functional Genomics.Current opinion in systems biology · 2017
    Article
  20. 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 4 institutions in 1 country.

Amit AnandCenter for Behavioral Health, Cleveland Clinic, 9500 Euclid Avenue/P57, Cleveland, OH 44195 United States; Department of Psychiatry, Indiana University School of Medicine, United States. Electronic address: ananda@ccf.org.
Daniel L KollerDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, United States.
William B LawsonDepartment of Psychiatry, Howard University, United States.
Elliot S GershonDepartment of Psychiatry, University of Chicago, United States.
John I NurnbergerDepartment of Psychiatry, Indiana University School of Medicine, United States; Department of Medical and Molecular Genetics, Indiana University School of Medicine, United States; Institute of Psychiatric Research, Department of Psychiatry, Indiana University School of Medicine, United States.
BiGS Collaborative
University School · USHoward University · USIndiana University · USUniversity of Chicago · US

Funding

Genomic Association Study of Bipolar DisorderR01MH078151 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KELSOE, JOHN R. · 2007 to 2009
$5.5M
Stability of Biotypes: a Longitudinal Evaluation (STABLE)R01MH103368 · NIMH · UNIVERSITY OF CHICAGO · PI GERSHON, ELLIOT S, KEEDY, SARAH K · 2015 to 2019
$4.5M
NIMH NIH HHS R01 MH078151NIMH NIH HHS R01 MH103368
6 · The paper itself

Abstract

introductionThis study investigated whether early life trauma mediates genetic effects on the age at onset (AAO) of bipolar disorder.

methodData from the BiGS Consortium case samples (N=1119) were used. Childhood traumatic events were documented using the Childhood Life Events Scale (CLES). Interaction between occurrence of childhood trauma and common genetic variants throughout the genome was tested to identify single nucleotide polymorphic gene variants (SNPs) whose effects on bipolar AAO differ between individuals clearly exposed (CLES≥2) and not exposed (CLES=0) to childhood trauma.

resultsThe modal response to the CLES was 0 (N=480), but an additional 276 subjects had CLES=1, and 363 subjects reported 2 or more traumatic lifetime events. The distribution of age at onset showed a broad peak between ages 12 and 18, with the majority of subjects having onset during that period, and a significant decrease in age of onset with the number of traumatic events. No single SNP showed a statistically significant interaction with the presence of traumatic events to impact bipolar age at onset. However, SNPs in or near genes coding for calcium channel activity-related proteins (Gene Ontology: 0005262) were found to be more likely than other SNPs to show evidence of interaction using the INRICH method (p<0.001). LIMITATIONS: Retrospective ascertainment of trauma and AAO.

conclusionInteraction effects of early life trauma with genotype may have a significant effect on the development and manifestation of bipolar disorder. These effects may be mediated in part by genes involved in calcium signaling.

Indexed as

Gene-Environment InteractionAdult Survivors of Child AbuseAge DistributionAge of OnsetBipolar DisorderCalcium ChannelsCase-Control StudiesFemaleGenome-Wide Association StudyGenotypeHumansMalePolymorphism, Single NucleotidePsychological TraumaRetrospective StudiesRisk FactorsCalcium ChannelsAge of onsetBipolar disorderCalciumChildhood traumaGeneticGWAS

Identifiers

PMID25837715
PMCPMC5845791
OpenAlexW2153341829

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.