Evidence map›Paper›PMID 24703166›Full record

ArticlePsychoneuroendocrinology2014

Oxytocin receptor gene polymorphism (rs53576) moderates the intergenerational transmission of depression.

Sarah M Thompson, Constance Hammen, Lisa R Starr, Jake M Najman

Abstract read
In one paragraph

Article in Psychoneuroendocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
12.4field-weighted citation impact, top 1% 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

30 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Intertwined associations between oxytocin, immune system and major depressive disorder.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2023
    Review
  5. Review
  6. Roles of the Oxytocin Receptor (OXTR) in Human Diseases.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Article
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  17. Article
  18. TheDiabetes, metabolic syndrome and obesity : targets and therapy · 2019
    Article
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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

4 authors at 3 institutions in 2 countries.

Sarah M ThompsonDepartment of Psychology, University of California, Los Angeles, Los Angeles, CA, United States. Electronic address: smt44@ucla.edu.
Constance HammenDepartment of Psychology, University of California, Los Angeles, Los Angeles, CA, United States.
Lisa R StarrDepartment of Clinical and Social Sciences in Psychology, University of Rochester, Rochester, NY, United States.
Jake M NajmanSchool of Social Science, University of Queensland, St Lucia, Queensland, Australia.
University of California, Los Angeles · USUniversity of Queensland · AUUniversity of Rochester · US

Funding

TRANSITION TO ADULTHOOD IN YOUTH AT RISK FOR DEPRESSIONR01MH052239 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BRENNAN, PATRICIA A · 1995 to 2004
$1.8M
NIMH NIH HHS R01 MH052239NIMH NIH HHS R01MH052239
6 · The paper itself

Abstract

Maternal depression serves as a potent source of stress among offspring, greatly enhancing the risk of numerous adverse outcomes including youth depression. Several factors moderate the transmission of depression from mothers to offspring. However, the role of genetic characteristics in this process merits further exploration. Consistent with an interpersonal perspective on depression, the present study focused on a genetic polymorphism that has been shown to be relevant to social functioning, the rs53576 polymorphism of the oxytocin receptor gene (OXTR). In a community sample of 441 youth, OXTR genotype moderated the association between maternal depression in early childhood and youth depressive symptoms in adolescence, such that youth possessing at least one A allele of OXTR who also had a history of maternal depression exhibited the highest levels of depressive symptoms at age 15. In order to explore possible interpersonal mediators of this effect, conditional process analyses examined the role of youth social functioning in adolescence. Results suggest that OXTR genotype may partially account for the transmission of maternal depression to youth and support the role of dysfunctional social processes as a mechanism through which OXTR influences the development of depressive symptoms.

Indexed as

AdolescentChildDepressionFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMothersPolymorphism, GeneticReceptors, OxytocinSocial BehaviorYoung AdultReceptors, OxytocinAdolescentsIntergenerational transmission of depressionMaternal depressionOXTROxytocin receptor geneSocial functioning

Identifiers

PMID24703166
PMCPMC3979470
OpenAlexW1996996506

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.