Evidence map›Paper›PMID 25244972›Full record

ArticleSchizophrenia research2014

Associations between oxytocin receptor genotypes and social cognitive performance in individuals with schizophrenia.

Michael C Davis, William P Horan, Erika L Nurmi, Shemra Rizzo, Wendy Li, Catherine A Sugar, Michael F Green

Abstract read
In one paragraph

Article in Schizophrenia research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Genetic and epigenetic signatures associated with plasma oxytocin levels in children and adolescents with autism spectrum disorder.Autism research : official journal of the International Society for Autism Research · 2023
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  18. Oxytocin ReceptorMolecular neuropsychiatry · 2016
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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 2 institutions in 1 country.

Michael C DavisUCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, United States; VA Desert Pacific Mental Illness Research, Education, and Clinical Center, Los Angeles, CA, United States.
William P HoranUCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, United States; VA Desert Pacific Mental Illness Research, Education, and Clinical Center, Los Angeles, CA, United States.
Erika L NurmiUCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, United States.
Shemra RizzoDepartment of Biostatistics, UCLA Fielding School of Public Health, Los Angeles, CA, United States.
Wendy LiUCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, United States.
Catherine A SugarUCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, United States; Department of Biostatistics, UCLA Fielding School of Public Health, Los Angeles, CA, United States.
Michael F GreenUCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, United States; VA Desert Pacific Mental Illness Research, Education, and Clinical Center, Los Angeles, CA, United States. Electronic address: mgreen@ucla.edu.
West Los Angeles College · USUCLA Health · US

Funding

EARLY VISUAL PROCESSING IN SCHIZOPHRENIAR01MH043292 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GREEN, MICHAEL F. · 1996 to 2010
$3.5M
Next generation risk variant discovery in a highly penetrant OCD subtypeK23MH094613 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NURMI, ERIKA L · 2011 to 2014
$721k
EARLY VISUAL PROCESSING IN SCHIZOPHRENIAR29MH043292 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GREEN, MICHAEL F · 1988 to 1992
–
NIMH NIH HHS K23 MH094613NIMH NIH HHS MH043292NIMH NIH HHS MH094613-01NIMH NIH HHS R01 MH043292NIMH NIH HHS R29 MH043292
6 · The paper itself

Abstract

Individuals with schizophrenia often show substantial deficits in social cognitive abilities, which are strongly associated with social functioning. To advance our understanding of the genetic variation that is associated with social cognitive deficits in schizophrenia, we genotyped 74 schizophrenia outpatients who completed social cognitive performance measures assessing mentalizing, social perception, and emotional intelligence, as well as clinical symptoms. We assessed seven single nucleotide polymorphisms (SNPs) of the oxytocin receptor (OXTR) previously found to show replicable associations with socio-emotional processes. For one of the seven SNPs, rs2268493, the 'T' allele was significantly associated with poorer performance on a composite social cognition index, as well as specific tests of mentalizing and social perception. None of the SNPs were associated with clinical symptoms. Though the sample size is small, these findings provide initial support for the involvement of genetic variants of the OXTR in social cognitive impairments in schizophrenia.

Indexed as

Social PerceptionAdolescentAdultAnalysis of VarianceCognition DisordersFemaleGenotypeHumansMaleMiddle AgedNeuropsychological TestsPolymorphism, Single NucleotidePsychiatric Status Rating ScalesReceptors, OxytocinSchizophreniaYoung AdultOXTR protein, humanReceptors, OxytocinOxytocinOxytocin receptorSchizophreniaSingle nucleotide polymorphismSocial cognition

Identifiers

PMID25244972
PMCPMC4254299
OpenAlexW2122556992

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.