Evidence map›Paper›PMID 18692992›Full record

SynthesisSchizophrenia research2008

Effect of Rhesus D incompatibility on schizophrenia depends on offspring sex.

Christina G S Palmer, Erin Mallery, Joni A Turunen, Hsin-Ju Hsieh, Leena Peltonen, Jouko Lonnqvist, J Arthur Woodward, Janet S Sinsheimer

Open access · hybridAbstract readMeta-Analysis
In one paragraph

Synthesis in Schizophrenia research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

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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

8 authors at 7 institutions in 3 countries.

Christina G S PalmerDepartment of Psychiatry & Biobehavioral Sciences, University of California, Los Angeles, CA, 90095, USA. cpalmer@mednet.ucla.edu
Erin Mallery
Joni A Turunen
Hsin-Ju Hsieh
Leena Peltonen
Jouko Lonnqvist
J Arthur Woodward
Janet S Sinsheimer
University of California, Los Angeles · USFinnish Foundation for Alcohol Studies · FIGenentechInstitute for Molecular Medicine Finland · FINeurobehavioral Systems · USUniversity of California, Merced · USWellcome Sanger Institute · GB

Funding

STATISTICAL METHODS FOR GENE MAPPINGR01GM053275 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LANGE, KENNETH L · 1995 to 2019
$9.3M
Maternal/fetal genotype incompatibility in schizophreniaR21MH066001 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SINSHEIMER, JANET S · 2002 to 2003
$305k
NIGMS NIH HHS GM53275NIGMS NIH HHS R01 GM053275NIMH NIH HHS MH066001NIMH NIH HHS R21 MH066001Wellcome Trust 089061
6 · The paper itself

Abstract

Rhesus D incompatibility increases risk for schizophrenia, with some evidence that risk is limited to male offspring. The purpose of this study is to determine whether risk for schizophrenia due to Rhesus D incompatibility differs by offspring sex using a nuclear family-based candidate gene approach and a meta-analysis approach. The genetic study is based on a sample of 277 nuclear families with RHD genotype data on at least one parent and at least one child diagnosed with schizophrenia or related disorder. Meta-analysis inclusion criteria were (1) well-defined sample of schizophrenia patients with majority born before 1970, (2) Rhesus D incompatibility phenotype or genotype data available on mother and offspring, and by offspring sex. Two of ten studies, plus the current genetic study sample, fulfilled these criteria, for a total of 358 affected males and 226 affected females. The genetic study found that schizophrenia risk for incompatible males was significantly greater than for compatible offspring (p=0.03), while risk for incompatible and compatible females was not significantly different (p=.32). Relative risks for incompatible males and females were not significantly different from each other. Meta-analysis using a larger number of affected males and females supports their difference. Taken together, these results provide further support that risk of schizophrenia due to Rhesus D incompatibility is limited to incompatible males, although a weak female incompatibility effect cannot be excluded. Sex differences during fetal neurodevelopment should be investigated to fully elucidate the etiology of schizophrenia.

Indexed as

FemaleFetal DiseasesGenetic Predisposition to DiseaseGenetic TestingGenotypeHumansMaleMothersPhenotypePregnancyRh-Hr Blood-Group SystemSchizophreniaSiblingsRh-Hr Blood-Group SystemRho(D) antigen

Identifiers

PMID18692992
PMCPMC2572267
OpenAlexW2048573699

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.