Evidence map›Paper›PMID 17522711›Full record

ArticleMolecular psychiatry2007

Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia.

T Lencz, T V Morgan, M Athanasiou, B Dain, C R Reed, J M Kane, R Kucherlapati, A K Malhotra

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01844700 (1/2-MC4R Genotype and Pediatric Antipsychotic Drug- Induced Weight Gain), which is not on this map. Cited by 114 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed, 9 pooled it
0.1field-weighted citation impact, top 55% 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.

NCT01844700 phase4terminatednot on this mapstarted 2013, after this paper: background citation

1/2-MC4R Genotype and Pediatric Antipsychotic Drug- Induced Weight Gain

TypeinterventionalSponsorNorthwell HealthRan2013 to 2014Enrolled14ConditionsHigh Risk MC4R Genotype, Low Risk MC4R Genotype, One Week or Less Antipsychotic Lifetime ExposureArmsZiprasidone, aripiprazole, quetiapine, or risperidone
3 · Its place in the literature

Who cites it

114 citing papers in PubMed, 9 syntheses or guidelines pooled it, 278 citations in OpenAlex.

  1. Pooled it
  2. Association between aBioMed research international · 2020
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  8. IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2010
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  12. Proof-of-concept trial with the neurosteroid pregnenolone targeting cognitive and negative symptoms in schizophrenia.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2009
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54 more citing papers are in PubMed but not listed here.

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 5 institutions in 1 country.

T LenczDepartment of Psychiatry Research, The Zucker Hillside Hospital, Division of the North Shore-Long Island Jewish Health System, Glen Oaks, NY 11004, USA. lencz@lij.edu
T V Morgan
M Athanasiou
B Dain
C R Reed
J M Kane
R Kucherlapati
A K Malhotra
MaineHealth · USCenter for Human Genetics · USFeinstein Institute for Medical Research · USNorthwell Health · USYeshiva University · US

Funding

Trials Operation UnitP30MH074543 · NIMH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI KANE, JOHN M · 2005 to 2009
$8.1M
Identifying &Characterizing Prodromal SchizophreniaK01MH065580 · NIMH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI LENCZ, TODD · 2003 to 2007
$675k
CLINICAL TRIALS IN SCHIZOPHRENIA--MOLECULAR APPROACHESK23MH001760 · NIMH · LONG ISLAND JEWISH MEDICAL CENTER · PI MALHOTRA, ANIL K · 1999 to 2003
$621k
NIMH NIH HHS MH001760NIMH NIH HHS MH065580NIMH NIH HHS MH074543
6 · The paper itself

Abstract

Schizophrenia is a strongly heritable disorder, and identification of potential candidate genes has accelerated in recent years. Genomewide scans have identified multiple large linkage regions across the genome, with fine-mapping studies and other investigations of biologically plausible targets demonstrating several promising candidate genes of modest effect. The recent introduction of technological platforms for whole-genome association (WGA) studies can provide an opportunity to rapidly identify novel targets, although no WGA studies have been reported in the psychiatric literature to date. We report results of a case-control WGA study in schizophrenia, examining approximately 500 000 markers, which revealed a strong effect (P=3.7 x 10(-7)) of a novel locus (rs4129148) near the CSF2RA (colony stimulating factor, receptor 2 alpha) gene in the pseudoautosomal region. Sequencing of CSF2RA and its neighbor, IL3RA (interleukin 3 receptor alpha) in an independent case-control cohort revealed both common intronic haplotypes and several novel, rare missense variants associated with schizophrenia. The presence of cytokine receptor abnormalities in schizophrenia may help explain prior epidemiologic data relating the risk for this illness to altered rates of autoimmune disorders, prenatal infection and familial leukemia.

Indexed as

Case-Control StudiesCohort StudiesFemaleGenetic LinkageGenome, HumanHaplotypesHumansInterleukin-3 Receptor alpha SubunitMaleMutation, MissensePolymorphism, Single NucleotideReceptors, Granulocyte-Macrophage Colony-Stimulating FactorReceptors, Interleukin-3SchizophreniaSex FactorsCSF2RA protein, humanIL3RA protein, humanInterleukin-3 Receptor alpha SubunitReceptors, Granulocyte-Macrophage Colony-Stimulating FactorReceptors, Interleukin-3

Identifiers

PMID17522711
OpenAlexW2142244624

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.