Evidence map›Paper›PMID 20838396›Full record

SynthesisMolecular psychiatry2011

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.

X Chen, G Lee, B S Maher, A H Fanous, J Chen, Z Zhao, A Guo, E van den Oord, P F Sullivan, J Shi and 54 more

4 registry-linked trialsAbstract readMeta-Analysis
In one paragraph

Synthesis in Molecular psychiatry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT02897739 completednot on this mapstarted 2015, after this paper: background citation

Pathogenesis of Acute Stress Induced (Tako-tsubo) Cardiomyopathy: Energy Shut-Down or Intense Inflammation? The TERRIFIC Study

Typeobservational_patient_registrySponsorUniversity of AberdeenRan2015 to 2019Enrolled77ConditionsTako-tsubo CardiomyopathyArmsMagnetic resonance imaging, Acute Inflammatory Activation study, PET CT, Psychological assessment
NCT02989454 completednot on this mapstarted 2015, after this paper: background citation

Persistent Symptoms and Early Incomplete Recovery After Acute Stress-induced Cardiomyopathy: Is There Ongoing Heart Distress? The HEROIC Study

TypeobservationalSponsorUniversity of AberdeenRan2015 to 2017Enrolled42ConditionsTako-tsubo CardiomyopathyArmsAssessment of exercise capacity and cardiac energetics
NCT03299569 recruitingnot on this mapstarted 2016, after this paper: background citation

Establishing the Incidence of Tako-tsubo Cardiomyopathy in Scotland - the STARR Study

Typeobservational_patient_registrySponsorUniversity of AberdeenRan2016 to 2028Enrolled800ConditionsTakotsubo Cardiomyopathy, Myocardial Infarction
NCT04425785 nacompletednot on this mapstarted 2019, after this paper: background citation

Physical Exercise and Mental Wellbeing Rehabilitation for Acute Stress-induced Takotsubo Cardiomyopathy: The PLEASE Study

TypeinterventionalSponsorUniversity of AberdeenRan2019 to 2023Enrolled76ConditionsTakotsubo CardiomyopathyArmsPhysical Exercise Program, Cognitive Behavioural Therapy
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Review
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  14. A GluD Coming-Of-Age Story.Trends in neurosciences · 2017
    Review
  15. Article
  16. Article
  17. Currently recognized genes for schizophrenia: High-resolution chromosome ideogram representation.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2016
    Article
  18. Review
  19. 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

64 authors.

X ChenDepartment of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA 23298-0424, USA. xchen@vcu.edu
G Lee
B S Maher
A H Fanous
J Chen
Z Zhao
A Guo
E van den Oord
P F Sullivan
J Shi
D F Levinson
P V Gejman
A Sanders
J Duan
M J Owen
N J Craddock
M C O'Donovan
J Blackman
D Lewis
G K Kirov
W Qin
S Schwab
D Wildenauer
K Chowdari
V Nimgaonkar
R E Straub
D R Weinberger
F A O'Neill
D Walsh
M Bronstein
A Darvasi
T Lencz
A K Malhotra
D Rujescu
I Giegling
T Werge
T Hansen
A Ingason
M M Nöethen
M Rietschel
S Cichon
S Djurovic
O A Andreassen
R M Cantor
R Ophoff
A Corvin
D W Morris
M Gill
C N Pato
M T Pato
A Macedo
H M D Gurling
A McQuillin
J Pimm
C Hultman
P Lichtenstein
P Sklar
S M Purcell
E Scolnick
D St Clair
D H R Blackwood
K S Kendler
GROUP investigators
International Schizophrenia Consortium

Funding

A Neurobehavioral Family Study of SchizophreniaR01MH063480 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIMGAONKAR, VISHWAJIT LAXMIKANT · 2001 to 2018
$6.1M
THE GENETIC EPIDEMIOLOGY OF SCHIZOPHRENIA IN IRELANDR01MH041953 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI KENDLER, KENNETH SEEDMAN · 1987 to 2008
$5.2M
High-density Genome-wide Association Study SchizophreniaR01MH078075 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI OPHOFF, ROEL A · 2006 to 2009
$3.7M
Genetic Susceptibility in SchizophreniaR01MH056242 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIMGAONKAR, VISHWAJIT LAXMIKANT · 2002 to 2007
$2.9M
GENETIC SUSCEPTIBILITY IN SCHIZOPHRENIAR10MH056242 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIMGAONKAR, VISHWAJIT LAXMIKANT · 1997 to 2001
$1.2M
Replication of Schizophrenia Associations in CATIER01MH074027 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2006 to 2007
$715k
Pop-Track NIMHZ01MH900001 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI POP-TRACK, IC · 2002 to 2003
–
Medical Research Council G0800509NIMH NIH HHS MH074027NIMH NIH HHS MH078075NIMH NIH HHS MH41953NIMH NIH HHS MH56242NIMH NIH HHS MH63480NIMH NIH HHS N01 MH900001NIMH NIH HHS R01 MH041953NIMH NIH HHS R01 MH056242NIMH NIH HHS R01 MH063480NIMH NIH HHS R01 MH074027NIMH NIH HHS R01 MH078075NIMH NIH HHS R10 MH056242Wellcome Trust
6 · The paper itself

Abstract

We conducted data-mining analyses using the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) and molecular genetics of schizophrenia genome-wide association study supported by the genetic association information network (MGS-GAIN) schizophrenia data sets and performed bioinformatic prioritization for all the markers with P-values ≤0.05 in both data sets. In this process, we found that in the CMYA5 gene, there were two non-synonymous markers, rs3828611 and rs10043986, showing nominal significance in both the CATIE and MGS-GAIN samples. In a combined analysis of both the CATIE and MGS-GAIN samples, rs4704591 was identified as the most significant marker in the gene. Linkage disequilibrium analyses indicated that these markers were in low LD (3 828 611-rs10043986, r(2)=0.008; rs10043986-rs4704591, r(2)=0.204). In addition, CMYA5 was reported to be physically interacting with the DTNBP1 gene, a promising candidate for schizophrenia, suggesting that CMYA5 may be involved in the same biological pathway and process. On the basis of this information, we performed replication studies for these three single-nucleotide polymorphisms. The rs3828611 was found to have conflicting results in our Irish samples and was dropped out without further investigation. The other two markers were verified in 23 other independent data sets. In a meta-analysis of all 23 replication samples (family samples, 912 families with 4160 subjects; case-control samples, 11 380 cases and 15 021 controls), we found that both markers are significantly associated with schizophrenia (rs10043986, odds ratio (OR)=1.11, 95% confidence interval (CI)=1.04-1.18, P=8.2 × 10(-4) and rs4704591, OR=1.07, 95% CI=1.03-1.11, P=3.0 × 10(-4)). The results were also significant for the 22 Caucasian replication samples (rs10043986, OR=1.11, 95% CI=1.03-1.17, P=0.0026 and rs4704591, OR=1.07, 95% CI=1.02-1.11, P=0.0015). Furthermore, haplotype conditioned analyses indicated that the association signals observed at these two markers are independent. On the basis of these results, we concluded that CMYA5 is associated with schizophrenia and further investigation of the gene is warranted.

Indexed as

Genome-Wide Association StudyPolymorphism, Single NucleotideBlack or African AmericanCarrier ProteinsCase-Control StudiesData MiningDysbindinDystrophin-Associated ProteinsGermanyHumansIrelandJewsLinkage DisequilibriumMuscle ProteinsPennsylvaniaRiskCarrier ProteinsCMYA5 protein, humanDTNBP1 protein, humanDysbindinDystrophin-Associated ProteinsMuscle Proteins

Identifiers

PMID20838396
PMCPMC3443634

What OpenQuestion holds

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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.