TY - JOUR
T1 - Genome-wide association study of suicide attempts in mood disorder patients
AU - Perlis, Roy H.
AU - Huang, Jie
AU - Purcell, Shaun
AU - Fava, Maurizio
AU - Rush, A. John
AU - Sullivan, Patrick F.
AU - Hamilton, Steven P.
AU - McMahon, Francis Joseph
AU - Schulze, Thomas
AU - Potash, James B.
AU - Zandi, Peter P.
AU - Willour, Virginia L.
AU - Penninx, Brenda W.
AU - Boomsma, Dorret I.
AU - Vogelzangs, Nicole
AU - Middeldorp, Christel M.
AU - Rietschel, Marcella
AU - Nöthen, Markus
AU - Cichon, Sven
AU - Gurling, Hugh
AU - Bass, Nick
AU - McQuillin, Andrew
AU - Hamshere, Marian
AU - Craddock, Nick
AU - Sklar, Pamela
AU - Smoller, Jordan W.
PY - 2010/12
Y1 - 2010/12
N2 - Objective: Family and twin studies suggest that liability for suicide attempts is heritable and distinct from mood disorder susceptibility. The authors therefore examined the association between common genomewide variation and lifetime suicide attempts. Method: The authors analyzed data on lifetime suicide attempts from genomewide association studies of bipolar I and II disorder as well as major depressive disorder. Bipolar disorder subjects were drawn from the Systematic Treatment Enhancement Program for Bipolar Disorder cohort, the Wellcome Trust Case Control Consortium bipolar cohort, and the University College London cohort. Replication was pursued in the NIMH Genetic Association Information Network bipolar disorder project and a German clinical cohort. Depression subjects were drawn from the Sequential Treatment Alternatives to Relieve Depression cohort, with replication in the Netherlands Study of Depression and Anxiety/Netherlands Twin Register depression cohort. Results: Strongest evidence of association for suicide attempt in bipolar disorder was observed in a region without identified genes (rs1466846); five loci also showed suggestive evidence of association. In major depression, strongest evidence of association was observed for a single nucleotide polymorphism in ABI3BP, with six loci also showing suggestive association. Replication cohorts did not provide further support for these loci. However, meta-analysis incorporating approximately 8,700 mood disorder subjects identified four additional regions that met the threshold for suggestive association, including the locus containing the gene coding for protein kinase C-epsilon, previously implicated in models of mood and anxiety. Conclusions: The results suggest that inherited risk for suicide among mood disorder patients is unlikely to be the result of individual common variants of large effect. They nonetheless provide suggestive evidence for multiple loci, which merit further investigation.
AB - Objective: Family and twin studies suggest that liability for suicide attempts is heritable and distinct from mood disorder susceptibility. The authors therefore examined the association between common genomewide variation and lifetime suicide attempts. Method: The authors analyzed data on lifetime suicide attempts from genomewide association studies of bipolar I and II disorder as well as major depressive disorder. Bipolar disorder subjects were drawn from the Systematic Treatment Enhancement Program for Bipolar Disorder cohort, the Wellcome Trust Case Control Consortium bipolar cohort, and the University College London cohort. Replication was pursued in the NIMH Genetic Association Information Network bipolar disorder project and a German clinical cohort. Depression subjects were drawn from the Sequential Treatment Alternatives to Relieve Depression cohort, with replication in the Netherlands Study of Depression and Anxiety/Netherlands Twin Register depression cohort. Results: Strongest evidence of association for suicide attempt in bipolar disorder was observed in a region without identified genes (rs1466846); five loci also showed suggestive evidence of association. In major depression, strongest evidence of association was observed for a single nucleotide polymorphism in ABI3BP, with six loci also showing suggestive association. Replication cohorts did not provide further support for these loci. However, meta-analysis incorporating approximately 8,700 mood disorder subjects identified four additional regions that met the threshold for suggestive association, including the locus containing the gene coding for protein kinase C-epsilon, previously implicated in models of mood and anxiety. Conclusions: The results suggest that inherited risk for suicide among mood disorder patients is unlikely to be the result of individual common variants of large effect. They nonetheless provide suggestive evidence for multiple loci, which merit further investigation.
UR - http://www.scopus.com/inward/record.url?scp=78649743723&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78649743723&partnerID=8YFLogxK
U2 - 10.1176/appi.ajp.2010.10040541
DO - 10.1176/appi.ajp.2010.10040541
M3 - Article
C2 - 21041247
AN - SCOPUS:78649743723
SN - 0002-953X
VL - 167
SP - 1499
EP - 1507
JO - American Journal of Psychiatry
JF - American Journal of Psychiatry
IS - 12
ER -