Testing The Role of Circadian Genes in Conferring Risk for Psychiatric Disorders

被引:32
作者
Byrne, Enda M. [1 ]
Heath, Andrew C. [2 ]
Madden, Pamela A. F. [2 ]
Pergadia, Michele L. [2 ]
Hickie, Ian B. [3 ]
Montgomery, Grant W. [4 ]
Martin, Nicholas G. [4 ]
Wray, Naomi R. [1 ]
机构
[1] Univ Queensland, Queensland Brain Inst, St Lucia, Qld 4072, Australia
[2] Washington Univ Sch Med, Dept Psychiat, St Louis, MO USA
[3] Univ Sydney, Brain & Mind Res Inst, Sydney, NSW 2006, Australia
[4] Queensland Inst Med Res, Brisbane, Qld 4006, Australia
基金
英国医学研究理事会;
关键词
circadian; clock; mood; GENOME-WIDE ASSOCIATION; BIPOLAR-I-DISORDER; SCHIZOAFFECTIVE DISORDER; CLOCK; DEPRESSION; PROLACTIN; SLEEP;
D O I
10.1002/ajmg.b.32230
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Disturbed sleep and disrupted circadian rhythms are a common feature of psychiatric disorders, and many groups have postulated an association between genetic variants in circadian clock genes and psychiatric disorders. Using summary data from the association analyses of the Psychiatric Genomics Consortia (PGC) for schizophrenia, bipolar disorder and major depressive disorder, we evaluated the evidence that common SNPs in genes encoding components of the molecular clock influence risk to psychiatric disorders. Initially, gene-based and SNP P-values were analyzed for 21 core circadian genes. Subsequently, an expanded list of genes linked to control of circadian rhythms was analyzed. After correcting for multiple comparisons, none of the circadian genes were significantly associated with any of the three disorders. Several genes previously implicated in the etiology of psychiatric disorders harbored no SNPs significant at the nominal level of P<0.05, and none of the the variants identified in candidate studies of clock genes that were included in the PGC datasets were significant after correction for multiple testing. There was no evidence of an enrichment of associations in genes linked to control of circadian rhythms in human cells. Our results suggest that genes encoding components of the molecular clock are not good candidates for harboring common variants that increase risk to bipolar disorder, schizophrenia, or major depressive disorder. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:254 / 260
页数:7
相关论文
共 30 条
[1]   A length polymorphism in the circadian clock gene Per3 influences age at onset of bipolar disorder [J].
Benedetti, Francesco ;
Dallaspezia, Sara ;
Colombo, Cristina ;
Pirovano, Adele ;
Marino, Elena ;
Smeraldi, Enrico .
NEUROSCIENCE LETTERS, 2008, 445 (02) :184-187
[2]   A genome-wide association study of sleep habits and insomnia [J].
Byrne, Enda M. ;
Gehrman, Philip R. ;
Medland, Sarah E. ;
Nyholt, Dale R. ;
Heath, Andrew C. ;
Madden, Pamela A. F. ;
Hickie, Ian B. ;
Van Duijn, Cornelia M. ;
Henders, Anjali K. ;
Montgomery, Grant W. ;
Martin, Nicholas G. ;
Wray, Naomi R. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2013, 162B (05) :439-451
[3]   Phenotypic Effects of a Bipolar Liability Gene Among Individuals With Major Depressive Disorder [J].
Casamassima, Francesco ;
Huang, Jie ;
Fava, Maurizio ;
Sachs, Gary S. ;
Smoller, Jordan W. ;
Cassano, Giovanni B. ;
Lattanzi, Lorenzo ;
Fagerness, Jes ;
Stange, Jonathan P. ;
Perlis, Roy H. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2010, 153B (01) :303-309
[4]   Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results [J].
Collins, A. L. ;
Kim, Y. ;
Sklar, P. ;
O'Donovan, M. C. ;
Sullivan, P. F. .
PSYCHOLOGICAL MEDICINE, 2012, 42 (03) :607-616
[5]   Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder [J].
Ferreira, Manuel A. R. ;
O'Donovan, Michael C. ;
Meng, Yan A. ;
Jones, Ian R. ;
Ruderfer, Douglas M. ;
Jones, Lisa ;
Fan, Jinbo ;
Kirov, George ;
Perlis, Roy H. ;
Green, Elaine K. ;
Smoller, Jordan W. ;
Grozeva, Detelina ;
Stone, Jennifer ;
Nikolov, Ivan ;
Chambert, Kimberly ;
Hamshere, Marian L. ;
Nimgaonkar, Vishwajit L. ;
Moskvina, Valentina ;
Thase, Michael E. ;
Caesar, Sian ;
Sachs, Gary S. ;
Franklin, Jennifer ;
Gordon-Smith, Katherine ;
Ardlie, Kristin G. ;
Gabriel, Stacey B. ;
Fraser, Christine ;
Blumenstiel, Brendan ;
Defelice, Matthew ;
Breen, Gerome ;
Gill, Michael ;
Morris, Derek W. ;
Elkin, Amanda ;
Muir, Walter J. ;
McGhee, Kevin A. ;
Williamson, Richard ;
MacIntyre, Donald J. ;
MacLean, Alan W. ;
Clair, David St ;
Robinson, Michelle ;
Van Beck, Margaret ;
Pereira, Ana C. P. ;
Kandaswamy, Radhika ;
McQuillin, Andrew ;
Collier, David A. ;
Bass, Nicholas J. ;
Young, Allan H. ;
Lawrence, Jacob ;
Ferrier, I. Nicol ;
Anjorin, Adebayo ;
Farmer, Anne .
NATURE GENETICS, 2008, 40 (09) :1056-1058
[6]   Genome-wide association of sleep and circadian phenotypes [J].
Gottlieb, Daniel J. ;
O'Connor, George T. ;
Wilk, Jemma B. .
BMC MEDICAL GENETICS, 2007, 8
[7]   CLOCK may Predict the Response to Fluvoxamine Treatment in Japanese Major Depressive Disorder Patients [J].
Kishi, Taro ;
Kitajima, Tsuyoshi ;
Ikeda, Masashi ;
Yamanouchi, Yoshio ;
Kinoshita, Yoko ;
Kawashima, Kunihiro ;
Okochi, Tomo ;
Okumura, Takenori ;
Tsunoka, Tomoko ;
Ozaki, Norio ;
Iwata, Nakao .
NEUROMOLECULAR MEDICINE, 2009, 11 (02) :53-57
[8]  
Kripke Daniel F, 2009, J Circadian Rhythms, V7, P2, DOI 10.1186/1740-3391-7-2
[9]   PER2 Variantion Is Associated With Depression Vulnerability [J].
Lavebratt, Catharina ;
Sjoholm, Louise K. ;
Partonen, Timo ;
Schalling, Martin ;
Forsell, Yvonne .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2010, 153B (02) :570-581
[10]  
LINKOWSKI P, 1989, ARCH GEN PSYCHIAT, V46, P813