Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder

被引:51
作者
Cohen-Woods, Sarah [1 ]
Gaysina, Daria [1 ]
Craddock, Nick [2 ]
Farmer, Anne [1 ]
Gray, Joanna [1 ]
Gunasinghe, Cerisse [1 ]
Hoda, Farzana [1 ]
Jones, Lisa [3 ]
Knight, Jo [1 ]
Korszun, Ania [4 ]
Owen, Michael J. [2 ]
Sterne, Abram [1 ]
Craig, Ian W. [1 ]
McGuffin, Peter [1 ]
机构
[1] Kings Coll London, MRC, SGDP Ctr, Inst Psychiat, London SES 8AF, England
[2] Cardiff Univ, Dept Psychol Med, Sch Med, Cardiff CF14 4XN, S Glam, Wales
[3] Univ Birmingham, Div Neurosci, Dept Psychiat, Birmingham B15 2FG, W Midlands, England
[4] Wolfson Inst Prevent Med, Ctr Psychiat, London EC1M 6BQ, England
基金
奥地利科学基金会; 英国医学研究理事会;
关键词
ALCOHOL DEPENDENCE; ALZHEIMERS-DISEASE; ASSOCIATION; PSYCHOPATHOLOGY; SAMPLE; CORTEX; RISK; MAIL; MICE; DNA;
D O I
10.1093/hmg/ddp051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has been suggested that alteration in the muscarinic-cholinergic system is involved in modulation of mood. Three studies have reported linkage on chromosome 7 with major depressive disorder (MDD) in or close to a region containing the muscarinic receptor CHRM2 gene. A haplotype of SNPs located in CHRM2 (rs1824024-rs2061174-rs324650) has been significantly associated with MDD in a previous study. We report the first study investigating this gene in a large, adequately powered, clinical depression case-control sample (n = 1420 cases, 1624 controls). Our data fail to support association with the CHRM2 polymorphisms previously implicated in the genetic aetiology of depression. It is possible our failure to replicate may be a consequence of differences in definition of the MDD phenotype and/or ethnic differences.
引用
收藏
页码:1504 / 1509
页数:6
相关论文
共 40 条
  • [1] American Psychiatric Association, 1994, DSM, VIV
  • [2] Cognitive functions of the basal forebrain
    Baxter, MG
    Chiba, AA
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (02) : 178 - 183
  • [3] BECK AT, 1984, J CLIN PSYCHOL, V40, P1365, DOI 10.1002/1097-4679(198411)40:6<1365::AID-JCLP2270400615>3.0.CO
  • [4] 2-D
  • [5] Association of the muscarinic cholinergic 2 receptor (CHRM2) gene with major depression in women
    Comings, DE
    Wu, S
    Rostamkhani, M
    McGue, M
    Iacono, WG
    MacMurray, JP
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (05): : 527 - 529
  • [6] Using dimensional models of externalizing psychopathology to aid in gene identification
    Dick, Danielle M.
    Aliev, Fazil
    Wang, Jen C.
    Grucza, Richard A.
    Schuckit, Marc
    Kuperman, Samuel
    Kramer, John
    Hinrichs, Anthony
    Bertelsen, Sarah
    Budde, John P.
    Hesselbrock, Victor
    Porjesz, Bernice
    Edenberg, Howard J.
    Bierut, Laura Jean
    Goate, Alison
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 2008, 65 (03) : 310 - 318
  • [7] Association of CHRM2 with IQ:: Converging evidence for a gene influencing intelligence
    Dick, Danielle M.
    Aliev, Fazil
    Kramer, John
    Wang, Jen C.
    Hinrichs, Anthony
    Bertelsen, Sarah
    Kuperman, Sam
    Schuckit, Marc
    Nurnberger, John, Jr.
    Edenberg, Howard J.
    Porjesz, Bernice
    Begleiter, Henri
    Hesselbrock, Victor
    Goate, Alison
    Bierut, Laura
    [J]. BEHAVIOR GENETICS, 2007, 37 (02) : 265 - 272
  • [8] PATHOPHYSIOLOGY OF CHOLINOCEPTOR SUPERSENSITIVITY IN AFFECTIVE-DISORDERS
    DILSAVER, SC
    [J]. BIOLOGICAL PSYCHIATRY, 1986, 21 (8-9) : 813 - 829
  • [9] Pedigree disequilibrium tests for multilocus haplotypes
    Dudbridge, F
    [J]. GENETIC EPIDEMIOLOGY, 2003, 25 (02) : 115 - 121
  • [10] POWER AND SAMPLE-SIZE CALCULATIONS - A REVIEW AND COMPUTER-PROGRAM
    DUPONT, WD
    PLUMMER, WD
    [J]. CONTROLLED CLINICAL TRIALS, 1990, 11 (02): : 116 - 128