Literature DB >> 22080789

The CLOCK gene and mood disorders: a case-control study and meta-analysis.

Taro Kishi1, Reiji Yoshimura, Yasuhisa Fukuo, Tsuyoshi Kitajima, Tomo Okochi, Shinji Matsunaga, Toshiya Inada, Hiroshi Kunugi, Tadafumi Kato, Takeo Yoshikawa, Hiroshi Ujike, Wakako Umene-Nakano, Jun Nakamura, Norio Ozaki, Alessandro Serretti, Christoph U Correll, Nakao Iwata.   

Abstract

The clock gene (CLOCK) is considered to be a good candidate gene for the pathophysiology of mood disorders, including bipolar disorder (BP) and major depressive disorder (MDD). rs1801260 (T3111C) has been detected at position 3111 in the CLOCK mRNA 3' untranslated region, and was reported to be associated with a substantial delay in preferred timing for activity and sleep in a human study. As for function, rs1801260 has been speculated to affect mRNA. Therefore, the authors investigated the association between the three tagging single-nucleotide polymorphisms (SNPs) (rs3736544, rs1801260, and rs3749474) in CLOCK and risk of BP (n=867) and MDD (n=139) compared to controls (n=889) in the Japanese population. In addition, we also performed an updated meta-analysis of nine published, genetic association studies investigating the relationship between rs1801260 and mood disorder risk, comprising 3321 mood disorders cases and 3574 controls. We did not detect any associations between tagging SNPs in CLOCK and BP or MDD in the allele, genotype, or haplotype analysis (global p(BP)=.605 and global p(MDD)=.211). Moreover, rs1801260 was also not associated with BP, MDD, or any mood disorders in the meta-analysis. In conclusion, these data suggest that CLOCK does not play a major role in the pathophysiology of mood disorders.

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Year:  2011        PMID: 22080789     DOI: 10.3109/07420528.2011.609951

Source DB:  PubMed          Journal:  Chronobiol Int        ISSN: 0742-0528            Impact factor:   2.877


  15 in total

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Journal:  J Neural Transm (Vienna)       Date:  2012-04-27       Impact factor: 3.575

3.  Major depressive disorder: a loss of circadian synchrony?

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Journal:  Proc Natl Acad Sci U S A       Date:  2016-02-22       Impact factor: 11.205

5.  Clock gene variants differentiate mood disorders.

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6.  Mitochondria, Metabolism, and Redox Mechanisms in Psychiatric Disorders.

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Review 7.  Genetics Factors in Major Depression Disease.

Authors:  Maria Shadrina; Elena A Bondarenko; Petr A Slominsky
Journal:  Front Psychiatry       Date:  2018-07-23       Impact factor: 4.157

Review 8.  The genetics of major depression.

Authors:  Jonathan Flint; Kenneth S Kendler
Journal:  Neuron       Date:  2014-02-05       Impact factor: 17.173

9.  Molecular analyses of circadian gene variants reveal sex-dependent links between depression and clocks.

Authors:  S-q Shi; M J White; H M Borsetti; J S Pendergast; A Hida; C M Ciarleglio; P A de Verteuil; A G Cadar; C Cala; D G McMahon; R C Shelton; S M Williams; C H Johnson
Journal:  Transl Psychiatry       Date:  2016-03-01       Impact factor: 6.222

10.  The wnt pathway in mood disorders.

Authors:  Gabriele Sani; Flavia Napoletano; Alberto Maria Forte; Giorgio D Kotzalidis; Isabella Panaccione; Giulio Maria Porfiri; Alessio Simonetti; Matteo Caloro; Nicoletta Girardi; Carla Ludovica Telesforo; Giulia Serra; Silvia Romano; Giovanni Manfredi; Valeria Savoja; Stefano Maria Tamorri; Alexia E Koukopoulos; Daniele Serata; Chiara Rapinesi; Antonio Del Casale; Ferdinando Nicoletti; Paolo Girardi
Journal:  Curr Neuropharmacol       Date:  2012-09       Impact factor: 7.363

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