Literature DB >> 20560707

T3111C clock single nucleotide polymorphism and mood disorders: a meta-analysis.

Raffaella Calati1, Enrique Gaspar-Barba, Adina Yukler, Alessandro Serretti.   

Abstract

It has been hypothesized that abnormalities in the molecular clock underlie the development of mood disorders, in the direction of higher prevalence in individuals with a reduced flexibility to adapt to important regulations of mood in response to changes in seasons, stress levels, sleep schedules, and time zones. In particular, a T/C change (rs1801260) at the 3111 position of the circadian locomotor output cycles kaput (CLOCK) gene has been explored in psychiatry disorders. This meta-analysis has been undertaken to investigate the association between rs1801260 and both mood disorders and depression severity, shedding light on previous controversial results and providing better power to detect smaller effect sizes. PubMed and ISI databases were searched for studies focused on the association between rs1801260 and mood disorders spectrum. Quality of studies was assessed. We found no association between CLOCK genotypes and mood disorders, even when we separately investigated ethnical homogeneous or unipolar disorder studies. No association was found regarding severity of depression either. The methodological quality of the studies has been found to be medium-high. Our meta-analysis shows no association between rs1801260 and mood disorders (as a complete phenotype) or depression severity and points out the necessity of further research in order to better understand the underlying biological machinery of circadian dysfunction in subjects affected by mood disorders.

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Year:  2010        PMID: 20560707     DOI: 10.3109/07420521003681480

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


  7 in total

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Authors:  Alexander Dueck; Johannes Thome; Frank Haessler
Journal:  J Neural Transm (Vienna)       Date:  2012-06-06       Impact factor: 3.575

Review 2.  Clock gene variants in mood and anxiety disorders.

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

3.  Clock gene variants differentiate mood disorders.

Authors:  Monika Paulina Dmitrzak-Weglarz; Joanna Maria Pawlak; Malgorzata Maciukiewicz; Jerzy Moczko; Monika Wilkosc; Anna Leszczynska-Rodziewicz; Dorota Zaremba; Joanna Hauser
Journal:  Mol Biol Rep       Date:  2014-09-26       Impact factor: 2.316

Review 4.  The serotonin 1A receptor gene confer susceptibility to mood disorders: results from an extended meta-analysis of patients with major depression and bipolar disorder.

Authors:  Taro Kishi; Reiji Yoshimura; Yasuhisa Fukuo; Tomo Okochi; Shinji Matsunaga; Wakako Umene-Nakano; Jun Nakamura; Alessandro Serretti; Christoph U Correll; John M Kane; Nakao Iwata
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2012-07-03       Impact factor: 5.270

5.  Circadian pathway genes in relation to glioma risk and outcome.

Authors:  Melissa H Madden; Gabriella M Anic; Reid C Thompson; L Burton Nabors; Jeffrey J Olson; James E Browning; Alvaro N Monteiro; Kathleen M Egan
Journal:  Cancer Causes Control       Date:  2013-10-18       Impact factor: 2.506

6.  Mood disorders, circadian rhythms, melatonin and melatonin agonists.

Authors:  M A Quera Salva; S Hartley
Journal:  J Cent Nerv Syst Dis       Date:  2012-01-04

7.  Clinical and genetic factors associated with anxiety and depression in breast cancer patients: a cross-sectional study.

Authors:  Aline Hajj; Roula Hachem; Rita Khoury; Souheil Hallit; Bashar ElJEBBAWI; Fady Nasr; Fadi El Karak; Georges Chahine; Joseph Kattan; Lydia Rabbaa Khabbaz
Journal:  BMC Cancer       Date:  2021-07-30       Impact factor: 4.638

  7 in total

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