Literature DB >> 15952199

Insomnia improvement during antidepressant treatment and CLOCK gene polymorphism.

Alessandro Serretti1, Cristina Cusin, Francesco Benedetti, Laura Mandelli, Adele Pirovano, Raffaella Zanardi, Cristina Colombo, Enrico Smeraldi.   

Abstract

Sleep disturbances are commonly observed in mood disorders, and sleep manipulations can influence the clinical status. In the present study, we investigated the possible effect of the 3111 T/C circadian locomotor output cycles kaput (CLOCK) gene polymorphism on insomnia symptomatology during antidepressant treatment. One hundred seventy-eight inpatients were treated with fluvoxamine 300 mg/day (n = 147) or paroxetine 20-40 mg/day (n = 31), and either placebo or pindolol in a double blind design for 6 weeks. The severity of depressive symptoms was weekly assessed with the Hamilton Rating Scale for Depression (HAM-D). We observed a significantly higher presence of insomnia throughout the trial in homozygotes for the C variant (P = 0.026). Other demographic and clinical features were found not to be related with CLOCK polymorphisms. Overall, our findings may suggest that CLOCK genotype influences the time course of insomnia during antidepressant treatment. This, together with previous findings on this polymorphism could lead to a further dissection of the complexity of mood disorders. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15952199     DOI: 10.1002/ajmg.b.30130

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  37 in total

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Review 4.  Diversity of human clock genotypes and consequences.

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Review 6.  Melatonin, circadian rhythms, and the clock genes in bipolar disorder.

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7.  Genetic differences in human circadian clock genes among worldwide populations.

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8.  Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance.

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9.  CLOCK is suggested to associate with comorbid alcohol use and depressive disorders.

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Journal:  J Circadian Rhythms       Date:  2010-01-21

10.  Incomplete coverage of candidate genes: a poorly considered bias.

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