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Influence of CLOCK gene polymorphism on circadian mood fluctuation and illness recurrence in bipolar depression. | LitMetric

Influence of CLOCK gene polymorphism on circadian mood fluctuation and illness recurrence in bipolar depression.

Am J Med Genet B Neuropsychiatr Genet

Department of Neuropsychiatric Sciences, University of Vita-Salute San Raffaele, School of Medicine, Milano, Italy.

Published: November 2003

AI Article Synopsis

  • Recent research indicates that a specific genetic variation in the CLOCK gene is linked to people’s preference for being "evening types," which might impact mood fluctuations, especially during depressive episodes.
  • A study involving 101 patients with bipolar disorder examined mood levels at different times of the day, initially finding no significant differences based on genetic variations.
  • However, when focusing on patients with a longer illness duration, those with two copies of the C variant exhibited a nearly doubled recurrence rate of depressive episodes, suggesting a potential role for the CLOCK gene in long-term mood regulation, warranting further investigation.

Article Abstract

Recent studies showed that a polymorphism (T to C nucleotide substitution) in the 3' flanking region of the human CLOCK gene is associated with diurnal preferences of human healthy subjects, with higher "eveningness" in subjects carrying at least one copy of the C allele. We investigated the possible role of CLOCK gene polymorphism in the regulation of diurnal mood fluctuations during a major depressive episode. Sample (n = 101) was collected, in the context of previously reported trials, among patients affected by bipolar disorder type I, depressive episode without psychotic features, free of psychotropic medications. Perceived mood levels were assessed three times a day with self-administered visual analogue scales. Genotype groups showed no significant difference in diurnal mood fluctuations. When stratifying the sample by including only patients with an adequate period of observation (duration of illness higher than 5 years, n = 69), we post-hoc observed a significantly higher recurrence rate in homozygotes for the C variant, which was almost double than that of the other genotype groups. This preliminary observation leads to hypothesize a role for the CLOCK gene polymorphism in the regulation of long-term illness recurrence in bipolar disorder. Given the post-hoc nature of the finding, replication in independent samples is necessary to confirm it.

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Source
http://dx.doi.org/10.1002/ajmg.b.20038DOI Listing

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