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Possible association of prokineticin 2 receptor gene (PROKR2) with mood disorders in the Japanese population.
- Source :
-
Neuromolecular medicine [Neuromolecular Med] 2009; Vol. 11 (2), pp. 114-22. Date of Electronic Publication: 2009 Jun 20. - Publication Year :
- 2009
-
Abstract
- Several investigations have suggested that disruption of circadian rhythms may provide the foundation for the development of mood disorders such as bipolar disorder (BP) and major depressive disorder (MDD). Recent animal studies reported that prokineticin 2 or prokineticin 2 receptor gene deficient mice showed disruptions in circadian and homeostatic regulation of sleep. This evidence indicates that prokineticin 2 gene (PROK2) and prokineticin 2 receptor gene (PROKR2) are good candidate genes for the pathogenesis of mood disorders. To evaluate the association between PROK2, PROKR2, and mood disorders, we conducted a case-control study of Japanese samples (151 bipolar patients, 319 major depressive disorder patients, and 340 controls) with four and five tagging SNPs in PROK2 or PROKR2, respectively, selected by HapMap database. We detected a significant association between PROKR2 and major depressive disorder and bipolar disorder in the Japanese population. In conclusion, our findings suggest that PROKR2 may play a role in the pathophysiology of mood disorders in the Japanese population. However, because our samples were small, it will be important to replicate and confirm these findings in other independent studies using larger samples.
- Subjects :
- Adult
Animals
Exons
Female
Gastrointestinal Hormones genetics
Gastrointestinal Hormones metabolism
Genetic Predisposition to Disease
Genotype
Haplotypes
Humans
Male
Mice
Middle Aged
Neuropeptides genetics
Neuropeptides metabolism
Receptors, G-Protein-Coupled metabolism
Receptors, Peptide metabolism
Young Adult
Asian People genetics
Mood Disorders genetics
Polymorphism, Single Nucleotide
Receptors, G-Protein-Coupled genetics
Receptors, Peptide genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1559-1174
- Volume :
- 11
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Neuromolecular medicine
- Publication Type :
- Academic Journal
- Accession number :
- 19544013
- Full Text :
- https://doi.org/10.1007/s12017-009-8067-0