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CRY2 Is Associated with Depression
BACKGROUND: Abnormalities in the circadian clockwork often characterize patients with major depressive and bipolar disorders. Circadian clock genes are targets of interest in these patients. CRY2 is a circadian gene that participates in regulation of the evening oscillator. This is of interest in mo...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2827563/ https://www.ncbi.nlm.nih.gov/pubmed/20195522 http://dx.doi.org/10.1371/journal.pone.0009407 |
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author | Lavebratt, Catharina Sjöholm, Louise K. Soronen, Pia Paunio, Tiina Vawter, Marquis P. Bunney, William E. Adolfsson, Rolf Forsell, Yvonne Wu, Joseph C. Kelsoe, John R. Partonen, Timo Schalling, Martin |
author_facet | Lavebratt, Catharina Sjöholm, Louise K. Soronen, Pia Paunio, Tiina Vawter, Marquis P. Bunney, William E. Adolfsson, Rolf Forsell, Yvonne Wu, Joseph C. Kelsoe, John R. Partonen, Timo Schalling, Martin |
author_sort | Lavebratt, Catharina |
collection | PubMed |
description | BACKGROUND: Abnormalities in the circadian clockwork often characterize patients with major depressive and bipolar disorders. Circadian clock genes are targets of interest in these patients. CRY2 is a circadian gene that participates in regulation of the evening oscillator. This is of interest in mood disorders where a lack of switch from evening to morning oscillators has been postulated. PRINCIPAL FINDINGS: We observed a marked diurnal variation in human CRY2 mRNA levels from peripheral blood mononuclear cells and a significant up-regulation (P = 0.020) following one-night total sleep deprivation, a known antidepressant. In depressed bipolar patients, levels of CRY2 mRNA were decreased (P = 0.029) and a complete lack of increase was observed following sleep deprivation. To investigate a possible genetic contribution, we undertook SNP genotyping of the CRY2 gene in two independent population-based samples from Sweden (118 cases and 1011 controls) and Finland (86 cases and 1096 controls). The CRY2 gene was significantly associated with winter depression in both samples (haplotype analysis in Swedish and Finnish samples: OR = 1.8, P = 0.0059 and OR = 1.8, P = 0.00044, respectively). CONCLUSIONS: We propose that a CRY2 locus is associated with vulnerability for depression, and that mechanisms of action involve dysregulation of CRY2 expression. |
format | Text |
id | pubmed-2827563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-28275632010-03-02 CRY2 Is Associated with Depression Lavebratt, Catharina Sjöholm, Louise K. Soronen, Pia Paunio, Tiina Vawter, Marquis P. Bunney, William E. Adolfsson, Rolf Forsell, Yvonne Wu, Joseph C. Kelsoe, John R. Partonen, Timo Schalling, Martin PLoS One Research Article BACKGROUND: Abnormalities in the circadian clockwork often characterize patients with major depressive and bipolar disorders. Circadian clock genes are targets of interest in these patients. CRY2 is a circadian gene that participates in regulation of the evening oscillator. This is of interest in mood disorders where a lack of switch from evening to morning oscillators has been postulated. PRINCIPAL FINDINGS: We observed a marked diurnal variation in human CRY2 mRNA levels from peripheral blood mononuclear cells and a significant up-regulation (P = 0.020) following one-night total sleep deprivation, a known antidepressant. In depressed bipolar patients, levels of CRY2 mRNA were decreased (P = 0.029) and a complete lack of increase was observed following sleep deprivation. To investigate a possible genetic contribution, we undertook SNP genotyping of the CRY2 gene in two independent population-based samples from Sweden (118 cases and 1011 controls) and Finland (86 cases and 1096 controls). The CRY2 gene was significantly associated with winter depression in both samples (haplotype analysis in Swedish and Finnish samples: OR = 1.8, P = 0.0059 and OR = 1.8, P = 0.00044, respectively). CONCLUSIONS: We propose that a CRY2 locus is associated with vulnerability for depression, and that mechanisms of action involve dysregulation of CRY2 expression. Public Library of Science 2010-02-24 /pmc/articles/PMC2827563/ /pubmed/20195522 http://dx.doi.org/10.1371/journal.pone.0009407 Text en Lavebratt et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lavebratt, Catharina Sjöholm, Louise K. Soronen, Pia Paunio, Tiina Vawter, Marquis P. Bunney, William E. Adolfsson, Rolf Forsell, Yvonne Wu, Joseph C. Kelsoe, John R. Partonen, Timo Schalling, Martin CRY2 Is Associated with Depression |
title |
CRY2 Is Associated with Depression |
title_full |
CRY2 Is Associated with Depression |
title_fullStr |
CRY2 Is Associated with Depression |
title_full_unstemmed |
CRY2 Is Associated with Depression |
title_short |
CRY2 Is Associated with Depression |
title_sort | cry2 is associated with depression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2827563/ https://www.ncbi.nlm.nih.gov/pubmed/20195522 http://dx.doi.org/10.1371/journal.pone.0009407 |
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