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CLOCK is suggested to associate with comorbid alcohol use and depressive disorders
BACKGROUND: Depression and alcohol abuse or dependence (AUD) co-occur in the general population more frequently than expected by chance. Alcohol use influences the circadian rhythms generated by the central pacemaker in the suprachiasmatic nucleus, and circadian rhythm alterations in turn are common...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854106/ https://www.ncbi.nlm.nih.gov/pubmed/20180986 http://dx.doi.org/10.1186/1740-3391-8-1 |
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author | Sjöholm, Louise K Kovanen, Leena Saarikoski, Sirkku T Schalling, Martin Lavebratt, Catharina Partonen, Timo |
author_facet | Sjöholm, Louise K Kovanen, Leena Saarikoski, Sirkku T Schalling, Martin Lavebratt, Catharina Partonen, Timo |
author_sort | Sjöholm, Louise K |
collection | PubMed |
description | BACKGROUND: Depression and alcohol abuse or dependence (AUD) co-occur in the general population more frequently than expected by chance. Alcohol use influences the circadian rhythms generated by the central pacemaker in the suprachiasmatic nucleus, and circadian rhythm alterations in turn are common in depressive disorders as well as among persons addicted to alcohol. METHODS: 32 SNPs in 19 circadian clockwork related genes were analyzed using DNA from 76 individuals with comorbid depression and AUD, 446 individuals with AUD and 517 healthy controls with no psychiatric diagnosis. The individuals participated in a nationwide health examination study, representative of the general population aged 30 and over in Finland. RESULTS: The CLOCK haplotype TTGC formed by SNPs rs3805151, rs2412648, rs11240 and rs2412646, was associated with increased risk for comorbidity (OR = 1.65, 95% CI = 1.14-2.28, P = 0.0077). The SNPs of importance for this suggestive association were rs2412646 and rs11240 indicating location of the functional variation in the block downstream rs2412648. There was no indication for association between CLOCK and AUD. CONCLUSION: Our findings suggest an association between the CLOCK gene and the comorbid condition of alcohol use and depressive disorders. Together with previous reports it indicates that the CLOCK variations we found here may be a vulnerability factor to depression given the exposure to alcohol in individuals having AUD. |
format | Text |
id | pubmed-2854106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28541062010-04-14 CLOCK is suggested to associate with comorbid alcohol use and depressive disorders Sjöholm, Louise K Kovanen, Leena Saarikoski, Sirkku T Schalling, Martin Lavebratt, Catharina Partonen, Timo J Circadian Rhythms Research BACKGROUND: Depression and alcohol abuse or dependence (AUD) co-occur in the general population more frequently than expected by chance. Alcohol use influences the circadian rhythms generated by the central pacemaker in the suprachiasmatic nucleus, and circadian rhythm alterations in turn are common in depressive disorders as well as among persons addicted to alcohol. METHODS: 32 SNPs in 19 circadian clockwork related genes were analyzed using DNA from 76 individuals with comorbid depression and AUD, 446 individuals with AUD and 517 healthy controls with no psychiatric diagnosis. The individuals participated in a nationwide health examination study, representative of the general population aged 30 and over in Finland. RESULTS: The CLOCK haplotype TTGC formed by SNPs rs3805151, rs2412648, rs11240 and rs2412646, was associated with increased risk for comorbidity (OR = 1.65, 95% CI = 1.14-2.28, P = 0.0077). The SNPs of importance for this suggestive association were rs2412646 and rs11240 indicating location of the functional variation in the block downstream rs2412648. There was no indication for association between CLOCK and AUD. CONCLUSION: Our findings suggest an association between the CLOCK gene and the comorbid condition of alcohol use and depressive disorders. Together with previous reports it indicates that the CLOCK variations we found here may be a vulnerability factor to depression given the exposure to alcohol in individuals having AUD. BioMed Central 2010-01-21 /pmc/articles/PMC2854106/ /pubmed/20180986 http://dx.doi.org/10.1186/1740-3391-8-1 Text en Copyright ©2010 Sjöholm et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Sjöholm, Louise K Kovanen, Leena Saarikoski, Sirkku T Schalling, Martin Lavebratt, Catharina Partonen, Timo CLOCK is suggested to associate with comorbid alcohol use and depressive disorders |
title | CLOCK is suggested to associate with comorbid alcohol use and depressive disorders |
title_full | CLOCK is suggested to associate with comorbid alcohol use and depressive disorders |
title_fullStr | CLOCK is suggested to associate with comorbid alcohol use and depressive disorders |
title_full_unstemmed | CLOCK is suggested to associate with comorbid alcohol use and depressive disorders |
title_short | CLOCK is suggested to associate with comorbid alcohol use and depressive disorders |
title_sort | clock is suggested to associate with comorbid alcohol use and depressive disorders |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854106/ https://www.ncbi.nlm.nih.gov/pubmed/20180986 http://dx.doi.org/10.1186/1740-3391-8-1 |
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