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Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking

Several genome-wide association and candidate gene studies have linked chromosome 15q24–q25.1 (a region including the CHRNA5-CHRNA3-CHRNB4 gene cluster) with alcohol dependence, nicotine dependence and smoking-related illnesses such as lung cancer and chronic obstructive pulmonary disease. To furthe...

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Autores principales: Kapoor, Manav, Wang, Jen-Chyong, Bertelsen, Sarah, Bucholz, Kathy, Budde, John P., Hinrichs, Anthony, Agrawal, Arpana, Brooks, Andrew, Chorlian, David, Dick, Danielle, Hesselbrock, Victor, Foroud, Tatiana, Kramer, John, Kuperman, Samuel, Manz, Niklas, Nurnberger, John, Porjesz, Bernice, Rice, John, Tischfield, Jay, Xuei, Xiaoling, Schuckit, Marc, Edenberg, Howard J., Bierut, Laura J., Goate, Alison M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306405/
https://www.ncbi.nlm.nih.gov/pubmed/22438940
http://dx.doi.org/10.1371/journal.pone.0033513
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author Kapoor, Manav
Wang, Jen-Chyong
Bertelsen, Sarah
Bucholz, Kathy
Budde, John P.
Hinrichs, Anthony
Agrawal, Arpana
Brooks, Andrew
Chorlian, David
Dick, Danielle
Hesselbrock, Victor
Foroud, Tatiana
Kramer, John
Kuperman, Samuel
Manz, Niklas
Nurnberger, John
Porjesz, Bernice
Rice, John
Tischfield, Jay
Xuei, Xiaoling
Schuckit, Marc
Edenberg, Howard J.
Bierut, Laura J.
Goate, Alison M.
author_facet Kapoor, Manav
Wang, Jen-Chyong
Bertelsen, Sarah
Bucholz, Kathy
Budde, John P.
Hinrichs, Anthony
Agrawal, Arpana
Brooks, Andrew
Chorlian, David
Dick, Danielle
Hesselbrock, Victor
Foroud, Tatiana
Kramer, John
Kuperman, Samuel
Manz, Niklas
Nurnberger, John
Porjesz, Bernice
Rice, John
Tischfield, Jay
Xuei, Xiaoling
Schuckit, Marc
Edenberg, Howard J.
Bierut, Laura J.
Goate, Alison M.
author_sort Kapoor, Manav
collection PubMed
description Several genome-wide association and candidate gene studies have linked chromosome 15q24–q25.1 (a region including the CHRNA5-CHRNA3-CHRNB4 gene cluster) with alcohol dependence, nicotine dependence and smoking-related illnesses such as lung cancer and chronic obstructive pulmonary disease. To further examine the impact of these genes on the development of substance use disorders, we tested whether variants within and flanking the CHRNA5-CHRNA3-CHRNB4 gene cluster affect the transition to daily smoking (individuals who smoked cigarettes 4 or more days per week) in a cross sectional sample of adolescents and young adults from the COGA (Collaborative Study of the Genetics of Alcoholism) families. Subjects were recruited from families affected with alcoholism (either as a first or second degree relative) and the comparison families. Participants completed the SSAGA interview, a comprehensive assessment of alcohol and other substance use and related behaviors. Using the Quantitative trait disequilibrium test (QTDT) significant association was detected between age at onset of daily smoking and variants located upstream of CHRNB4. Multivariate analysis using a Cox proportional hazards model further revealed that these variants significantly predict the age at onset of habitual smoking among daily smokers. These variants were not in high linkage disequilibrium (0.28<r(2)<0.56) with variants that have previously been reported to affect risk for nicotine dependence and smoking related diseases in adults. The data suggests that an age-associated relationship underlies the association of SNPs in CHRNB4 with onset of chronic smoking behaviors in adolescents and young adults and may improve genetic information that will lead to better prevention and intervention for substance use disorders among adolescents and young adults.
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spelling pubmed-33064052012-03-21 Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking Kapoor, Manav Wang, Jen-Chyong Bertelsen, Sarah Bucholz, Kathy Budde, John P. Hinrichs, Anthony Agrawal, Arpana Brooks, Andrew Chorlian, David Dick, Danielle Hesselbrock, Victor Foroud, Tatiana Kramer, John Kuperman, Samuel Manz, Niklas Nurnberger, John Porjesz, Bernice Rice, John Tischfield, Jay Xuei, Xiaoling Schuckit, Marc Edenberg, Howard J. Bierut, Laura J. Goate, Alison M. PLoS One Research Article Several genome-wide association and candidate gene studies have linked chromosome 15q24–q25.1 (a region including the CHRNA5-CHRNA3-CHRNB4 gene cluster) with alcohol dependence, nicotine dependence and smoking-related illnesses such as lung cancer and chronic obstructive pulmonary disease. To further examine the impact of these genes on the development of substance use disorders, we tested whether variants within and flanking the CHRNA5-CHRNA3-CHRNB4 gene cluster affect the transition to daily smoking (individuals who smoked cigarettes 4 or more days per week) in a cross sectional sample of adolescents and young adults from the COGA (Collaborative Study of the Genetics of Alcoholism) families. Subjects were recruited from families affected with alcoholism (either as a first or second degree relative) and the comparison families. Participants completed the SSAGA interview, a comprehensive assessment of alcohol and other substance use and related behaviors. Using the Quantitative trait disequilibrium test (QTDT) significant association was detected between age at onset of daily smoking and variants located upstream of CHRNB4. Multivariate analysis using a Cox proportional hazards model further revealed that these variants significantly predict the age at onset of habitual smoking among daily smokers. These variants were not in high linkage disequilibrium (0.28<r(2)<0.56) with variants that have previously been reported to affect risk for nicotine dependence and smoking related diseases in adults. The data suggests that an age-associated relationship underlies the association of SNPs in CHRNB4 with onset of chronic smoking behaviors in adolescents and young adults and may improve genetic information that will lead to better prevention and intervention for substance use disorders among adolescents and young adults. Public Library of Science 2012-03-16 /pmc/articles/PMC3306405/ /pubmed/22438940 http://dx.doi.org/10.1371/journal.pone.0033513 Text en Kapoor 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
Kapoor, Manav
Wang, Jen-Chyong
Bertelsen, Sarah
Bucholz, Kathy
Budde, John P.
Hinrichs, Anthony
Agrawal, Arpana
Brooks, Andrew
Chorlian, David
Dick, Danielle
Hesselbrock, Victor
Foroud, Tatiana
Kramer, John
Kuperman, Samuel
Manz, Niklas
Nurnberger, John
Porjesz, Bernice
Rice, John
Tischfield, Jay
Xuei, Xiaoling
Schuckit, Marc
Edenberg, Howard J.
Bierut, Laura J.
Goate, Alison M.
Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking
title Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking
title_full Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking
title_fullStr Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking
title_full_unstemmed Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking
title_short Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking
title_sort variants located upstream of chrnb4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smoking
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306405/
https://www.ncbi.nlm.nih.gov/pubmed/22438940
http://dx.doi.org/10.1371/journal.pone.0033513
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