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CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy

Background: The large individual variability in response to drugs for smoking cessation suggests that specific treatments can be more effective in particular subgroups of smokers. In the context of personalized medicine, the main aim of the present study was to evaluate whether the CHRNA4 and CHRNB2...

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Autores principales: Rocha Santos, Juliana, Tomaz, Paulo R. X., Issa, Jaqueline S., Abe, Tânia O., Krieger, José E., Pereira, Alexandre C., Santos, Paulo C. J. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4343187/
https://www.ncbi.nlm.nih.gov/pubmed/25774163
http://dx.doi.org/10.3389/fgene.2015.00046
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author Rocha Santos, Juliana
Tomaz, Paulo R. X.
Issa, Jaqueline S.
Abe, Tânia O.
Krieger, José E.
Pereira, Alexandre C.
Santos, Paulo C. J. L.
author_facet Rocha Santos, Juliana
Tomaz, Paulo R. X.
Issa, Jaqueline S.
Abe, Tânia O.
Krieger, José E.
Pereira, Alexandre C.
Santos, Paulo C. J. L.
author_sort Rocha Santos, Juliana
collection PubMed
description Background: The large individual variability in response to drugs for smoking cessation suggests that specific treatments can be more effective in particular subgroups of smokers. In the context of personalized medicine, the main aim of the present study was to evaluate whether the CHRNA4 and CHRNB2 polymorphisms are associated with response to smoking cessation therapies in patients from a smoker assistance program. Methods: This cohort study enrolled 483 smoking patients who received behavioral counseling and drug treatment (varenicline, bupropion, and/or nicotine replacement therapy). Smoking cessation success was considered for patients who completed 6 months of continuous abstinence. Fagerström test for nicotine dependence (FTND) and Issa situational smoking scores were analyzed for nicotine dependence. The CHRNA4 (rs1044396 and rs2236196) and CHRNB2 (rs2072660 and rs2072661) polymorphisms were genotyped by high resolution melting analysis. Results: Patients with rs1044396 CC genotype had lower success rate in treatment with varenicline (29.5%) compared with carriers of CT or TT genotypes (50.9%; p = 0.007, n = 167). The CT or TT genotypes were associated with higher odds ratio for success (OR = 1.67, 95% CI = 1.10–2.53, p = 0.02), in a multivariate model. We did not observe significant differences in the FTND and Issa scores according to the studied polymorphisms. Conclusion: The CHRNA4 rs1044396 is associated with smoking cessation in individuals on varenicline therapy. We suggest that this polymorphism influences the varenicline response, but replications of this finding are needed.
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spelling pubmed-43431872015-03-13 CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy Rocha Santos, Juliana Tomaz, Paulo R. X. Issa, Jaqueline S. Abe, Tânia O. Krieger, José E. Pereira, Alexandre C. Santos, Paulo C. J. L. Front Genet Genetics Background: The large individual variability in response to drugs for smoking cessation suggests that specific treatments can be more effective in particular subgroups of smokers. In the context of personalized medicine, the main aim of the present study was to evaluate whether the CHRNA4 and CHRNB2 polymorphisms are associated with response to smoking cessation therapies in patients from a smoker assistance program. Methods: This cohort study enrolled 483 smoking patients who received behavioral counseling and drug treatment (varenicline, bupropion, and/or nicotine replacement therapy). Smoking cessation success was considered for patients who completed 6 months of continuous abstinence. Fagerström test for nicotine dependence (FTND) and Issa situational smoking scores were analyzed for nicotine dependence. The CHRNA4 (rs1044396 and rs2236196) and CHRNB2 (rs2072660 and rs2072661) polymorphisms were genotyped by high resolution melting analysis. Results: Patients with rs1044396 CC genotype had lower success rate in treatment with varenicline (29.5%) compared with carriers of CT or TT genotypes (50.9%; p = 0.007, n = 167). The CT or TT genotypes were associated with higher odds ratio for success (OR = 1.67, 95% CI = 1.10–2.53, p = 0.02), in a multivariate model. We did not observe significant differences in the FTND and Issa scores according to the studied polymorphisms. Conclusion: The CHRNA4 rs1044396 is associated with smoking cessation in individuals on varenicline therapy. We suggest that this polymorphism influences the varenicline response, but replications of this finding are needed. Frontiers Media S.A. 2015-02-27 /pmc/articles/PMC4343187/ /pubmed/25774163 http://dx.doi.org/10.3389/fgene.2015.00046 Text en Copyright © 2015 Rocha Santos, Tomaz, Issa, Abe, Krieger, Pereira and Santos. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Rocha Santos, Juliana
Tomaz, Paulo R. X.
Issa, Jaqueline S.
Abe, Tânia O.
Krieger, José E.
Pereira, Alexandre C.
Santos, Paulo C. J. L.
CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy
title CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy
title_full CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy
title_fullStr CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy
title_full_unstemmed CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy
title_short CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy
title_sort chrna4 rs1044396 is associated with smoking cessation in varenicline therapy
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4343187/
https://www.ncbi.nlm.nih.gov/pubmed/25774163
http://dx.doi.org/10.3389/fgene.2015.00046
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