Genetic variation in CHRNA7 and CHRFAM7A is associated with nicotine dependence and response to varenicline treatment. (December 2018)
- Record Type:
- Journal Article
- Title:
- Genetic variation in CHRNA7 and CHRFAM7A is associated with nicotine dependence and response to varenicline treatment. (December 2018)
- Main Title:
- Genetic variation in CHRNA7 and CHRFAM7A is associated with nicotine dependence and response to varenicline treatment
- Authors:
- Cameli, Cinzia
Bacchelli, Elena
Paola, Maria
Giucastro, Giuliano
Cifiello, Stefano
Collo, Ginetta
Cainazzo, Maria
Pini, Luigi
Maestrini, Elena
Zoli, Michele - Abstract:
- Abstract The role of nicotinic acetylcholine receptors (nAChR) in nicotine dependence (ND) is well established;CHRNA7, encoding the α7 subunit, has a still uncertain role in ND, although it is implicated in a wide range of neuropsychiatric conditions.CHRFAM7A, a hybrid gene containing a partial duplication ofCHRNA7, is possibly involved in modulating α7 nAChR function. The aim of this study was to investigate the role ofCHRNA7 andCHRFAM7A genetic variants in ND and to test the hypothesis that α7 nAChR variation may modulate the efficacy of varenicline treatment in smoking cessation. We assessedCHRNA7 andCHRFAM7A copy number, CHRFAM7A exon 6 ∆2 bp polymorphism, and sequence variants in theCHRNA7 proximal promoter in an Italian sample of 408 treatment-seeking smokers. We conducted case-control and quantitative association analyses using two smoking measures (cigarettes per day, CPD, and Fagerström Test for Nicotine Dependence, FTND). Next, driven by the hypothesis that varenicline may exert some of its therapeutic effects through activation of α7 nAChRs, we restricted the analysis to a subgroup of 142 smokers who received varenicline treatment. TheCHRNA7 promoter variant rs28531779 showed association with both smoking quantitative measures (FNTDp = 0.026, β = 0.89, 95% CI 0.11–1.67; CPDp = 0.006, β = 4.82 95% CI 1.42–8.22). Moreover, in the varenicline-treated subgroup we observed association ofCHRFAM7A copy number with 6 months smoking abstinence (p = 0.035, OR = 3.18,Abstract The role of nicotinic acetylcholine receptors (nAChR) in nicotine dependence (ND) is well established;CHRNA7, encoding the α7 subunit, has a still uncertain role in ND, although it is implicated in a wide range of neuropsychiatric conditions.CHRFAM7A, a hybrid gene containing a partial duplication ofCHRNA7, is possibly involved in modulating α7 nAChR function. The aim of this study was to investigate the role ofCHRNA7 andCHRFAM7A genetic variants in ND and to test the hypothesis that α7 nAChR variation may modulate the efficacy of varenicline treatment in smoking cessation. We assessedCHRNA7 andCHRFAM7A copy number, CHRFAM7A exon 6 ∆2 bp polymorphism, and sequence variants in theCHRNA7 proximal promoter in an Italian sample of 408 treatment-seeking smokers. We conducted case-control and quantitative association analyses using two smoking measures (cigarettes per day, CPD, and Fagerström Test for Nicotine Dependence, FTND). Next, driven by the hypothesis that varenicline may exert some of its therapeutic effects through activation of α7 nAChRs, we restricted the analysis to a subgroup of 142 smokers who received varenicline treatment. TheCHRNA7 promoter variant rs28531779 showed association with both smoking quantitative measures (FNTDp = 0.026, β = 0.89, 95% CI 0.11–1.67; CPDp = 0.006, β = 4.82 95% CI 1.42–8.22). Moreover, in the varenicline-treated subgroup we observed association ofCHRFAM7A copy number with 6 months smoking abstinence (p = 0.035, OR = 3.18, 95% CI = 1.09–9.30). Thus, our study points to a possible role of genetic variation inCHRNA7 andCHRFAM7A in tobacco addiction mechanisms and response to varenicline treatment. … (more)
- Is Part Of:
- European journal of human genetics. Volume 26:Number 12(2018)
- Journal:
- European journal of human genetics
- Issue:
- Volume 26:Number 12(2018)
- Issue Display:
- Volume 26, Issue 12 (2018)
- Year:
- 2018
- Volume:
- 26
- Issue:
- 12
- Issue Sort Value:
- 2018-0026-0012-0000
- Page Start:
- 1824
- Page End:
- 1831
- Publication Date:
- 2018-12
- Subjects:
- Human genetics -- Periodicals
Medical genetics -- Periodicals
616.042 - Journal URLs:
- http://www.nature.com/ejhg/index.html ↗
https://www.karger.com/Journal/Home/224162 ↗
http://www.nature.com/ ↗ - DOI:
- 10.1038/s41431-018-0223-2 ↗
- Languages:
- English
- ISSNs:
- 1018-4813
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.730020
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11054.xml