Influence of a dopamine pathway additive genetic efficacy score on smoking cessation

Results from two randomized clinical trials of bupropion

Sean P. David, David R. Strong, Adam M. Leventhal, Molly A. Lancaster, John E. Mcgeary, Marcus R. Munafò, Andrew W. Bergen, Gary E. Swan, Neal L. Benowitz, Rachel F. Tyndale, David V. Conti, Richard A. Brown, Caryn Lerman, Raymond Niaura

Research output: Contribution to journalArticle

Abstract

Aims: To evaluate the associations of treatment and an additive genetic efficacy score (AGES) based on dopamine functional polymorphisms with time to first smoking lapse and point prevalence abstinence at end of treatment among participants enrolled into two randomized clinical trials of smoking cessation therapies. Design: Double-blind pharmacogenetic efficacy trials randomizing participants to active or placebo bupropion. Study 1 also randomized participants to cognitive-behavioral smoking cessation treatment (CBT) or this treatment with CBT for depression. Study 2 provided standardized behavioural support. Setting: Two hospital-affiliated clinics (study 1), and two university-affiliated clinics (study 2). Participants: A total of 792 self-identified white treatment-seeking smokers aged ≥18 years smoking ≥10 cigarettes per day over the last year. Measurements: Age, gender, Fagerström Test for Nicotine Dependence, dopamine pathway genotypes (rs1800497 [ANKK1E713K], rs4680 [COMT V158M], DRD4 exon 3 variable number of tandem repeats polymorphism [DRD4VNTR], SLC6A3,3′VNTR) analyzed both separately and as part of an AGES, time to first lapse and point prevalence abstinence at end of treatment. Findings: Significant associations of the AGES (hazard ratio [HR]=1.10, 95% confidence interval [CI]=1.06-1.14, P=0.009) and of the DRD4VNTR (HR=1.29, 95% CI=1.17-1.41, P=0.0073) were observed with time to first lapse. A significant AGES by pharmacotherapy interaction was observed (β standard error=-0.18 [0.07], P=0.016), such that AGES predicted risk for time to first lapse only for individuals randomized to placebo. Conclusions: A score based on functional polymorphisms relating to dopamine pathways appears to predict lapse to smoking following a quit attempt, and the association is mitigated in smokers using bupropion.

Original languageEnglish (US)
Pages (from-to)2202-2211
Number of pages10
JournalAddiction
Volume108
Issue number12
DOIs
StatePublished - Dec 2013

Fingerprint

Bupropion
Smoking Cessation
Dopamine
Randomized Controlled Trials
Minisatellite Repeats
Smoking
Exons
Therapeutics
Placebos
Confidence Intervals
Tobacco Use Disorder
Withholding Treatment
Pharmacogenetics
Genotype
Depression
Drug Therapy

Keywords

  • Bupropion
  • First lapse
  • Genetic
  • Pharmacogenetic analysis
  • Randomized clinical trial

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Psychiatry and Mental health

Cite this

Influence of a dopamine pathway additive genetic efficacy score on smoking cessation : Results from two randomized clinical trials of bupropion. / David, Sean P.; Strong, David R.; Leventhal, Adam M.; Lancaster, Molly A.; Mcgeary, John E.; Munafò, Marcus R.; Bergen, Andrew W.; Swan, Gary E.; Benowitz, Neal L.; Tyndale, Rachel F.; Conti, David V.; Brown, Richard A.; Lerman, Caryn; Niaura, Raymond.

In: Addiction, Vol. 108, No. 12, 12.2013, p. 2202-2211.

Research output: Contribution to journalArticle

David, SP, Strong, DR, Leventhal, AM, Lancaster, MA, Mcgeary, JE, Munafò, MR, Bergen, AW, Swan, GE, Benowitz, NL, Tyndale, RF, Conti, DV, Brown, RA, Lerman, C & Niaura, R 2013, 'Influence of a dopamine pathway additive genetic efficacy score on smoking cessation: Results from two randomized clinical trials of bupropion', Addiction, vol. 108, no. 12, pp. 2202-2211. https://doi.org/10.1111/add.12325
David, Sean P. ; Strong, David R. ; Leventhal, Adam M. ; Lancaster, Molly A. ; Mcgeary, John E. ; Munafò, Marcus R. ; Bergen, Andrew W. ; Swan, Gary E. ; Benowitz, Neal L. ; Tyndale, Rachel F. ; Conti, David V. ; Brown, Richard A. ; Lerman, Caryn ; Niaura, Raymond. / Influence of a dopamine pathway additive genetic efficacy score on smoking cessation : Results from two randomized clinical trials of bupropion. In: Addiction. 2013 ; Vol. 108, No. 12. pp. 2202-2211.
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abstract = "Aims: To evaluate the associations of treatment and an additive genetic efficacy score (AGES) based on dopamine functional polymorphisms with time to first smoking lapse and point prevalence abstinence at end of treatment among participants enrolled into two randomized clinical trials of smoking cessation therapies. Design: Double-blind pharmacogenetic efficacy trials randomizing participants to active or placebo bupropion. Study 1 also randomized participants to cognitive-behavioral smoking cessation treatment (CBT) or this treatment with CBT for depression. Study 2 provided standardized behavioural support. Setting: Two hospital-affiliated clinics (study 1), and two university-affiliated clinics (study 2). Participants: A total of 792 self-identified white treatment-seeking smokers aged ≥18 years smoking ≥10 cigarettes per day over the last year. Measurements: Age, gender, Fagerstr{\"o}m Test for Nicotine Dependence, dopamine pathway genotypes (rs1800497 [ANKK1E713K], rs4680 [COMT V158M], DRD4 exon 3 variable number of tandem repeats polymorphism [DRD4VNTR], SLC6A3,3′VNTR) analyzed both separately and as part of an AGES, time to first lapse and point prevalence abstinence at end of treatment. Findings: Significant associations of the AGES (hazard ratio [HR]=1.10, 95{\%} confidence interval [CI]=1.06-1.14, P=0.009) and of the DRD4VNTR (HR=1.29, 95{\%} CI=1.17-1.41, P=0.0073) were observed with time to first lapse. A significant AGES by pharmacotherapy interaction was observed (β standard error=-0.18 [0.07], P=0.016), such that AGES predicted risk for time to first lapse only for individuals randomized to placebo. Conclusions: A score based on functional polymorphisms relating to dopamine pathways appears to predict lapse to smoking following a quit attempt, and the association is mitigated in smokers using bupropion.",
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AU - Lancaster, Molly A.

AU - Mcgeary, John E.

AU - Munafò, Marcus R.

AU - Bergen, Andrew W.

AU - Swan, Gary E.

AU - Benowitz, Neal L.

AU - Tyndale, Rachel F.

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