A greater understanding of individual differences in the neurobiology of tobacco use is integral to developing more effective tobacco interventions. Understanding these individual differences would facilitate matching individuals with a specific biological vulnerability (e.g., genetic variation that alters nicotine receptor function), to an intervention that targets that vulnerability (e.g., a medication that targets nicotinic receptor function, like varenicline). Our previous studies clearly indicate the critical role of specific genetic variation in the gene (CHRNA4) that codes for the 14 subunit of the 1422 nicotinic receptor. This proposed research will extend our previous work by testing whether this genetic variation influences brain activation in response to smoking cues and influences the clinical effects of varenicline. Specifically, the first aim is to determine whether a functional single nucleotide polymorphism (SNP) in the CHRNA4 gene influences the acute effects of smoking and influences mesocorticolimbic activation in response to smoking cues.
The second aim i s to replicate the finding that varenicline increases abstinence and identify brain based measures that predict treatment outcome.
The third aim i s to determine whether the CHRNA4 SNP moderates the effects of varenicline on abstinence. To accomplish these aims, 216 treatment seeking smokers will participate in a 12 week, placebo controlled trial of varenicline with a neuroimaging assessment at baseline and behavioral assessments at baseline, 2, 6, and 12 weeks and a 6 month follow-up. The proposed research on genetic variation that predicts responses to varenicline is expected to have significant clinical implications.
Despite rapid advances in our understanding of the human genome, the identification of genetic factors that influence the etiology and treatment of tobacco dependence has yet to materialize. This research is designed to identify specific genetic variations that are related to how people respond to tobacco and identify how they are related to tobacco dependence. This research will also test whether these genetic variations predict the effectiveness of varenicline, which is currently the most effective medication for smoking cessation. Improvements in our understanding of genetic factors and neurobiological mechanisms that influence the etiology of tobacco dependence is expected to have implications for new prevention and treatment approaches.
|Thayer, Rachel E; Hagerty, Sarah L; Sabbineni, Amithrupa et al. (2016) Negative and interactive effects of sex, aging, and alcohol abuse on gray matter morphometry. Hum Brain Mapp 37:2276-92|
|Weiland, Barbara J; Sabbineni, Amithrupa; Calhoun, Vince D et al. (2015) Reduced executive and default network functional connectivity in cigarette smokers. Hum Brain Mapp 36:872-82|
|Weiland, Barbara J; Sabbineni, Amithrupa; Calhoun, Vince D et al. (2014) Reduced left executive control network functional connectivity is associated with alcohol use disorders. Alcohol Clin Exp Res 38:2445-53|
|Claus, Eric D; Blaine, Sara K; Filbey, Francesca M et al. (2013) Association between nicotine dependence severity, BOLD response to smoking cues, and functional connectivity. Neuropsychopharmacology 38:2363-72|
|Karoly, Hollis C; Harlaar, Nicole; Hutchison, Kent E (2013) Substance use disorders: a theory-driven approach to the integration of genetics and neuroimaging. Ann N Y Acad Sci 1282:71-91|
|Karoly, Hollis C; Stevens, Courtney J; Thayer, Rachel E et al. (2013) Aerobic exercise moderates the effect of heavy alcohol consumption on white matter damage. Alcohol Clin Exp Res 37:1508-15|
|Shoemaker, J M; Holdsworth, M T; Aine, C et al. (2011) A practical approach to incidental findings in neuroimaging research. Neurology 77:2123-7|