The American Journal of Medicine
Volume 121, Issue 4, Supplement , Pages S32-S42, April 2008

Efficacy and Safety of Varenicline for Smoking Cessation

  • J. Taylor Hays, MD

      Affiliations

    • Corresponding Author InformationRequests for reprints should be addressed to J. Taylor Hays, MD, Nicotine Dependence Center, Mayo Clinic, 200 First Street SW, Rochester, Minnesota 55905.
  • ,
  • Jon O. Ebbert, MD
  • ,
  • Amit Sood, MD

Nicotine Dependence Center, Mayo Clinic College of Medicine, Mayo Clinic, Rochester, Minnesota, USA

Abstract 

Effective treatment of nicotine addiction is essential for reducing the substantial current and predicted morbidity and mortality associated with tobacco smoking. Despite the availability of effective treatments for smoking cessation, such as nicotine replacement therapy and bupropion sustained-release (SR), abstinence rates remain less than optimal. Varenicline is the first in a new class of agents for smoking cessation, the α4β2 nicotinic acetylcholine receptor (nAChR) partial agonists. Nicotine addiction is mediated by stimulation of central α4β2 nAChRs by nicotine, which causes the release of dopamine, ultimately leading to the pleasurable effects of smoking. As a nAChR partial agonist, varenicline attenuates the craving and withdrawal symptoms that occur with abstinence from nicotine and also reduces the rewarding effects of nicotine obtained from smoking in patients who lapse. Thus, varenicline offers a new therapeutic option for the treatment of nicotine addiction. Clinical trials have demonstrated superior efficacy of this agent over placebo and bupropion-SR for achieving abstinence from smoking, and varenicline has also been shown to significantly delay smoking relapse. As the newest agent approved for smoking cessation, the mechanism of action, efficacy, and safety of varenicline.

Keywords: α4β2 nicotinic acetylcholine receptor, Partial agonist, Smoking cessation, Varenicline

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 Statement of conflict of interest: Please see Author Disclosures section at the end of this article.

PII: S0002-9343(08)00106-X

doi:10.1016/j.amjmed.2008.01.017

The American Journal of Medicine
Volume 121, Issue 4, Supplement , Pages S32-S42, April 2008