4.4 Article

Menstrual cycle phase at quit date and smoking abstinence at 6 weeks in an open label trial of bupropion

Journal

DRUG AND ALCOHOL DEPENDENCE
Volume 114, Issue 1, Pages 68-72

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.drugalcdep.2010.07.024

Keywords

Smoking cessation; Gender; Menstrual cycle phase; Bupropion

Funding

  1. National Institute on Drug Abuse
  2. National Institute on Alcohol Abuse and Alcoholism at the National Institutes of Health [P50DA013334-9005, P50AA015632-9002]
  3. Pfizer
  4. Abbott Laboratories
  5. Eli Lilly
  6. Janssen
  7. Schering Plough
  8. Lundbeck
  9. Glaxo-Smith Kline
  10. Alkermes
  11. NABI Biopharmaceutical

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Background: Quit attempts may have different outcomes based on menstrual cycle phase on quit day. This is the first preliminary study examining whether smoking cessation outcomes vary by menstrual cycle phase of quit date in women receiving a 6-week open trial of sustained release (SR) bupropion. Methods: Thirty-three treatment-seeking premenopausal women were studied. Abstinence outcomes were compared for women quitting during the luteal versus follicular phase. Results: Women receiving bupropion SR whose self-selected quit date occurred in the luteal phase had significantly higher rates of point prevalence abstinence during the final week of a 6-week post-quit treatment period than women quitting in the follicular phase (62.5% versus 29.4%; p <0.05). A similar, but non-significant, pattern of findings was demonstrated for continuous abstinence during the treatment phase and for point prevalence abstinence at 3-month follow-up. Conclusions: Women receiving bupropion SR were significantly more likely to be abstinent at treatment completion if quitting occurred during the luteal phase. This is consistent with recent findings of outcome related to cycle phase at quit date in the absence of pharmacotherapy, and differs from findings utilizing nicotine replacement. Results add to emerging data suggesting that smoking cessation interventions with varying mechanisms of action may result in different outcomes for premenopausal women based on gonadal hormones at quit date. (C) 2010 Elsevier Ireland Ltd. All rights reserved.

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