4.7 Article

Nicotine treatment of mild cognitive impairment A 6-month double-blind pilot clinical trial

Journal

NEUROLOGY
Volume 78, Issue 2, Pages 91-101

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e31823efcbb

Keywords

-

Funding

  1. AstraZeneca
  2. Eli Lilly and Company
  3. Targacept, Inc.
  4. NIH (NIA)
  5. NIH (NIDA)
  6. NIH (NIAMS)
  7. Pfizer Inc
  8. Bayer Schering Pharma
  9. Baxter International Inc.
  10. Merck Serono
  11. sanofi-aventis
  12. Astellas Pharma Inc.
  13. Pharmaton(R)
  14. Novartis
  15. Gilead Sciences, Inc.
  16. Philip Morris-USA
  17. EPA
  18. Wallace Research Foundation
  19. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR000109] Funding Source: NIH RePORTER
  20. NATIONAL INSTITUTE ON AGING [R01AG022462] Funding Source: NIH RePORTER

Ask authors/readers for more resources

Objective: To preliminarily assess the safety and efficacy of transdermal nicotine therapy on cognitive performance and clinical status in subjects with mild cognitive impairment (MCI). Methods: Nonsmoking subjects with amnestic MCI were randomized to transdermal nicotine (15 mg per day or placebo) for 6 months. Primary outcome variables were attentional improvement assessed with Connors Continuous Performance Test (CPT), clinical improvement as measured by clinical global impression, and safety measures. Secondary measures included computerized cognitive testing and patient and observer ratings. Results: Of 74 subjects enrolled, 39 were randomized to nicotine and 35 to placebo. 67 subjects completed (34 nicotine, 33 placebo). The primary cognitive outcome measure (CPT) showed a significant nicotine-induced improvement. There was no statistically significant effect on clinician-rated global improvement. The secondary outcome measures showed significant nicotine-associated improvements in attention, memory, and psychomotor speed, and improvements were seen in patient/informant ratings of cognitive impairment. Safety and tolerability for transdermal nicotine were excellent. Conclusion: This study demonstrated that transdermal nicotine can be safely administered to nonsmoking subjects with MCI over 6 months with improvement in primary and secondary cognitive measures of attention, memory, and mental processing, but not in ratings of clinician-rated global impression. We conclude that this initial study provides evidence for nicotine-induced cognitive improvement in subjects with MCI; however, whether these effects are clinically important will require larger studies. Classification of evidence: This study provides Class I evidence that 6 months of transdermal nicotine (15 mg/day) improves cognitive test performance, but not clinical global impression of change, in nonsmoking subjects with amnestic MCI. Neurology (R) 2012; 78:91-101

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available