White Heidi K, Levin Edward D
Department of Medicine, Duke University Medical Center, Box no. 3003, Durham, NC 27710, USA.
Psychopharmacology (Berl). 2004 Feb;171(4):465-71. doi: 10.1007/s00213-003-1614-8. Epub 2003 Oct 8.
Chronic transdermal nicotine has been found to improve attentional performance in patients with Alzheimer's disease (AD), but little is known about chronic nicotine effects in age-associated memory impairment (AAMI), a milder form of cognitive dysfunction. The current study was performed to determine the clinical and neuropsychological effects of chronic transdermal nicotine in AAMI subjects over a 4-week period.
The double-blind, placebo-controlled, cross-over study consisted of two 4-week periods separated by a 2-week washout period.
An outpatient setting was used.
The subjects ( n=11) met criteria for AAMI.
The subjects were given nicotine patches (Nicotrol) to wear for 16 h a day at the following doses: 5 mg/day during week 1, 10 mg/day during week 2 and week 3 and 5 mg/day during week 4.
The effects of nicotine treatment were determined with the clinical global impressions questionnaire, Conners' Continuous Performance test, and the automated neuropsychologic assessment metrics (ANAM) computerized neuropsychology battery.
Nicotine significantly improved the clinical global impression score as assessed by participants, as well as objective tests of attentional function on the Connors' Continuous Performance Test and decision reaction time on the neuropsychology test battery. Nicotine did not improve performance on other tests measuring motor and memory function.
Chronic transdermal nicotine treatment in AAMI subjects caused a sustained improvement in clinical symptoms and objective computerized tests of attention. These results support the further investigation of nicotinic treatment as a promising therapy for AAMI.
已发现慢性经皮给予尼古丁可改善阿尔茨海默病(AD)患者的注意力表现,但对于年龄相关性记忆障碍(AAMI,一种较轻形式的认知功能障碍)中慢性尼古丁的作用知之甚少。本研究旨在确定慢性经皮给予尼古丁在4周时间内对AAMI受试者的临床和神经心理学影响。
双盲、安慰剂对照、交叉研究包括两个4周周期,中间有2周的洗脱期。
采用门诊环境。
受试者(n = 11)符合AAMI标准。
给予受试者尼古丁贴片(Nicotrol),每天佩戴16小时,剂量如下:第1周5毫克/天,第2周和第3周10毫克/天,第4周5毫克/天。
通过临床总体印象问卷、康纳斯连续作业测试以及自动化神经心理评估指标(ANAM)计算机化神经心理测试组来确定尼古丁治疗的效果。
尼古丁显著改善了参与者评估的临床总体印象评分,以及康纳斯连续作业测试中注意力功能的客观测试和神经心理测试组中的决策反应时间。尼古丁并未改善其他测量运动和记忆功能的测试表现。
对AAMI受试者进行慢性经皮尼古丁治疗可使临床症状以及注意力的客观计算机化测试得到持续改善。这些结果支持进一步研究将烟碱治疗作为AAMI的一种有前景的治疗方法。