Jenike M A, Albert M S, Baer L
Division on Aging, Massachusetts General Hospital, Boston 02114.
Alzheimer Dis Assoc Disord. 1990 Winter;4(4):226-31. doi: 10.1097/00002093-199040400-00004.
Six patients with dementia of the Alzheimer type (DAT), treated with oral physostigmine and followed from 9 to 27 months (mean +/- SD, 17.8 +/- 7.3 months), were matched for sex, age, initial degree of dementia, and length of follow-up with six control patients who did not receive oral physostigmine. The small sample size precluded drawing definite conclusions about overall efficacy; however, three in the physostigmine group did not deteriorate during the course of follow-up while all of the controls deteriorated although the difference was nonsignificant. The data generated in these patients provides evidence of the safety of long-term trials of oral physostigmine. The possible role of cholinesterase inhibition in retarding the progression of DAT is discussed.
六名患有阿尔茨海默型痴呆(DAT)的患者接受了口服毒扁豆碱治疗,并进行了9至27个月(平均±标准差,17.8±7.3个月)的随访。将这六名患者与六名未接受口服毒扁豆碱的对照患者进行性别、年龄、初始痴呆程度和随访时间匹配。样本量较小,无法就总体疗效得出明确结论;然而,毒扁豆碱组中有三名患者在随访期间病情未恶化,而所有对照患者病情均恶化,尽管差异不显著。这些患者产生的数据为口服毒扁豆碱长期试验的安全性提供了证据。讨论了胆碱酯酶抑制在延缓DAT进展中的可能作用。