Trinh Nhi-Ha, Hoblyn Jennifer, Mohanty Subhanjoy, Yaffe Kristine
Department of Psychiatry, Massachusetts General Hospital, Boston, USA.
JAMA. 2003 Jan 8;289(2):210-6. doi: 10.1001/jama.289.2.210.
Cholinesterase inhibitors are the primary treatment for the cognitive symptoms of Alzheimer disease (AD). Cholinergic dysfunction is also associated with neuropsychiatric and functional deficits, but results from randomized controlled trials of cholinesterase inhibitors are conflicting.
To conduct a systematic review and meta-analysis to quantify the efficacy of cholinesterase inhibitors for neuropsychiatric and functional outcomes in patients with mild to moderate AD.
We performed a literature search of trials using MEDLINE (January 1966-December 2001), Dissertations Abstracts On-line, PSYCHINFO, BIOSIS, PubMed, and the Cochrane Controlled Trials Register. We retrieved English- and non-English-language articles for review and collected references from bibliographies of reviews, original research articles, and other articles of interest. We searched for both published and unpublished trials, contacting researchers and pharmaceutical companies.
We included 29 parallel-group or crossover randomized, double-blind, placebo-controlled trials of outpatients who were diagnosed as having mild to moderate probable AD and were treated for at least 1 month with a cholinesterase inhibitor. Sixteen trials included neuropsychiatric and 18 included functional measures.
Two investigators (N.H.T. and J.H.) independently extracted study methods, sources of bias, and outcomes. Neuropsychiatric outcomes were measured with the Neuropsychiatric Inventory (NPI, 0-120 points) and the Alzheimer Disease Assessment Scale, noncognitive (ADAS-noncog, 0-50 points) and were analyzed with the weighted mean difference method. Functional outcomes were measured with several activities of daily living (ADL) and instrumental activities of daily living (IADL) scales and analyzed with the standardized mean difference method.
For neuropsychiatric outcomes, 10 trials included the ADAS-noncog and 6 included the NPI. Compared with placebo, patients randomized to cholinesterase inhibitors improved 1.72 points on the NPI (95% confidence interval [CI], 0.87-2.57 points), and 0.03 points on the ADAS-noncog (95% CI, 0.00-0.05 points). For functional outcomes, 14 trials used ADL and 13 trials used IADL scales. Compared with placebo, patients randomized to cholinesterase inhibitors improved 0.1 SDs on ADL scales (95% CI, 0.00-0.19 SDs), and 0.09 SDs on IADL scales (95% CI, 0.01 to 0.17 SDs). There was no difference in efficacy among various cholinesterase inhibitors.
These results indicate that cholinesterase inhibitors have a modest beneficial impact on neuropsychiatric and functional outcomes for patients with AD. Future research should focus on how such improvements translate into long-term outcomes such as patient quality of life, institutionalization, and caregiver burden.
胆碱酯酶抑制剂是治疗阿尔茨海默病(AD)认知症状的主要药物。胆碱能功能障碍也与神经精神和功能缺陷有关,但胆碱酯酶抑制剂随机对照试验的结果相互矛盾。
进行系统评价和荟萃分析,以量化胆碱酯酶抑制剂对轻至中度AD患者神经精神和功能结局的疗效。
我们使用MEDLINE(1966年1月至2001年12月)、《在线学位论文摘要》、PSYCHINFO、BIOSIS、PubMed和Cochrane对照试验注册库对试验进行了文献检索。我们检索了英文和非英文文章进行综述,并从综述、原始研究文章和其他相关文章的参考文献中收集资料。我们搜索了已发表和未发表的试验,并联系了研究人员和制药公司。
我们纳入了29项平行组或交叉随机、双盲、安慰剂对照试验,这些试验的门诊患者被诊断为患有轻至中度可能的AD,并接受胆碱酯酶抑制剂治疗至少1个月。16项试验纳入了神经精神测量指标,18项试验纳入了功能测量指标。
两名研究人员(N.H.T.和J.H.)独立提取研究方法、偏倚来源和结局指标。神经精神结局用神经精神量表(NPI,0 - 120分)和阿尔茨海默病评估量表非认知部分(ADAS - noncog,0 - 50分)进行测量,并采用加权均数差法进行分析。功能结局用几种日常生活活动(ADL)和工具性日常生活活动(IADL)量表进行测量,并采用标准化均数差法进行分析。
对于神经精神结局,10项试验纳入了ADAS - noncog,6项试验纳入了NPI。与安慰剂相比,随机接受胆碱酯酶抑制剂治疗的患者在NPI上改善了1.72分(95%置信区间[CI],0.87 - 2.57分),在ADAS - noncog上改善了0.03分(95% CI,0.00 - 0.05分)。对于功能结局,14项试验使用了ADL量表,13项试验使用了IADL量表。与安慰剂相比,随机接受胆碱酯酶抑制剂治疗的患者在ADL量表上改善了0.1个标准差(95% CI,0.00 - 0.19个标准差),在IADL量表上改善了0.09个标准差(95% CI,0.01 - 0.17个标准差)。各种胆碱酯酶抑制剂之间的疗效没有差异。
这些结果表明,胆碱酯酶抑制剂对AD患者的神经精神和功能结局有适度的有益影响。未来的研究应关注这些改善如何转化为长期结局,如患者生活质量、住院情况和照顾者负担。