Leinonen Anne, Koponen Marjaana, Hartikainen Sirpa
University of Eastern Finland, Faculty of Health Sciences, School of Pharmacy, Kuopio, Finland.
PLoS One. 2015 May 1;10(5):e0124500. doi: 10.1371/journal.pone.0124500. eCollection 2015.
To determine whether there are differences in age and sex distribution and presence of comorbidities between participants included in randomized controlled trials of acetylcholinesterase inhibitors and nationwide cohort of persons with Alzheimer's disease.
PubMed, Scopus and Cochrane Library databases were searched for original articles from their inception to January 4, 2015. Double-blind randomized controlled trials with donepezil, rivastigmine or galantamine compared to placebo in participants with Alzheimer's disease were included. Data from a nationwide cohort of persons with clinically verified diagnoses of Alzheimer's disease was defined as a reference population.
128 full-text articles were assessed for eligibility, 31 of them fulfilled criteria. Mean age of participants in randomized controlled trials (n = 15,032) was 5.8 years lower (95% CI 5.7 to 5.9, P < 0.001), compared to the mean age of 79.7 years in the reference population with Alzheimer's disease (n = 28,093). Most of the articles did not report age distribution of participants. The proportion of women was 63.2% (9,475/14,991) in randomized controlled trials and 67.8% (19,043/28,093) (P < 0.001) in the reference population. Information on comorbidities and use of concomitant drugs were lacking or poorly reported in most articles.
There is a discrepancy between participants in randomized controlled trials of acetylcholinesterase inhibitors and real-life population with Alzheimer's disease. Participants in randomized controlled trials were significantly younger. Further, more detailed reporting of age distribution, comorbidities and concomitant drugs would be important information for clinicians when evaluating conclusions from randomized controlled trials to real-life practice. The existing recommendations of inclusion of older people should be followed to ensure safe pharmacotherapy for older people.
确定在乙酰胆碱酯酶抑制剂随机对照试验中的参与者与全国范围的阿尔茨海默病患者队列之间,年龄和性别分布以及合并症的存在情况是否存在差异。
检索PubMed、Scopus和Cochrane图书馆数据库,查找从建库至2015年1月4日的原始文章。纳入在阿尔茨海默病患者中进行的、将多奈哌齐、卡巴拉汀或加兰他敏与安慰剂进行比较的双盲随机对照试验。来自全国范围经临床确诊为阿尔茨海默病患者队列的数据被定义为参考人群。
评估了128篇全文文章的 eligibility,其中31篇符合标准。随机对照试验(n = 15,032)参与者的平均年龄为79.7岁,比阿尔茨海默病参考人群(n = 28,093)的平均年龄低5.8岁(95% CI 5.7至5.9,P < 0.001)。大多数文章未报告参与者的年龄分布。随机对照试验中女性比例为63.2%(9,475/14,991),参考人群中为67.8%(19,043/28,093)(P < 0.001)。大多数文章缺乏关于合并症和伴随药物使用的信息或报告不充分。
乙酰胆碱酯酶抑制剂随机对照试验中的参与者与现实生活中的阿尔茨海默病患者人群之间存在差异。随机对照试验中的参与者明显更年轻。此外,更详细地报告年龄分布、合并症和伴随药物,对于临床医生在从随机对照试验结论评估到现实生活实践时将是重要信息。应遵循纳入老年人的现有建议,以确保老年人的安全药物治疗。