INSERM UMR 1027, Toulouse, France; University of Toulouse III, Toulouse, France; Department of Epidemiology and Public Health, CHU Toulouse, Toulouse, France.
INSERM UMR 1027, Toulouse, France; University of Toulouse III, Toulouse, France; Gérontopôle, Department of Geriatrics, CHU Toulouse, Purpan University Hospital, Toulouse, France.
Lancet Neurol. 2017 May;16(5):377-389. doi: 10.1016/S1474-4422(17)30040-6. Epub 2017 Mar 27.
No large trials have been done to investigate the efficacy of an intervention combining a specific compound and several lifestyle interventions compared with placebo for the prevention of cognitive decline. We tested the effect of omega 3 polyunsaturated fatty acid supplementation and a multidomain intervention (physical activity, cognitive training, and nutritional advice), alone or in combination, compared with placebo, on cognitive decline.
The Multidomain Alzheimer Preventive Trial was a 3-year, multicentre, randomised, placebo-controlled superiority trial with four parallel groups at 13 memory centres in France and Monaco. Participants were non-demented, aged 70 years or older, and community-dwelling, and had either relayed a spontaneous memory complaint to their physician, limitations in one instrumental activity of daily living, or slow gait speed. They were randomly assigned (1:1:1:1) to either the multidomain intervention (43 group sessions integrating cognitive training, physical activity, and nutrition, and three preventive consultations) plus omega 3 polyunsaturated fatty acids (ie, two capsules a day providing a total daily dose of 800 mg docosahexaenoic acid and 225 mg eicosapentaenoic acid), the multidomain intervention plus placebo, omega 3 polyunsaturated fatty acids alone, or placebo alone. A computer-generated randomisation procedure was used to stratify patients by centre. All participants and study staff were blinded to polyunsaturated fatty acid or placebo assignment, but were unblinded to the multidomain intervention component. Assessment of cognitive outcomes was done by independent neuropsychologists blinded to group assignment. The primary outcome was change from baseline to 36 months on a composite Z score combining four cognitive tests (free and total recall of the Free and Cued Selective Reminding test, ten Mini-Mental State Examination orientation items, Digit Symbol Substitution Test, and Category Naming Test) in the modified intention-to-treat population. The trial was registered with ClinicalTrials.gov (NCT00672685).
1680 participants were enrolled and randomly allocated between May 30, 2008, and Feb 24, 2011. In the modified intention-to-treat population (n=1525), there were no significant differences in 3-year cognitive decline between any of the three intervention groups and the placebo group. Between-group differences compared with placebo were 0·093 (95% CI 0·001 to 0·184; adjusted p=0·142) for the combined intervention group, 0·079 (-0·012 to 0·170; 0·179) for the multidomain intervention plus placebo group, and 0·011 (-0·081 to 0·103; 0·812) for the omega 3 polyunsaturated fatty acids group. 146 (36%) participants in the multidomain plus polyunsaturated fatty acids group, 142 (34%) in the multidomain plus placebo group, 134 (33%) in the polyunsaturated fatty acids group, and 133 (32%) in the placebo group had at least one serious emerging adverse event. Four treatment-related deaths were recorded (two in the multidomain plus placebo group and two in the placebo group). The interventions did not raise any safety concerns and there were no differences between groups in serious or other adverse events.
The multidomain intervention and polyunsaturated fatty acids, either alone or in combination, had no significant effects on cognitive decline over 3 years in elderly people with memory complaints. An effective multidomain intervention strategy to prevent or delay cognitive impairment and the target population remain to be determined, particularly in real-world settings.
French Ministry of Health, Pierre Fabre Research Institute, Gerontopole, Exhonit Therapeutics, Avid Radiopharmaceuticals.
尚未开展大型试验来调查特定化合物与几种生活方式干预相结合的干预措施与安慰剂相比在预防认知能力下降方面的疗效。我们测试了ω-3 多不饱和脂肪酸补充剂和多领域干预(体力活动、认知训练和营养建议)单独或联合使用与安慰剂相比对认知能力下降的影响。
多领域阿尔茨海默病预防试验是一项为期 3 年的多中心、随机、安慰剂对照的优势试验,在法国和摩纳哥的 13 个记忆中心有四个平行组。参与者为非痴呆,年龄在 70 岁或以上,居住在社区,且向医生报告了记忆障碍、一项日常活动受限或步态缓慢。他们以 1:1:1:1 的比例随机分配到多领域干预组(43 个整合认知训练、体力活动和营养的小组会议和 3 次预防性咨询)加ω-3 多不饱和脂肪酸(即每天 2 粒胶囊,提供 800 毫克二十二碳六烯酸和 225 毫克二十碳五烯酸的总日剂量)、多领域干预加安慰剂、ω-3 多不饱和脂肪酸单独或安慰剂单独。采用计算机生成的随机化程序按中心对患者进行分层。所有参与者和研究人员对多不饱和脂肪酸或安慰剂的分配均不知情,但对多领域干预成分不知情。认知结果的评估由独立的神经心理学家进行,他们对分组不知情。主要结局是在修改后的意向治疗人群中,从基线到 36 个月时,四项认知测试(自由和总回忆自由和线索选择性回忆测试、十个迷你精神状态检查定向项目、数字符号替代测试和类别命名测试)的复合 Z 评分的变化。该试验在 ClinicalTrials.gov(NCT00672685)注册。
2008 年 5 月 30 日至 2011 年 2 月 24 日期间,共纳入并随机分配了 1680 名参与者。在修改后的意向治疗人群(n=1525)中,与安慰剂组相比,任何一组干预组的 3 年认知下降均无显著差异。与安慰剂相比,联合干预组差异为 0.093(95%CI 0.001 至 0.184;调整后的 p=0.142),多领域干预加安慰剂组为 0.079(-0.012 至 0.170;0.179),ω-3 多不饱和脂肪酸组为 0.011(-0.081 至 0.103;0.812)。多领域加多不饱和脂肪酸组 146(36%)名、多领域加安慰剂组 142(34%)名、多不饱和脂肪酸组 134(33%)名和安慰剂组 133(32%)名至少有一次严重的新发不良事件。记录了 4 例与治疗相关的死亡(多领域加安慰剂组 2 例,安慰剂组 2 例)。干预措施未引起任何安全问题,各组之间的严重或其他不良事件无差异。
在有记忆障碍的老年人中,多领域干预和多不饱和脂肪酸单独或联合使用在 3 年内对认知能力下降没有显著影响。需要确定一种有效的多领域干预策略来预防或延迟认知障碍,特别是在实际环境中。
法国卫生部、皮埃尔·法布研究所、老年医学研究中心、埃克诺蒂克斯治疗公司、阿维德放射性药物公司。