Institute of Clinical Medicine/Neurology, University of Eastern Finland, Kuopio, Finland.
Aging Research Center, Karolinska Institutet, Stockholm University, Stockholm, Sweden.
JAMA Neurol. 2018 Apr 1;75(4):462-470. doi: 10.1001/jamaneurol.2017.4365.
IMPORTANCE: The role of the apolipoprotein E (APOE) ε4 allele as an effect modifier in lifestyle interventions to prevent cognitive impairment is still unclear. OBJECTIVE: To examine whether the APOE ε4 allele modifies the previously reported significant cognitive benefits of a multidomain lifestyle intervention (prespecified subgroup analysis). DESIGN, SETTING, AND PARTICIPANTS: The Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability (FINGER) was a randomized clinical trial in 6 centers across Finland (screening and randomization performed from September 7, 2009, through November 24, 2011; intervention duration, 2 years). Data analysis was performed from August 1, 2015, to March 31, 2016. The study population was at-risk older individuals from the general population. Inclusion criteria were age of 60 to 77 years; Cardiovascular Risk Factors, Aging, and Dementia risk score of at least 6 points; and cognition at a mean level or slightly lower than expected for age. Individuals with dementia or substantial cognitive impairment and conditions that prevented cooperation or safe engagement in the intervention were excluded. APOE genotype data were available for 1175 of the 1260 participants. INTERVENTIONS: Participants were randomly assigned in a 1:1 ratio to a multidomain intervention group (diet, exercise, cognitive training, and vascular risk management) or a control group (general health advice). Group allocation was not actively disclosed to participants, and outcome assessors were masked to group allocation. MAIN OUTCOMES AND MEASURES: Primary outcome was change in cognition measured through a comprehensive neuropsychological test battery. Analysis was based on modified intention to treat (participants with at least 1 postbaseline assessment). RESULTS: A total of 1109 participants (mean [SD] age, 69.3 [4.7] years; 514 [46.3%] female) were included in the analysis: 362 APOE ε4 allele carriers (173 intervention and 189 control) and 747 noncarriers (380 intervention and 367 control). The APOE ε4 carriers and noncarriers were not significantly different at baseline (except for serum cholesterol level). The difference between the intervention and control groups in annual neuropsychological test battery total score change was 0.037 (95% CI, 0.001 to 0.073) among carriers and 0.014 (95% CI, -0.011 to 0.039) among noncarriers. Intervention effect was not significantly different between carriers and noncarriers (0.023; 95% CI, -0.021 to 0.067). CONCLUSIONS AND RELEVANCE: Healthy lifestyle changes may be beneficial for cognition in older at-risk individuals even in the presence of APOE-related genetic susceptibility to dementia. Whether such benefits are more pronounced in APOE ε4 carriers compared with noncarriers should be further investigated. The findings also emphasize the importance of early prevention strategies that target multiple modifiable risk factors simultaneously. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT01041989.
重要性:载脂蛋白 E(APOE)ε4 等位基因作为生活方式干预预防认知障碍的效应修饰因子的作用仍不清楚。 目的:检验 APOE ε4 等位基因是否改变了先前报道的多领域生活方式干预对认知有显著益处的结果(预先指定的亚组分析)。 设计、地点和参与者:芬兰老年干预研究预防认知障碍和残疾(FINGER)是一项在芬兰 6 个中心进行的随机临床试验(筛选和随机化于 2009 年 9 月 7 日至 2011 年 11 月 24 日进行;干预持续时间 2 年)。数据分析于 2015 年 8 月 1 日至 2016 年 3 月 31 日进行。研究人群为来自普通人群的高危老年人。纳入标准为年龄 60 至 77 岁;心血管危险因素、衰老和痴呆风险评分至少为 6 分;认知能力处于平均水平或略低于预期年龄。排除痴呆或严重认知障碍以及存在妨碍合作或安全参与干预的条件的个体。1175 名参与者中有 APOE 基因型数据。 干预措施:参与者以 1:1 的比例随机分配到多领域干预组(饮食、运动、认知训练和血管风险管理)或对照组(一般健康建议)。组分配未主动向参与者披露,结果评估者对组分配进行了盲法。 主要结果和测量:主要结果是通过全面的神经心理学测试量表来衡量认知的变化。分析基于改良的意向治疗(至少有 1 次基线后评估的参与者)。 结果:共有 1109 名参与者(平均[SD]年龄 69.3[4.7]岁;514[46.3%]为女性)纳入分析:362 名 APOE ε4 等位基因携带者(173 名干预组和 189 名对照组)和 747 名非携带者(380 名干预组和 367 名对照组)。APOE ε4 携带者和非携带者在基线时没有明显差异(除血清胆固醇水平外)。在干预组和对照组中,每年神经心理学测试量表总分的变化分别为携带者组 0.037(95%CI,0.001 至 0.073)和非携带者组 0.014(95%CI,-0.011 至 0.039)。携带者和非携带者之间的干预效果无显著差异(0.023;95%CI,-0.021 至 0.067)。 结论和相关性:健康的生活方式改变可能对高危老年人的认知有益,即使存在与痴呆相关的 APOE 遗传易感性。APOE ε4 携带者与非携带者相比,这种益处是否更明显,应进一步研究。研究结果还强调了早期预防策略的重要性,这些策略同时针对多个可改变的风险因素。 试验注册:ClinicalTrials.gov 标识符:NCT01041989。
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