文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

载脂蛋白 E 基因型对多领域生活方式干预期间认知变化的影响:一项随机临床试验的亚组分析。

Effect of the Apolipoprotein E Genotype on Cognitive Change During a Multidomain Lifestyle Intervention: A Subgroup Analysis of a Randomized Clinical Trial.

机构信息

Institute of Clinical Medicine/Neurology, University of Eastern Finland, Kuopio, Finland.

Aging Research Center, Karolinska Institutet, Stockholm University, Stockholm, Sweden.

出版信息

JAMA Neurol. 2018 Apr 1;75(4):462-470. doi: 10.1001/jamaneurol.2017.4365.


DOI:10.1001/jamaneurol.2017.4365
PMID:29356827
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5885273/
Abstract

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.

摘要

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。

相似文献

[1]
Effect of the Apolipoprotein E Genotype on Cognitive Change During a Multidomain Lifestyle Intervention: A Subgroup Analysis of a Randomized Clinical Trial.

JAMA Neurol. 2018-4-1

[2]
A 2 year multidomain intervention of diet, exercise, cognitive training, and vascular risk monitoring versus control to prevent cognitive decline in at-risk elderly people (FINGER): a randomised controlled trial.

Lancet. 2015-3-12

[3]
Telomere Length Change in a Multidomain Lifestyle Intervention to Prevent Cognitive Decline: A Randomized Clinical Trial.

J Gerontol A Biol Sci Med Sci. 2021-2-25

[4]
Association between white matter hyperintensity severity and cognitive impairment according to the presence of the apolipoprotein E (APOE) ε4 allele in the elderly: retrospective analysis of data from the CREDOS study.

J Clin Psychiatry. 2012-10-30

[5]
Cognitive domain decline in healthy apolipoprotein E epsilon4 homozygotes before the diagnosis of mild cognitive impairment.

Arch Neurol. 2007-9

[6]
Association of APOE ε4 genotype and lifestyle with cognitive function among Chinese adults aged 80 years and older: A cross-sectional study.

PLoS Med. 2021-6

[7]
Multidomain lifestyle intervention benefits a large elderly population at risk for cognitive decline and dementia regardless of baseline characteristics: The FINGER trial.

Alzheimers Dement. 2017-10-19

[8]
Association Between Apolipoprotein E ε2 vs ε4, Age, and β-Amyloid in Adults Without Cognitive Impairment.

JAMA Neurol. 2021-2-1

[9]
Association of β-Amyloid and Apolipoprotein E ε4 With Memory Decline in Preclinical Alzheimer Disease.

JAMA Neurol. 2018-4-1

[10]
Baseline Telomere Length and Effects of a Multidomain Lifestyle Intervention on Cognition: The FINGER Randomized Controlled Trial.

J Alzheimers Dis. 2017

引用本文的文献

[1]
Reallocation of time between accelerometer-derived movement behaviors, genetic susceptibility, and risk of incident dementia, mortality, and premature death: a longitudinal cohort study.

Int J Behav Nutr Phys Act. 2025-8-21

[2]
Dual Inhibitors of Acetylcholinesterase and Monoamine Oxidase-B for the Treatment of Alzheimer's Disease.

Molecules. 2025-7-15

[3]
Baseline cognition and demographic, lifestyle, and cardiovascular risk factors in US POINTER.

Alzheimers Dement. 2025-7

[4]
The relationship between the APOE genotypes and memory performance of young adults and its neural basis.

Sci Rep. 2025-7-11

[5]
SubgroupTE: Advancing Treatment Effect Estimation with Subgroup Identification.

ACM Trans Intell Syst Technol. 2025-6

[6]
Multidomain interventions for preventing cognitive decline in older adults with type 2 diabetes and mild cognitive impairment: Secondary analysis of the J-MINT: Multidomain intervention in type 2 diabetes.

JAR Life. 2025-6-9

[7]
Multidomain interventions for prevention of dementia: Achievements, challenges and future perspectives.

Geriatr Gerontol Int. 2025-8

[8]
Genetic background and multidomain interventions in mild cognitive impairment.

Alzheimers Res Ther. 2025-6-10

[9]
Intervention Role of APOE in CNS Diseases: APOE Actions and APOE Neurogenesis Capability.

Mol Neurobiol. 2025-5-22

[10]
Multi-pathway blood biomarkers to target and monitor multidimensional prevention of cognitive and functional decline (nested in the IN-TeMPO study framed within the world-wide FINGERS network).

Front Aging Neurosci. 2025-5-7

本文引用的文献

[1]
Defeating Alzheimer's disease and other dementias: a priority for European science and society.

Lancet Neurol. 2016-4

[2]
Statins for the prevention of dementia.

Cochrane Database Syst Rev. 2016-1-4

[3]
Cognitive Effects of Intentional Weight Loss in Elderly Obese Individuals With Mild Cognitive Impairment.

J Clin Endocrinol Metab. 2016-3

[4]
Effects of a process-based cognitive training intervention for patients with stress-related exhaustion.

Stress. 2015

[5]
A 2 year multidomain intervention of diet, exercise, cognitive training, and vascular risk monitoring versus control to prevent cognitive decline in at-risk elderly people (FINGER): a randomised controlled trial.

Lancet. 2015-3-12

[6]
The effect of galantamine on brain atrophy rate in subjects with mild cognitive impairment is modified by apolipoprotein E genotype: post-hoc analysis of data from a randomized controlled trial.

Alzheimers Res Ther. 2014-7-21

[7]
The Study of Mental and Resistance Training (SMART) study—resistance training and/or cognitive training in mild cognitive impairment: a randomized, double-blind, double-sham controlled trial.

J Am Med Dir Assoc. 2014-10-23

[8]
Computerized cognitive training in cognitively healthy older adults: a systematic review and meta-analysis of effect modifiers.

PLoS Med. 2014-11-18

[9]
Recruitment and baseline characteristics of participants in the Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability (FINGER)-a randomized controlled lifestyle trial.

Int J Environ Res Public Health. 2014-9-10

[10]
Apolipoprotein E: structure and function in lipid metabolism, neurobiology, and Alzheimer's diseases.

Neurobiol Dis. 2014-12

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索