APOE4基因型对运动干预随机对照试验中生理和认知健康的影响:系统回顾和荟萃分析

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-01-20 DOI:10.1186/s13063-024-08696-4
Felicity S E Spencer, Richard J Elsworthy, Leigh Breen, Jon R B Bishop, Connor Dunleavy, Sarah Aldred
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引用次数: 0

摘要

背景:阿尔茨海默病是由可改变和不可改变的危险因素引起的。随机对照试验调查了阿尔茨海默病最强的遗传风险因素APOE4是否会影响运动对健康的影响。系统评价还没有评估运动对APOE基因型参与者的身体和认知结果的影响。需要对这些随机对照试验进行质量评估,以了解基因型对干预潜在成功的影响。本系统综述旨在确定APOE4基因型是否影响基于运动的随机对照试验的有效性。方法:检索MEDLINE、EMBASE和PsycINFO,确定符合条件的基于运动的随机对照试验,纳入不同认知能力的参与者。进行了质量评估。结果:19项研究符合系统评价的纳入标准,3项研究符合meta分析的纳入标准。极低到中等质量的证据表明,APOE4携带者在运动后的认知(如执行功能、学习)和身体(如相对端粒长度)结果上比非APOE4携带者受益更多;APOE4非携带者在生理指标(血清BDNF、步态速度)和认知指标(全局认知、言语记忆)方面比携带者受益。在meta分析中,极低质量的证据表明APOE4携带者和非携带者在身体功能结局上没有差异。研究设计和报告的几个方面,包括相对运动强度的维持和完整的统计报告,被认为需要改进。讨论:本系统综述发现非常有限的证据表明,运动干预可以使APOE4携带者和非携带者同样受益,尽管结论受到证据质量的限制。需要进一步的随机对照试验,根据APOE状态对参与者进行分层,以更好地了解APOE基因型与运动对健康相关结果的影响之间的关系。试验注册:本综述在PROSPERO注册(CRD42023436842)。于2023年6月16日注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of the APOE4 genotype on physiological and cognitive health in randomised controlled trials with an exercise intervention: a systematic review and meta-analysis.

Background: Alzheimer's disease is caused by modifiable and non-modifiable risk factors. Randomised controlled trials have investigated whether the strongest genetic risk factor for Alzheimer's disease, APOE4, impacts the effectiveness of exercise on health. Systematic reviews are yet to evaluate the effect of exercise on physical and cognitive outcomes in APOE genotyped participants. A quality assessment of these randomised controlled trials is needed to understand the impact genotype has on the potential success of intervention. This systematic review aimed to determine if the APOE4 genotype influences the effectiveness of exercise-based randomised controlled trials.

Method: Searches on MEDLINE, EMBASE, and PsycINFO identified eligible exercise based randomised controlled trials incorporating participants with varied cognitive abilities. Quality assessments were conducted.

Results: Nineteen studies met the inclusion criteria for systematic review, and 3 for the meta-analysis. Very low to moderate quality evidence showed that APOE4 carriers benefitted more than APOE4 non-carriers on cognitive (e.g. executive function, learning) and physical (e.g. relative telomere length) outcomes after exercise; and that APOE4 non-carriers benefited over carriers for physical (serum BDNF, gait speed) and cognitive (global cognition, verbal memory) markers. Very low quality evidence indicated that there was no evidence of difference between APOE4 carriers and non-carriers on physical function outcomes in meta-analysis. Several areas of study design and reporting, including maintenance of relative exercise intensity and complete statistical reporting, were identified as needing improvement.

Discussion: This systematic review found very limited evidence to suggest that exercise interventions can benefit APOE4 carriers and non-carriers equally, though conclusions were limited by evidence quality. Further randomised controlled trials, stratifying participants by APOE status are required to better understand the relationship between APOE genotype and the effect of exercise on health-related outcomes.

Trial registration: This review was registered with PROSPERO (CRD42023436842). Registered on June 16, 2023.

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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