Effects of intensive lifestyle changes on the progression of mild cognitive impairment or early dementia due to Alzheimer's disease: a randomized, controlled clinical trial.

IF 7.9 1区 医学 Q1 CLINICAL NEUROLOGY
Dean Ornish, Catherine Madison, Miia Kivipelto, Colleen Kemp, Charles E McCulloch, Douglas Galasko, Jon Artz, Dorene Rentz, Jue Lin, Kim Norman, Anne Ornish, Sarah Tranter, Nancy DeLamarter, Noel Wingers, Carra Richling, Rima Kaddurah-Daouk, Rob Knight, Daniel McDonald, Lucas Patel, Eric Verdin, Rudolph E Tanzi, Steven E Arnold
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引用次数: 0

Abstract

Background: Evidence links lifestyle factors with Alzheimer's disease (AD). We report the first randomized, controlled clinical trial to determine if intensive lifestyle changes may beneficially affect the progression of mild cognitive impairment (MCI) or early dementia due to AD.

Methods: A 1:1 multicenter randomized controlled phase 2 trial, ages 45-90 with MCI or early dementia due to AD and a Montreal Cognitive Assessment (MoCA) score of 18 or higher. The primary outcome measures were changes in cognition and function tests: Clinical Global Impression of Change (CGIC), Alzheimer's Disease Assessment Scale (ADAS-Cog), Clinical Dementia Rating-Sum of Boxes (CDR-SB), and Clinical Dementia Rating Global (CDR-G) after 20 weeks of an intensive multidomain lifestyle intervention compared to a wait-list usual care control group. ADAS-Cog, CDR-SB, and CDR-Global scales were compared using a Mann-Whitney-Wilcoxon rank-sum test, and CGIC was compared using Fisher's exact test. Secondary outcomes included plasma Aβ42/40 ratio, other biomarkers, and correlating lifestyle with the degree of change in these measures.

Results: Fifty-one AD patients enrolled, mean age 73.5. No significant differences in any measures at baseline. Only two patients withdrew. All patients had plasma Aβ42/40 ratios <0.0672 at baseline, strongly supporting AD diagnosis. After 20 weeks, significant between-group differences in the CGIC (p= 0.001), CDR-SB (p= 0.032), and CDR Global (p= 0.037) tests and borderline significance in the ADAS-Cog test (p= 0.053). CGIC, CDR Global, and ADAS-Cog showed improvement in cognition and function and CDR-SB showed significantly less progression, compared to the control group which worsened in all four measures. Aβ42/40 ratio increased in the intervention group and decreased in the control group (p = 0.003). There was a significant correlation between lifestyle and both cognitive function and the plasma Aβ42/40 ratio. The microbiome improved only in the intervention group (p <0.0001).

Conclusions: Comprehensive lifestyle changes may significantly improve cognition and function after 20 weeks in many patients with MCI or early dementia due to AD.

Trial registration: Approved by Western Institutional Review Board on 12/31/2017 (#20172897) and by Institutional Review Boards of all sites. This study was registered retrospectively with clinicaltrials.gov on October 8, 2020 (NCT04606420, ID: 20172897).

深入改变生活方式对阿尔茨海默氏症所致轻度认知障碍或早期痴呆症进展的影响:随机对照临床试验。
背景:有证据表明,生活方式因素与阿尔茨海默病(AD)有关。我们报告了第一项随机对照临床试验,以确定深入改变生活方式是否会对轻度认知障碍(MCI)或因阿氏痴呆症导致的早期痴呆症的进展产生有益影响:一项1:1多中心随机对照2期试验,研究对象为年龄在45-90岁之间、患有轻度认知障碍(MCI)或因注意力缺陷导致的早期痴呆症、蒙特利尔认知评估(MoCA)得分在18分或以上的患者。主要结果指标为认知和功能测试的变化:与等待名单上的常规护理对照组相比,强化多领域生活方式干预 20 周后,认知和功能测试:临床总体变化印象 (CGIC)、阿尔茨海默病评估量表 (ADAS-Cog)、临床痴呆评级-方框总和 (CDR-SB) 和临床痴呆评级-总体 (CDR-G)。ADAS-Cog、CDR-SB和CDR-Global量表的比较采用曼-惠特尼-威尔库克森秩和检验,CGIC的比较采用费雪精确检验。次要结果包括血浆Aβ42/40比值、其他生物标志物以及生活方式与这些指标变化程度的相关性:51名AD患者参加了此次研究,平均年龄为73.5岁。基线测量结果无明显差异。只有两名患者退出。所有患者的血浆 Aβ42/40 比值均有变化:全面改变生活方式可在20周后明显改善许多MCI或AD导致的早期痴呆患者的认知和功能:2017年12月31日获得西部机构审查委员会批准(#20172897),并获得所有研究地点机构审查委员会的批准。本研究于2020年10月8日在clinicaltrials.gov进行了回顾性注册(NCT04606420,ID:20172897)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
期刊介绍: Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.
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