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一项针对早期阿尔茨海默病的个性化多模式生活方式干预的系统生物学临床试验。

A systems-biology clinical trial of a personalized multimodal lifestyle intervention for early Alzheimer's disease.

作者信息

McEwen Sarah C, Merrill David A, Bramen Jennifer, Porter Verna, Panos Stella, Kaiser Scott, Hodes John, Ganapathi Aarthi, Bell Lesley, Bookheimer Tess, Glatt Ryan, Rapozo Molly, Ross Mary Kay, Price Nathan D, Kelly Daniel, Funk Cory C, Hood Leroy, Roach Jared C

机构信息

Pacific Neuroscience Institute Pacific Brain Health Center Santa Monica California USA.

Providence Saint John's Cancer Institute Department of Translational Neurosciences and Neurotherapeutics Santa Monica California USA.

出版信息

Alzheimers Dement (N Y). 2021 Jul 20;7(1):e12191. doi: 10.1002/trc2.12191. eCollection 2021.

Abstract

INTRODUCTION

There is an urgent need to develop effective interventional treatments for people with Alzheimer's disease (AD). AD results from a complex multi-decade interplay of multiple interacting dysfunctional biological systems that have not yet been fully elucidated. Epidemiological studies have linked several modifiable lifestyle factors with increased incidence for AD. Because monotherapies have failed to prevent or ameliorate AD, interventional studies should deploy multiple, targeted interventions that address the dysfunctional systems that give rise to AD.

METHODS

This randomized controlled trial (RCT) will examine the efficacy of a 12-month personalized, multimodal, lifestyle intervention in 60 mild cognitive impairment (MCI) and early stage AD patients (aged 50+, amyloid positivity). Both groups receive data-driven, lifestyle recommendations designed to target multiple systemic pathways implicated in AD. One group receives these personalized recommendations without coaching. The other group receives personalized recommendations with health coaching, dietary counseling, exercise training, cognitive stimulation, and nutritional supplements. We collect clinical, proteomic, metabolomic, neuroimaging, and genetic data to fuel systems-biology analyses. We will examine effects on cognition and hippocampal volume. The overarching goal of the study is to longitudinally track biological systems implicated in AD to reveal the dynamics between these systems during the intervention to understand differences in treatment response.

RESULTS

We have developed and implemented a protocol for a personalized, multimodal intervention program for early AD patients. We began enrollment in September 2019; we have enrolled a third of our target (20 of 60) with a 95% retention and 86% compliance rate.

DISCUSSION

This study presents a paradigm shift in designing multimodal, lifestyle interventions to reduce cognitive decline, and how to elucidate the biological systems being targeted. Analytical efforts to explain mechanistic or causal underpinnings of individual trajectories and the interplay between multi-omic variables will inform the design of future hypotheses and development of effective precision medicine trials.

摘要

引言

迫切需要为阿尔茨海默病(AD)患者开发有效的干预治疗方法。AD是由多个相互作用的功能失调生物系统历经数十年的复杂相互作用导致的,这些系统尚未完全阐明。流行病学研究已将多种可改变的生活方式因素与AD发病率增加联系起来。由于单一疗法未能预防或改善AD,干预研究应采用多种有针对性的干预措施,以解决导致AD的功能失调系统。

方法

这项随机对照试验(RCT)将研究一项为期12个月的个性化、多模式生活方式干预对60名轻度认知障碍(MCI)和早期AD患者(年龄50岁以上,淀粉样蛋白呈阳性)的疗效。两组患者均接受以数据为驱动的生活方式建议,旨在针对与AD相关的多个全身途径。一组在没有指导的情况下接受这些个性化建议。另一组在接受健康指导、饮食咨询、运动训练、认知刺激和营养补充剂的同时接受个性化建议。我们收集临床、蛋白质组学、代谢组学、神经影像学和基因数据,以推动系统生物学分析。我们将研究对认知和海马体积的影响。该研究的总体目标是纵向追踪与AD相关的生物系统,以揭示干预期间这些系统之间的动态变化,从而了解治疗反应的差异。

结果

我们已经为早期AD患者制定并实施了一项个性化、多模式干预计划的方案。我们于2019年9月开始招募;我们已经招募了三分之一的目标患者(60名中的20名),保留率为95%,依从率为86%。

讨论

本研究在设计多模式生活方式干预以减少认知衰退以及如何阐明目标生物系统方面呈现出范式转变。解释个体轨迹的机制或因果基础以及多组学变量之间相互作用的分析工作将为未来假设的设计和有效精准医学试验的开发提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/206b/8290633/6a3cdeebfb59/TRC2-7-e12191-g001.jpg

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