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FIT-AD试验中运动干预对阿尔茨海默病血浆生物标志物的可行性及初步效果:一项针对患有阿尔茨海默病痴呆症老年人的随机试点研究

Feasibility and preliminary effects of exercise interventions on plasma biomarkers of Alzheimer's disease in the FIT-AD trial: a randomized pilot study in older adults with Alzheimer's dementia.

作者信息

Yu Fang, Han Seung Yong, Salisbury Dereck, Pruzin Jeremy J, Geda Yonas, Caselli Richard J, Li Danni

机构信息

Edson College of Nursing and Health Innovation, Arizona State University, Phoenix, AZ, USA.

Adult and Gerontological Health Cooperative, School of Nursing, University of Minnesota, Minneapolis, MN, USA.

出版信息

Pilot Feasibility Stud. 2022 Dec 2;8(1):243. doi: 10.1186/s40814-022-01200-2.

Abstract

BACKGROUND

Alzheimer's disease (AD) biomarkers have provided a unique opportunity to understand AD pathogenesis and monitor treatment responses. However, exercise trials show mixed effects on imagining and cerebrospinal fluid biomarkers of AD. The feasibility and effects of exercise on plasma biomarkers remain unknown. The primary objective of this study was to examine the feasibility of recruitment, retention, and blood sample collection in community-dwelling older adults with mild-to-moderate AD dementia. Secondarily, it estimated the preliminary effects of 6-month aerobic and stretching exercise on plasma amyloid-β and Aβ (Aβ) ratio, phosphorylated tau (p-tau) 181, and total tau (t-tau).

METHODS

This pilot study was implemented in year 2 of the 2-parallel group FIT-AD trial that randomized 96 participants on a 2:1 allocation ratio to moderate-intensity cycling or low-intensity stretching for 20-50 min, 3 times/week for 6 months with 6-month follow-up. Investigators (except for the statistician) and data collectors were blinded to group assignment. Fasting blood samples were collected from 26 participants at baseline and 3 and 6 months. Plasma Aβ, Aβ, p-tau181, and t-tau were measured using Simoa™ assays. Data were analyzed using intention-to-treat, Cohen's d, and linear mixed models.

RESULTSS

The sample averaged 77.6±6.99 years old and 15.4±3.00 years of education with 65% being male and 96.2% being apolipoprotein epsilon 4 gene carriers. The recruitment rate was 76.5%. The retention rate was 100% at 3 months and 96.2% at 6 months. The rate of blood collection was 88.5% at 3 months and 96.2% at 6 months. Means (standard deviation) of within-group 6-month difference in the stretching and cycling group were 0.001 (0.012) and -0.001 (0.010) for Aβ ratio, 0.609 (1.417) pg/mL and 0.101(1.579) pg/mL for p-tau181, and -0.020 (0.279) pg/mL and -0.075 (0.215) pg/mL for t-tau. Effect sizes for within-group 6-month difference were observed for p-tau181 in stretching (d=0.43 [-0.33, 1.19]) and t-tau in cycling (-0.35 [-0.87, 0.17]).

CONCLUSIONS

Blood collections with fasting were well received by participants and feasible with high recruitment and retention rates. Plasma biomarkers of AD may be modifiable by exercise intervention. Important design considerations are provided for future Phase III trials.

TRIALS REGISTRATION

ClinicalTrials.gov Identifier: NCT01954550 and posted on October 1, 2013.

摘要

背景

阿尔茨海默病(AD)生物标志物为了解AD发病机制和监测治疗反应提供了独特机会。然而,运动试验对AD的影像学和脑脊液生物标志物的影响不一。运动对血浆生物标志物的可行性和影响尚不清楚。本研究的主要目的是检验在社区居住的轻至中度AD痴呆老年人中招募、留存和采集血样的可行性。其次,评估6个月有氧运动和伸展运动对血浆淀粉样蛋白-β(Aβ)、Aβ比值、磷酸化tau蛋白(p-tau)181和总tau蛋白(t-tau)的初步影响。

方法

本试点研究在2组平行的FIT-AD试验的第2年实施,该试验将96名参与者按2:1的分配比例随机分为中等强度骑行组或低强度伸展组,每次运动20 - 50分钟,每周3次,共6个月,并进行6个月的随访。研究者(统计学家除外)和数据收集者对分组情况不知情。在基线、3个月和6个月时从26名参与者中采集空腹血样。使用Simoa™检测法测量血浆Aβ、Aβ、p-tau181和t-tau。采用意向性分析、科恩d值和线性混合模型进行数据分析。

结果

样本的平均年龄为77.6±6.99岁,平均受教育年限为15.4±3.00年,65%为男性,96.2%为载脂蛋白ε4基因携带者。招募率为76.5%。3个月时留存率为100%,6个月时为96.2%。3个月时采血率为88.5%,6个月时为96.2%。伸展组和骑行组6个月内组内差异的均值(标准差),Aβ比值分别为0.001(0.012)和 -0.001(0.010),p-tau181分别为0.609(1.417)pg/mL和0.101(1.579) pg/mL,t-tau分别为 -0.020(0.279)pg/mL和 -0.075(0.215)pg/mL。在伸展组中观察到p-tau181的6个月内组内差异效应量(d = 0.43 [-0.33, 1.19]),在骑行组中观察到t-tau的6个月内组内差异效应量(-0.35 [-0.87, 0.17])。

结论

参与者对空腹采血接受度良好,且具有较高的招募率和留存率,采血可行。AD的血浆生物标志物可能可通过运动干预进行调节。为未来的III期试验提供了重要的设计考量。

试验注册

ClinicalTrials.gov标识符:NCT01954550,于2013年10月1日发布。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/9716660/80e910614ffd/40814_2022_1200_Fig1_HTML.jpg

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