Cerebral Metabolic Rate of Oxygen and Accelerometry-Based Fatigability in Community-Dwelling Older Adults.

IF 8 1区 医学 Q1 CELL BIOLOGY
Aging Cell Pub Date : 2025-06-13 DOI:10.1111/acel.70121
Emma L Gay, Caterina Rosano, Paul M Coen, Nicholaas Bohnen, Theodore Huppert, Yujia Susanna Qiao, Nancy W Glynn
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Abstract

Alterations in energy metabolism may drive fatigue in older age, but prior research primarily focused on skeletal muscle energetics without assessing other systems and utilized self-reported measures of fatigue. We tested the association between energy metabolism in the brain and an objective measure of fatigability in the Study of Muscle, Mobility and Aging (N = 119, age 76.8 ± 4.0 years, 59.7% women). Total brain cerebral metabolic rate of oxygen (CMRO2) was measured using arterial spin labeling and T2-relaxation under spin tagging MRI protocols. Accelerometry-based fatigability status during a fast-paced 400 m walk was determined using the Pittsburgh Performance Fatigability Index (PPFI, higher = worse). Confounders included skeletal muscle energetics, measured in vivo using spectroscopy and ex vivo using respirometry, cardiorespiratory fitness (VO2peak), weight, medication count, and multimorbidity. Multivariable logistic regression models were used to estimate the association (odds ratio (OR)) of CMRO2 with PPFI > 0 compared to the referent group PPFI = 0. Models were first adjusted for age and sex and further adjusted for confounders. In this sample, 41.2% had PPFI > 0 (median 3.3% [0.4%-8.0%]). Higher CMRO2 was associated with exhibiting performance fatigability (age- and sex-adjusted OR = 1.61, 95% CI: 1.06, 2.45, p = 0.03). This association remained significant after adjusting for in vivo skeletal muscle energetics and VO2peak, suggesting that performance fatigability is associated with multi-system impairments in older adults.

社区居住老年人脑氧代谢率和基于加速度计的疲劳。
能量代谢的改变可能会导致老年人疲劳,但之前的研究主要集中在骨骼肌能量学上,而没有评估其他系统,并利用自我报告的疲劳测量方法。我们在肌肉、运动和衰老研究中测试了大脑能量代谢与疲劳的客观测量之间的关系(N = 119,年龄76.8±4.0岁,59.7%为女性)。在自旋标记MRI方案下,采用动脉自旋标记和t2松弛法测量脑总脑氧代谢率(cro2)。使用匹兹堡疲劳指数(PPFI,越高=越差)来确定快节奏400米步行过程中基于加速度计的疲劳状态。混杂因素包括骨骼肌能量学,体内用光谱学测量,体外用呼吸计测量,心肺适能(vo2峰值),体重,药物计数和多病。采用多变量logistic回归模型估计与参照组PPFI = 0相比,cmor2与PPFI >的相关性(比值比(OR))。模型首先根据年龄和性别进行调整,并进一步根据混杂因素进行调整。在该样本中,41.2%的患者有PPFI bb0(中位数为3.3%[0.4%-8.0%])。较高的cmoro2与表现出疲劳表现相关(经年龄和性别调整的OR = 1.61, 95% CI: 1.06, 2.45, p = 0.03)。在调整体内骨骼肌能量和vo2峰值后,这种关联仍然显著,这表明老年人的表现疲劳与多系统损伤有关。
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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
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