Emma L Gay, Caterina Rosano, Paul M Coen, Nicholaas Bohnen, Theodore Huppert, Yujia Susanna Qiao, Nancy W Glynn
{"title":"社区居住老年人脑氧代谢率和基于加速度计的疲劳。","authors":"Emma L Gay, Caterina Rosano, Paul M Coen, Nicholaas Bohnen, Theodore Huppert, Yujia Susanna Qiao, Nancy W Glynn","doi":"10.1111/acel.70121","DOIUrl":null,"url":null,"abstract":"<p><p>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 (CMRO<sub>2</sub>) was measured using arterial spin labeling and T<sub>2</sub>-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 (VO<sub>2</sub>peak), weight, medication count, and multimorbidity. Multivariable logistic regression models were used to estimate the association (odds ratio (OR)) of CMRO<sub>2</sub> 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 CMRO<sub>2</sub> 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 VO<sub>2</sub>peak, suggesting that performance fatigability is associated with multi-system impairments in older adults.</p>","PeriodicalId":119,"journal":{"name":"Aging Cell","volume":" ","pages":"e70121"},"PeriodicalIF":8.0000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cerebral Metabolic Rate of Oxygen and Accelerometry-Based Fatigability in Community-Dwelling Older Adults.\",\"authors\":\"Emma L Gay, Caterina Rosano, Paul M Coen, Nicholaas Bohnen, Theodore Huppert, Yujia Susanna Qiao, Nancy W Glynn\",\"doi\":\"10.1111/acel.70121\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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 (CMRO<sub>2</sub>) was measured using arterial spin labeling and T<sub>2</sub>-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 (VO<sub>2</sub>peak), weight, medication count, and multimorbidity. Multivariable logistic regression models were used to estimate the association (odds ratio (OR)) of CMRO<sub>2</sub> 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 CMRO<sub>2</sub> was associated with exhibiting performance fatigability (age- and sex-adjusted OR = 1.61, 95% CI: 1.06, 2.45, p = 0.03). 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Cerebral Metabolic Rate of Oxygen and Accelerometry-Based Fatigability in Community-Dwelling Older Adults.
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.
Aging CellBiochemistry, 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:
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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.