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      Exercise intolerance and rapid skeletal muscle energetic decline in human age-associated frailty

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          Abstract

          BACKGROUND

          Physical frailty in older individuals is characterized by subjective symptoms of fatigue and exercise intolerance (EI). Objective abnormalities in skeletal muscle (SM) mitochondrial high-energy phosphate (HEP) metabolism contribute to EI in inherited myopathies; however, their presence or link to EI in the frail older adult is unknown.

          METHODS

          Here, we studied 3 groups of ambulatory, community-dwelling adults with no history of significant coronary disease: frail older (FO) individuals (81 ± 2.7 years, mean ± SEM), nonfrail older (NFO) individuals (79 ± 2.0 years), and healthy middle-aged individuals, who served as controls (CONT, 51 ± 2.1 years). Lower extremity SM HEP levels and mitochondrial function were measured with 31P magnetic resonance (MR) techniques during graded multistage plantar flexion exercise (PFE). EI was quantified by a 6-minute walk (6MW) and peak oxygen consumption during cardiopulmonary testing (peak VO 2).

          RESULTS

          During graded exercise, FO, NFO, and CONT individuals all fatigued at similar SM HEP levels, as measured by 31P-MR. However, FO individuals fatigued fastest, with several-fold higher rates of PFE-induced HEP decline that correlated closely with shorter exercise duration in the MR scanner and with 6MW distance and lower peak oxygen consumption on cardiopulmonary testing ( P < 0.001 for all). SM mitochondrial oxidative capacity was lower in older individuals and correlated with rapid HEP decline but less closely with EI.

          CONCLUSION

          Several-fold faster SM energetic decline during exercise occurs in FO individuals and correlates closely with multiple measures of EI. Rapid energetic decline represents an objective, functional measure of SM metabolic changes and a potential new target for mitigating frailty-associated physical limitations.

          FUNDING

          This work was supported by NIH R21 AG045634, R01 AG063661, R01 HL61912, the Johns Hopkins University Claude D. Pepper Older Americans Independence Center P30AG021334, and the Clarence Doodeman Endowment in Cardiology at Johns Hopkins.

          Abstract

          Abstract

          Rapid exercise-induced skeletal muscle high-energy phosphate decline occurs in frail, older individuals and is closely linked to exercise intolerance and fatigue.

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          Most cited references71

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          Frailty in Older Adults: Evidence for a Phenotype

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            Psychophysical bases of perceived exertion

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              Decline in skeletal muscle mitochondrial function with aging in humans.

              Cumulative mtDNA damage occurs in aging animals, and mtDNA mutations are reported to accelerate aging in mice. We determined whether aging results in increased DNA oxidative damage and reduced mtDNA abundance and mitochondrial function in skeletal muscle of human subjects. Studies performed in 146 healthy men and women aged 18-89 yr demonstrated that mtDNA and mRNA abundance and mitochondrial ATP production all declined with advancing age. Abundance of mtDNA was positively related to mitochondrial ATP production rate, which in turn, was closely associated with aerobic capacity and glucose tolerance. The content of several mitochondrial proteins was reduced in older muscles, whereas the level of the oxidative DNA lesion, 8-oxo-deoxyguanosine, was increased, supporting the oxidative damage theory of aging. These results demonstrate that age-related muscle mitochondrial dysfunction is related to reduced mtDNA and muscle functional changes that are common in the elderly.
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                Author and article information

                Contributors
                Journal
                JCI Insight
                JCI Insight
                JCI Insight
                JCI Insight
                American Society for Clinical Investigation
                2379-3708
                15 October 2020
                15 October 2020
                15 October 2020
                : 5
                : 20
                : e141246
                Affiliations
                [1 ]Division of Cardiology, Department of Medicine, and
                [2 ]Division of Magnetic Resonance Research, Department of Radiology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
                [3 ]Philips Healthcare Germany, Hamburg, Germany.
                [4 ]Key Laboratory for Biomedical Engineering of Ministry of Education, Department of Biomedical Engineering, College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou, Zhejiang, China.
                [5 ]Divison of Geriatric Medicine and Gerontology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
                Author notes
                Address correspondence to: Robert G. Weiss, Blalock 544, Johns Hopkins Hospital, 600 N. Wolfe Street, Baltimore, Maryland 21287-6568, USA. Phone: 410.955.1703; Email: rweiss@ 123456jhmi.edu .
                Author information
                http://orcid.org/0000-0003-4295-4585
                http://orcid.org/0000-0002-7044-9941
                http://orcid.org/0000-0002-0071-0155
                http://orcid.org/0000-0001-7638-1864
                Article
                141246
                10.1172/jci.insight.141246
                7605538
                32941181
                21065bcf-a117-4a78-8447-e933c175aa4e
                © 2020 Lewsey et al.

                This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 12 June 2020
                : 9 September 2020
                Funding
                Funded by: National Institutes of Health, https://doi.org/10.13039/100000002;
                Award ID: R21 AG045634,R01 AG063661,R01 HL61912,P30AG021334
                Funded by: Johns Hopkins University, https://doi.org/10.13039/100007880;
                Award ID: Clarence Doodeman Endowment in Cardiology
                Categories
                Clinical Medicine

                aging,bioenergetics,mitochondria
                aging, bioenergetics, mitochondria

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