Higher skeletal muscle mitochondrial oxidative capacity is associated with preserved brain structure up to over a decade
Qu Tian (),
Erin E. Greig,
Christos Davatzikos,
Bennett A. Landman,
Susan M. Resnick and
Luigi Ferrucci
Additional contact information
Qu Tian: National Institute on Aging
Erin E. Greig: National Institute on Aging
Christos Davatzikos: University of Pennsylvania
Bennett A. Landman: Vanderbilt University
Susan M. Resnick: National Institute on Aging
Luigi Ferrucci: National Institute on Aging
Nature Communications, 2024, vol. 15, issue 1, 1-12
Abstract:
Abstract Impaired muscle mitochondrial oxidative capacity is associated with future cognitive impairment, and higher levels of PET and blood biomarkers of Alzheimer’s disease and neurodegeneration. Here, we examine its associations with up to over a decade-long changes in brain atrophy and microstructure. Higher in vivo skeletal muscle oxidative capacity via MR spectroscopy (post-exercise recovery rate, kPCr) is associated with less ventricular enlargement and brain aging progression, and less atrophy in specific regions, notably primary sensorimotor cortex, temporal white and gray matter, thalamus, occipital areas, cingulate cortex, and cerebellum white matter. Higher kPCr is also associated with less microstructural integrity decline in white matter around cingulate, including superior longitudinal fasciculus, corpus callosum, and cingulum. Higher in vivo muscle oxidative capacity is associated with preserved brain structure up to over a decade, particularly in areas important for cognition, motor function, and sensorimotor integration.
Date: 2024
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-55009-z
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DOI: 10.1038/s41467-024-55009-z
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