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1.
Clin Nutr ; 35(6): 1359-1365, 2016 12.
Article in English | MEDLINE | ID: mdl-27010836

ABSTRACT

BACKGROUND & AIMS: Cancer patients frequently experience weight loss, with negative consequences for functionality and prognosis. The extent to which muscle atrophy contributes to weight loss, however, is not clear, as few studies have directly measured muscle fiber morphology in cancer patients. METHODS: Whole body and regional tissue composition were measured, along with the cross-sectional area (CSA) and fiber type of mechanically-isolated, single muscle fibers, in 19 cancer patients (8 with a history of weight loss, 11 weight-stable) and 15 non-diseased controls. RESULTS: Whole body fat mass was reduced in cancer patients with a history of weight loss, but no differences in whole body or leg fat-free mass were apparent. In contrast, reductions (∼20%) in single muscle fiber CSA were found in both slow-twitch, myosin heavy chain (MHC) I and fast-twitch, MHC IIA fibers in both weight-stable patients and those with a history of weight loss. Fiber type distribution showed a shift towards a fast-twitch phenotype compared to controls, which may preserve muscle function in cancer patients despite atrophy, as positive relationships were found between the fractions of hybrid MHC IIAX and I/IIA fibers and 6-min walk performance. CONCLUSIONS: Our results suggest that, although not apparent from whole body or regional measurements, cancer is associated with reduced skeletal muscle fiber size independent of weight loss history and a shift towards fast-twitch fibers, phenotypes that resemble adaptations to muscle disuse.


Subject(s)
Muscle Fibers, Skeletal/classification , Muscle Fibers, Skeletal/pathology , Neoplasms/pathology , Aged , Female , Humans , Male , Middle Aged , Muscle Fibers, Fast-Twitch/pathology , Muscle Fibers, Skeletal/chemistry , Muscle Fibers, Slow-Twitch/pathology , Muscular Atrophy/etiology , Muscular Atrophy/pathology , Myosin Heavy Chains/analysis , Neoplasms/complications , Neoplasms/physiopathology , Prognosis , Weight Loss
2.
Am J Physiol Cell Physiol ; 308(11): C932-43, 2015 Jun 01.
Article in English | MEDLINE | ID: mdl-25810256

ABSTRACT

In older adults, we examined the effect of chronic muscle disuse on skeletal muscle structure at the tissue, cellular, organellar, and molecular levels and its relationship to muscle function. Volunteers with advanced-stage knee osteoarthritis (OA, n = 16) were recruited to reflect the effects of chronic lower extremity muscle disuse and compared with recreationally active controls (n = 15) without knee OA but similar in age, sex, and health status. In the OA group, quadriceps muscle and single-fiber cross-sectional area were reduced, with the largest reduction in myosin heavy chain IIA fibers. Myosin heavy chain IIAX fibers were more prevalent in the OA group, and their atrophy was sex-specific: men showed a reduction in cross-sectional area, and women showed no differences. Myofibrillar ultrastructure, myonuclear content, and mitochondrial content and morphology generally did not differ between groups, with the exception of sex-specific adaptations in subsarcolemmal (SS) mitochondria, which were driven by lower values in OA women. SS mitochondrial content was also differently related to cellular and molecular functional parameters by sex: greater SS mitochondrial content was associated with improved contractility in women but reduced function in men. Collectively, these results demonstrate sex-specific structural phenotypes at the cellular and organellar levels with chronic disuse in older adults, with novel associations between energetic and contractile systems.


Subject(s)
Knee/physiopathology , Muscle Contraction , Muscle Fibers, Skeletal/pathology , Muscular Atrophy/physiopathology , Osteoarthritis, Knee/physiopathology , Quadriceps Muscle/physiopathology , Aged , Case-Control Studies , Exercise , Female , Gene Expression , Humans , Knee/pathology , Male , Mitochondria/metabolism , Mitochondria/ultrastructure , Muscle Fibers, Skeletal/metabolism , Muscle Fibers, Skeletal/ultrastructure , Muscular Atrophy/complications , Muscular Atrophy/metabolism , Muscular Atrophy/pathology , Myosin Heavy Chains/genetics , Myosin Heavy Chains/metabolism , Osteoarthritis, Knee/complications , Osteoarthritis, Knee/metabolism , Osteoarthritis, Knee/pathology , Protein Isoforms/genetics , Protein Isoforms/metabolism , Quadriceps Muscle/metabolism , Quadriceps Muscle/ultrastructure , Sex Factors
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