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Association between vitamin D deficiency and exercise capacity in patients with CKD, a cross-sectional analysis

Abstract

BACKGROUND: Evidence is growing for a role of vitamin D in regulating skeletal muscle mass, strength and functional capacity. Given the role the kidneys play in activating total vitamin D, and the high prevalence of vitamin D deficiency in Chronic Kidney Disease (CKD), it is possible that deficiency contributes to the low levels of physical function and muscle mass in these patients. METHODS: This is a secondary cross-sectional analysis of previously published interventional study, with in vitro follow up work. 34 CKD patients at stages G3b-5 (eGFR 25.5 +/- 8.3 mL/min/1.73m2; age 61 +/- 12 years) were recruited, with a sub-group (n = 20) also donating a muscle biopsy. Vitamin D and associated metabolites were analysed in plasma by liquid chromatography tandem-mass spectroscopy and correlated to a range of physiological tests of muscle size, function, exercise capacity and body composition. The effects of 1alpha,25(OH)2D3 supplementation on myogenesis and myotube size was investigated in primary skeletal muscle cells from vitamin D deficient donors. RESULTS: In vivo, there was no association between total or active vitamin D and muscle size or strength, but a significant correlation with VO2Peak was seen with total vitamin D (25OHD). in vitro, 1alpha,25(OH)2D3 supplementation reduced IL-6 mRNA expression, but had no effect upon proliferation, differentiation or myotube diameter. CONCLUSIONS: Vitamin D deficiency is not a prominent factor driving the loss of muscle mass in CKD, but may play a role in reduced exercise capacity.

Type Journal
ISBN 1879-1220 (Electronic) 0960-0760 (Linking)
Authors Watson, E. L.; Wilkinson, T. J.; O'Sullivan, T. F.; Baker, L. A.; Gould, D. W.; Xenophontos, S.; Graham-Brown, M.; Major, R.; Jenkinson, C.; Hewison, M.; Philp, A.; Smith, A. C.
Responsible Garvan Author Dr Andy Philp
Publisher Name JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
Published Date 2021-03-03
Published Volume 210
Published Pages 105861
Status Always Electronic
DOI 10.1016/j.jsbmb.2021.105861
URL link to publisher's version https://www.ncbi.nlm.nih.gov/pubmed/33675951