Resistance training increases muscle mitochondrial biogenesis in patients with chronic kidney disease

Clin J Am Soc Nephrol. 2010 Jun;5(6):996-1002. doi: 10.2215/CJN.09141209. Epub 2010 May 24.

Abstract

Background and objectives: Muscle wasting, a common complication in chronic kidney disease (CKD), contributes to poor outcomes. Mitochondrial biogenesis is critical for the maintenance of skeletal muscle function and structural integrity. The present study--a secondary analysis from a published randomized controlled trial--examined the effect of resistance exercise training on skeletal muscle mitochondrial (mt)DNA copy number and determined its association with skeletal muscle phenotype (muscle mass and strength).

Design, setting, participants, & measurements: Twenty-three patients with moderate-to-severe CKD were randomized to resistance training (n = 13) or an attention-control (n = 10) group for 12 weeks. After a run-in period of a low-protein diet that continued during the intervention, mtDNA copy number in the vastus lateralis muscle was estimated by quantitative real-time PCR at baseline and 12 weeks.

Results: Participants mean age was 64 +/- 10 (SD) years and median (interquartile range, IQR) GFR 27.5 (37.0) ml/min. There were no differences between groups at baseline. Median (IQR) mtDNA copy number was 13,713 (10,618). There was a significant increase in muscle mtDNA with exercise compared with controls (1306 [13306] versus -3747 [15467], P = 0.01). The change in muscle mtDNA copy number was positively correlated with previously reported changes in types I and II muscle fiber cross-sectional area.

Conclusions: In this pilot study, resistance training was highly effective in enhancing mitochondrial content in patients with moderate-to-severe CKD. This finding suggests that the mitochondrial dysfunction observed with chronic disease could potentially be restored with this exercise modality and should be investigated further.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aged
  • Biopsy
  • Chronic Disease
  • DNA, Mitochondrial / biosynthesis*
  • Diet, Protein-Restricted
  • Female
  • Humans
  • Kidney Diseases / complications
  • Kidney Diseases / genetics
  • Kidney Diseases / physiopathology
  • Kidney Diseases / therapy*
  • Male
  • Middle Aged
  • Mitochondria, Muscle / metabolism*
  • Muscle Strength
  • Muscular Atrophy / etiology
  • Muscular Atrophy / genetics
  • Muscular Atrophy / physiopathology
  • Muscular Atrophy / therapy*
  • Organ Size
  • Pilot Projects
  • Polymerase Chain Reaction
  • Quadriceps Muscle / metabolism*
  • Quadriceps Muscle / pathology
  • Quadriceps Muscle / physiopathology
  • Resistance Training*
  • Severity of Illness Index
  • Time Factors
  • Treatment Outcome

Substances

  • DNA, Mitochondrial