4.4 Article

Serum myostatin levels and grip strength in normal subjects and patients on maintenance haemodialysis

Journal

CLINICAL ENDOCRINOLOGY
Volume 75, Issue 6, Pages 857-863

Publisher

WILEY-BLACKWELL
DOI: 10.1111/j.1365-2265.2011.04120.x

Keywords

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Funding

  1. National Taiwan University Hospital (NTUH) [94S-67, 97N-965, 99M1401]
  2. National Science Council, of Taiwan [97-2314-B-002-014-MY3]
  3. New Century Health Promotion Foundation

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Objective Myostatin, a negative regulator of skeletal muscle growth, may modulate grip strength, an indicator of muscle function. Its serum levels could be modulated by maintenance haemodialysis (MHD). Design A descriptive cross-sectional study. Patients Forty-one normal controls and 60 MHD patients using different dialyzers at a medical centre. Measurements The grip strength of the dominant hand, body composition, and the predialysis and postdialysis serum myostatin and IGF-1 levels were measured. Results The MHD patients had lower body mass index, IGF-1 level, and grip strength than the normal controls. The patients using the high-flux dialyzer had better grip strength than those using the low-flux dialyzer (25.5 vs 19.2 kg). The predialysis myostatin level was higher in low-flux dialyzer than high-flux dialyzer (31.0 vs 18.5 mu g/ml). Interestingly, the high-flux dialyzer reduced the serum myostatin by 36%, whereas low-flux dialyzer increased it by 25%. The myostatin was inversely related to age and the use of high-flux dialyzer. Furthermore, the grip strength was negatively related to age, female gender, muscle mass, myostatin levels and haemodialysis, but positively to the use of high-flux dialyzer in linear regression. The risk of low grip strength was 7.6 times higher in those with higher serum myostatin with the adjustment of age, gender, muscle mass, haemodialysis and mode of dialysis in a logistic regression. Conclusions The mode of dialyzer modulates the blood levels of myostatin. Higher myostatin is associated with lower muscle function. The use of myostatin assay in various clinical settings merits further investigation.

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