Abstract

AimsMyostatin is a negative regulator of skeletal muscle mass and may also modulate energy metabolism secondarily. We aim to investigate the relationship between serum myostatin and the metabolic variables in diabetic (DM) and non-diabetic subjects.Materials and MethodsA cross-sectional study recruiting 246 consecutive DM patients and 82 age- and gender-matched non-diabetic individuals at a medical center was conducted. The variables of anthropometry and blood chemistry were obtained. Serum myostatin level was measured with enzyme immunoassay.ResultsDM group had lower serum myostatin compared with non-diabetics (7.82 versus 9.28 ng/ml, p<0.01). Sixty-two percent of the recruited individuals had metabolic syndrome (MetS). The patients with MetS had significantly lower serum myostatin than those without (7.39 versus 9.49 ng/ml, p<0.001). The serum myostatin level decreased with increasing numbers of the MetS components (p for trend<0.001). The patients with higher body mass index, larger abdominal girth, lower high-density lipoprotein cholesterol (HDL-C), and higher triglycerides had lower serum myostatin than those without. The serum myostatin level was independently negatively related to larger abdominal girth, higher triglycerides, and lower HDL-C after adjustment. The odds ratios for MetS, central obesity, low HDL-C, high triglycerides, and DM were 0.85, 0.88, 0.89, 0.85, and 0.92, respectively, when serum myostatin increased per 1 ng/mL, in the binary logistic regression models.ConclusionsLower serum myostatin independently associated with MetS, central obesity, low HDL-C, and high triglycerides after adjustment. Higher serum myostatin is associated with favorable metabolic profiles.

Highlights

  • Myostatin, a member of the transforming growth factor-b (TGF-b) superfamily, is a novel muscle-secreted biofactor that was demonstrated to modulate growth and differentiation of skeletal muscles [1]

  • The serum myostatin level decreased with increasing numbers of the metabolic syndrome (MetS) components (p for trend,0.001)

  • The odds ratios for MetS, central obesity, low high-density lipoprotein cholesterol (HDL-C), high triglycerides, and diabetes mellitus (DM) were 0.85, 0.88, 0.89, 0.85, and 0.92, respectively, when serum myostatin increased per 1 ng/mL, in the binary logistic regression models

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Summary

Introduction

A member of the transforming growth factor-b (TGF-b) superfamily, is a novel muscle-secreted biofactor that was demonstrated to modulate growth and differentiation of skeletal muscles [1]. Myostatin is mainly expressed in the skeletal muscles, released into extracellular space and blood circulation to exert its paracrine and endocrine effects [2,3]. Myostatin-deficient mice had a phenotype of increased myogenesis, and decreased fat mass [4,5]. Nude mice expressing highlevel of recombinant myostatin had a cachexia-like phenotype with reduction in both muscle and fat [9]. Taken together, these results suggest that myostatin is a negative regulator of skeletal muscle mass in development and regeneration to prevent muscle hyperplasia and hypertrophy. Myostatin may reduce fat mass by its direct anti-adipogenic effect or indirectly via increasing muscle mass by lessening its inhibition

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