» Articles » PMID: 22886966

Increased Circulating Myostatin in Patients with Type 2 Diabetes Mellitus

Overview
Specialty General Medicine
Date 2012 Aug 14
PMID 22886966
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

The changes of plasma myostatin levels in patients with type 2 diabetes mellitus (T2D) and their clinical correlation were investigated. We recruited 43 T2D patients and 20 age-matched healthy subjects. Plasma myostatin, lipid and glucose, and serum insulin were determined. T2D patients showed significantly higher fasting plasma glucose (FPG), serum insulin and triglyceride levels, and lower high-density lipoprotein levels than normal control subjects (P<0.01). Mean plasma myostatin level in T2D patients and health controls was (66.5±17.8) and (46.2±13.8) ng/mL, respectively. An unpaired t test showed that the increase of myostatin in the T2D patients was significant (P<0.001). In both healthy control and T2D groups, the female subjects showed higher myostatin levels than the male subjects. In the T2D patients, plasma level of myostatin was negatively correlated with body mass index (BMI, r=-0.42, P<0.01) and FPG (r=-0.51, P[Symbol: see text]0.01), but positively correlated with insulin resistance index (HOMA-IR, r=0.48, P<0.01). Up-regulation of plasma myostatin in the T2D patients and its correlation with BMI, FPG and blood insulin sensitivity suggests that plasma myostatin may be implicated in the pathogenesis of T2D and thus presented as a therapeutic target for treating the disease. Furthermore, circulating myostatin levels may be used as a biomarker for the disease.

Citing Articles

Therapeutic applications and challenges in myostatin inhibition for enhanced skeletal muscle mass and functions.

Wetzlich B, Nyakundi B, Yang J Mol Cell Biochem. 2024; 480(3):1535-1553.

PMID: 39340593 PMC: 11842502. DOI: 10.1007/s11010-024-05120-y.


Targeting Molecular Mechanisms of Obesity- and Type 2 Diabetes Mellitus-Induced Skeletal Muscle Atrophy with Nerve Growth Factor.

Jun L, Ding X, Robinson M, Jafari H, Knight E, Geetha T Int J Mol Sci. 2024; 25(8).

PMID: 38673892 PMC: 11050157. DOI: 10.3390/ijms25084307.


Diabetes Mellitus Should Be Considered While Analysing Sarcopenia-Related Biomarkers.

Rentflejsz J, Wojszel Z J Clin Med. 2024; 13(4).

PMID: 38398421 PMC: 10889814. DOI: 10.3390/jcm13041107.


[Adipomyokines in children with obesity].

Burmitskaya Y, Vasyukova O, Okorokov P, Zuraeva Z, Bezlepkina O Probl Endokrinol (Mosk). 2023; 69(4):87-95.

PMID: 37694871 PMC: 10520902. DOI: 10.14341/probl13250.


The bidirectional relationship between AMPK pathway activation and myokine secretion in skeletal muscle: How it affects energy metabolism.

Ahsan M, Garneau L, Aguer C Front Physiol. 2022; 13:1040809.

PMID: 36479347 PMC: 9721351. DOI: 10.3389/fphys.2022.1040809.


References
1.
Lee S . Genetic analysis of the role of proteolysis in the activation of latent myostatin. PLoS One. 2008; 3(2):e1628. PMC: 2237902. DOI: 10.1371/journal.pone.0001628. View

2.
Reardon K, Davis J, Kapsa R, Choong P, Byrne E . Myostatin, insulin-like growth factor-1, and leukemia inhibitory factor mRNAs are upregulated in chronic human disuse muscle atrophy. Muscle Nerve. 2001; 24(7):893-9. DOI: 10.1002/mus.1086. View

3.
Welle S, Burgess K, Mehta S . Stimulation of skeletal muscle myofibrillar protein synthesis, p70 S6 kinase phosphorylation, and ribosomal protein S6 phosphorylation by inhibition of myostatin in mature mice. Am J Physiol Endocrinol Metab. 2009; 296(3):E567-72. PMC: 2660146. DOI: 10.1152/ajpendo.90862.2008. View

4.
McPherron A, Lee S . Suppression of body fat accumulation in myostatin-deficient mice. J Clin Invest. 2002; 109(5):595-601. PMC: 150888. DOI: 10.1172/JCI13562. View

5.
Hill J, Qiu Y, Hewick R, Wolfman N . Regulation of myostatin in vivo by growth and differentiation factor-associated serum protein-1: a novel protein with protease inhibitor and follistatin domains. Mol Endocrinol. 2003; 17(6):1144-54. DOI: 10.1210/me.2002-0366. View