Skeletal muscle as a therapeutic target for delaying type 1 diabetic complications.

World J Diabetes

Samantha K Coleman, Irena A Rebalka, Donna M D'Souza, Thomas J Hawke, Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON L8S 4L8, Canada.

Published: December 2015

AI Article Synopsis

  • Type 1 diabetes mellitus (T1DM) is an autoimmune disease that attacks pancreatic beta-cells, leading to insulin deficiency and high blood sugar, resulting in long-term health issues like blindness and kidney failure.
  • T1DM negatively impacts skeletal muscle health, affecting insulin sensitivity and metabolic functions, which complicates disease management for patients.
  • The review explores how T1DM affects skeletal muscle, examines potential therapies alongside insulin treatment, and aims to improve muscle health and delay other diabetic complications.

Article Abstract

Type 1 diabetes mellitus (T1DM) is a chronic autoimmune disease targeting the pancreatic beta-cells and rendering the person hypoinsulinemic and hyperglycemic. Despite exogenous insulin therapy, individuals with T1DM will invariably develop long-term complications such as blindness, kidney failure and cardiovascular disease. Though often overlooked, skeletal muscle is also adversely affected in T1DM, with both physical and metabolic derangements reported. As the largest metabolic organ in the body, impairments to skeletal muscle health in T1DM would impact insulin sensitivity, glucose/lipid disposal and basal metabolic rate and thus affect the ability of persons with T1DM to manage their disease. In this review, we discuss the impact of T1DM on skeletal muscle health with a particular focus on the proposed mechanisms involved. We then identify and discuss established and potential adjuvant therapies which, in association with insulin therapy, would improve the health of skeletal muscle in those with T1DM and thereby improve disease management- ultimately delaying the onset and severity of other long-term diabetic complications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673386PMC
http://dx.doi.org/10.4239/wjd.v6.i17.1323DOI Listing

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