Mechanisms of Muscle Atrophy in Type 2 Diabetes Mellitus: Factors Dysregulating Muscle Protein Synthesis and Breakdown.

Moses Jeong, Taylor McColl, David Clarke
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Abstract

Type 2 diabetes mellitus (T2DM) is rising in prevalence and incidence, which is leading to increased burden on healthcare systems. A less recognized consequence of T2DM is the accelerated loss of skeletal muscle, which can reduce quality of life and further exacerbate T2DM progression. Insulin resistance disrupts skeletal muscle maintenance by impairing insulin- and leucine-mediated signalling - processes challenging to study due to the number and complexity of dysregulated components. Several key areas in this field remain underexplored, such as the causal relationship between T2DM and muscle atrophy, the impact of insulin resistance on muscle protein balance, and the mechanisms driving muscle atrophy in humans with T2DM. Advancing understanding in these areas requires the integration of evidence from experimental, prospective, and computational studies to more precisely characterize the mechanisms and progression of T2DM-related muscle atrophy and to inform targeted interventions to mitigate muscle loss.

2型糖尿病肌肉萎缩的机制:调节肌肉蛋白合成和分解的因素。
2型糖尿病(T2DM)的患病率和发病率正在上升,这导致卫生保健系统的负担增加。T2DM的一个鲜为人知的后果是骨骼肌的加速损失,这可能降低生活质量并进一步加剧T2DM的进展。胰岛素抵抗通过损害胰岛素和亮氨酸介导的信号传导过程来破坏骨骼肌的维持,由于失调成分的数量和复杂性,研究具有挑战性。该领域的几个关键领域仍未得到充分研究,如T2DM与肌肉萎缩之间的因果关系,胰岛素抵抗对肌肉蛋白平衡的影响,以及T2DM患者肌肉萎缩的机制。推进对这些领域的理解需要整合来自实验、前瞻性和计算研究的证据,以更准确地表征t2dm相关肌肉萎缩的机制和进展,并为有针对性的干预提供信息,以减轻肌肉损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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