Price S Russ, Mitch William E, Garibotto Giacomo
Department of Biochemistry & Molecular Biology, Brody School of Medicine at East Carolina University, Greenville, North Carolina; Department of Internal Medicine, Brody School of Medicine at East Carolina University, Greenville, North Carolina.
Nephrology Division, Department of Medicine, Baylor College of Medicine, Houston, Texas.
J Ren Nutr. 2023 Nov;33(6S):S88-S92. doi: 10.1053/j.jrn.2022.09.009. Epub 2022 Sep 29.
This perspective reviews the seminal clinical and experimental observations that led to today's current mechanistic model of muscle protein loss (wasting) in patients with chronic kidney disease (CKD).
Early International Society of Renal Nutrition and Metabolism (ISRNM) meetings facilitated discussions and hypotheses about the causes of muscle wasting in CKD. It became widely recognized that wasting is common and correlated with increased risks of mortality and morbidity. Although anorexia and dietary restrictions contribute to muscle loss, several features of CKD-associated wasting cannot be explained by malnutrition alone. The protein catabolism-inducing actions of metabolic acidosis, inflammation, insulin resistance, endocrine disorders and uremic toxins were progressively identified. Continued research to understand the interactions of inflammation, anabolic resistance, mitochondrial dysfunction, exercise, and nutrition on muscle protein turnover in patients with CKD will hopefully accelerate discoveries and treatments to ameliorate muscle wasting as well as the progression of CKD.
本综述回顾了一些具有开创性的临床和实验观察结果,这些结果促成了当今慢性肾脏病(CKD)患者肌肉蛋白丢失(消瘦)的机制模型。
早期的国际肾脏营养与代谢学会(ISRNM)会议推动了关于CKD患者肌肉消瘦原因的讨论和假设。人们逐渐认识到消瘦很常见,且与死亡率和发病率增加相关。尽管厌食和饮食限制会导致肌肉流失,但CKD相关消瘦的一些特征不能仅用营养不良来解释。代谢性酸中毒、炎症、胰岛素抵抗、内分泌紊乱和尿毒症毒素的蛋白分解诱导作用逐渐被发现。持续开展研究以了解炎症、合成代谢抵抗、线粒体功能障碍、运动和营养对CKD患者肌肉蛋白周转的相互作用,有望加速改善肌肉消瘦以及CKD进展的发现和治疗。