Department of Medical, Technological and Translational Sciences, Clinica Medica, University of Trieste, Ospedale Cattinara, Strada di Fiume 447, Trieste, Italy.
J Ren Nutr. 2011 Jan;21(1):2-6. doi: 10.1053/j.jrn.2010.10.008.
Chronic uremia is often characterized by wasting of muscle and fat mass, which has been defined as protein-energy wasting (PEW), and is responsible for substantial worsening of patient outcome in terms of morbidity and mortality, mostly from cardiovascular events. Despite major advances in patient treatment, nutritional outcome in patients with end-stage renal disease has not improved substantially in recent years. Extensive research in this field has provided plausible explanations for this limitation by indicating that the pathogenesis of PEW in kidney disease is complex and multifactorial. Complexity involves underlying metabolic alterations, including inflammation, oxidative stress, and insulin resistance. In addition, patient heterogeneity is increasing with large numbers of obese individuals as a result of the ongoing obesity epidemics. Several tissues are involved in cross-talk and contribute to metabolic derangements, including adipose tissue, the gut, and the central nervous system, with novel mediators including the gastric hormone ghrelin. Acknowledging its complex pathogenesis may favor the development of novel and more effective therapeutic tools for PEW. These should ideally be effective in treating the underlying common mechanisms of wasting, which appear to include oxidative stress, inflammation, and insulin resistance.
慢性尿毒症常伴有肌肉和脂肪量的消耗,这被定义为蛋白质能量消耗(PEW),并导致患者的发病率和死亡率大幅恶化,主要是由于心血管事件。尽管患者的治疗取得了重大进展,但近年来终末期肾病患者的营养状况并没有得到实质性改善。该领域的广泛研究通过表明肾脏疾病中 PEW 的发病机制复杂且多因素,为这一局限性提供了合理的解释。这种复杂性涉及潜在的代谢改变,包括炎症、氧化应激和胰岛素抵抗。此外,由于肥胖症的持续流行,肥胖患者的数量不断增加,患者的异质性也在增加。包括脂肪组织、肠道和中枢神经系统在内的多种组织参与了相互作用,并导致代谢紊乱,新的介质包括胃激素 ghrelin。认识到其复杂的发病机制可能有利于开发针对 PEW 的新型、更有效的治疗工具。这些治疗方法在治疗潜在的消耗的共同机制方面应该是有效的,这些机制似乎包括氧化应激、炎症和胰岛素抵抗。