Jia Ting, Stenvinkel Peter, Lindholm Bengt
G Ital Nefrol. 2013 May-Jun;30(3).
Chronic kidney disease (CKD) is characterized by numerous metabolic, nutritional and cardiovascular complications including loss of muscle mass, osteoporosis and vascular calcification contributing to the high mortality among these patients. Factors involved in the underlying pathology processes resulting in these complications such as insulin-like growth factor-1 system, calcium and phosphate homeostasis, fibrosis growth factor-23/parathyroid hormone pathway, receptor activator of nuclear-factor B system and osteoprotegerin pathway are closely interrelated and may act synergistically. Thus, the regulation of protein degradation, bone loss and vascular calcification share several common mediators and mechanisms, underlining the need for research approaches focusing on these shared mechanisms and pathways. This brief review aims at summarizing advances in our current understanding of the basis for development of muscle loss, osteoporosis and vascular calcification and also the possible connections among them in the CKD patients.
慢性肾脏病(CKD)的特征是存在众多代谢、营养和心血管并发症,包括肌肉量减少、骨质疏松和血管钙化,这些导致了此类患者的高死亡率。导致这些并发症的潜在病理过程所涉及的因素,如胰岛素样生长因子-1系统、钙和磷稳态、成纤维细胞生长因子-23/甲状旁腺激素途径、核因子κB受体激活剂系统和骨保护素途径,相互密切关联且可能协同作用。因此,蛋白质降解、骨质流失和血管钙化的调节共享几种常见的介质和机制,这突出了专注于这些共享机制和途径的研究方法的必要性。本简要综述旨在总结我们目前对CKD患者肌肉减少、骨质疏松和血管钙化发生基础的理解进展,以及它们之间可能的联系。