FGF23/Klotho在骨质疏松与血管钙化共病机制中的研究进展  

Research progress of FGF23-Klotho axis in common pathogenesis of osteoporosis and vascular calcification

作　　者：张元霞[1] 周萍[1] 马兰[1] 王丽平[1] 王秋军[1] 林琳[1] 

机构地区：[1]哈尔滨医科大学附属第二医院老年病科

出　　处：《中华老年多器官疾病杂志》2016年第11期873-876,共4页Chinese Journal of Multiple Organ Diseases in the Elderly

基　　金：黑龙江省科技厅课题(12521210)~~

摘　　要：骨质疏松和血管钙化均为伴随衰老而发病率增高的退行性疾病，受多种因素影响。两者的发生发展都与钙磷代谢密切相关。近年来，涌现出许多关于骨质疏松和动脉硬化共同发病机制的研究报道，成纤维细胞生长因子23（ FGF23）／Klotho轴是热点之一，本文将对其在骨质疏松和血管钙化中的作用进行阐述。Osteoporosis and vascular calcification are both degenerative diseases associated with aging , and affected by a variety of factors.The occurrence and development of the 2 diseases are closely related to calcium and phosphorus metabolism .Recently, there are many studies concerning their common pathogenesis .One of the hot spots is fibroblast growth factor-23 （ FGF23）-Klotho axis.This article mainly elaborated its roles in the comorbidity of osteoporosis and vascular calcification .

关 键 词：成纤维细胞生长因子23 骨质疏松 血管钙化 钙磷代谢 

分 类 号：R68[医药卫生—骨科学] R543[医药卫生—外科学]