NorthShore University HealthSystem, Division of Nephrology and Hypertension, Pritzker School of Medicine, University of Chicago, Evanston, IL 60201, USA.
Adv Chronic Kidney Dis. 2013 Sep;20(5):423-6. doi: 10.1053/j.ackd.2013.06.007.
Development of CKD-mineral and bone disorder (MBD) increases morbidity and mortality in men and women with CKD. The corresponding link among bone disease, fracture, and extraskeletal calcifications has been the subject of much focus. In the general population, the incidence of cardiovascular disease is higher in men than women, and this gender differences in degree of calcification and morbidity is maintained in kidney disease. Gender differences in phosphorus and fibroblast growth factor-23 (FGF-23) have been described. Increases in both have been linked with increasing likelihood of death in the CKD population as a whole; however, this link is not as well described when looking at women alone. The clinical significance of these differences, and the potential associated outcomes, are poorly understood. Traditional understanding of bone disease in women without kidney disease may not be fully applicable in women with CKD. Use of bone densitometry is limited in this population, and the traditional preventative interventions may not be fully transferrable to women with CKD.
慢性肾脏病矿物质和骨异常(CKD-MBD)的发生增加了男女 CKD 患者的发病率和死亡率。骨骼疾病、骨折和骨骼外钙化之间的相关联系一直是关注的焦点。在普通人群中,心血管疾病的发病率男性高于女性,而在肾脏病患者中,这种程度的钙化和发病率的性别差异是保持不变的。已经描述了磷和成纤维细胞生长因子 23(FGF-23)的性别差异。在整个 CKD 人群中,这两者的增加都与死亡率的增加有关;然而,当单独观察女性时,这种联系并没有得到很好的描述。这些差异的临床意义以及潜在的相关结果尚不清楚。在没有肾脏病的女性中,对骨骼疾病的传统理解可能不完全适用于 CKD 女性。在该人群中,骨密度测定的使用受到限制,传统的预防干预措施可能不完全适用于 CKD 女性。