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慢性肾脏病与骨代谢

Chronic kidney disease and bone metabolism.

作者信息

Kazama Junichiro James, Matsuo Koji, Iwasaki Yoshiko, Fukagawa Masafumi

机构信息

Division of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan,

出版信息

J Bone Miner Metab. 2015 May;33(3):245-52. doi: 10.1007/s00774-014-0639-x. Epub 2015 Feb 5.

Abstract

Chronic kidney disease-related mineral and bone disease (CKD-MBD) is a syndrome defined as a systemic mineral metabolic disorder associated with CKD, and the term renal osteodystrophy indicates a pathomorphological concept of bone lesions associated with CKD-MBD. Cortical bone thinning, abnormalities in bone turnover and primary/secondary mineralization, elevated levels of circulating sclerostin, increased apoptosis in osteoblasts and osteocytes, disturbance of the coupling phenomenon, iatrogenic factors, accumulated micro-crackles, crystal/collagen disorientation, and chemical modification of collagen crosslinks are all possible candidates found in CKD that could promote osteopenia and/or bone fragility. Some of above factors are the consequences of abnormal systemic mineral metabolism but for others it seem unlikely. We have used the term uremic osteoporosis to describe the uremia-induced bone fragility which is not derived from abnormal systemic mineral metabolism. Interestingly, the disease aspect of uremic osteoporosis appears to be similar to that of senile osteoporosis.

摘要

慢性肾脏病相关的矿物质和骨疾病(CKD-MBD)是一种被定义为与慢性肾脏病相关的全身性矿物质代谢紊乱的综合征,术语肾性骨营养不良表明了与CKD-MBD相关的骨病变的病理形态学概念。皮质骨变薄、骨转换和原发性/继发性矿化异常、循环中硬化蛋白水平升高、成骨细胞和骨细胞凋亡增加、耦合现象紊乱、医源性因素、累积的微裂纹、晶体/胶原取向紊乱以及胶原交联的化学修饰都是在慢性肾脏病中发现的可能促进骨质减少和/或骨脆性增加的因素。上述一些因素是全身性矿物质代谢异常的后果,但其他因素似乎并非如此。我们使用术语尿毒症性骨质疏松来描述并非源于全身性矿物质代谢异常的尿毒症诱导的骨脆性。有趣的是,尿毒症性骨质疏松的疾病表现似乎与老年性骨质疏松相似。

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