Kidney and Metabolic Bone Diseases Vol.32 No.1(9)

Theme Uremia and bone
Title Changes in type 1 collagen and bone material properties with chronic kidney disease
Publish Date 2019/01
Author Akiko Tajiri Division of Kidney and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine
Author Taketo Uchiyama Division of Kidney and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine
Author Ichiro Ohkido Division of Kidney and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine
[ Summary ] The mechanisms related to bone fragility in patients with chronic kidney disease (CKD) are widely known, and the causes of bone fragility are diverse. Among those causes, it is a very interesting concept that bone fragility in patients with CKD is caused by changes in bone material characteristics resulting from changes of type 1 collagen. There are two types of collagen crosslinking. One is "enzyme-dependent crosslinking". The other is "advanced glycation-product crosslinking". Renal dysfunction causes a decrease in enzyme-dependent crosslinking, whereas there is an increase in advanced glycation-product crosslinking. The causes of these changes in collagen crosslinking, such as accumulation of uremic toxins, hyper-homocysteinemia, vitamin D activation disorders, and enhancement of oxidative stress, have been reported. In this article, we will describe how renal dysfunction causes changes in type 1 collagen and bone material properties in terms of changes in collagen crosslinking.
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