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.