Vascular calcification and bone disease: the calcification paradox

被引:298
作者
Persy, Veerle [1 ]
D'Haese, Patrick [1 ]
机构
[1] Univ Antwerp, Lab Pathophysiol, B-2020 Antwerp, Belgium
关键词
SMOOTH-MUSCLE-CELLS; CORONARY-ARTERY CALCIFICATION; STAGE RENAL-DISEASE; ABDOMINAL AORTIC CALCIFICATION; CHRONIC KIDNEY-DISEASE; PULSE-WAVE VELOCITY; KAPPA-B LIGAND; MINERAL DENSITY; IN-VITRO; MEDIAL ELASTOCALCINOSIS;
D O I
10.1016/j.molmed.2009.07.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Vascular calcification or ectopic mineralization in blood vessels is an active, cell-regulated process, increasingly recognized as a general cardiovascular risk factor. Remarkably, ectopic artery mineralization is frequently accompanied by decreased bone mineral density or disturbed bone turnover. This contradictory association, observed mainly in osteoporosis and chronic kidney disease, is called the 'calcification paradox'. Here, we review recent advances in our understanding of the calcification paradox, including protein expression patterns governing both normal and ectopic mineralization, the conversion of vascular smooth muscle cells to bone-like cells, and the regulatory pathways involved in both bone and vessel mineralization. Further elucidation of the mechanisms underlying the calcification paradox is crucial in order to develop preventive and therapeutic strategies to deal with vascular calcification and reduce the associated cardiovascular risk.
引用
收藏
页码:405 / 416
页数:12
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