Calcification in atherosclerosis: Bone biology and chronic inflammation at the arterial crossroads

被引:367
作者
Doherty, TM
Asotra, K
Fitzpatrick, LA
Qiao, JH
Wilkin, DJ
Detrano, RC
Dunstan, CR
Shah, PK
Rajavashisth, TB
机构
[1] Univ Calif Los Angeles, Cedars Sinai Med Ctr, David Geffen Sch Med, Atherosclerosis Res Ctr,Div Cardiol, Los Angeles, CA 90048 USA
[2] Univ Calif Los Angeles, Cedars Sinai Med Ctr, Burns & Allen Res Inst, Div Cardiol,Dept Med, Los Angeles, CA 90048 USA
[3] Mayo Clin & Mayo Fdn, Dept Internal Med, Div Endocrinol Diabet Metab & Nutr, Rochester, MN 55905 USA
[4] Univ Calif Los Angeles, Los Angeles Cty Harbor Med Ctr, Res & Educ Inst, Dept Med,Div Cardiol, Torrance, CA 90502 USA
[5] Amgen Inc, Dept Dev, Thousand Oaks, CA 91320 USA
关键词
D O I
10.1073/pnas.1932554100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dystrc phic or ectopic mineral deposition occurs in many pathologic conditions, including atherosclerosis. Calcium mineral deposits that frequent y accompany atherosclerosis are readily quantifiable radiographically, serve as a surrogate marker for the disease, and predict a higher risk of myocardial infarction and death. Accelerating research interest has been propelled by a clear need to understand how plaquo structure, composition, and stability lead to devastating cardiovascular events. In atherosclerotic plaque, accumulating evidence is consistent with the notion that calcification involves the participation of arterial osteoblasts and osteoclasts. Here we summarize current models of intimal arterial plaque calcification and highlight intriguing questions that require further investigation. Because atherosclerosis is a chronic vascular inflammation, we propose that arterial plaque calcification is best conceptualized as a convergence of bone biology with vascular inflammatory pathobiology.
引用
收藏
页码:11201 / 11206
页数:6
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