Genetic determinants of arterial calcification associated with atherosclerosis

被引:49
作者
Doherty, TM
Fitzpatrick, LA
Shaheen, A
Rajavashisth, TB
Detrano, RC
机构
[1] Mayo Clin & Mayo Fdn, Coll Med, Endocrine Res Unit, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Coll Med, Div Endocrinol Diabet Metab Nutr & Internal Med, Rochester, MN 55905 USA
[3] Cedars Sinai Med Ctr, Dept Med, Div Cardiol, Atherosclerosis Res Ctr, Los Angeles, CA USA
[4] Cedars Sinai Med Ctr, Dept Med, Div Cardiol, Burns & Allen Res Inst, Los Angeles, CA USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA USA
关键词
D O I
10.4065/79.2.197
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Increasing research interest has focused on arterial calcification in the setting of atherosclerosis. Many features of atherosclerosis-related calcification provide useful clinical information. For example, calcium mineral,deposits frequently form in atherosclerotic plaque, and intimal arterial calcification can be used as a surrogate marker for atherosclerosis; also, calcium deposits are readily and noninvasively quantified, which is useful because greater amounts of coronary calcification predict a higher risk of myocardial infarction and death. Several mechanisms leading to calcification associated with atherosclerosis have been proposed; however, no direct testing of proposed mechanisms has yet been reported. Studies in genetically altered animals and in humans have shed light on potential genetic determinants, which in turn could form the basis for a more comprehensive understanding of the factors affecting calcification within plaque and the associated pathobiologic implications. We review proposed molecular and cellular mechanisms of atherosclerosis-associated arterial calcification, summarize genetic influences, and suggest areas in which further investigation is needed. Understanding the molecular and genetic determinants of specific structural plaque components such as calcification can provide a solid foundation for the development of novel therapeutic approaches to favorably alter plaque structure and minimize vulnerability to arterial rupture.
引用
收藏
页码:197 / 210
页数:14
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