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Shockwave Intravascular Lithotripsy for the Treatment of Severe Vascular Calcification.冲击波血管内碎石术治疗严重血管钙化。
Angiology. 2020 Sep;71(8):677-688. doi: 10.1177/0003319720932455. Epub 2020 Jun 22.
2
Vascular Calcification-New Insights Into Its Mechanism.血管钙化——机制的新见解。
Int J Mol Sci. 2020 Apr 13;21(8):2685. doi: 10.3390/ijms21082685.
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Downregulation of miR-542-3p promotes osteogenic transition of vascular smooth muscle cells in the aging rat by targeting BMP7.miR-542-3p 的下调通过靶向 BMP7 促进衰老大鼠血管平滑肌细胞的成骨转化。
Hum Genomics. 2019 Dec 11;13(1):67. doi: 10.1186/s40246-019-0245-z.
4
Understanding Vulnerable Plaques: Current Status and Future Directions.了解易损斑块:现状与未来方向。
Korean Circ J. 2019 Dec;49(12):1115-1122. doi: 10.4070/kcj.2019.0211.
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The Vicious Cycle of Arterial Stiffness and Arterial Media Calcification.动脉僵硬度与动脉中膜钙化的恶性循环。
Trends Mol Med. 2019 Dec;25(12):1133-1146. doi: 10.1016/j.molmed.2019.08.006. Epub 2019 Sep 12.
6
Interactive and Multifactorial Mechanisms of Calcific Vascular and Valvular Disease.钙化性血管和瓣膜疾病的相互作用和多因素机制。
Trends Endocrinol Metab. 2019 Sep;30(9):646-657. doi: 10.1016/j.tem.2019.06.001. Epub 2019 Jul 3.
7
2018 Guidelines for the management of dyslipidemia.2018年血脂异常管理指南。
Korean J Intern Med. 2019 Jul;34(4):723-771. doi: 10.3904/kjim.2019.188. Epub 2019 Jul 1.
8
Angiotensin II Type 1 Receptor Blocker, Fimasartan, Reduces Vascular Smooth Muscle Cell Senescence by Inhibiting the CYR61 Signaling Pathway.血管紧张素II 1型受体阻滞剂菲马沙坦通过抑制CYR61信号通路减轻血管平滑肌细胞衰老。
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9
The Key Role of Phosphate on Vascular Calcification.磷酸盐在血管钙化中的关键作用。
Toxins (Basel). 2019 Apr 9;11(4):213. doi: 10.3390/toxins11040213.
10
Calcifications in atherosclerotic plaques and impact on plaque biomechanics.动脉粥样硬化斑块中的钙化及对斑块生物力学的影响。
J Biomech. 2019 Apr 18;87:1-12. doi: 10.1016/j.jbiomech.2019.03.005. Epub 2019 Mar 18.

炎症在动脉钙化中的作用。

Role of Inflammation in Arterial Calcification.

作者信息

Lee Hae Young, Lim Soyeon, Park Sungha

机构信息

Department of Internal Medicine and Cardiovascular Center, Seoul National University Hospital, Seoul, Korea.

Institute for Bio-Medical Convergence, College of Medicine, Catholic Kwandong University, Gangneung, Korea.

出版信息

Korean Circ J. 2021 Feb;51(2):114-125. doi: 10.4070/kcj.2020.0517.

DOI:10.4070/kcj.2020.0517
PMID:33525066
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7853899/
Abstract

Arterial calcification, characterized by calcium phosphate deposition in the arteries, can be divided into intimal calcification and medial calcification. The former is the predominant form of calcification in coronary artery plaques; the latter mostly affects peripheral arteries and aortas. Both forms of arterial calcification have strong correlations with adverse cardiovascular events. Intimal microcalcification is associated with increased risk of plaque disruption while the degree of burden of coronary calcification, measured by coronary calcium score, is a marker of overall plaque burden. Continuous research on vascular calcification has been performed during the past few decades, and several cellular and molecular mechanisms and therapeutic targets were identified. However, despite clinical trials to evaluate the efficacy of drug therapies to treat vascular calcification, none have been shown to have efficacy until the present. Therefore, more extensive research is necessary to develop appropriate therapeutic strategies based on a thorough understanding of vascular calcification. In this review, we mainly focus on intimal calcification, namely the pathobiology of arterial calcification, and its clinical implications.

摘要

动脉钙化,其特征为动脉中磷酸钙沉积,可分为内膜钙化和中膜钙化。前者是冠状动脉斑块中钙化的主要形式;后者主要影响外周动脉和主动脉。两种形式的动脉钙化都与不良心血管事件密切相关。内膜微钙化与斑块破裂风险增加有关,而通过冠状动脉钙化积分测量的冠状动脉钙化负担程度是总体斑块负担的一个指标。在过去几十年里,对血管钙化进行了持续研究,确定了几种细胞和分子机制以及治疗靶点。然而,尽管进行了评估药物治疗血管钙化疗效的临床试验,但迄今为止尚无一种药物显示出疗效。因此,有必要进行更广泛的研究,以便在全面了解血管钙化的基础上制定适当的治疗策略。在本综述中,我们主要关注内膜钙化,即动脉钙化的病理生物学及其临床意义。