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血管钙化:分子机制与治疗干预

Vascular calcification: Molecular mechanisms and therapeutic interventions.

作者信息

Pan Wei, Jie Wei, Huang Hui

机构信息

Department of Cardiology, the Eighth Affiliated Hospital Sun Yat-sen University Shenzhen Guangdong China.

Joint Laboratory of Guangdong-Hong Kong-Macao Universities for Nutritional Metabolism and Precise Prevention and Control of Major Chronic Disease Sun Yat-sen University Shenzhen Guangdong China.

出版信息

MedComm (2020). 2023 Jan 3;4(1):e200. doi: 10.1002/mco2.200. eCollection 2023 Feb.

DOI:10.1002/mco2.200
PMID:36620697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9811665/
Abstract

Vascular calcification (VC) is recognized as a pathological vascular disorder associated with various diseases, such as atherosclerosis, hypertension, aortic valve stenosis, coronary artery disease, diabetes mellitus, as well as chronic kidney disease. Therefore, it is a life-threatening state for human health. There were several studies targeting mechanisms of VC that revealed the importance of vascular smooth muscle cells transdifferentiating, phosphorous and calcium milieu, as well as matrix vesicles on the progress of VC. However, the underlying molecular mechanisms of VC need to be elucidated. Though there is no acknowledged effective therapeutic strategy to reverse or cure VC clinically, recent evidence has proved that VC is not a passive irreversible comorbidity but an active process regulated by many factors. Some available approaches targeting the underlying molecular mechanism provide promising prospects for the therapy of VC. This review aims to summarize the novel findings on molecular mechanisms and therapeutic interventions of VC, including the role of inflammatory responses, endoplasmic reticulum stress, mitochondrial dysfunction, iron homeostasis, metabolic imbalance, and some related signaling pathways on VC progression. We also conclude some recent studies on controversial interventions in the clinical practice of VC, such as calcium channel blockers, renin-angiotensin system inhibitions, statins, bisphosphonates, denosumab, vitamins, and ion conditioning agents.

摘要

血管钙化(VC)被认为是一种与多种疾病相关的病理性血管疾病,如动脉粥样硬化、高血压、主动脉瓣狭窄、冠状动脉疾病、糖尿病以及慢性肾脏病。因此,它对人类健康构成了威胁生命的状态。有几项针对VC机制的研究揭示了血管平滑肌细胞转分化、磷和钙环境以及基质小泡在VC进展中的重要性。然而,VC的潜在分子机制仍有待阐明。尽管临床上尚无公认的有效治疗策略来逆转或治愈VC,但最近的证据表明,VC并非被动的不可逆合并症,而是一个受多种因素调节的活跃过程。一些针对潜在分子机制的可用方法为VC的治疗提供了有前景的前景。本综述旨在总结VC分子机制和治疗干预的新发现,包括炎症反应、内质网应激、线粒体功能障碍、铁稳态、代谢失衡以及一些相关信号通路在VC进展中的作用。我们还总结了最近关于VC临床实践中有争议干预措施的一些研究,如钙通道阻滞剂、肾素 - 血管紧张素系统抑制剂、他汀类药物、双膦酸盐、地诺单抗、维生素和离子调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef3/9811665/a69e65b62e1f/MCO2-4-e200-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef3/9811665/7fd8d164afb8/MCO2-4-e200-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef3/9811665/2b52d23c5068/MCO2-4-e200-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef3/9811665/4f893a1ebeee/MCO2-4-e200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef3/9811665/a69e65b62e1f/MCO2-4-e200-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef3/9811665/7fd8d164afb8/MCO2-4-e200-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef3/9811665/2b52d23c5068/MCO2-4-e200-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef3/9811665/4f893a1ebeee/MCO2-4-e200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef3/9811665/a69e65b62e1f/MCO2-4-e200-g001.jpg

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