Suppr超能文献

导致血管钙化的促动脉粥样硬化途径。

Proatherogenic pathways leading to vascular calcification.

作者信息

Mazzini Michael J, Schulze P Christian

机构信息

Department of Cardiology, Boston University Medical Center, Boston, MA 02118-2526, USA.

出版信息

Eur J Radiol. 2006 Mar;57(3):384-9. doi: 10.1016/j.ejrad.2005.12.025. Epub 2006 Feb 2.

Abstract

Cardiovascular disease is the leading cause of morbidity and mortality in the western world and atherosclerosis is the major common underlying disease. The pathogenesis of atherosclerosis involves local vascular injury, inflammation and oxidative stress as well as vascular calcification. Vascular calcification has long been regarded as a degenerative process leading to mineral deposition in the vascular wall characteristic for late stages of atherosclerosis. However, recent studies identified vascular calcification in early stages of atherosclerosis and its occurrence has been linked to clinical events in patients with cardiovascular disease. Its degree correlates with local vascular inflammation and with the overall impact and the progression of atherosclerosis. Over the last decade, diverse and highly regulated molecular signaling cascades controlling vascular calcification have been described. Local and circulating molecules such as osteopontin, osteoprogerin, leptin and matrix Gla protein were identified as critical regulators of vascular calcification. We here review the current knowledge on molecular pathways of vascular calcification and their relevance for the progression of cardiovascular disease.

摘要

心血管疾病是西方世界发病和死亡的主要原因,动脉粥样硬化是主要的常见基础疾病。动脉粥样硬化的发病机制涉及局部血管损伤、炎症、氧化应激以及血管钙化。长期以来,血管钙化一直被视为一种导致矿物质在血管壁沉积的退行性过程,这是动脉粥样硬化晚期的特征。然而,最近的研究发现动脉粥样硬化早期就存在血管钙化,其发生与心血管疾病患者的临床事件有关。其程度与局部血管炎症以及动脉粥样硬化的总体影响和进展相关。在过去十年中,已经描述了多种高度调控的控制血管钙化的分子信号级联反应。局部和循环分子,如骨桥蛋白、骨保护素、瘦素和基质Gla蛋白,被确定为血管钙化的关键调节因子。我们在此综述目前关于血管钙化分子途径的知识及其与心血管疾病进展的相关性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验