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心脏代谢干预——关注转录调节因子。

Cardiometabolic interventions - focus on transcriptional regulators.

作者信息

Chai Joshua T, Choudhury Robin P

机构信息

Division of Cardiovascular Medicine, Radcliffe Department of Medicine University of Oxford, United Kingdom.

出版信息

Eur J Cardiovasc Med. 2013 Aug 13;2(3):212-218. doi: 10.5083/ejcm.20424884.102.

Abstract

Cardiovascular disease (CVD) remains the largest healthcare burden in the Western world; and the increasing prevalence of type II diabetes mellitus, at least partially driven by a trend in lifestyle changes associated with global economic development, is likely to fuel this CVD burden worldwide. Over the past two decades, there has been an increased awareness of the convergence of risk factors contributing to both cardiovascular disease and diabetes leading to the concept of the metabolic syndrome, and the realisation of the opportunity to intervene at this intersection to simultaneously target CVD and metabolic dysfunction. This brings together the fields of cardiovascular medicine, diabetology, and increasingly clinical immunology for a unified and concerted effort to reduce risk for both conditions simultaneously. The discovery of the targeted pathways of drugs already in clinical use such as fibrates and thiazolidinediones (TZD) has led to accelerated basic and clinical research into selective and dual PPAR-α and PPAR-γ agonists, which can theoretically target glucose, lipid and lipoprotein metabolism, as well as potentially exerting inhibitoryeffects in vascular inflammation, all of which might be predicted to reduce atherosclerosis. In this article, we will discuss the basic science as well as recent clinical development in the pursuit of optimal cardiometabolic intervention along with insight into strategies for future drug development.

摘要

心血管疾病(CVD)仍然是西方世界最大的医疗负担;II型糖尿病患病率不断上升,至少部分是由与全球经济发展相关的生活方式变化趋势驱动的,这可能会加剧全球范围内的心血管疾病负担。在过去二十年中,人们越来越意识到导致心血管疾病和糖尿病的危险因素相互交织,从而产生了代谢综合征的概念,并且认识到在这个交叉点进行干预以同时针对心血管疾病和代谢功能障碍的机会。这将心血管医学、糖尿病学以及越来越多的临床免疫学领域汇聚在一起,为同时降低这两种疾病的风险而进行统一和协同的努力。已在临床使用的药物(如贝特类药物和噻唑烷二酮类药物(TZD))的靶向途径的发现,促使针对选择性和双重PPAR-α和PPAR-γ激动剂的基础和临床研究加速进行,理论上这些激动剂可以靶向葡萄糖、脂质和脂蛋白代谢,以及可能在血管炎症中发挥抑制作用,所有这些都可能被预测为可减少动脉粥样硬化。在本文中,我们将讨论在寻求最佳心脏代谢干预方面的基础科学以及近期临床进展,并深入了解未来药物开发的策略。

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