Cardiometabolic interventions - focus on transcriptional regulators.

Joshua T Chai, Robin P Choudhury
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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.

心脏代谢干预--关注转录调节因子。
心血管疾病(CVD)仍然是西方世界最大的医疗负担;而 II 型糖尿病患病率的上升(至少部分原因是与全球经济发展相关的生活方式改变趋势)很可能会加重全球的心血管疾病负担。在过去的二十年里,人们越来越意识到导致心血管疾病和糖尿病的风险因素趋于一致,从而产生了代谢综合征的概念,并意识到有机会在这一交叉点上进行干预,以同时解决心血管疾病和代谢功能障碍问题。这就将心血管医学、糖尿病学以及越来越多的临床免疫学领域结合在一起,为同时降低这两种疾病的风险做出统一而协调的努力。由于发现了纤维酸盐和噻唑烷二酮类(TZD)等已在临床上使用的药物的靶向途径,加速了对选择性和双重 PPAR-α 和 PPAR-γ 激动剂的基础和临床研究,这些药物理论上可以靶向葡萄糖、脂质和脂蛋白代谢,并可能对血管炎症产生抑制作用,所有这些都可望减少动脉粥样硬化。在本文中,我们将讨论在追求最佳心脏代谢干预方面的基础科学和最新临床发展,并深入探讨未来药物开发的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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