Sanin Veronika, Pfetsch Vanessa, Koenig Wolfgang
Deutsches Herzzentrum München, Technische Universität München, Lazarettstr. 36, 80636, Munich, Germany.
DZHK (German Centre for Cardiovascular Research), Partner Site Munich Heart Alliance, Munich, Germany.
Curr Cardiol Rep. 2017 Jul;19(7):61. doi: 10.1007/s11886-017-0869-3.
This study aimed to present the current information on the genetic background of dyslipidemias and provide insights into the complex pathophysiological role of several plasma lipids/lipoproteins in the pathogenesis of atherosclerotic cardiovascular disease. Furthermore, we aim to summarize established therapies and describe the scientific rationale for the development of novel therapeutic strategies.
Evidence from genetic studies suggests that besides lowering low-density lipoprotein cholesterol, pharmacological reduction of triglyceride-rich lipoproteins, or lipoprotein(a) will reduce risk for coronary heart disease. Dyslipidemia, in particular hypercholesterolemia, is a common clinical condition and represents an important determinant of atherosclerotic vascular disease. Treatment decisions are currently guided by the causative lipid phenotype and the presence of other risk factors suggesting a very high cardiovascular risk. Therefore, the identification of lipid disorders and the optimal combination of therapeutic strategies provide an outstanding opportunity for reducing the onset and burden of cardiovascular disease.
本研究旨在介绍血脂异常的遗传背景的当前信息,并深入了解几种血浆脂质/脂蛋白在动脉粥样硬化性心血管疾病发病机制中的复杂病理生理作用。此外,我们旨在总结已确立的疗法,并描述新型治疗策略开发的科学依据。
遗传研究的证据表明,除了降低低密度脂蛋白胆固醇外,药物降低富含甘油三酯的脂蛋白或脂蛋白(a)将降低冠心病风险。血脂异常,尤其是高胆固醇血症,是一种常见的临床病症,是动脉粥样硬化性血管疾病的重要决定因素。目前的治疗决策以致病脂质表型和其他提示心血管风险极高的危险因素的存在为指导。因此,识别脂质紊乱和治疗策略的最佳组合为降低心血管疾病的发生和负担提供了绝佳机会。