医学
保健品
临床试验
重症监护医学
脂蛋白(a)
动脉粥样硬化性心血管疾病
脂蛋白
生物信息学
疾病
内科学
胆固醇
生物
病理
作者
Karam Kostner,Gerhard M. Kostner
标识
DOI:10.1097/mco.0000000000000994
摘要
Purpose of review Lp(a) is one of the most atherogenic lipoproteins, and significant progress has been made to understand its pathophysiology over the last 20 years. There are now selective therapies in late-stage clinical trials to lower Lp(a). Yet there are many outstanding questions about Lp(a). This review outlines 10 of the most burning questions and tries to answer some of them. Recent findings Antisense oligonucleotide (ASO) treatment is currently the most advanced therapy to lower plasma Lp(a) by 60–80%. There are, however, also two small molecule medications in early stage of development with similar efficacy. Summary This review aims to answer important preclinical and clinical questions about the metabolism and physiological role of Lp(a) and also outlines possible therapeutic approaches with nutraceuticals, currently available lipid-lowering therapies and new medications. In addition, ways are illustrated to use Lp(a) as a marker to better predict cardiovascular risk.
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