医学
不利影响
背景(考古学)
剩余风险
临床试验
甘油三酯
疾病
他汀类
内科学
生物信息学
胆固醇
药理学
古生物学
生物
作者
Waqas Malick,Ori Waksman,Ron Do,Wolfgang Köenig,Aruna D. Pradhan,Erik S.G. Stroes,Robert S. Rosenson
标识
DOI:10.1016/j.jacc.2023.02.034
摘要
Triglyceride-rich lipoproteins (TRLs) are a source of residual risk in patients with atherosclerotic cardiovascular disease, and are indirectly correlated with triglyceride (TG) levels. Previous clinical trials studying TG-lowering therapies have either failed to reduce major adverse cardiovascular events or shown no linkage of TG reduction with event reduction, particularly when these agents were tested on a background of statin therapy. Limitations in trial design may explain this lack of efficacy. With the advent of new RNA-silencing therapies in the TG metabolism pathway, there is renewed focus on reducing TRLs for major adverse cardiovascular event reduction. In this context, the pathophysiology of TRLs, pharmacological effects of TRL-lowering therapies, and optimal design of cardiovascular outcomes trials are major considerations.
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