Australian Atherosclerosis Society Position Statement on Lipoprotein(a): Clinical and Implementation Recommendations

医学 脂蛋白(a) 以兹提米比 内科学 人口 动脉粥样硬化性心血管疾病 脂蛋白 社会心理的 疾病 风险因素 他汀类 胆固醇 心脏病学 环境卫生 精神科
作者
Natalie C. Ward,Gerald F. Watts,Warrick Bishop,David Colquhoun,Christian Hamilton‐Craig,David L. Hare,Nadarajah Kangaharan,Karam Kostner,Leonard Kritharides,Richard O’Brien,Trevor A. Mori,Paul J. Nestel,Stephen J. Nicholls,Peter J. Psaltis,Natalie Raffoul,Harvey D. White,David Sullivan
出处
期刊:Heart Lung and Circulation [Elsevier BV]
卷期号:32 (3): 287-296 被引量:27
标识
DOI:10.1016/j.hlc.2022.11.015
摘要

This position statement provides guidance to cardiologists and related specialists on the management of adult patients with elevated lipoprotein(a) [Lp(a)]. Elevated Lp(a) is an independent and causal risk factor for atherosclerotic cardiovascular disease (ASCVD) and calcific aortic valve disease (CAVD). While circulating Lp(a) levels are largely determined by ancestry, they are also influenced by ethnicity, hormones, renal function, and acute inflammatory events, such that measurement should be done after accounting for these factors. Further, circulating Lp(a) concentrations should be estimated using an apo(a)-isoform independent assay that employs appropriate calibrators and reports the results in molar units (nmol/L). Selective screening strategies of high-risk patients are recommended, but universal screening of the population is currently not advised. Testing for elevated Lp(a) is recommended in all patients with premature ASCVD and those considered to be at intermediate-to-high risk of ASCVD. Elevated Lp(a) should be employed to assess and stratify risk and to enable a decision on initiation or intensification of preventative treatments, such as cholesterol lowering therapy. In adult patients with elevated Lp(a) at intermediate-to-high risk of ASCVD, absolute risk should be reduced by addressing all modifiable behavioural, lifestyle, psychosocial and clinical risk factors, including maximising cholesterol-lowering with statin and ezetimibe and, where appropriate, PCSK9 inhibitors. Apheresis should be considered in patients with progressive ASCVD. New ribonucleic acid (RNA)-based therapies which directly lower Lp(a) are undergoing clinical trials.
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