Aortic stenosisLandmark
HEART UK consensus statement on Lp(a): a call to action (Cegla et al., Atherosclerosis 2019)
Original title: HEART UK consensus statement on Lipoprotein(a): A call to action
Ten statements for UK practice: measure Lp(a) in adults with personal or family history of premature ASCVD, first-degree relatives with Lp(a) above 200 nmol/L, familial hypercholesterolaemia, calcific aortic valve stenosis and borderline 10-year risk; manage by lowering overall risk, targeting non-HDL-C below 2.5 mmol/L and considering apheresis. Notably reported in nmol/L with a 90 to 200 nmol/L risk gradient.
Original abstract
Lipoprotein(a), Lp(a), is a modified atherogenic low-density lipoprotein particle that contains apolipoprotein(a). Its levels are highly heritable and variable in the population. This consensus statement by HEART UK is based on the evidence that Lp(a) is an independent cardiovascular disease (CVD) risk factor, provides recommendations for its measurement in clinical practice and reviews current and emerging therapeutic strategies to reduce CVD risk. Ten statements summarise the most salient points for practitioners and patients with high Lp(a). HEART UK recommends that Lp(a) is measured in adults as follows: 1) those with a personal or family history of premature atherosclerotic CVD; 2) those with first-degree relatives who have Lp(a) levels >200 nmol/l; 3) patients with familial hypercholesterolemia; 4) patients with calcific aortic valve stenosis and 5) those with borderline (but <15%) 10-year risk of a cardiovascular event. The management of patients with raised Lp(a) levels should include: 1) reducing overall atherosclerotic risk; 2) controlling dyslipidemia with a desirable non-HDL-cholesterol level of <100 mg/dl (2.5 mmol/l) and 3) consideration of lipoprotein apheresis.
aortic stenosiscascade screeningconsensusfamilial hypercholesterolaemiageneticsguidelinestesting
Summary written by lp-a.org from the published abstract; figures as published. Page updated 17 August 2026. Methods.