HEART UK consensus statement on Lipoprotein(a): A call to action.


Journal

Atherosclerosis
ISSN: 1879-1484
Titre abrégé: Atherosclerosis
Pays: Ireland
ID NLM: 0242543

Informations de publication

Date de publication:
12 2019
Historique:
received: 15 02 2019
revised: 08 10 2019
accepted: 10 10 2019
pubmed: 11 11 2019
medline: 4 8 2020
entrez: 10 11 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 31704552
pii: S0021-9150(19)31528-X
doi: 10.1016/j.atherosclerosis.2019.10.011
pii:
doi:

Substances chimiques

Biomarkers 0
Hypolipidemic Agents 0
LPA protein, human 0
Lipoprotein(a) 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

62-70

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Jaimini Cegla (J)

Division of Diabetes, Endocrinology and Metabolism, Imperial College London, London, UK. Electronic address: j.cegla@imperial.ac.uk.

R Dermot G Neely (RDG)

Department of Blood Sciences and NIHR MedTech and IVD Centre, Newcastle Upon Tyne Hospitals, Newcastle Upon Tyne, UK.

Michael France (M)

Department of Clinical Biochemistry, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.

Gordon Ferns (G)

Department of Medical Education, Brighton and Sussex Medical School, Brighton, UK.

Chris D Byrne (CD)

Department of Nutrition and Metabolism, Faculty of Medicine, University of Southampton, UK; Southampton National Institute for Health Research Biomedical Research Centre, University Hospital Southampton, Southampton, UK.

Julian Halcox (J)

Swansea University (Prifysgol Abertawe), College of Medicine, Swansea, UK.

Dev Datta (D)

Lipid Unit, University Hospital Llandough, Cardiff, UK.

Nigel Capps (N)

Department of Clinical Biochemistry, The Shrewsbury and Telford Hospital NHS Trust, Telford, UK.

Carol Shoulders (C)

William Harvey Research Institute, Queen Mary University of London, London, UK.

Nadeem Qureshi (N)

Division of Primary Care, University of Nottingham, Nottingham, UK.

Alan Rees (A)

HEART UK, Maidenhead, UK.

Linda Main (L)

HEART UK, Maidenhead, UK.

Robert Cramb (R)

University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Adie Viljoen (A)

Lister Hospital, Stevenage, UK.

Jules Payne (J)

HEART UK, Maidenhead, UK.

Handrean Soran (H)

Department of Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, UK.

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Classifications MeSH