Lipoprotein(a) - Marker for cardiovascular risk and target for lipoprotein apheresis.


Journal

Atherosclerosis. Supplements
ISSN: 1878-5050
Titre abrégé: Atheroscler Suppl
Pays: Netherlands
ID NLM: 100973461

Informations de publication

Date de publication:
Dec 2019
Historique:
entrez: 11 12 2019
pubmed: 11 12 2019
medline: 26 5 2020
Statut: ppublish

Résumé

Lipoprotein(a) (Lp(a)) consists of an LDL particle whose apolipoprotein B (apoB) is covalently bound to apolipoprotein(a) (apo[a]). An increased Lp(a) concentration is a causal, independent risk factor for atherosclerotic cardiovascular disease (ASCVD) and a predictor of incident or recurrent cardiovascular events. Although Lp(a) was first described as early as 1963, only the more recent results of epidemiological, molecular, and genetic studies have led to this unequivocal conclusion. More than 20% of Western populations have elevated Lp(a) values. Lp(a) concentrations should be always part of the lipid profile when ASCVD risk is assessed. However, presence of other risk factors, laboratory findings, medical history and family history must be considered to conclude on its clinical relevance in an individual patient. Early or progressive ASCVD or a familial predisposition are key findings which can be associated with elevated Lp(a). The cholesterol portion contained in Lp(a) is also included in the various methods of LDL-C measurement. To assess proximity to the cardiovascular risk related target value for LDL-C, appropriate correction should be applied when high Lp(a) values are obtained to estimate the LDL-C that can actually be treated by lipid lowering drugs. Initial study data show that antisense oligonucleotides, which selectively decrease apolipoprotein(a), are promising as future treatment options. Currently, lipoprotein apheresis, which has a reimbursement guideline in Germany, is the therapy of choice for patients with Lp(a)-associated progressive ASCVD, with the aim of sustained prevention of further cardiovascular events.

Identifiants

pubmed: 31818445
pii: S1567-5688(19)30060-1
doi: 10.1016/j.atherosclerosissup.2019.08.037
pii:
doi:

Substances chimiques

Biomarkers 0
Lipoprotein(a) 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

17-22

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Reinhard Klingel (R)

Apheresis Research Institute, Cologne, Germany; First Department of Internal Medicine, University of Mainz, Mainz, Germany. Electronic address: klingel@apheresis-research.org.

Franz Heigl (F)

Medical Care Center Kempten-Allgäu, Kempten, Germany.

Volker Schettler (V)

Center of Nephrology Göttingen, Göttingen, Germany.

Eberhard Roeseler (E)

Center of Nephrology, Hypertension and Metabolic Diseases, Hannover, Germany.

Peter Grützmacher (P)

Medical Clinic II, Agaplesion Markus Hospital, Frankfurt, Germany.

Bernd Hohenstein (B)

Nephrological Center Villingen-Schwenningen, Villingen-Schwenningen, Germany; Department of Internal Medicine III, University Hospital Carl Gustav Carus at the Technische Universität Dresden, Germany.

Anja Vogt (A)

Medizinische Klinik IV, Klinikum der Universität München, Germany.

Cordula Fassbender (C)

Apheresis Research Institute, Cologne, Germany.

Andreas Heibges (A)

Apheresis Research Institute, Cologne, Germany.

Ulrich Julius (U)

Department of Internal Medicine III, University Hospital Carl Gustav Carus at the Technische Universität Dresden, Germany.

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Classifications MeSH