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Published in: Current Atherosclerosis Reports 7/2019

Open Access 01-07-2019 | Nonstatin Drugs (R. Carmena, Section Editor)

Current Role of Lipoprotein Apheresis

Authors: Gilbert Thompson, Klaus G. Parhofer

Published in: Current Atherosclerosis Reports | Issue 7/2019

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Abstract

Purpose of Review

Lipoprotein apheresis is a very efficient but time-consuming and expensive method of lowering levels of low-density lipoprotein cholesterol, lipoprotein(a)) and other apoB containing lipoproteins, including triglyceride-rich lipoproteins. First introduced almost 45 years ago, it has long been a therapy of “last resort” for dyslipidaemias that cannot otherwise be managed. In recent years new, very potent lipid-lowering drugs have been developed and the purpose of this review is to define the role of lipoprotein apheresis in the current setting.

Recent Findings

Lipoprotein apheresis still plays an important role in managing patients with homozygous FH and some patients with other forms of hypercholesterolaemia and cardiovascular disease. In particular, patients not achieving treatment goals despite modern lipid-lowering drugs, either because these are not tolerated or the response is insufficient. Recently, lipoprotein(a) has emerged as an important cardiovascular risk factor and lipoprotein apheresis has been used to decrease lipoprotein(a) concentrations in patients with marked elevations and cardiovascular disease. However, there is considerable heterogeneity concerning the recommendations by scientific bodies as to which patient groups should be treated with lipoprotein apheresis.

Summary

Lipoprotein apheresis remains an important tool for the management of patients with severe drug-resistant dyslipidaemias, especially those with homozygous FH.
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Metadata
Title
Current Role of Lipoprotein Apheresis
Authors
Gilbert Thompson
Klaus G. Parhofer
Publication date
01-07-2019
Publisher
Springer US
Published in
Current Atherosclerosis Reports / Issue 7/2019
Print ISSN: 1523-3804
Electronic ISSN: 1534-6242
DOI
https://doi.org/10.1007/s11883-019-0787-5
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