Literature DB >> 28572002

Toward an international consensus-Integrating lipoprotein apheresis and new lipid-lowering drugs.

Claudia Stefanutti1, Ulrich Julius2, Gerald F Watts3, Mariko Harada-Shiba4, Maria Cossu5, Volker J Schettler6, Giustina De Silvestro7, Handrean Soran8, Jeanine Roeters Van Lennep9, Livia Pisciotta10, Hans U Klör11, Kurt Widhalm12, Patrick M Moriarty13.   

Abstract

BACKGROUND: Despite advances in pharmacotherapy of lipid disorders, many dyslipidemic patients do not attain sufficient lipid lowering to mitigate risk of atherosclerotic cardiovascular disease. Several classes of novel lipid-lowering agents are being evaluated to reduce atherosclerotic cardiovascular disease risk. Lipoprotein apheresis (LA) is effective in acutely lowering the plasma concentrations of atherogenic lipoproteins including low-density lipoprotein cholesterol and lipoprotein(a), and novel lipid-lowering drugs may dampen the lipid rebound effect of LA, with the possibility that LA frequency may be decreased, in some cases even be discontinued. SOURCES OF MATERIAL: This document builds on current American Society for Apheresis guidelines and, for the first time, makes recommendations from summarized data of the emerging lipid-lowering drug classes (inhibitors of proprotein convertase subtilisin/kexin type 9 or microsomal triglyceride transfer protein, high-density lipoprotein mimetic), including the available evidence on combination therapy with LA with respect to the management of patients with dyslipidemia. ABSTRACT OF
FINDINGS: Recommendations for different indications are given based on the latest evidence. However, except for lomitapide in homozygous familial hypercholesterolemia and alirocumab/evolocumab in heterozygous familial hypercholesterolemia subjects, limited data are available on the effectiveness and safety of combination therapy. More studies on combining LA with novel lipid-lowering drugs are needed.
CONCLUSION: Novel lipid-lowering agents have potential to improve the performance of LA, but more evidence is needed. The Multidisciplinary International Group for Hemapheresis TherapY and Metabolic DIsturbances Contrast scientific society aims to establish an international registry of clinical experience on LA combination therapy to expand the evidence on this treatment in individuals at high cardiovascular disease risk.
Copyright © 2017 National Lipid Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Dyslipidemia; Familial hypercholesterolemia; HDL mimetic; LDL-cholesterol; Lipoprotein apheresis; Lipoproteins; Lp(a) hyperlipoproteinemia; MTP inhibition; PCSK9 inhibition

Mesh:

Substances:

Year:  2017        PMID: 28572002     DOI: 10.1016/j.jacl.2017.04.114

Source DB:  PubMed          Journal:  J Clin Lipidol        ISSN: 1876-4789            Impact factor:   4.766


  20 in total

1.  Generation and characterization of LPA-KIV9, a murine monoclonal antibody binding a single site on apolipoprotein (a).

Authors:  Ayelet Gonen; Xiaohong Yang; Calvin Yeang; Elena Alekseeva; Marlys Koschinsky; Joseph L Witztum; Michael Boffa; Sotirios Tsimikas
Journal:  J Lipid Res       Date:  2020-07-08       Impact factor: 5.922

Review 2.  Looking at Lp(a) and Related Cardiovascular Risk: from Scientific Evidence and Clinical Practice.

Authors:  Thomas M Stulnig; Claudia Morozzi; Roman Reindl-Schwaighofer; Claudia Stefanutti
Journal:  Curr Atheroscler Rep       Date:  2019-07-27       Impact factor: 5.113

3.  Plasmapheresis for hypertriglyceridemia: The association between blood viscosity and triglyceride clearance rate.

Authors:  Hung-Chieh Wu; Lin-Chien Lee; Wei-Jie Wang
Journal:  J Clin Lab Anal       Date:  2018-10-15       Impact factor: 2.352

Review 4.  Knowns and unknowns in the care of pediatric familial hypercholesterolemia.

Authors:  Andrew C Martin; Samuel S Gidding; Albert Wiegman; Gerald F Watts
Journal:  J Lipid Res       Date:  2017-07-12       Impact factor: 5.922

Review 5.  [Lipoprotein apheresis : State of the art and case report of the longest HELP treatment worldwide].

Authors:  Adrienn Tünnemann-Tarr; Julius Ludwig Katzmann; Joachim Thiery; Ulrich Laufs
Journal:  Herz       Date:  2022-04-22       Impact factor: 1.443

Review 6.  Familial hypercholesterolaemia: evolving knowledge for designing adaptive models of care.

Authors:  Gerald F Watts; Samuel S Gidding; Pedro Mata; Jing Pang; David R Sullivan; Shizuya Yamashita; Frederick J Raal; Raul D Santos; Kausik K Ray
Journal:  Nat Rev Cardiol       Date:  2020-01-23       Impact factor: 32.419

Review 7.  Women Living with Familial Hypercholesterolemia: Challenges and Considerations Surrounding Their Care.

Authors:  Sujana Balla; Eson P Ekpo; Katherine A Wilemon; Joshua W Knowles; Fatima Rodriguez
Journal:  Curr Atheroscler Rep       Date:  2020-08-20       Impact factor: 5.113

Review 8.  Current Approach to the Diagnosis and Treatment of Heterozygote and Homozygous FH Children and Adolescents.

Authors:  Hofit Cohen; Claudia Stefanutti
Journal:  Curr Atheroscler Rep       Date:  2021-05-08       Impact factor: 5.113

Review 9.  Lomitapide-a Microsomal Triglyceride Transfer Protein Inhibitor for Homozygous Familial Hypercholesterolemia.

Authors:  Claudia Stefanutti
Journal:  Curr Atheroscler Rep       Date:  2020-06-18       Impact factor: 5.113

10.  Hypercholesterolaemia - practical information for non-specialists.

Authors:  Handrean Soran; Safwaan Adam; Jamal B Mohammad; Jan H Ho; Jonathan D Schofield; See Kwok; Tarza Siahmansur; Yifen Liu; Akheel A Syed; Shaishav S Dhage; Claudia Stefanutti; Rachelle Donn; Rayaz A Malik; Maciej Banach; Paul N Durrington
Journal:  Arch Med Sci       Date:  2017-12-19       Impact factor: 3.318

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