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Managing of Dyslipidaemia Characterized by Accumulation of Triglyceride-Rich Lipoproteins
PURPOSE OF REVIEW: The accumulation of triglyceride-rich lipoproteins (TRLs) in plasma in patients with familial chylomicronaemia syndrome (FCS) or severe hypertriglyceridemia is associated with an increased risk of potentially life-threatening pancreatitis. Elevated TRL levels have also been sugges...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924084/ https://www.ncbi.nlm.nih.gov/pubmed/35107764 http://dx.doi.org/10.1007/s11883-022-00979-y |
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author | Visser, Jolien van Zwol, Willemien Kuivenhoven, Jan Albert |
author_facet | Visser, Jolien van Zwol, Willemien Kuivenhoven, Jan Albert |
author_sort | Visser, Jolien |
collection | PubMed |
description | PURPOSE OF REVIEW: The accumulation of triglyceride-rich lipoproteins (TRLs) in plasma in patients with familial chylomicronaemia syndrome (FCS) or severe hypertriglyceridemia is associated with an increased risk of potentially life-threatening pancreatitis. Elevated TRL levels have also been suggested to contribute to atherosclerotic cardiovascular disease (ASCVD). This review provides the latest progress that has been made in this field of research. RECENT FINDINGS: Apolipoprotein C-III and angiopoietin-like protein 3 play key roles in the metabolism of TRLs. Targeting their production in the liver or their presence in the circulation effectively reduces triglycerides in patients with FCS or severe hypertriglyceridemia. Attempts to reduce triglyceride synthesis in the small intestine have been halted. Early studies with a fibroblast growth factor 21 agonist have shown to reduce plasma triglycerides and hepatic steatosis and improve glucose homeostasis. SUMMARY: New drugs have recently been shown to effectively reduce plasma triglycerides which render hope for treating the risk of pancreatitis. Studies that have just been initiated will learn whether this unmet clinical will be met. It is too early to evaluate the potential of these drugs to reduce the risk of atherosclerosis through the reduction of triglycerides. |
format | Online Article Text |
id | pubmed-8924084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-89240842022-03-17 Managing of Dyslipidaemia Characterized by Accumulation of Triglyceride-Rich Lipoproteins Visser, Jolien van Zwol, Willemien Kuivenhoven, Jan Albert Curr Atheroscler Rep Nonstatin Drugs (M. Vrablik, Section Editor) PURPOSE OF REVIEW: The accumulation of triglyceride-rich lipoproteins (TRLs) in plasma in patients with familial chylomicronaemia syndrome (FCS) or severe hypertriglyceridemia is associated with an increased risk of potentially life-threatening pancreatitis. Elevated TRL levels have also been suggested to contribute to atherosclerotic cardiovascular disease (ASCVD). This review provides the latest progress that has been made in this field of research. RECENT FINDINGS: Apolipoprotein C-III and angiopoietin-like protein 3 play key roles in the metabolism of TRLs. Targeting their production in the liver or their presence in the circulation effectively reduces triglycerides in patients with FCS or severe hypertriglyceridemia. Attempts to reduce triglyceride synthesis in the small intestine have been halted. Early studies with a fibroblast growth factor 21 agonist have shown to reduce plasma triglycerides and hepatic steatosis and improve glucose homeostasis. SUMMARY: New drugs have recently been shown to effectively reduce plasma triglycerides which render hope for treating the risk of pancreatitis. Studies that have just been initiated will learn whether this unmet clinical will be met. It is too early to evaluate the potential of these drugs to reduce the risk of atherosclerosis through the reduction of triglycerides. Springer US 2022-02-02 2022 /pmc/articles/PMC8924084/ /pubmed/35107764 http://dx.doi.org/10.1007/s11883-022-00979-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Nonstatin Drugs (M. Vrablik, Section Editor) Visser, Jolien van Zwol, Willemien Kuivenhoven, Jan Albert Managing of Dyslipidaemia Characterized by Accumulation of Triglyceride-Rich Lipoproteins |
title | Managing of Dyslipidaemia Characterized by Accumulation of Triglyceride-Rich Lipoproteins |
title_full | Managing of Dyslipidaemia Characterized by Accumulation of Triglyceride-Rich Lipoproteins |
title_fullStr | Managing of Dyslipidaemia Characterized by Accumulation of Triglyceride-Rich Lipoproteins |
title_full_unstemmed | Managing of Dyslipidaemia Characterized by Accumulation of Triglyceride-Rich Lipoproteins |
title_short | Managing of Dyslipidaemia Characterized by Accumulation of Triglyceride-Rich Lipoproteins |
title_sort | managing of dyslipidaemia characterized by accumulation of triglyceride-rich lipoproteins |
topic | Nonstatin Drugs (M. Vrablik, Section Editor) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924084/ https://www.ncbi.nlm.nih.gov/pubmed/35107764 http://dx.doi.org/10.1007/s11883-022-00979-y |
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