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Statin-Associated Autoimmune Myopathy: Current Perspectives

Although generally well tolerated, statin users frequently report muscle-related side effects, ranging from self-limiting myalgias to rhabdomyolysis or the rare clinical entity of statin-associated immune-mediated necrotizing myopathy (IMNM). Statin-associated IMNM is based on the development of aut...

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Autor principal: Tiniakou, Eleni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7266943/
https://www.ncbi.nlm.nih.gov/pubmed/32581543
http://dx.doi.org/10.2147/TCRM.S197941
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author Tiniakou, Eleni
author_facet Tiniakou, Eleni
author_sort Tiniakou, Eleni
collection PubMed
description Although generally well tolerated, statin users frequently report muscle-related side effects, ranging from self-limiting myalgias to rhabdomyolysis or the rare clinical entity of statin-associated immune-mediated necrotizing myopathy (IMNM). Statin-associated IMNM is based on the development of autoantibodies against 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR), the rate-limiting enzyme in cholesterol synthesis and the pharmacologic target of statins, and leads to a necrotizing myopathy requiring immunosuppressive therapy. This review attempts to recapitulate the diverse aspects of anti-HMGCR IMNM, including clinical presentation, diagnostic modalities, genetic risk associations, therapeutic options and potential pathogenetic pathways.
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spelling pubmed-72669432020-06-23 Statin-Associated Autoimmune Myopathy: Current Perspectives Tiniakou, Eleni Ther Clin Risk Manag Review Although generally well tolerated, statin users frequently report muscle-related side effects, ranging from self-limiting myalgias to rhabdomyolysis or the rare clinical entity of statin-associated immune-mediated necrotizing myopathy (IMNM). Statin-associated IMNM is based on the development of autoantibodies against 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR), the rate-limiting enzyme in cholesterol synthesis and the pharmacologic target of statins, and leads to a necrotizing myopathy requiring immunosuppressive therapy. This review attempts to recapitulate the diverse aspects of anti-HMGCR IMNM, including clinical presentation, diagnostic modalities, genetic risk associations, therapeutic options and potential pathogenetic pathways. Dove 2020-05-27 /pmc/articles/PMC7266943/ /pubmed/32581543 http://dx.doi.org/10.2147/TCRM.S197941 Text en © 2020 Tiniakou. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Tiniakou, Eleni
Statin-Associated Autoimmune Myopathy: Current Perspectives
title Statin-Associated Autoimmune Myopathy: Current Perspectives
title_full Statin-Associated Autoimmune Myopathy: Current Perspectives
title_fullStr Statin-Associated Autoimmune Myopathy: Current Perspectives
title_full_unstemmed Statin-Associated Autoimmune Myopathy: Current Perspectives
title_short Statin-Associated Autoimmune Myopathy: Current Perspectives
title_sort statin-associated autoimmune myopathy: current perspectives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7266943/
https://www.ncbi.nlm.nih.gov/pubmed/32581543
http://dx.doi.org/10.2147/TCRM.S197941
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