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Statin use in patients with non‐HMGCR idiopathic inflammatory myopathies: A retrospective study

BACKGROUND: Statins are the most widely used lipid lowering therapies which reduce cardiovascular risk, but are associated with muscular adverse events (AEs). Idiopathic inflammatory myopathies (IIM) are autoimmune diseases of the muscle with higher risk of cardiovascular disease. More data is neede...

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Autores principales: Bae, Sangmee Sharon, Oganesian, Buzand, Golub, Ilana, Charles‐Schoeman, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368310/
https://www.ncbi.nlm.nih.gov/pubmed/32432360
http://dx.doi.org/10.1002/clc.23375
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author Bae, Sangmee Sharon
Oganesian, Buzand
Golub, Ilana
Charles‐Schoeman, Christina
author_facet Bae, Sangmee Sharon
Oganesian, Buzand
Golub, Ilana
Charles‐Schoeman, Christina
author_sort Bae, Sangmee Sharon
collection PubMed
description BACKGROUND: Statins are the most widely used lipid lowering therapies which reduce cardiovascular risk, but are associated with muscular adverse events (AEs). Idiopathic inflammatory myopathies (IIM) are autoimmune diseases of the muscle with higher risk of cardiovascular disease. More data is needed regarding statin safety in patients with intrinsic muscle disease such as IIM. HYPOTHESIS: Statins are tolerated in patients with IIM without leading to significant increase in muscular AEs. METHODS: Statin use was retrospectively examined in a longitudinal IIM cohort. Safety analysis included assessment of muscular and nonmuscular AEs by chart review. IIM patients receiving a statin during the cohort follow‐up period were matched to IIM patients not receiving a statin for comparative analysis of longitudinal outcomes. RESULTS: 33/214 patients had a history of statin use. 63% started for primary prevention, while others were started for clinical ASCVD events, vascular surgery, IIM related heart failure, and cardiac transplantation. A high intensity statin was used in nine patients with non‐HMGCR myositis, and tolerated in 8/9 patients. Statin related muscular AE was noted in three patients. There were no cases of rhabdomyolysis, or statin related nonmuscular AEs in a median observation period of 5 years. In patients newly started on statins during cohort follow‐up (n = 7) there was no change in disease activity after statin initiation. Long term outcomes were not different between statin and nonstatin IIM control groups. CONCLUSION: Statins were well tolerated in patients with non‐HMGCR positive IIM. Given the accelerated atherosclerotic risk in IIM patients, further prospective studies of statin safety in IIM patients are warranted.
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spelling pubmed-73683102020-07-20 Statin use in patients with non‐HMGCR idiopathic inflammatory myopathies: A retrospective study Bae, Sangmee Sharon Oganesian, Buzand Golub, Ilana Charles‐Schoeman, Christina Clin Cardiol Clinical Investigations BACKGROUND: Statins are the most widely used lipid lowering therapies which reduce cardiovascular risk, but are associated with muscular adverse events (AEs). Idiopathic inflammatory myopathies (IIM) are autoimmune diseases of the muscle with higher risk of cardiovascular disease. More data is needed regarding statin safety in patients with intrinsic muscle disease such as IIM. HYPOTHESIS: Statins are tolerated in patients with IIM without leading to significant increase in muscular AEs. METHODS: Statin use was retrospectively examined in a longitudinal IIM cohort. Safety analysis included assessment of muscular and nonmuscular AEs by chart review. IIM patients receiving a statin during the cohort follow‐up period were matched to IIM patients not receiving a statin for comparative analysis of longitudinal outcomes. RESULTS: 33/214 patients had a history of statin use. 63% started for primary prevention, while others were started for clinical ASCVD events, vascular surgery, IIM related heart failure, and cardiac transplantation. A high intensity statin was used in nine patients with non‐HMGCR myositis, and tolerated in 8/9 patients. Statin related muscular AE was noted in three patients. There were no cases of rhabdomyolysis, or statin related nonmuscular AEs in a median observation period of 5 years. In patients newly started on statins during cohort follow‐up (n = 7) there was no change in disease activity after statin initiation. Long term outcomes were not different between statin and nonstatin IIM control groups. CONCLUSION: Statins were well tolerated in patients with non‐HMGCR positive IIM. Given the accelerated atherosclerotic risk in IIM patients, further prospective studies of statin safety in IIM patients are warranted. Wiley Periodicals, Inc. 2020-05-20 /pmc/articles/PMC7368310/ /pubmed/32432360 http://dx.doi.org/10.1002/clc.23375 Text en © 2020 The Authors. Clinical Cardiology published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Bae, Sangmee Sharon
Oganesian, Buzand
Golub, Ilana
Charles‐Schoeman, Christina
Statin use in patients with non‐HMGCR idiopathic inflammatory myopathies: A retrospective study
title Statin use in patients with non‐HMGCR idiopathic inflammatory myopathies: A retrospective study
title_full Statin use in patients with non‐HMGCR idiopathic inflammatory myopathies: A retrospective study
title_fullStr Statin use in patients with non‐HMGCR idiopathic inflammatory myopathies: A retrospective study
title_full_unstemmed Statin use in patients with non‐HMGCR idiopathic inflammatory myopathies: A retrospective study
title_short Statin use in patients with non‐HMGCR idiopathic inflammatory myopathies: A retrospective study
title_sort statin use in patients with non‐hmgcr idiopathic inflammatory myopathies: a retrospective study
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368310/
https://www.ncbi.nlm.nih.gov/pubmed/32432360
http://dx.doi.org/10.1002/clc.23375
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