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Effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis: Post-hoc analysis of a randomised controlled trial

OBJECTIVE: Populations with knee osteoarthritis (KOA) are at increased risk of cardiovascular disease, due to higher prevalence of risk factors including dyslipidaemia, where statins are commonly prescribed. However, the effect of statins on muscles and symptoms in this population is unknown. Thus,...

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Autores principales: Lim, Yuan Z., Cicuttini, Flavia M., Wluka, Anita E., Jones, Graeme, Hill, Catherine L., Forbes, Andrew B., Tonkin, Andrew, Berezovskaya, Sofia, Tan, Lynn, Ding, Changhai, Wang, Yuanyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9452814/
https://www.ncbi.nlm.nih.gov/pubmed/36091679
http://dx.doi.org/10.3389/fmed.2022.939800
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author Lim, Yuan Z.
Cicuttini, Flavia M.
Wluka, Anita E.
Jones, Graeme
Hill, Catherine L.
Forbes, Andrew B.
Tonkin, Andrew
Berezovskaya, Sofia
Tan, Lynn
Ding, Changhai
Wang, Yuanyuan
author_facet Lim, Yuan Z.
Cicuttini, Flavia M.
Wluka, Anita E.
Jones, Graeme
Hill, Catherine L.
Forbes, Andrew B.
Tonkin, Andrew
Berezovskaya, Sofia
Tan, Lynn
Ding, Changhai
Wang, Yuanyuan
author_sort Lim, Yuan Z.
collection PubMed
description OBJECTIVE: Populations with knee osteoarthritis (KOA) are at increased risk of cardiovascular disease, due to higher prevalence of risk factors including dyslipidaemia, where statins are commonly prescribed. However, the effect of statins on muscles and symptoms in this population is unknown. Thus, this study examined the effect of atorvastatin on muscle properties in patients with symptomatic KOA. DESIGN: Post-hoc analysis of a 2-year multicentre randomised, double-blind, placebo-controlled trial. SETTING: Australian community. PARTICIPANTS: Participants aged 40–70 years (mean age 55.7 years, 55.6% female) with KOA who met the American College of Rheumatology clinical criteria received atorvastatin 40 mg daily (n = 151) or placebo (n = 153). MAIN OUTCOME MEASURES: Levels of creatinine kinase (CK), aspartate transaminase (AST), and alanine transaminase (ALT) at 1, 6, 12, and 24 months; muscle strength (by dynamometry) at 12 and 24 months; vastus medialis cross-sectional area (CSA) on magnetic resonance imaging at 24 months; and self-reported myalgia. RESULTS: There were no significant between-group differences in CK and AST at all timespoints. The atorvastatin group had higher ALT than placebo group at 1 (median 26 vs. 21, p = 0.004) and 6 (25 vs. 22, p = 0.007) months without significant between-group differences at 12 and 24 months. Muscle strength increased in both groups at 24 months without between-group differences [mean 8.2 (95% CI 3.5, 12.9) vs. 5.9 (1.3, 10.4), p = 0.49]. Change in vastus medialis CSA at 24 months favoured the atorvastatin group [0.11 (−0.10, 0.31) vs. −0.23 (−0.43, −0.03), p = 0.02] but of uncertain clinical significance. There was a trend for more myalgia in the atorvastatin group (8/151 vs. 2/153, p = 0.06) over 2 years, mostly occurring within 6 months (7/151 vs. 1/153, p = 0.04). CONCLUSIONS: In those with symptomatic KOA, despite a trend for more myalgia, there was no clear evidence of an adverse effect of atorvastatin on muscles, including those most relevant to knee joint health.
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spelling pubmed-94528142022-09-09 Effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis: Post-hoc analysis of a randomised controlled trial Lim, Yuan Z. Cicuttini, Flavia M. Wluka, Anita E. Jones, Graeme Hill, Catherine L. Forbes, Andrew B. Tonkin, Andrew Berezovskaya, Sofia Tan, Lynn Ding, Changhai Wang, Yuanyuan Front Med (Lausanne) Medicine OBJECTIVE: Populations with knee osteoarthritis (KOA) are at increased risk of cardiovascular disease, due to higher prevalence of risk factors including dyslipidaemia, where statins are commonly prescribed. However, the effect of statins on muscles and symptoms in this population is unknown. Thus, this study examined the effect of atorvastatin on muscle properties in patients with symptomatic KOA. DESIGN: Post-hoc analysis of a 2-year multicentre randomised, double-blind, placebo-controlled trial. SETTING: Australian community. PARTICIPANTS: Participants aged 40–70 years (mean age 55.7 years, 55.6% female) with KOA who met the American College of Rheumatology clinical criteria received atorvastatin 40 mg daily (n = 151) or placebo (n = 153). MAIN OUTCOME MEASURES: Levels of creatinine kinase (CK), aspartate transaminase (AST), and alanine transaminase (ALT) at 1, 6, 12, and 24 months; muscle strength (by dynamometry) at 12 and 24 months; vastus medialis cross-sectional area (CSA) on magnetic resonance imaging at 24 months; and self-reported myalgia. RESULTS: There were no significant between-group differences in CK and AST at all timespoints. The atorvastatin group had higher ALT than placebo group at 1 (median 26 vs. 21, p = 0.004) and 6 (25 vs. 22, p = 0.007) months without significant between-group differences at 12 and 24 months. Muscle strength increased in both groups at 24 months without between-group differences [mean 8.2 (95% CI 3.5, 12.9) vs. 5.9 (1.3, 10.4), p = 0.49]. Change in vastus medialis CSA at 24 months favoured the atorvastatin group [0.11 (−0.10, 0.31) vs. −0.23 (−0.43, −0.03), p = 0.02] but of uncertain clinical significance. There was a trend for more myalgia in the atorvastatin group (8/151 vs. 2/153, p = 0.06) over 2 years, mostly occurring within 6 months (7/151 vs. 1/153, p = 0.04). CONCLUSIONS: In those with symptomatic KOA, despite a trend for more myalgia, there was no clear evidence of an adverse effect of atorvastatin on muscles, including those most relevant to knee joint health. Frontiers Media S.A. 2022-08-25 /pmc/articles/PMC9452814/ /pubmed/36091679 http://dx.doi.org/10.3389/fmed.2022.939800 Text en Copyright © 2022 Lim, Cicuttini, Wluka, Jones, Hill, Forbes, Tonkin, Berezovskaya, Tan, Ding and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Lim, Yuan Z.
Cicuttini, Flavia M.
Wluka, Anita E.
Jones, Graeme
Hill, Catherine L.
Forbes, Andrew B.
Tonkin, Andrew
Berezovskaya, Sofia
Tan, Lynn
Ding, Changhai
Wang, Yuanyuan
Effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis: Post-hoc analysis of a randomised controlled trial
title Effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis: Post-hoc analysis of a randomised controlled trial
title_full Effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis: Post-hoc analysis of a randomised controlled trial
title_fullStr Effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis: Post-hoc analysis of a randomised controlled trial
title_full_unstemmed Effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis: Post-hoc analysis of a randomised controlled trial
title_short Effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis: Post-hoc analysis of a randomised controlled trial
title_sort effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis: post-hoc analysis of a randomised controlled trial
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9452814/
https://www.ncbi.nlm.nih.gov/pubmed/36091679
http://dx.doi.org/10.3389/fmed.2022.939800
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