TY - JOUR
T1 - Effect of atorvastatin on skeletal muscles of patients with knee osteoarthritis
T2 - Post-hoc analysis of a randomised controlled trial
AU - Lim, Yuan Z.
AU - Cicuttini, Flavia M.
AU - Wluka, Anita E.
AU - Jones, Graeme
AU - Hill, Catherine L.
AU - Forbes, Andrew B.
AU - Tonkin, Andrew
AU - Berezovskaya, Sofia
AU - Tan, Lynn
AU - Ding, Changhai
AU - Wang, Yuanyuan
N1 - Funding Information:
The study was funded by a project grant from the National Health and Medical Research Council of Australia (NHMRC, APP1048581). YL was the recipient of NHMRC Clinical Postgraduate Scholarship (APP1133903) and Royal Australasian College of Physicians Woolcock Scholarship. FC was the recipient of NHMRC Investigator Grant (APP1194829). AW was the recipient of the Royal Australian College of Physicians Fellows Career Development Fellowship. GJ was the recipient of NHMRC Practitioner Fellowship. YW was the recipient of NHMRC Translating Research into Practice Fellowship (APP1168185).
Funding Information:
The study was funded by a project grant from the National Health and Medical Research Council of Australia (NHMRC, APP1048581). YL was the recipient of NHMRC Clinical Postgraduate Scholarship (APP1133903) and Royal Australasian College of Physicians Woolcock Scholarship. FC was the recipient of NHMRC Investigator Grant (APP1194829). AW was the recipient of the Royal Australian College of Physicians Fellows Career Development Fellowship. GJ was the recipient of NHMRC Practitioner Fellowship. YW was the recipient of NHMRC Translating Research into Practice Fellowship (APP1168185).
Publisher Copyright:
Copyright © 2022 Lim, Cicuttini, Wluka, Jones, Hill, Forbes, Tonkin, Berezovskaya, Tan, Ding and Wang.
PY - 2022/8/25
Y1 - 2022/8/25
N2 - 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.
AB - 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.
KW - knee
KW - muscles
KW - myalgia
KW - osteoarthritis
KW - statins
UR - http://www.scopus.com/inward/record.url?scp=85137896539&partnerID=8YFLogxK
U2 - 10.3389/fmed.2022.939800
DO - 10.3389/fmed.2022.939800
M3 - Article
C2 - 36091679
AN - SCOPUS:85137896539
VL - 9
JO - Frontiers in Medicine
JF - Frontiers in Medicine
SN - 2296-858X
M1 - 939800
ER -