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
School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Front Med (Lausanne). 2022 Aug 25;9:939800. doi: 10.3389/fmed.2022.939800. eCollection 2022.
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.
analysis of a 2-year multicentre randomised, double-blind, placebo-controlled trial.
Australian community.
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 ( = 151) or placebo ( = 153).
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.
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, = 0.004) and 6 (25 vs. 22, = 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), = 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), = 0.02] but of uncertain clinical significance. There was a trend for more myalgia in the atorvastatin group (8/151 vs. 2/153, = 0.06) over 2 years, mostly occurring within 6 months (7/151 vs. 1/153, = 0.04).
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.
膝关节骨关节炎(KOA)患者患心血管疾病的风险增加,这是由于包括血脂异常在内的危险因素患病率较高,而他汀类药物是常用的处方药。然而,他汀类药物对该人群肌肉和症状的影响尚不清楚。因此,本研究探讨了阿托伐他汀对有症状KOA患者肌肉特性的影响。
对一项为期2年的多中心随机、双盲、安慰剂对照试验进行分析。
澳大利亚社区。
年龄在40 - 70岁(平均年龄55.7岁,55.6%为女性)且符合美国风湿病学会临床标准的KOA患者,接受每日40毫克阿托伐他汀治疗(n = 151)或安慰剂治疗(n = 153)。
在1、6、12和24个月时的肌酸激酶(CK)、天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)水平;在12和24个月时的肌肉力量(通过测力计测量);在24个月时通过磁共振成像测量的股内侧肌横截面积(CSA);以及自我报告的肌痛。
在所有时间点,两组之间的CK和AST无显著差异。阿托伐他汀组在1个月(中位数26对21,P = 0.004)和6个月(25对22,P = 0.007)时的ALT高于安慰剂组,在12和24个月时两组之间无显著差异。两组在24个月时肌肉力量均增加,组间无差异[平均值8.2(95%CI 3.5,12.9)对5.9(1.3,10.4),P = 0.49]。24个月时股内侧肌CSA的变化有利于阿托伐他汀组[0.11(-0.10,0.31)对-0.23(-0.43,-0.03),P = 0.02],但临床意义不确定。在2年期间,阿托伐他汀组有更多肌痛的趋势(8/151对2/153,P = 0.06),大多发生在6个月内(7/151对1/153,P = 0.04)。
在有症状的KOA患者中,尽管有更多肌痛的趋势,但没有明确证据表明阿托伐他汀对肌肉有不良影响,包括那些与膝关节健康最相关的肌肉。