Rheumatology, Reade, Amsterdam Rheumatology and Immunology Center, Amsterdam, Noord-Holland, The Netherlands
Rheumatology, Reade, Amsterdam Rheumatology and Immunology Center, Amsterdam, Noord-Holland, The Netherlands.
RMD Open. 2021 Mar;7(1). doi: 10.1136/rmdopen-2021-001591.
Persons at high risk of rheumatoid arthritis (RA) might benefit from a low-risk pharmacological intervention aimed at primary prevention. Previous studies demonstrated disease-modifying effects of statins in patients with RA as well as an association between statin use and a decreased risk of RA development. A randomised, double-blind, placebo-controlled trial investigated whether atorvastatin could prevent arthritis development in high-risk individuals.
Arthralgia patients with anticitrullinated protein antibody (ACPA) >3 xULN or ACPA and rheumatoid factor, without (a history of) arthritis, were randomised to receive atorvastatin 40 mg daily or placebo for 3 years. The calculated sample size was 220 participants. The primary endpoint was clinical arthritis. Cox regression analysis was used to determine the effect of atorvastatin on arthritis development.
Due to a low inclusion rate, mainly because of an unwillingness to participate, the trial was prematurely stopped. Data of the 62 randomised individuals were analysed. Median follow-up was 14 (inner quartiles 6-35) months. Fifteen individuals (24%) developed arthritis: 9/31 (29%) in the atorvastatin group; 6/31 (19%) in the placebo group: HR 1.40, 95% CI 0.50 to 3.95.
In this small set of randomised high-risk individuals, we did not demonstrate a protective effect of atorvastatin on arthritis development. The main reason for the low inclusion was unwillingness to participate; this may also impede other RA prevention trials. Further research to investigate and solve barriers for prevention trial participation is needed.
类风湿关节炎(RA)高危人群可能受益于旨在进行初级预防的低风险药物干预。先前的研究表明,他汀类药物在 RA 患者中有改善疾病的作用,以及他汀类药物的使用与 RA 发病风险降低之间存在关联。一项随机、双盲、安慰剂对照试验研究了阿托伐他汀是否可以预防高危人群的关节炎发展。
抗瓜氨酸蛋白抗体(ACPA)>3×正常值上限或 ACPA 和类风湿因子阳性、无(有过)关节炎的关节痛患者被随机分配接受阿托伐他汀 40mg 每日或安慰剂治疗 3 年。计算的样本量为 220 名参与者。主要终点是临床关节炎。Cox 回归分析用于确定阿托伐他汀对关节炎发展的影响。
由于纳入率低,主要是由于不愿意参与,试验提前停止。对 62 名随机分配的个体的数据进行了分析。中位随访时间为 14 个月(内四分位数 6-35)。15 名个体(24%)发生关节炎:阿托伐他汀组 9/31(29%);安慰剂组 6/31(19%):HR 1.40,95%CI 0.50 至 3.95。
在这一小部分随机高危人群中,我们没有证明阿托伐他汀对关节炎发展有保护作用。低纳入率的主要原因是不愿意参与;这也可能阻碍其他 RA 预防试验。需要进一步研究以调查和解决预防试验参与的障碍。