The Rheumatoid Arthritis and MUScle (RAMUS) Study: Protocol for an observational single-arm study of skeletal muscle in patients with rheumatoid arthritis receiving tofacitinib.

Joshua L Bennett, Maha Egail, Amy E Anderson, Richard Dodds, Catherine Feeney, Gráinne S Gorman, Arthur G Pratt, Avan A Sayer, Kieren G Hollingsworth, John D Isaacs
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引用次数: 1

Abstract

People with rheumatoid arthritis (RA) are disproportionately affected by sarcopenia, the generalised loss of muscle strength and mass, consequently facing an increased risk of falls, functional decline and death. Currently, there are no approved pharmacological treatments for sarcopenia. RA patients who start tofacitinib (a Janus kinase inhibitor) develop small increases in serum creatinine that are not explained by renal function changes and could reflect sarcopenia improvement. The RAMUS Study is a proof of concept, single-arm observational study in which patients with RA who commence tofacitinib according to routine care will be offered participation according to eligibility criteria. Participants will undergo lower limb quantitative magnetic resonance imaging, whole-body dual energy x-ray absorptiometry, joint examination, muscle function testing and blood tests at three time points: prior to starting tofacitinib and 1 and 6 months afterwards. Muscle biopsy will be performed before and 6 months after starting tofacitinib. The primary outcome will be lower limb muscle volume changes following treatment initiation. The RAMUS Study will investigate whether muscle health improves following tofacitinib treatment for RA. Identifying a potential pharmacological treatment for sarcopenia could have important implications for individuals with RA and for older people in general. ISRCTN registry ID: 13364395.

Abstract Image

类风湿关节炎和肌肉(RAMUS)研究:接受托法替尼治疗的类风湿关节炎患者骨骼肌观察性单臂研究方案。
类风湿性关节炎(RA)患者受到肌肉减少症(肌肉力量和质量的普遍丧失)的影响不成比例,因此面临摔倒、功能下降和死亡的风险增加。目前,还没有批准的药物治疗肌肉减少症。开始使用托法替尼(一种Janus激酶抑制剂)的RA患者血清肌酐小幅升高,这不能用肾功能改变来解释,可能反映了肌肉减少症的改善。RAMUS研究是一项概念验证,单臂观察性研究,根据常规护理开始使用托法替尼的RA患者将根据资格标准参与研究。参与者将在三个时间点接受下肢定量磁共振成像、全身双能x线吸收仪、关节检查、肌肉功能测试和血液检查:开始使用托法替尼之前和开始使用托法替尼后1个月和6个月。肌肉活检将在开始使用托法替尼之前和6个月后进行。主要结果将是治疗开始后下肢肌肉体积的变化。RAMUS研究将调查托法替尼治疗RA后肌肉健康是否得到改善。确定肌肉减少症的潜在药物治疗可能对RA患者和一般老年人具有重要意义。ISRCTN注册表ID: 13364395。
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