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MERINO研究方案:一项随机安慰剂对照试验,评估甲氨蝶呤对侵蚀性手部骨关节炎患者的疗效、安全性和成本效益。

Protocol for the MERINO study: A randomized placebo-controlled trial assessing the efficacy, safety, and cost-effectiveness of methotrexate in people with erosive hand osteoarthritis.

作者信息

Mathiessen Alexander, Gaundal Line, Sexton Joseph, Sjølie Dag, Steen Pettersen Pernille, Slatkowsky-Christensen Barbara, Haugen Ida Kristin

机构信息

Center for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway.

Department of Radiology, Diakonhjemmet Hospital, Oslo, Norway.

出版信息

Osteoarthr Cartil Open. 2024 Dec 15;7(1):100558. doi: 10.1016/j.ocarto.2024.100558. eCollection 2025 Mar.

DOI:10.1016/j.ocarto.2024.100558
PMID:39807424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11728867/
Abstract

OBJECTIVE

Previous studies on the efficacy of methotrexate in people with hand osteoarthritis (OA) have shown conflicting results. The MERINO trial aims to investigate the efficacy and safety of methotrexate in people with painful inflammatory erosive hand OA.

DESIGN

In total 163 participants with erosive hand OA, synovitis by ultrasound, and finger joint pain of 40-80 ​mm on a visual analogue scale (VAS) will be recruited from a rheumatology outpatient clinic. Participants are randomized 1:1 to receive either encapsulated oral methotrexate 20 ​mg/week or placebo for 12 months in a double-blind manner. The primary endpoint is VAS finger joint pain at 6 months. Key secondary outcomes are hand function by the Australian/Canadian hand index (AUSCAN) at 6 months and radiographic progression by the Verbruggen-Veys anatomical phase scoring system at 12 months. Other secondary endpoints include hand stiffness, disease activity, health-related quality of life, grip strength, clinical joint counts, synovitis by ultrasound and MRI, bone marrow lesions by MRI, cost-effectiveness, and symptoms in knees and hips. Adverse events will be recorded. The primary analysis will be performed on full analysis set.

CONCLUSIONS

The findings of this trial will be clinically relevant for patients with erosive hand OA and may influence future treatment recommendations.

CLINICAL TRIAL REGISTRATION

EU CT number: 2023-510523-30-00, NCT04579848.

摘要

目的

先前关于甲氨蝶呤对手部骨关节炎(OA)患者疗效的研究结果相互矛盾。MERINO试验旨在研究甲氨蝶呤对伴有疼痛性炎性侵蚀性手部OA患者的疗效和安全性。

设计

将从风湿病门诊招募总共163名患有侵蚀性手部OA、超声显示滑膜炎且视觉模拟量表(VAS)上手指关节疼痛为40-80毫米的参与者。参与者以1:1的比例随机分组,接受每周20毫克的胶囊装口服甲氨蝶呤或安慰剂,为期12个月,采用双盲方式。主要终点是6个月时的VAS手指关节疼痛。关键次要结局是6个月时澳大利亚/加拿大手部指数(AUSCAN)评估的手部功能以及12个月时Verbruggen-Veys解剖分期评分系统评估的影像学进展。其他次要终点包括手部僵硬、疾病活动度、健康相关生活质量、握力、临床关节计数、超声和MRI检查的滑膜炎、MRI检查的骨髓病变、成本效益以及膝关节和髋关节的症状。将记录不良事件。主要分析将在全分析集上进行。

结论

该试验的结果对于侵蚀性手部OA患者具有临床相关性,可能会影响未来的治疗建议。

临床试验注册

欧盟临床试验编号:2023-510523-30-00,美国国立医学图书馆临床试验注册编号:NCT04579848。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfd/11728867/c285cad03fe3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfd/11728867/61de1cae2622/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfd/11728867/c285cad03fe3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfd/11728867/61de1cae2622/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfd/11728867/c285cad03fe3/gr2.jpg

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本文引用的文献

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