Methotrexate treatment in hand osteoarthritis refractory to usual treatments: A randomised, double-blind, placebo-controlled trial

医学 安慰剂 骨关节炎 双盲 甲氨蝶呤 耐火材料(行星科学) 内科学 物理疗法 临床试验 病理 物理 替代医学 天体生物学
作者
S. Ferrero,Ruth Wittoek,Edem Allado,Coralie Cruzel,Éric Fontas,Véronique Breuil,L. Euller Ziegler,Joel M. Kremer,Damien Lœuille,C. Roux
出处
期刊:Seminars in Arthritis and Rheumatism [Elsevier BV]
卷期号:51 (4): 831-838 被引量:65
标识
DOI:10.1016/j.semarthrit.2021.04.016
摘要

To examine the effect of methotrexate (MTX) on pain and structural progression in symptomatic erosive hand osteoarthritis (HOA). This 1-year prospective, single-centre, randomised, double-blind, placebo-controlled study (www.ClinicalTrial.gov, NCT01068405) followed up patients with symptomatic erosive HOA. Patients were randomised into two groups based on the drug that was administered: 10 mg methotrexate (MTX) per week or a placebo. The primary endpoint was the change in pain (determined using a visual analogue scale [VAS]) from baseline to 3 months. The secondary endpoints were pain VAS score at 12 months, clinical features (pain VAS score and function), radiographic features (the anatomical radiographic Verbruggen–Veys [VV] score and Gent University Score System), and magnetic resonance imaging (MRI) at 12 months. Sixty-four patients with HOA were randomised into either the placebo or MTX group. At 3 months, there was no significant difference in the mean decrease in the pain VAS score (mm) (MTX: 21.1 [standard deviation, 27.4], placebo: 11.7 [24.3]; p = 0.2). At 12 months, according to the VV score, erosive joints progressed significantly more to a remodelling phase in the MTX group than in the placebo group (27% vs 15%; p = 0.03). Joints with space loss appeared to be eroding less in the MTX group compared to the placebo group (8% vs 29%; p = 0.2). Synovitis on MRI at baseline could be associated with the erosive structural evolution of non-erosive joints (p = 0.02). Weekly doses of 10-mg MTX showed no superiority over the placebo in terms of pain relief at 3 or 12 months. Clinical Trial Registration Number: This study was registered at www.ClinicalTrial.gov (NCT01068405).
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