Robin François, Ghossan Roba, Mehsen-Cetre Nadia, Triquet Louise, Larid Guillaume, Coiffier Guillaume, Mina Marine, Pickering Marie Eva, Barthe Claire, Paccou Julien, Herman Julien, Massy Emmanuel, Roitg Isabelle, Branquet Martine, Lasnier Siron Julien, Guillouard Manon, Desmonet Trousset Camille, Aubrun Aurore, Godfrin Bertrand, Hauzeur Jean-Philippe, Chatelus Emmanuel, Koumakis Eugénie, Legrand Jean-Louis, Schaeverbeke Thierry, Leloix Alexia, Masson Maeva, Nicolau Julia, Ghiringhelli Charles, Decrock Marijke, Durel Cécile-Audrey, Bouvard Béatrice, Cortet Bernard, Casadepax-Soulet Charlotte, Malaise Olivier, Javier Rose-Marie, Briot Karine, Guggenbuhl Pascal
Univ Rennes, INSERM, INRAE, CHU Rennes, UMR 1317 1341, Institut NuMeCan (Nutrition Metabolisms and Cancer), Rennes, France
Rheumatology department, Rennes University Hospital, Rennes, France.
RMD Open. 2025 Sep 25;11(3):e005941. doi: 10.1136/rmdopen-2025-005941.
Methotrexate-induced osteopathy (MTX-IO) is a rare condition typically involving the lower limbs, especially tibia or foot fractures, among patients with well-controlled rheumatoid arthritis (RA) or psoriatic arthritis (PsA). This study aimed to identify the affected population, describe fracture characteristics and identify risk factors for poor clinical outcome. A multicentre retrospective study included patients with MTX-IO diagnosed by bone specialists or identified through French pharmacovigilance. The data collected included clinical presentation, imaging features, bone mineral density and biochemical markers. Between 2012 and 2024, 92 patients were included, predominantly postmenopausal women with seropositive RA. A history of major fractures was noted for 22% of the patients, and 56% presented osteoporosis at diagnosis. Fractures were most common in the tibial metaphysis (distal and proximal) (88%) and the foot bones (49%), with multiple fractures often present at diagnosis (76%), and frequently repeated fractures in the patients' recent histories (63%). Diagnosis was conducted using MRI of the painful sites (84%), but bone scintigraphy was also used (41 patients, 45%). Management involved methotrexate discontinuation in 79% of the cases. Fracture healing and pain relief were achieved in 77% of the cases, with a significant difference in outcomes between those who discontinued methotrexate (91%) versus those who continued (29%) (p<0.001). MTX-IO is a rare but significant condition, especially among postmenopausal women with RA or PsA. Early diagnoses via MRI or bone scintigraphy and the discontinuation of methotrexate are critical, as stopping the drug significantly improves outcomes and prevents further fractures.
甲氨蝶呤所致骨病(MTX-IO)是一种罕见病症,在类风湿关节炎(RA)或银屑病关节炎(PsA)病情得到良好控制的患者中,通常累及下肢,尤其是胫骨或足部骨折。本研究旨在确定受影响人群,描述骨折特征,并识别临床预后不良的危险因素。一项多中心回顾性研究纳入了由骨专科医生诊断或通过法国药物警戒识别出的MTX-IO患者。收集的数据包括临床表现、影像学特征、骨密度和生化指标。2012年至2024年期间,共纳入92例患者,主要是血清阳性RA的绝经后女性。22%的患者有重大骨折病史,56%在诊断时存在骨质疏松。骨折最常见于胫骨干骺端(远端和近端)(88%)和足部骨骼(49%),诊断时经常出现多处骨折(76%),且患者近期病史中经常有反复骨折(63%)。通过对疼痛部位进行MRI检查进行诊断(84%),但也使用了骨闪烁显像(41例患者,45%)。79%的病例采取了停用甲氨蝶呤的措施。77%的病例实现了骨折愈合和疼痛缓解,停用甲氨蝶呤的患者与继续使用的患者在预后方面存在显著差异(91%对29%)(p<0.001)。MTX-IO是一种罕见但严重的病症,尤其是在患有RA或PsA的绝经后女性中。通过MRI或骨闪烁显像进行早期诊断以及停用甲氨蝶呤至关重要,因为停药可显著改善预后并预防进一步骨折。