Department of Rheumatology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Beijing, China.
Department of Orthopedic Surgery, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Front Immunol. 2022 Mar 29;13:860646. doi: 10.3389/fimmu.2022.860646. eCollection 2022.
Chronic non-bacterial osteomyelitis (CNO) is a rare polygenic autoinflammatory bone disease. We aimed to characterize the clinical manifestations and gene variants of Chinese adult patients with CNO.
By reviewing data of all CNO patients being diagnosed and followed up at the Center for Adult Autoinflammation Diseases, Department of Rheumatology, Peking Union Medical College Hospital, clinical and genetic features of these patients were evaluated and concluded.
The median age of disease onset was 19 (6-64) years old, and adult-onset was observed in 6 (60%) patients. The mean time of diagnosis delay was 92 ± 78 months. The common symptoms were bone pain (10, 100%), fever (9, 90%), and arthritis (6, 60%). In total, there were 54 skeletal lesions, and each patient had no less than 2 lesions. The most frequently affected sites included lower limbs (20.5%), mandible, vertebrae and pelvis (17.5%, separately). Variants of 4 genes were detected in our study including , , and . In seven patients who were treated with combination therapy containing tumor necrosis factor (TNF) α inhibitors, five (55.6%) had a complete response and 2 (44.4%) had a partial response.
This is the first and largest case series of CNO in the Chinese adult patients. Four novel genetic mutations potentially associated with CNO were identified. Notably, CNO should be considered in the differential diagnosis of adult patients with long disease course and recurrent multifocal osteomyelitis of unknown cause, and these patients might benefit from combination therapy containing TNFα inhibitors.
慢性非细菌性骨髓炎(CNO)是一种罕见的多基因自身炎症性骨病。我们旨在描述中国成年 CNO 患者的临床表现和基因变异。
通过回顾北京协和医院风湿免疫科成人自身炎症性疾病中心诊断和随访的所有 CNO 患者的数据,评估和总结这些患者的临床和遗传特征。
疾病发病的中位年龄为 19 岁(6-64 岁),6 例(60%)为成年发病。平均诊断延迟时间为 92±78 个月。常见症状有骨痛(10 例,100%)、发热(9 例,90%)和关节炎(6 例,60%)。共有 54 处骨骼病变,每位患者至少有 2 处病变。最常受累的部位包括下肢(20.5%)、下颌骨、脊柱和骨盆(分别为 17.5%)。在我们的研究中检测到 4 个基因的变异,包括 、 、 和 。在接受包含肿瘤坏死因子(TNF)α抑制剂的联合治疗的 7 例患者中,5 例(55.6%)完全缓解,2 例(44.4%)部分缓解。
这是首例也是最大的中国成年 CNO 患者病例系列研究。鉴定了 4 种潜在与 CNO 相关的新基因变异。值得注意的是,对于病程长、反复发作、病因不明的多灶性骨髓炎的成年患者,应考虑 CNO 的鉴别诊断,这些患者可能受益于包含 TNFα抑制剂的联合治疗。