Department of Internal Medicine, Martinique University Hospital, Fort-de France, France.
Department of Rheumatology, Martinique University Hospital, Fort-de-France, France; EpiCliV Research Unit, University of French West Indies, Martinique, France.
J Autoimmun. 2023 Sep;139:103086. doi: 10.1016/j.jaut.2023.103086. Epub 2023 Jun 23.
To describe the epidemiology, characteristics, response to initial treatment, and outcomes of Adult-Onset Still's disease (AOSD) in the Afro-Caribbean population of Martinique with free and easy access to specialised care.
We conducted a retrospective study from 2004 to 2022 in the island of Martinique, French West-Indies which total population was 354 800 in 2021. Patients were identified from multiple sources including standardised databases. To be included, patients had to be residents of the island and fulfilled Yamaguchi and/or Fautrel's criteria for AOSD, or have a compatible disease course, without a diagnosis of cancer, auto-immune disease or another auto-inflammatory disorder. Date of diagnosis, clinical and biological characteristics, treatments, and outcomes were collected.
The prevalence was 7.6/100 000 inhabitants in 2021. The mean incidence was 0.4/100 000 during study period. Thirty-three patients (70.6% females) with a median follow-up of 35 months [7.5 to 119] were included. Twenty-six patients (78.8%) had a systemic pattern. Patients with a systemic monocyclic pattern had significantly more polyarticular involvement than patients with systemic polycyclic pattern (p = 0.016). Pulmonary involvement occurred in 51.5% of patients at diagnosis and systemic Pouchot score has been identified as an independent predictive factor for pulmonary involvement; OR of 3.29 [CI 95% 1.20; 9.01]. At first flare, all patients but one received oral glucocorticoids, 11 patients (32.4%) received intravenous glucocorticoids pulse and 12 patients (33%) received anti-IL1 therapy. Nineteen patients (57%) relapsed in a median time of 9 months [6 to 12] Three patients (9%) developed hemophagocytosis lymphohistiocytosis, fatal in 1 case. All deceased patients (n = 4, 11.76%) belonged to the systemic polycyclic pattern, with an event-free survival of 13.6 months [IQR 5.7; 29.5] CONCLUSION: AOSD in the Afro-Caribbean population of Martinique shares some similarities with other ethnic groups, but exhibit differences, such as a high proportion of lung involvement. Comparative studies are needed to confirm these results.
描述法属西印度群岛马提尼克岛非裔加勒比人群中成人Still 病(AOSD)的流行病学、特征、初始治疗反应和结局,该人群可自由便捷地获得专业治疗。
我们进行了一项回顾性研究,时间范围为 2004 年至 2022 年,研究对象为法属西印度群岛马提尼克岛的居民,该岛 2021 年的总人口为 354800 人。患者通过包括标准化数据库在内的多种来源确定。纳入标准为:必须为该岛居民,符合 Yamaguchi 和/或 Fautrel 的 AOSD 标准,或具有类似的疾病过程,且没有癌症、自身免疫性疾病或其他自身炎症性疾病的诊断。收集患者的诊断日期、临床和生物学特征、治疗方法和结局。
2021 年,该人群的患病率为 7.6/100000 居民。研究期间,平均发病率为 0.4/100000。共纳入 33 名患者(70.6%为女性),中位随访时间为 35 个月[7.5 至 119]。26 名患者(78.8%)存在全身模式。具有全身单环型模式的患者多关节受累明显多于全身多环型模式的患者(p=0.016)。诊断时,51.5%的患者存在肺部受累,全身 Pouchot 评分被确定为肺部受累的独立预测因素;比值比为 3.29[95%CI 95% 1.20;9.01]。首次发病时,除 1 名患者外,所有患者均接受了口服糖皮质激素治疗,11 名患者(32.4%)接受了静脉糖皮质激素冲击治疗,12 名患者(33%)接受了抗 IL1 治疗。19 名患者(57%)在中位时间 9 个月[6 至 12]时复发。3 名患者(9%)发生噬血细胞性淋巴组织细胞增生症,其中 1 例死亡。所有死亡患者(n=4,11.76%)均为全身多环型模式,无事件生存时间为 13.6 个月[IQR 5.7;29.5]。
马提尼克岛非裔加勒比人群中的 AOSD 与其他人群有一些相似之处,但也存在一些差异,例如肺部受累的比例较高。需要开展比较研究来证实这些结果。