Ma Kevin Sheng-Kai, Lee Chee-Ming, Chen Po-Hung, Yang Yan, Dong Yi Wei, Wang Yu-Hsun, Wei James Cheng-Chung, Zheng Wen Jie
Department of Pediatrics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Center for Global Health, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Front Med (Lausanne). 2022 Jun 13;9:903608. doi: 10.3389/fmed.2022.903608. eCollection 2022.
Optic neuritis is (ON) is believed to be an immune-mediated disease; however, the association between optic neuritis and autoimmune diseases remains unclear. This study aimed to identify the incidence rate and adjusted hazard ratio (aHR) of autoimmune diseases in patients with optic neuritis.
This nationwide, population-based, retrospective cohort study collected patients' data between 1999 and 2013 from the National Health Insurance Research Database in Taiwan. A total of 9,235 patients were included. Using 1:4 propensity scoring, 1,847 patients were enrolled in the optic neuritis group and 7,388 in the non-optic neuritis group according to age, sex, comorbidities, and corticosteroid use. Follow-up was started from the index date and the endpoint was a diagnosis of new-onset autoimmune diseases including, myasthenia gravis (MG), psoriatic arthritis (PsA), systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), and ankylosing spondylitis (AS).
The Kaplan-Meier curves depicted that patients with optic neuritis had a higher cumulative incidence of autoimmune diseases than patients without optic neuritis. Cox proportional hazard regression showed that patients with optic neuritis were at a high risk of autoimmune diseases (aHR: 1.40; 95% C.I., 1.05-1.87), including MG (aHR: 4.16, 95% C.I.: 1.33-12.94), SLE (aHR: 3.33, 95% C.I.: 1.24-8.97), and AS (aHR: 2.86, 95% C.I.: 1.54-5.31). Subgroup analysis provided that patients with optic neuritis aged below 65 years (aHR: 1.42, 95% C.I.: 1.03-1.96) or who were females (aHR: 1.59, 95% C.I.: 1.11-2.27) had a significantly increased risk of autoimmune diseases compared to respective controls. The use of corticosteroids reduced the risk of autoimmune diseases in patients with optic neuritis (aHR for corticosteroids non-users: 1.46, 95% C.I.: 1.03-2.07).
Patients with optic neuritis presented with a high risk of autoimmune diseases such as MG, SLE, and AS, especially patients with optic neuritis who were young or females. Corticosteroids attenuated the link between optic neuritis and subsequent autoimmune diseases.
视神经炎(ON)被认为是一种免疫介导的疾病;然而,视神经炎与自身免疫性疾病之间的关联仍不明确。本研究旨在确定视神经炎患者自身免疫性疾病的发病率及调整后的风险比(aHR)。
这项基于全国人群的回顾性队列研究收集了1999年至2013年台湾地区国民健康保险研究数据库中的患者数据。共纳入9235例患者。采用1:4倾向评分法,根据年龄、性别、合并症和皮质类固醇使用情况,将1847例患者纳入视神经炎组,7388例患者纳入非视神经炎组。随访从索引日期开始,终点为新发自身免疫性疾病的诊断,包括重症肌无力(MG)、银屑病关节炎(PsA)、系统性红斑狼疮(SLE)、类风湿关节炎(RA)和强直性脊柱炎(AS)。
Kaplan-Meier曲线显示,视神经炎患者自身免疫性疾病的累积发病率高于非视神经炎患者。Cox比例风险回归显示,视神经炎患者患自身免疫性疾病的风险较高(aHR:1.40;95%置信区间,1.05 - 1.87),包括MG(aHR:4.16,95%置信区间:1.33 - 12.94)、SLE(aHR:3.33,95%置信区间:1.24 - 8.97)和AS(aHR:2.86,95%置信区间:1.54 - 5.31)。亚组分析表明,年龄低于65岁的视神经炎患者(aHR:1.42,95%置信区间:1.03 - 1.96)或女性视神经炎患者(aHR:1.59,95%置信区间:1.11 - 2.27)与各自的对照组相比,患自身免疫性疾病的风险显著增加。使用皮质类固醇可降低视神经炎患者患自身免疫性疾病的风险(未使用皮质类固醇患者的aHR:1.46,95%置信区间:1.03 - 2.07)。
视神经炎患者患MG、SLE和AS等自身免疫性疾病的风险较高,尤其是年轻或女性视神经炎患者。皮质类固醇减弱了视神经炎与后续自身免疫性疾病之间的联系。