Department of Medicine 'B', Sheba Medical Centre, Tel-Hashomer, Israel; Zabludowicz Center for Autoimmune Diseases, Sheba Medical Centre, Tel-Hashomer, Israel; Sackler Faculty of Medicine, Tel-Aviv University, Israel; Section of Musculoskeletal Disease, NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Institute of Molecular Medicine, University of Leeds, Chapel Allerton Hospital, Leeds, UK.
Section of Musculoskeletal Disease, NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Institute of Molecular Medicine, University of Leeds, Chapel Allerton Hospital, Leeds, UK.
Pharmacol Res. 2022 Aug;182:106325. doi: 10.1016/j.phrs.2022.106325. Epub 2022 Jun 22.
Ankylosing spondylitis (AS) is a chronic progressive and debilitating form of arthritis with associated extra-articular features including uveitis, intestinal and lung apical inflammation and psoriasis. Putative associations between AS and neurologic disorders has been relatively overlooked. The purpose of this study is to assess the link between AS and major neurologic disorders and whether treatment with Tumor-Necrosis-Factor inhibitors (TNFi) has an impact on that association.
A retrospective cross-sectional study was carried out based on the Clalit Health Services (CHS) computerized database. AS patients were compared to age- and gender-matched controls with respect to the proportion of Alzheimer's disease (AD), Parkinson's disease (PD), epilepsy, and multiple sclerosis (MS). The impact of AS therapy (biologic vs conventional therapy) was assessed as well.
4082 AS patients and 20,397 age- and gender-matched controls were identified. AS was associated with a higher prevalence of AD (odds-ratio(OR) 1.46 [95%Confidence-interval(CI) 1.13-1.87], p = 0.003), epilepsy (OR 2.33 [95%CI 1.75-3.09] p < 0.0001) and PD (OR 2.75 [95%CI 2.04-3.72], p < 0.0001), whereas no statistically significant association was found for MS. Association with PD remained significant in the multivariate analysis (OR 1.49 [95%CI 1.05-2.13],p = 0.027). Within AS patients, the use of TNFi (OR 0.10 [95%CI 0.01-0.74], p = 0.024) were associated with a lowered risk of developing AD.
AS is positively associated with AD, PD, and epilepsy but not MS. AS patients treated with TNFi have lower rates of AD.
强直性脊柱炎(AS)是一种慢性进行性和使人虚弱的关节炎形式,伴有关节外特征,包括葡萄膜炎、肠和肺尖部炎症和银屑病。AS 与神经系统疾病之间的假定关联相对被忽视。本研究的目的是评估 AS 与主要神经系统疾病之间的联系,以及肿瘤坏死因子抑制剂(TNFi)治疗是否对该关联有影响。
基于 Clalit 健康服务(CHS)计算机数据库进行了回顾性横断面研究。AS 患者与年龄和性别匹配的对照组相比,比较了阿尔茨海默病(AD)、帕金森病(PD)、癫痫和多发性硬化症(MS)的比例。还评估了 AS 治疗(生物治疗与常规治疗)的影响。
确定了 4082 例 AS 患者和 20397 例年龄和性别匹配的对照组。AS 与 AD 的患病率较高相关(优势比(OR)1.46 [95%置信区间(CI)1.13-1.87],p=0.003)、癫痫(OR 2.33 [95%CI 1.75-3.09],p<0.0001)和 PD(OR 2.75 [95%CI 2.04-3.72],p<0.0001),而 MS 则没有统计学意义上的关联。在多变量分析中,与 PD 的关联仍然显著(OR 1.49 [95%CI 1.05-2.13],p=0.027)。在 AS 患者中,TNFi 的使用(OR 0.10 [95%CI 0.01-0.74],p=0.024)与 AD 发病风险降低相关。
AS 与 AD、PD 和癫痫呈正相关,但与 MS 无关。接受 TNFi 治疗的 AS 患者 AD 发生率较低。