Prasad Chandra Bhushan, Kopp Chirag Rajkumar, Naidu Gsrsnk, Sharma Vishal, Misra Durga Prasanna, Agarwal Vikas, Sharma Aman
Clinical Immunology and Rheumatology Unit, Department of Internal Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, Chandigarh, 160012, India.
Department of Adult Gastroenterology, Post Graduate Institute of Medical Education and Research, Chandigarh, Chandigarh, 160012, India.
Rheumatol Int. 2024 Dec;44(12):2807-2815. doi: 10.1007/s00296-023-05397-0. Epub 2023 Jul 27.
Central nervous system (CNS) involvement can occur in primary Sjögren's syndrome (pSS) due to co-existing neuromyelitis optica spectrum disorder (NMOSD) which has a highly relapsing course requiring indefinite immunosuppression, and if not diagnosed early, damage accrual occurs over time leading to permanent disability and morbidity. In this review, we describe and outline the clinical course and outcomes of anti-aquaporin 4 (AQP4) antibody seropositive NMOSD with pSS overlap cases. To investigate the co-existence of AQP4 + NMOSD with pSS, we conducted a review of individual patient data from case reports and case series found in major databases. The study extracted clinico-demographic features, imaging and laboratory profiles, treatment approaches, and outcomes of these patients. Inclusion criteria for the review required patients to have positivity for anti-AQP4 or NMO-IgG autoantibodies in the blood and/or cerebrospinal fluid (CSF) and exhibit at least one manifestation of both pSS and NMOSD. In this overlap between AQP4 + NMOSD and pSS, 44 patients were included of whom 41 (93.2%) were females. The mean age of pSS onset was 44.8 ± 18.4 years and NMOSD onset was 43.2 ± 19.8 years. In 20 (45.5%) patients, NMOSD preceded pSS onset, 13 (29.5%) NMOSD occurred after pSS onset, and 11 (25%) patients had a simultaneous presentation. 31 (70.5%) patients experienced acute transverse myelitis, 21 (47.7%) optic neuritis, 14 (31.8%) cerebral syndrome, 10 (22.7%) acute brainstem syndrome, 5 (11.4%) area postrema syndrome, and 2 (4.5%) diencephalic clinical syndromes. For the treatment of acute phase, 40 (90.9%) patients received intravenous methylprednisolone, 15 (34.1%) received plasma exchange, and 10 (22.7%) received intravenous immunoglobulin; and for the induction/maintenance therapy, 16 (36.4%) patients received cyclophosphamide, 6 (13.6%) received rituximab, 16 (36.4%) received azathioprine, and 10 (22.7%) received mycophenolate mofetil. Disease course was monophasic in 2 (4.5%) and relapsing in 27 (61.4%) patients. At median (IQR) follow-up duration of 2.4 (6) years, 39 (88.6%) patients showed improvement, 3 (6.8%) showed stabilization and 2 (4.5%) showed worsening of their NMOSD manifestations. In this overlap syndrome of AQP4 + NMOSD and pSS, patients have a neurologically disabling disorder that can mimic neurological manifestations of pSS, frequently occurs prior to the onset of pSS, has a relapsing course, responds well to immunosuppressants, and necessitates indefinite treatment. Collaborative multicentre studies are needed to clarify the natural history and outcomes of this rare overlap syndrome.
由于原发性干燥综合征(pSS)合并视神经脊髓炎谱系障碍(NMOSD)可导致中枢神经系统(CNS)受累,NMOSD具有高度复发的病程,需要长期免疫抑制治疗,若不及早诊断,随着时间推移会造成损害,导致永久性残疾和发病。在本综述中,我们描述并概述了抗水通道蛋白4(AQP4)抗体血清阳性的NMOSD与pSS重叠病例的临床病程及转归。为研究AQP4+NMOSD与pSS的共存情况,我们对主要数据库中病例报告和病例系列的个体患者数据进行了综述。该研究提取了这些患者的临床人口统计学特征、影像学和实验室检查结果、治疗方法及转归。综述的纳入标准要求患者血液和/或脑脊液(CSF)中的抗AQP4或NMO-IgG自身抗体呈阳性,且至少表现出pSS和NMOSD的一种症状。在AQP4+NMOSD与pSS的这种重叠情况中,共纳入44例患者,其中41例(93.2%)为女性。pSS发病的平均年龄为44.8±18.4岁,NMOSD发病的平均年龄为43.2±19.8岁。20例(45.5%)患者中,NMOSD先于pSS发病,13例(29.5%)NMOSD在pSS发病后出现,11例(25%)患者同时出现两种疾病表现。31例(70.5%)患者经历急性横贯性脊髓炎,21例(47.7%)患视神经炎,14例(31.8%)出现脑综合征,10例(22.7%)出现急性脑干综合征,5例(11.4%)出现最后区综合征,2例(4.5%)出现间脑临床综合征。急性期治疗时,40例(90.9%)患者接受静脉注射甲泼尼龙,15例(34.1%)接受血浆置换,10例(22.7%)接受静脉注射免疫球蛋白;诱导/维持治疗时,16例(36.4%)患者接受环磷酰胺,6例(13.6%)接受利妥昔单抗,16例(36.4%)接受硫唑嘌呤,10例(22.7%)接受霉酚酸酯。2例(4.5%)患者病程为单相,27例(61.4%)患者复发。在中位(四分位间距)随访2.4(6)年时,39例(88.6%)患者的NMOSD表现有所改善,3例(6.8%)稳定,2例(4.5%)恶化。在这种AQP4+NMOSD与pSS的重叠综合征中,患者患有神经系统致残性疾病,可模仿pSS的神经表现,常先于pSS发病,病程呈复发型,对免疫抑制剂反应良好,需要长期治疗。需要开展多中心合作研究以阐明这种罕见重叠综合征的自然病程和转归。