Rheumatology Unit, S. Anna Hospital - Ferrara (loc. Cona), Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
Division of Rheumatology, Department of Medicine and Department of Pathology, Queen Elizabeth II Health Sciences Center and Dalhousie University, Halifax, Nova Scotia, Canada.
Rheumatology (Oxford). 2020 Dec 5;59(Suppl5):v52-v62. doi: 10.1093/rheumatology/keaa404.
Neuropsychiatric (NP) events occur in the majority of patients with SLE and predominantly affect the CNS in addition to the peripheral and autonomic systems. Approximately 30% of all NP events are attributable to SLE (NPSLE) and present most frequently around the time of SLE onset. NPSLE is associated with increased morbidity and mortality and the proposed pathogenesis includes both ischaemic and neuroinflammatory mechanisms. Following diagnosis and causal attribution, the treatment of NPSLE is tailored to the type of NP event, the predominant putative pathogenic pathway and the activity and severity of the clinical event. There is a dearth of controlled clinical trials to guide management, but therapeutic options include symptomatic, antithrombotic and immunosuppressive agents that are supported by observational cohort studies. Our objective was to review what is currently known about NPSLE and to identify deficiencies in diagnostic biomarkers, novel therapies and clinical trials for this manifestation of SLE.
神经精神性(NP)事件发生在大多数 SLE 患者中,除了外周和自主神经系统外,主要还影响中枢神经系统。大约 30%的所有 NP 事件归因于 SLE(NPSLE),并最常出现在 SLE 发病时。NPSLE 与发病率和死亡率增加有关,其提出的发病机制包括缺血性和神经炎症机制。在诊断和因果归因后,NPSLE 的治疗根据 NP 事件的类型、主要假定的致病途径以及临床事件的活动和严重程度进行调整。目前缺乏对照临床试验来指导管理,但治疗选择包括症状性、抗血栓形成和免疫抑制剂,这些治疗选择得到了观察性队列研究的支持。我们的目的是回顾目前关于 NPSLE 的知识,并确定 SLE 这一表现的诊断生物标志物、新型疗法和临床试验的不足。