Ozgocmen Salih, Gur Ali
Division of Rheumatology, Department of Physical Medicine and Rehabilitation, Firat University, Faculty of Medicine, Elazig, Turkey.
Curr Pharm Des. 2008;14(13):1270-3. doi: 10.2174/138161208799316366.
Sjögren's syndrome (SS) is a chronic autoimmune disease that mainly affects the exocrine glands and usually presents with sicca symptoms of the main mucosal surfaces. The prevalence and the type of central nervous system (CNS) tissue damage caused by SS are debatable. The wide spectrum of CNS manifestations, different classification criteria used and unclear inclusion or exclusion criteria pose some difficulty reviewing these studies. Careful examination of the SS patients and to be aware of neurological findings which may be associated with suspicious CNS involvement is highly important. Central nervous system may also hypothetically have a role in the pathophysiology of SS. The wide spectrum of CNS involvement includes focal (sensorial and motor deficits, brain stem, cerebellar lesions, seizure, migraine etc.) or non-focal (encephalomyelitis, aseptic meningitis, neuropsychiatric dysfunctions), spinal cord (myelopathy, transverse myelitis, motor neuron disease etc.) findings or multiple sclerosis-like illness and optic neuritis. Evolving imaging techniques such as single photon emission computed tomography (SPECT), magnetic resonance spectroscopy or magnetization transfer imaging are promising for better understanding the nature of CNS involvement in SS. Treatments usually comprise symptomatic approach in milder cases however, pulse cyclophosphamide and steroids or other immunosuppressants (chlorambucil or azathioprine) are required in cases with progressive symptoms leading to neurological impairment. Anti-TNF agents (infliximab and etanercept) and B cell targeted therapies (rituximab and epratuzumab) are used in primary SS however their efficacy on CNS manifestation is still unclear. Randomized, multicenter studies are warranted to confirm the efficacy of treatment regimes which were reported to be effective in anecdotal reports or in small uncontrolled series. This article reviews the clinical approach to current therapy of CNS involvement in patients with primary SS.
干燥综合征(SS)是一种慢性自身免疫性疾病,主要影响外分泌腺,通常表现为主要黏膜表面的干燥症状。SS所致中枢神经系统(CNS)组织损伤的患病率及类型仍存在争议。CNS表现谱广泛、使用的分类标准不同以及纳入或排除标准不明确,给这些研究的综述带来了一定困难。仔细检查SS患者并留意可能与可疑CNS受累相关的神经学表现非常重要。中枢神经系统在SS的病理生理学中也可能起作用。CNS受累的广泛表现包括局灶性(感觉和运动功能障碍、脑干、小脑病变、癫痫、偏头痛等)或非局灶性(脑脊髓炎、无菌性脑膜炎、神经精神功能障碍)、脊髓(脊髓病、横贯性脊髓炎、运动神经元病等)表现或类似多发性硬化症的疾病及视神经炎。诸如单光子发射计算机断层扫描(SPECT)、磁共振波谱或磁化传递成像等不断发展的成像技术,有望更好地理解SS中CNS受累的本质。在较轻病例中,治疗通常采用对症方法,然而,对于出现导致神经功能损害的进行性症状的病例,需要使用脉冲环磷酰胺和类固醇或其他免疫抑制剂(苯丁酸氮芥或硫唑嘌呤)。抗TNF药物(英夫利昔单抗和依那西普)和B细胞靶向疗法(利妥昔单抗和依帕珠单抗)用于原发性SS,但它们对CNS表现的疗效仍不明确。需要进行随机、多中心研究,以证实据传闻报道或在小型非对照系列中有效的治疗方案的疗效。本文综述了原发性SS患者CNS受累的当前治疗的临床方法。