Ferro José M, Oliveira Santos Miguel
Serviço de Neurologia, Department of Neurological Sciences and Mental Health, Hospital de Santa Maria - CHULN, Lisboa, Portugal; Faculdade de Medicina, Universidade de Lisboa, Portugal; Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Portugal.
Serviço de Neurologia, Department of Neurological Sciences and Mental Health, Hospital de Santa Maria - CHULN, Lisboa, Portugal; Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Portugal.
J Neurol Sci. 2021 May 15;424:117426. doi: 10.1016/j.jns.2021.117426. Epub 2021 Mar 27.
Inflammatory bowel diseases (IBD) are chronic inflammatory conditions affecting the digestive system, comprising two main distinctive entities, ulcerative colitis (UC) and Crohn's disease (CD). Besides gastrointestinal manifestations, IBD causes extraintestinal manifestations in the central and peripheral nervous system. The incidence of neurological complications in IBD ranges from 0.25% to 47.5%. The pathophysiology of neurological manifestations of IBD is mostly immune mediated, but dysfunction of the brain-gut axis, arterial and venous thromboembolism, infections, nutritional deficiencies and side-effects of medications (steroids, metronidazole, sulfasalazine, anti-TNF-α, anti-integrin antibodies) are other contributory mechanisms. Patients with IBD have an increased risk of arterial and venous stroke, mainly during periods of exacerbations. Vasculitis is extremely rare. There is a bidirectional association between multiple sclerosis and IBD, with a relative risk for comorbidity of 1.54, being 1.53 for the risk of multiple sclerosis in IBD and 1.55 for the risk of IBD in multiple sclerosis patients. Anti-TNF-α therapy is contraindicated in the treatment of patients who have both IBD and multiple sclerosis. Demyelinating disorders can also be a rare complication of anti-TNF-α therapy. Optic neuritis, transverse myelitis, progressive myelopathy, central nervous system infections, epilepsy and encephalopathy are among other uncommon neurological complications. Peripheral nervous system manifestations include peripheral neuropathy, either demyelination and axonal, myasthenia gravis and polymyositis/dermatomyositis and localized forms of myositis.
炎症性肠病(IBD)是影响消化系统的慢性炎症性疾病,包括两个主要不同类型,即溃疡性结肠炎(UC)和克罗恩病(CD)。除胃肠道表现外,IBD还会导致中枢和外周神经系统出现肠外表现。IBD中神经并发症的发生率在0.25%至47.5%之间。IBD神经表现的病理生理学主要是免疫介导的,但脑-肠轴功能障碍、动静脉血栓栓塞、感染、营养缺乏以及药物(类固醇、甲硝唑、柳氮磺胺吡啶、抗TNF-α、抗整合素抗体)的副作用是其他促成机制。IBD患者发生动脉和静脉卒中的风险增加,主要在病情加重期间。血管炎极为罕见。多发性硬化症与IBD之间存在双向关联,合并症的相对风险为1.54,IBD患者患多发性硬化症的风险为1.53,多发性硬化症患者患IBD的风险为1.55。抗TNF-α治疗在同时患有IBD和多发性硬化症的患者中是禁忌的。脱髓鞘疾病也可能是抗TNF-α治疗的罕见并发症。视神经炎、横贯性脊髓炎、进行性脊髓病、中枢神经系统感染、癫痫和脑病是其他不常见的神经并发症。外周神经系统表现包括外周神经病变,无论是脱髓鞘性和轴索性、重症肌无力和多发性肌炎/皮肌炎以及局限性肌炎形式。
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