Dagur Ingi Jonsson, Olafur Sveinsson, Nina Moeini, Emir Pivac, Karin Wirdefeldt, Lou Brundin, Ellen Iacobaeus
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引用次数: 0
Abstract
Background and objectives: Myelitis is a relatively common clinical entity for neurologists, with diverse underlying causes. The aim of this study was to describe the incidence of myelitis, its causes, clinical presentation, and factors predicting functional outcomes and relapses.
Methods: Using the Swedish National Patient Registry, we identified all adult patients in Stockholm County between 2008 and 2018 using International Classification of Diseases, 10th Edition (ICD-10) codes likely to include myelitis. We collected medical records and classified patients using a modification of the 2002 Transverse Myelitis Consortium Group criteria. Long-term follow-up data were collected for patients not diagnosed with multiple sclerosis (MS) or neuromyelitis optica spectrum disorder as a result of the initial myelitis.
Results: We identified 2,321 individuals, of whom 461 were patients with myelitis. The crude mean incidence of all-cause myelitis was 24.9 (95% CI 16.7-33.9) cases per million person-years, of which idiopathic myelitis had an incidence of 8.0 (95% CI 3.8-12.1) cases per million person-years. Partial myelitis was found in 80% of patients. Poor functional outcome was found in 11% of the cohort and correlated, in a multivariate logistic model, with age older than 50 years (OR 4.26, 95% CI 1.75-10.40), transverse spinal cord lesions (odds ratio [OR] 6.85, 95% CI 2.68-17.52), elevated CSF count of polymorphonuclear cells (OR 6.09, 95% CI 1.56-23.72), and elevated CSF/serum albumin ratio (OR 3.17, 95% CI 1.23-8.17). The median follow-up time was 5.4 years. Relapses occurred in 27% of patients with idiopathic myelitis and 72% of patients with unspecified demyelinating disease of the CNS. An increased relapse rate after idiopathic myelitis was found to be associated, in a multivariate model, with the presence of oligoclonal bands (incidence rate ratio [IRR] 4.47, 95% CI 1.70-11.73), transverse spinal cord lesions (IRR 2.81, 95% CI 1.11-7.12), and multifocal spinal cord lesions (IRR 2.82, 95% CI 1.03-7.69). Around half (48%) of all patients with myelitis received MS diagnosis during the study period.
Discussion: This large population-wide study describes a relatively high incidence of myelitis and low risk of relapses after idiopathic myelitis. A complete diagnostic workup of myelitis, including MRI of the entire CNS and collection of CSF, is essential in evaluating underlying causes and prognosis.
背景和目的:脊髓炎是神经科医生比较常见的临床疾病,其病因多种多样。本研究的目的是描述脊髓炎的发病率,其原因,临床表现和预测功能结局和复发的因素。方法:使用瑞典国家患者登记处,我们使用可能包括脊髓炎的国际疾病分类第10版(ICD-10)代码确定了2008年至2018年斯德哥尔摩县的所有成年患者。我们收集了医疗记录,并使用2002年横脊髓炎联盟组标准的修改对患者进行了分类。长期随访数据收集了未被诊断为多发性硬化症(MS)或由初始脊髓炎引起的视神经脊髓炎谱系障碍的患者。结果:我们确定了2321例个体,其中461例为脊髓炎患者。全因脊髓炎的粗平均发病率为每百万人年24.9例(95% CI 16.7-33.9),其中特发性脊髓炎的发病率为每百万人年8.0例(95% CI 3.8-12.1)。80%的患者发现部分脊髓炎。在多变量logistic模型中,11%的队列中发现功能不良,并与年龄大于50岁(OR 4.26, 95% CI 1.75-10.40)、脊髓横向病变(比值比[OR] 6.85, 95% CI 2.68-17.52)、脑脊液多形核细胞计数升高(OR 6.09, 95% CI 1.56-23.72)和脑脊液/血清白蛋白比值升高(OR 3.17, 95% CI 1.23-8.17)相关。中位随访时间为5.4年。27%的特发性脊髓炎患者和72%的中枢神经系统不明脱髓鞘疾病患者复发。在多变量模型中,特发性脊髓炎后复发率的增加与存在寡克隆带(发病率比[IRR] 4.47, 95% CI 1.70-11.73)、脊髓横向病变(IRR 2.81, 95% CI 1.11-7.12)和多灶性脊髓病变(IRR 2.82, 95% CI 1.03-7.69)有关。在研究期间,大约一半(48%)的脊髓炎患者被诊断为多发性硬化症。讨论:这项大规模的人群研究描述了特发性脊髓炎后相对较高的发病率和较低的复发风险。脊髓炎的完整诊断检查,包括整个中枢神经系统的MRI检查和脑脊液的采集,对于评估潜在的病因和预后至关重要。
期刊介绍:
Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.