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急性部分横贯性脊髓炎:转化为多发性硬化症的危险因素。

Acute partial transverse myelitis: risk factors for conversion to multiple sclerosis.

作者信息

Sellner J, Lüthi N, Bühler R, Gebhardt A, Findling O, Greeve I, Mattle H P

机构信息

Department of Neurology, Inselspital, Bern University Hospital and University of Bern, Bern, Switzerland [corrected]

出版信息

Eur J Neurol. 2008 Apr;15(4):398-405. doi: 10.1111/j.1468-1331.2008.02088.x. Epub 2008 Feb 26.

Abstract

Acute partial transverse myelitis (APTM) may be the first clinical manifestation of multiple sclerosis (MS), of relapsing myelitis, or remain a monophasic event. Identification of risk factors associated with relapse or conversion to MS is important, as prognostic information might help to guide management. The objective of this study was to define clinical, laboratory and neuroimaging factors in patients with first-ever APTM that predict relapses or conversion to MS. We identified 73 patients with a first-ever APTM admitted to our institution from January 1999 to June 2005. The follow-up time ranged from 12 to 90 months (mean follow-up 46 months). Patient demographics, clinical impairment at onset and after 3 months, ancillary tests including cerebrospinal fluid (CSF), magnetic resonance imaging (MRI), evoked potentials, recurrent and new symptoms and signs during follow-up were analysed. APTM remained a monophasic event in 35 patients (47.9%), conversion to MS occurred in 32 (43.8%) and recurred as relapsing myelitis in six patients (8.2%). According to univariate analysis, a family history of MS (P = 0.02), higher expanded disability status scale (EDSS) at onset (P = 0.03) and lesions on brain MRI (P = 0.03) were predictive factors for conversion to MS. CSF-specific oligoclonal bands (P = 0.04) or abnormal IgG-index (P = 0.04) were associated with increased risk for MS as well. In patients with a first-ever APTM, a family history of MS, high EDSS at presentation, lesions on brain MRI, CSF-specific oligoclonal bands or abnormal IgG-index may indicate an increased risk for conversion to MS.

摘要

急性部分横贯性脊髓炎(APTM)可能是多发性硬化症(MS)、复发性脊髓炎的首发临床表现,或者一直是单相性疾病。识别与复发或转变为MS相关的危险因素很重要,因为预后信息可能有助于指导治疗。本研究的目的是确定首次发生APTM的患者中预测复发或转变为MS的临床、实验室和神经影像学因素。我们确定了1999年1月至2005年6月在我院首次发生APTM的73例患者。随访时间为12至90个月(平均随访46个月)。分析了患者的人口统计学资料、发病时和3个月后的临床损伤情况、包括脑脊液(CSF)、磁共振成像(MRI)、诱发电位等辅助检查结果,以及随访期间的复发和新出现的症状及体征。35例患者(47.9%)的APTM一直是单相性事件,32例(43.8%)转变为MS,6例(8.2%)复发为复发性脊髓炎。根据单因素分析,MS家族史(P = 0.02)、发病时较高的扩展残疾状态量表(EDSS)评分(P = 0.03)和脑部MRI病变(P = 0.03)是转变为MS的预测因素。CSF特异性寡克隆带(P = 0.04)或异常IgG指数(P = 0.04)也与MS风险增加相关。在首次发生APTM的患者中,MS家族史、发病时EDSS评分高、脑部MRI病变、CSF特异性寡克隆带或异常IgG指数可能提示转变为MS的风险增加。

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