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原发性进行性多发性硬化症中病变增强随时间而减弱。

Lesion enhancement diminishes with time in primary progressive multiple sclerosis.

机构信息

Department of Brain Repair and Rehabilitation, Institute of Neurology, University College London, London WC1N 3BG, UK.

出版信息

Mult Scler. 2010 Mar;16(3):317-24. doi: 10.1177/1352458509358090.

Abstract

Fewer gadolinium-enhancing lesions are seen in established primary progressive multiple sclerosis (PPMS) compared with other subtypes. Previously, we found unexpectedly high enhancement levels in early PPMS (42%), suggesting an early inflammatory phase. The objective of this study was to investigate whether this level of enhancement was maintained, and whether it influenced clinical progression, over 5 years. Forty-five patients with PPMS, within 5 years of onset, were scored on the Expanded Disability Status Scale (EDSS), Multiple Sclerosis Functional Composite (MSFC) and its subtests (including the timed walk test [TWT]) 6-monthly for 3 years, and at 5 years. T1-weighted brain and spinal cord images after triple dose gadolinium-DTPA, and T2-weighted brain sequences were also acquired. A mixed effect logistic model evaluated change in the percentage of patients with enhancing lesions. Ordinal logistic and multiple linear regression models identified predictors of progression, adjusted for T2 lesion load. The percentage of patients with enhancing lesions in the brain and spinal cord declined over 5 years (p = 0.03). Among patients with enhancement, more enhancing lesions at baseline predicted greater decline in mobility on the TWT over 5 years (p = 0.02). In conclusion, a proportion of patients with PPMS may undergo an early inflammatory phase, which has some impact on subsequent mobility.

摘要

与其他亚型相比,在已确诊的原发性进展型多发性硬化症(PPMS)中,增强病变的数量较少。此前,我们发现早期 PPMS 中增强水平出乎意料地高(42%),这表明存在早期炎症期。本研究的目的是调查这种增强水平是否持续存在,以及它是否会影响 5 年内的临床进展。45 名发病后 5 年内的 PPMS 患者,每隔 6 个月接受一次扩展残疾状态量表(EDSS)、多发性硬化功能综合量表(MSFC)及其子测试(包括定时步行测试[TWT])评分,持续 3 年,第 5 年再评分一次。在 3 年内,还获得了 T1 加权脑和脊髓图像,使用三重剂量钆-DTPA 增强,以及 T2 加权脑序列。混合效应逻辑模型评估了增强病变患者比例的变化。有序逻辑和多元线性回归模型确定了进展的预测因素,调整了 T2 病变负荷。脑和脊髓增强病变的患者比例在 5 年内下降(p=0.03)。在有增强的患者中,基线时更多的增强病变预示着 TWT 上移动能力在 5 年内下降更大(p=0.02)。总之,一部分 PPMS 患者可能经历早期炎症期,这对随后的移动能力有一定影响。

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