Department of Neurology and Center of Clinical Neuroscience, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.
PLoS One. 2012;7(11):e50101. doi: 10.1371/journal.pone.0050101. Epub 2012 Nov 15.
To compare clinical and MRI parameters between patients with clinically isolated syndrome and those converting to clinically definite multiple sclerosis within 2 years, to identify volumetric MRI predictors of this conversion and to assess effect of early relapses.
The SET study comprised 220 patients with clinically isolated syndrome treated with interferon beta (mean age, 29 years; Expanded Disability Status Scale, 1.5). Three patients with missing data were excluded from the analysis. Physical disability, time to clinically definite multiple sclerosis and volumetric MRI data were recorded for 2 years.
Patients reaching clinically definite multiple sclerosis showed impaired recovery of neurological function, faster decrease in corpus callosum cross-sectional area, higher T2 lesion volume and more contrast-enhancing lesions. Six-month decrease in corpus callosum cross-sectional area (≥ 1%) and baseline T2 lesion volume (≥ 5 cm(3)) predicted clinically definite multiple sclerosis within 2 years (hazard ratios 2.5 and 1.8, respectively). Of 22 patients fulfilling both predictive criteria, 83% reached clinically definite multiple sclerosis (hazard ratio 6.5). More relapses were associated with poorer recovery of neurological function and accelerated brain atrophy.
Neurological impairment is more permanent, brain atrophy is accelerated and focal inflammatory activity is greater in patients converting to clinically definite multiple sclerosis. Six-month corpus callosum atrophy and baseline T2 lesion volume jointly help predict individual risk of clinically definite multiple sclerosis. Early relapses contribute to permanent damage of the central nervous system.
比较临床孤立综合征患者和在 2 年内转化为临床确诊多发性硬化症患者的临床和 MRI 参数,确定容积 MRI 预测转化的指标,并评估早期复发的影响。
SET 研究纳入了 220 例接受干扰素-β治疗的临床孤立综合征患者(平均年龄 29 岁;扩展残疾状况量表评分为 1.5)。因数据缺失,3 例患者被排除在分析之外。记录了 2 年内的躯体残疾、转化为临床确诊多发性硬化症的时间和容积 MRI 数据。
转化为临床确诊多发性硬化症的患者神经功能恢复受损,胼胝体截面积下降更快,T2 病变体积更大,增强病变更多。6 个月时胼胝体截面积下降(≥1%)和基线 T2 病变体积(≥5cm³)可预测 2 年内的临床确诊多发性硬化症(风险比分别为 2.5 和 1.8)。在满足这两个预测指标的 22 例患者中,83%进展为临床确诊多发性硬化症(风险比为 6.5)。更多的复发与神经功能恢复较差和脑萎缩加速有关。
转化为临床确诊多发性硬化症的患者神经损伤更持久,脑萎缩加速,局灶性炎症活动更大。6 个月时的胼胝体萎缩和基线 T2 病变体积共同有助于预测临床确诊多发性硬化症的个体风险。早期复发会导致中枢神经系统的永久性损伤。