Department of Neurological and Behavioral Sciences, University of Siena, Italy.
Mult Scler. 2014 Feb;20(2):214-9. doi: 10.1177/1352458513494490. Epub 2013 Jul 22.
The accrual of brain focal pathology is considered a good substrate of disability in relapsing-remitting multiple sclerosis (RRMS). However, knowledge on long-term lesion evolution and its relationship with disability progression is poor.
The objective of this paper is to evaluate in RRMS the long-term clinical relevance of brain lesion evolution.
In 58 RRMS patients we acquired, using the same scanner and protocol, brain magnetic resonance imaging (MRI) at baseline and 10±0.5 years later. MRI data were correlated with disability changes as measured by the Expanded Disability Status Scale (EDSS).
The annualized 10-year lesion volume (LV) growth was +0.25±0.5 cm(3) (+6.7±8.7%) for T2-weighted (T2-W) lesions and +0.20±0.31 cm(3) (+11.5±12.3%) for T1-weighted (T1-W) lesions. The univariate analysis showed moderate correlations between baseline MRI measures and EDSS at 10 years (p < 0.001). Also, 10-year EDSS worsening correlated with LV growth and the number of new/enlarging lesions measured over the same period (p < 0.005). In the stepwise multiple regression analysis, EDSS worsening over 10 years was best correlated with the combination of baseline T1-W lesion count and increasing T1-W LV (R = 0.61, p < 0.001).
In RRMS patients, long-term brain lesion accrual is associated with worsening in clinical disability. This is particularly true for hypointense, destructive lesions.
脑局灶性病变的积累被认为是复发缓解型多发性硬化症(RRMS)残疾的良好基础。然而,关于长期病变演变及其与残疾进展的关系的知识却很有限。
本研究旨在评估 RRMS 中脑病变演变的长期临床相关性。
我们对 58 例 RRMS 患者进行了研究,这些患者在基线和 10±0.5 年后使用相同的扫描仪和方案进行了脑磁共振成像(MRI)检查。MRI 数据与扩展残疾状况量表(EDSS)测量的残疾变化相关联。
10 年的年度病变体积(LV)增长率为 T2 加权(T2-W)病变为+0.25±0.5 cm(3)(+6.7±8.7%),T1 加权(T1-W)病变为+0.20±0.31 cm(3)(+11.5±12.3%)。单变量分析显示基线 MRI 测量值与 10 年后的 EDSS 之间存在中度相关性(p < 0.001)。此外,10 年 EDSS 恶化与 LV 增长和同期新/扩大病变数量相关(p < 0.005)。在逐步多元回归分析中,10 年内 EDSS 的恶化与基线 T1-W 病变数和 T1-W LV 的增加的组合相关性最好(R = 0.61,p < 0.001)。
在 RRMS 患者中,长期脑病变的积累与临床残疾的恶化相关。对于低信号、破坏性病变尤其如此。