Kuhle Jens, Lindberg Raija L P, Regeniter Axel, Mehling Matthias, Hoffmann Francine, Reindl Markus, Berger Thomas, Radue Ernst W, Leppert David, Kappos Ludwig
Department of Neurology, University Hospital Basel, Petersgraben 4, 4031 Basel, Switzerland.
J Neurol. 2007 Feb;254(2):160-8. doi: 10.1007/s00415-006-0299-4.
We investigated the correlation of antimyelin oligodendrocyte glycoprotein-(anti-MOG) and anti-myelin basic protein antibodies (anti-MBP) in serum of CIS patients with inflammatory signs in MRI and in CSF and, as previously suggested,the incidence of more frequent and rapid progression to clinically definite MS (CDMS).
133CIS patients were analysed for anti-MOG and anti-MBP (Western blot). Routine CSF and cranial MRI (quantitatively and qualitatively) measures were analyzed. 55 patients had a follow-up of at least 12 months or until conversion to CDMS.
Patients with anti-MOG and anti-MBP had an increased intrathecal IgG production and CSF white blood cell count(p = 0.048 and p = 0.036). When anti-MBP alone, or both antibodies were present the cranial MRI showed significantly more T2 lesions (p = 0.007 and p = 0.01,respectively). There was a trend for more lesion dissemination in anti-MBP positive patients (p = 0.076).Conversely, anti-MOG- and/or anti-MBP failed to predict conversion to CDMS in our follow-up group (n = 55). Only in female patients with at least one MRI lesion (n = 34) did the presence of anti-MOG correlate with more frequent (p = 0.028) and more rapid (p = 0.0209) transition to CDMS.
Presence of anti-MOG or anti-MBP or both was not significantly associated with conversion to CDMS in our CIS cohort. However, patients with anti-MOG and anti-MBP had higher lesion load and more disseminated lesions in cranial MRI as well as higher values for CSF leucocytes and intrathecal IgG production. Our data support a correlation of anti-MOG and anti-MBP to inflammatory signs in MRI and CSF. The prognostic value of these antibodies for CDMS, however, seems to be less pronounced than previously reported.
我们研究了临床孤立综合征(CIS)患者血清中抗髓鞘少突胶质细胞糖蛋白抗体(抗MOG)和抗髓鞘碱性蛋白抗体(抗MBP)与MRI和脑脊液中炎症体征的相关性,以及如先前研究所提示的,进展为临床确诊多发性硬化症(CDMS)的更频繁和快速进展的发生率。
对133例CIS患者进行抗MOG和抗MBP检测(蛋白质印迹法)。分析常规脑脊液和头颅MRI(定量和定性)指标。55例患者进行了至少12个月的随访或直至转变为CDMS。
抗MOG和抗MBP阳性患者的鞘内IgG生成和脑脊液白细胞计数增加(p = 0.048和p = 0.036)。单独存在抗MBP或两种抗体均存在时,头颅MRI显示T2病变明显更多(分别为p = 0.007和p = 0.01)。抗MBP阳性患者有病变播散增多的趋势(p = 0.076)。相反,在我们的随访组(n = 55)中,抗MOG和/或抗MBP未能预测转变为CDMS。仅在至少有一个MRI病灶的女性患者(n = 34)中,抗MOG的存在与更频繁(p = 0.028)和更快(p = 0.0209)转变为CDMS相关。
在我们的CIS队列中,抗MOG或抗MBP或两者的存在与转变为CDMS无显著相关性。然而,抗MOG和抗MBP阳性患者在头颅MRI中有更高的病灶负荷和更多的播散性病变以及脑脊液白细胞和鞘内IgG生成的更高值。我们的数据支持抗MOG和抗MBP与MRI和脑脊液中的炎症体征相关。然而,这些抗体对CDMS的预后价值似乎不如先前报道的那么明显。