Neurology Service, Hospital Universitari La Fe, Valencia, Spain.
Mult Scler. 2010 Jul;16(7):810-5. doi: 10.1177/1352458510371961. Epub 2010 Jun 10.
The objective of this study was to investigate whether the presence of lipid-specific oligoclonal IgM bands (LS-OCMB) in cerebrospinal fluid (CSF) influences the response to treatment with beta-interferon in relapsing-remitting multiple sclerosis (RRMS) patients. We performed a collaborative prospective study including RRMS patients with brain MRI and LS-OCMB studies performed before starting interferon treatment. The primary endpoint was the risk of having a relapse after treatment initiation. Secondary endpoints included relapse rate, relapse-rate reduction, proportion of relapse-free patients and proportion of patients with sustained disability increase during follow-up. One-hundred and two patients were included. After a mean follow-up of 37.4 months, the risk of suffering a relapse was two-fold higher in patients with LS-OCMB (hazard ratio 2.0, 95% confidence interval 1.1-3.8). LS-OCMB+ patients showed lower reduction in relapse rate (51.8% versus 80.8%; p < 0.0001), higher relapse rate in the first year (0.8 versus 0.2; p = 0.001), lower proportion of relapse-free patients (25% versus 61.3%; p = 0.003), and higher proportion of patients with sustained 1.0 increase in the Expanded Disability Status Score (45% versus 12.9%; p = 0.0003). In conclusion, LS-OCMB can have an influence on the response to interferon treatment in RRMS patients. They could be used as a biological marker to predict high inflammatory activity after treatment.
本研究旨在探讨脑脊液(CSF)中是否存在脂质特异性寡克隆 IgM 带(LS-OCMB)是否会影响复发缓解型多发性硬化症(RRMS)患者接受β干扰素治疗的反应。我们进行了一项协作性前瞻性研究,纳入了接受脑 MRI 和 LS-OCMB 研究的 RRMS 患者,这些研究均在开始干扰素治疗前进行。主要终点是治疗开始后发生复发的风险。次要终点包括复发率、复发率降低、无复发患者的比例和随访期间持续残疾增加的患者比例。共纳入 102 例患者。平均随访 37.4 个月后,LS-OCMB 患者发生复发的风险增加了两倍(危险比 2.0,95%置信区间 1.1-3.8)。LS-OCMB+患者的复发率降低幅度较低(51.8%比 80.8%;p<0.0001),第一年的复发率较高(0.8 比 0.2;p=0.001),无复发患者的比例较低(25%比 61.3%;p=0.003),持续扩大残疾状态评分增加 1.0 的患者比例较高(45%比 12.9%;p=0.0003)。总之,LS-OCMB 可能会影响 RRMS 患者对干扰素治疗的反应。它们可以用作生物标志物,以预测治疗后的高炎症活性。