Patrucco Liliana, Rojas Juan Ignacio, Cristiano Edgardo
Sección de Enfermedades Desmielinizantes, Servicio de Neurología, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Rev Neurol. 2010 May 1;50(9):529-32.
To investigate the long-term impact of interferon-beta (IFNbeta) therapy on disease severity in relapsing-remitting multiple sclerosis (RRMS) patients.
We included 210 patients with RRMS and indication for immunomodulatory treatment followed up at least for nine years. We compared between treated and untreated groups: time since the beginning of the disease to reach EDSS 6.0 and time to conversion to secondary progressive multiple sclerosis. Log-rank test was used to compare outcomes between groups, p < 0.05 were considered significant.
160 patients were IFNbeta-treated, 50 untreated. The percentage of patients that converted to SPMS after 9 years of follow-up was 7.1% for treated vs. 21.7% for untreated (p = 0.022; RR = 0.32; 95% CI = 0.13-0.74). About 7.7% for IFNbeta-treated vs. 18.7% of untreated patients reached EDSS 6.0 after the period of follow-up (p = 0.032; RR = 0.4; 95% CI = 0.16-0.95). Mean time to reach EDSS 6.0 was 8.1 years for IFNbeta-treated vs. 5.8 years for untreated patients (p < 0.001).
Long term treatment with IFNbeta slows progression in MS measured by EDSS and time to conversion to secondary progressive multiple sclerosis.
探讨β-干扰素(IFNβ)治疗对复发缓解型多发性硬化症(RRMS)患者疾病严重程度的长期影响。
我们纳入了210例RRMS患者,这些患者有免疫调节治疗指征且随访至少9年。我们比较了治疗组和未治疗组:从疾病开始到扩展残疾状态量表(EDSS)达到6.0的时间以及转化为继发进展型多发性硬化症的时间。采用对数秩检验比较组间结果,p<0.05被认为具有统计学意义。
160例患者接受IFNβ治疗,50例未治疗。随访9年后转化为继发进展型多发性硬化症的患者百分比,治疗组为7.1%,未治疗组为21.7%(p = 0.022;风险比[RR]=0.32;95%置信区间[CI]=0.13 - 0.74)。随访期后,接受IFNβ治疗的患者中有7.7%达到EDSS 6.0,未治疗患者为18.7%(p = 0.032;RR = 0.4;95%CI = 0.16 - 0.95)。达到EDSS 6.0的平均时间,接受IFNβ治疗的患者为8.1年,未治疗患者为5.8年(p<0.001)。
IFNβ长期治疗可减缓以EDSS和转化为继发进展型多发性硬化症的时间衡量的MS疾病进展。