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在BENEFIT研究中,磁共振成像对转化为多发性硬化症的预测指标。

Magnetic resonance imaging predictors of conversion to multiple sclerosis in the BENEFIT study.

作者信息

Moraal Bastiaan, Pohl Christoph, Uitdehaag Bernard M J, Polman Chris H, Edan Gilles, Freedman Mark S, Hartung Hans-Peter, Kappos Ludwig, Miller David H, Montalban Xavier, Lanius Vivian, Sandbrink Rupert, Barkhof Frederik

机构信息

Department of Diagnostic Radiology, Multiple Sclerosis Center Amsterdam, Vrije University Medical Center, De Boelelaan 1117, 1081 HV Amsterdam, the Netherlands.

出版信息

Arch Neurol. 2009 Nov;66(11):1345-52. doi: 10.1001/archneurol.2009.243.

Abstract

BACKGROUND

Several studies have confirmed the predictive value of baseline and follow-up magnetic resonance (MR) imaging variables for conversion to clinically definite multiple sclerosis (CDMS), depending on the population, follow-up duration, and treatment intervention. However, the timing of follow-up imaging and the effect of treatment intervention on the predictive value of baseline MR imaging variables require further elucidation.

OBJECTIVES

To assess the prognostic value of baseline MR imaging variables for conversion to CDMS over 3 years and whether this was affected by treatment intervention and (2) to assess the increased risk for conversion posed by dissemination in time on follow-up MR imaging.

DESIGN

Cohort study.

SETTING

Multicenter randomized clinical trial.

PATIENTS

Four hundred sixty-eight patients with a clinically isolated syndrome who had an initial clinical demyelinating event within the past 60 days who received early treatment (3 years of interferon beta-1b) or delayed treatment (placebo first, followed by > or =1 year of interferon beta-1b). Intervention Magnetic resonance imaging. Main Outcome Measure Time to CDMS.

RESULTS

The overall conversion rate to CDMS was 42%. Barkhof criteria with the strongest prognostic value were the presence at baseline of at least 9 T2-weighted lesions (hazard ratio [HR], 1.64; 95% confidence interval [CI], 1.15-2.33; P = .006) and at least 3 periventricular lesions (1.66; 1.14-2.41; P = .009). No specific advantage was noted in using a fixed cutoff of at least 3 Barkhof criteria (HR, 1.31; 95% CI, 0.95-1.79; P = .10). The prognostic value of all MR imaging criteria was unaffected by treatment intervention (P > or = .20 for all). Dissemination in time resulted in increased risk for CDMS only in patients without dissemination in space at baseline and was most informative at the 9-month MR imaging (HR, 2.72; 95% CI, 1.26-5.87; P = .01).

CONCLUSIONS

The modified Barkhof criteria showed moderate predictive value for conversion to CDMS, although all patients had received interferon beta-1b therapy for at least 1 year. The predictive value was unaffected by treatment intervention. Follow-up MR imaging was most informative after 9 months in patients without dissemination in space at baseline.

摘要

背景

多项研究已证实,根据人群、随访时间和治疗干预情况,基线及随访磁共振(MR)成像变量对转化为临床确诊多发性硬化症(CDMS)具有预测价值。然而,随访成像的时间以及治疗干预对基线MR成像变量预测价值的影响尚需进一步阐明。

目的

(1)评估基线MR成像变量对3年内转化为CDMS的预后价值,以及这是否受治疗干预影响;(2)评估随访MR成像上时间扩散对转化风险增加的影响。

设计

队列研究。

设置

多中心随机临床试验。

患者

468例临床孤立综合征患者,在过去60天内发生首次临床脱髓鞘事件,接受早期治疗(3年β-1b干扰素)或延迟治疗(先使用安慰剂,随后使用≥1年β-1b干扰素)。干预措施为磁共振成像。主要观察指标为转化为CDMS的时间。

结果

转化为CDMS的总体转化率为42%。预后价值最强的Barkhof标准为基线时至少存在9个T2加权病灶(风险比[HR],1.64;95%置信区间[CI],1.15 - 2.33;P = 0.006)和至少3个脑室周围病灶(1.66;1.14 - 2.41;P = 0.009)。使用至少3条Barkhof标准的固定截断值未发现明显优势(HR,1.31;95% CI,0.95 - 1.79;P = 0.10)。所有MR成像标准的预后价值均不受治疗干预影响(所有P≥0.20)。仅在基线时无空间扩散的患者中,时间扩散会导致CDMS风险增加,且在9个月的MR成像时信息最丰富(HR,2.72;95% CI,1.26 - 5.87;P = 0.01)。

结论

改良的Barkhof标准对转化为CDMS显示出中等预测价值,尽管所有患者均接受了至少1年的β-1b干扰素治疗。预测价值不受治疗干预影响。对于基线时无空间扩散的患者,随访MR成像在9个月后信息最丰富。

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