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大剂量甲基强的松龙治疗多发性硬化症复发可减少增强病变进展为持续黑洞。

Treatment of multiple sclerosis relapses with high-dose methylprednisolone reduces the evolution of contrast-enhancing lesions into persistent black holes.

机构信息

Clinica Neurologica, Dipartimento di Medicina, Università degli Studi di Perugia, Ospedale S. Maria della Misericordia, 06156, Perugia, Italy.

S.C. Neuroradiologia, Azienda Ospedaliera di Perugia, Perugia, Italy.

出版信息

J Neurol. 2018 Mar;265(3):522-529. doi: 10.1007/s00415-017-8726-2. Epub 2018 Jan 11.

Abstract

INTRODUCTION

The MRI evidence of persistent black holes (pBHs) on T1-weighted images reflects brain tissue loss in multiple sclerosis (MS). The evolution of contrast-enhancing lesions (CELs) into pBHs probably depends on the degree and persistence of focal brain inflammation. The aim of our retrospective study was to evaluate the effect of a single cycle of intravenous methylprednisolone (IVMP), as for MS relapse treatment, on the risk of CELs' evolution into pBHs.

PATIENTS AND METHODS

We selected 57 patients with CELs on the baseline MRI scan. We evaluated the evolution of CELs into pBHs on a follow-up MRI scan performed after ≥ 6 months in patients exposed and not exposed to IVMP for the treatment of relapse after the baseline MRI.

RESULTS

In our cohort, 182 CELs were identified in the baseline MRI and 57 of them (31.3%) evolved into pBHs. In the multivariate analysis, the exposure of CELs to IVMP resulted to be a significant independent protective factor against pBHs' formation (OR 0.28, 95% CI 0.11-0.766, p = 0.005), while ring enhancement pattern and the fact of being symptomatic were significant risk factors for CELs' conversion into pBHs (OR 6.42, 95% CI 2.55-17.27, p < 0.001 and OR 13.19, 95% CI 1.56-288.87, p = 0.037).

CONCLUSIONS

The exposure of CELs to a cycle of IVMP as for relapse treatment is associated with a lower risk of CELs' evolution into pBHs. Future studies are required to confirm the potential independent protective effect of IVMP on CELs' evolution into pBHs.

摘要

简介

T1 加权图像上持续性黑洞(pBH)的 MRI 证据反映了多发性硬化症(MS)中的脑组织损失。对比增强病变(CEL)演变为 pBH 可能取决于局灶性脑炎症的程度和持续性。我们回顾性研究的目的是评估静脉注射甲基强的松龙(IVMP)作为 MS 复发治疗的单一周期对 CEL 演变为 pBH 的风险的影响。

患者和方法

我们在基线 MRI 扫描中选择了 57 例 CEL 患者。我们在基线 MRI 扫描后≥6 个月对接受和未接受 IVMP 治疗复发的患者进行随访 MRI 扫描,评估 CEL 演变为 pBH 的情况。

结果

在我们的队列中,基线 MRI 中发现了 182 个 CEL,其中 57 个(31.3%)演变为 pBH。在多变量分析中,CEL 暴露于 IVMP 是 pBH 形成的显著独立保护因素(OR 0.28,95%CI 0.11-0.766,p=0.005),而环形强化模式和症状性是 CEL 演变为 pBH 的显著危险因素(OR 6.42,95%CI 2.55-17.27,p<0.001 和 OR 13.19,95%CI 1.56-288.87,p=0.037)。

结论

CEL 暴露于 IVMP 作为复发治疗与 CEL 演变为 pBH 的风险降低相关。需要进一步的研究来证实 IVMP 对 CEL 演变为 pBH 的潜在独立保护作用。

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