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一项针对压力管理以预防多发性硬化症新脑部病变的随机试验。

A randomized trial of stress management for the prevention of new brain lesions in MS.

机构信息

Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

出版信息

Neurology. 2012 Jul 31;79(5):412-9. doi: 10.1212/WNL.0b013e3182616ff9. Epub 2012 Jul 11.

DOI:10.1212/WNL.0b013e3182616ff9
PMID:22786596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3405245/
Abstract

OBJECTIVES

This trial examined the efficacy of a stress management program in reducing neuroimaging markers of multiple sclerosis (MS) disease activity.

METHODS

A total of 121 patients with relapsing forms of MS were randomized to receive stress management therapy for MS (SMT-MS) or a wait-list control condition. SMT-MS provided 16 individual treatment sessions over 24 weeks, followed by a 24-week post-treatment follow-up. The primary outcome was the cumulative number of new gadolinium-enhancing (Gd+) brain lesions on MRI at weeks 8, 16, and 24. Secondary outcomes included new or enlarging T2 MRI lesions, brain volume change, clinical exacerbation, and stress.

RESULTS

SMT-MS resulted in a reduction in cumulative Gd+ lesions (p = 0.04) and greater numbers of participants remained free of Gd+ lesions during the treatment (76.8% vs 54.7%, p = 0.02), compared to participants receiving the control treatment. SMT-MS also resulted in significantly reduced numbers of cumulative new T2 lesions (p = 0.005) and a greater number of participants remaining free of new T2 lesions (69.5% vs 42.7%, p = 0.006). These effects were no longer detectable during the 24-week post-treatment follow-up period.

CONCLUSIONS

This trial indicates that SMT-MS may be useful in reducing the development of new MRI brain lesions while patients are in treatment.

CLASSIFICATION OF EVIDENCE

This study provides Class I evidence that SMT-MS, a manualized stress management therapy program, reduced the number of Gd+ lesions in patients with MS during a 24-week treatment period. This benefit was not sustained beyond 24 weeks, and there were no clinical benefits.

TRIAL REGISTRATION

ClinicalTrials.gov, number NCT00147446.

摘要

目的

本试验旨在研究一种应激管理方案对多发性硬化症(MS)疾病活动的神经影像学标志物的疗效。

方法

共 121 例复发性 MS 患者随机分为应激管理治疗 MS 组(SMT-MS)或等待名单对照组。SMT-MS 在 24 周内提供 16 次个体治疗,随后进行 24 周的治疗后随访。主要结局为第 8、16 和 24 周 MRI 上新钆增强(Gd+)脑病变的累积数量。次要结局包括新或扩大的 T2 MRI 病变、脑体积变化、临床恶化和应激。

结果

SMT-MS 可减少累积 Gd+病变(p=0.04),并且治疗期间有更多的参与者保持无 Gd+病变(76.8% vs 54.7%,p=0.02),与接受对照治疗的参与者相比。SMT-MS 还导致累积新 T2 病变的数量显著减少(p=0.005),并且更多的参与者保持无新 T2 病变(69.5% vs 42.7%,p=0.006)。这些影响在 24 周治疗后随访期间不再可检测到。

结论

本试验表明,SMT-MS 可能有助于减少新 MRI 脑病变的发生,同时患者正在接受治疗。

证据分类

本研究提供了 I 级证据,表明 SMT-MS,一种规范化的应激管理治疗方案,可减少 MS 患者在 24 周治疗期间 Gd+病变的数量。这种益处不能持续超过 24 周,并且没有临床益处。

临床试验注册

ClinicalTrials.gov,编号 NCT00147446。

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