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三十多年来,进展性多发性硬化症的研究人群变得更加年老和残疾,但临床试验中的进展率更低:43 项随机安慰剂对照试验的系统评价和荟萃分析。

Over three decades study populations in progressive multiple sclerosis have become older and more disabled, but have lower on-trial progression rates: A systematic review and meta-analysis of 43 randomised placebo-controlled trials.

机构信息

Centre for Neuroinflammation and Neurodegeneration, Faculty of Medicine, Imperial College London, London, UK.

Queen Square Multiple Sclerosis Centre, Department of Neuroinflammation, UCL Institute of Neurology, University College London, London, UK.

出版信息

Mult Scler. 2019 Oct;25(11):1462-1471. doi: 10.1177/1352458518794063. Epub 2018 Aug 24.

Abstract

BACKGROUND

Progression is the major driver of disability and cost in multiple sclerosis (MS). However, the search for treatments in progressive multiple sclerosis (PMS) has not mirrored the success in relapsing MS.

OBJECTIVES

To assess changes in PMS trials over time.

METHODS

PubMed, MEDLINE and Embase were searched to identify randomised, double-blind, placebo-controlled trials in PMS. Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were used, study quality was assessed and trends were examined by regression.

RESULTS

Placebo groups of 43 studies published between 1988 and 2018 were included. The mean age at trial entry increased by 9.8 years per decade (95% confidence interval (CI): [2.7; 4.9];  < 0.001). Mean baseline Expanded Disability Status Scale (EDSS) scores increased by 0.36 points (95% CI: [0.09; 0.62];  = 0.009) and disease durations at baseline were prolonged by 1.8 years (95% CI: [0.7; 2.9];  = 0.003) per decade. The trials became larger, specifically placebo groups increased by about 222 patients (95% CI: [36; 409];  = 0.021) and 88 patients (95% CI: [12; 165];  = 0.025) per decade for primary progressive multiple sclerosis (PPMS) and secondary progressive multiple sclerosis (SPMS), respectively. The proportion of patients on placebo experiencing disability progression within 24 months decreased by 7.6 percentage points (95% CI: [1.2; 14.1];  = 0.022) per year.

CONCLUSION

Over three decades, PMS trial populations changed and are now older, with a longer disease duration and more disability, with lower on-trial progression rates.

摘要

背景

进展是多发性硬化症(MS)导致残疾和费用的主要因素。然而,在进展型多发性硬化症(PMS)的治疗探索中,并没有取得与复发型多发性硬化症(RRMS)相同的成功。

目的

评估 PMS 试验随时间的变化。

方法

检索 PubMed、MEDLINE 和 Embase 以识别 PMS 的随机、双盲、安慰剂对照试验。采用系统评价和荟萃分析的 Preferred Reporting Items(PRISMA)指南,评估研究质量并通过回归分析检查趋势。

结果

纳入了 1988 年至 2018 年期间发表的 43 项研究的安慰剂组。试验入组时的平均年龄每 10 年增加 9.8 岁(95%置信区间(CI):[2.7;4.9]; < 0.001)。基线扩展残疾状况量表(EDSS)评分平均增加 0.36 分(95%CI:[0.09;0.62]; = 0.009),基线时疾病持续时间每 10 年延长 1.8 年(95%CI:[0.7;2.9]; = 0.003)。试验规模逐渐增大,特别是安慰剂组中,原发性进展型多发性硬化症(PPMS)和继发性进展型多发性硬化症(SPMS)的患者数量每 10 年分别增加了约 222 例(95%CI:[36;409]; = 0.021)和 88 例(95%CI:[12;165]; = 0.025)。在 24 个月内出现残疾进展的安慰剂组患者比例每年下降 7.6 个百分点(95%CI:[1.2;14.1]; = 0.022)。

结论

在过去的 30 年中,PMS 试验人群发生了变化,现在患者年龄更大,疾病持续时间更长,残疾程度更严重,且试验期间进展的比例更低。

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