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醛糖还原酶抑制剂雷帕霉素显著改善糖尿病多发性神经病的神经传导速度:日本的一项随机、双盲、安慰剂对照研究。

Aldose reductase inhibitor ranirestat significantly improves nerve conduction velocity in diabetic polyneuropathy: A randomized double-blind placebo-controlled study in Japan.

机构信息

Division of Neurology, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.

Department of Neurology, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

出版信息

J Diabetes Investig. 2019 Mar;10(2):466-474. doi: 10.1111/jdi.12890. Epub 2018 Aug 9.

Abstract

AIMS/INTRODUCTION: Diabetic polyneuropathy is one of the most frequent diabetic complications, and impairs patients' quality of life. We evaluated the efficacy and safety of ranirestat (40 mg/day) in patients with diabetic polyneuropathy.

MATERIALS AND METHODS

This was a multicenter, placebo-controlled, randomized double-blind, parallel-group, phase III study in which 557 patients were randomly assigned to either the ranirestat or placebo group and assessed for 52 weeks. The co-primary end-points were the changes in tibial motor nerve conduction velocity and total modified Toronto Clinical Neuropathy Score as a measure of clinical symptoms.

RESULTS

There was a significant increase in tibial motor nerve conduction velocity in the ranirestat group compared with the placebo group. The difference between groups in the change at last observation was 0.52 m/s (P = 0.021). Increases in nerve conduction velocity in the ranirestat group were found not only in the tibial motor nerves, but also in the median motor nerves, proximal median sensory nerves and distal median sensory nerves. No significant differences in modified Toronto Clinical Neuropathy Score or safety parameters were found between the two groups.

CONCLUSIONS

Ranirestat (40 mg/day) was well tolerated and improved nerve conduction velocity. Regarding symptoms and signs, no detectable benefits over the placebo were observed in the ranirestat group during the 52 weeks of treatment.

摘要

目的/引言:糖尿病多发性神经病是最常见的糖尿病并发症之一,会损害患者的生活质量。我们评估了瑞那度胺(40mg/天)治疗糖尿病多发性神经病患者的疗效和安全性。

材料和方法

这是一项多中心、安慰剂对照、随机、双盲、平行组、III 期研究,共 557 例患者随机分为瑞那度胺组或安慰剂组,评估 52 周。主要终点是胫神经运动传导速度和总改良多伦多临床神经病评分(作为临床症状的衡量标准)的变化。

结果

与安慰剂组相比,瑞那度胺组的胫神经运动传导速度显著增加。组间最后一次观察时的变化差异为 0.52m/s(P=0.021)。瑞那度胺组的神经传导速度增加不仅见于胫神经,还见于正中神经、近端正中感觉神经和远端正中感觉神经。两组间改良多伦多临床神经病评分或安全性参数无显著差异。

结论

瑞那度胺(40mg/天)耐受性良好,可改善神经传导速度。在 52 周的治疗期间,瑞那度胺组在症状和体征方面未观察到与安慰剂相比有可检测到的益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e93a/6400176/a276428baedb/JDI-10-466-g004.jpg

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