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一项双盲、随机、安慰剂对照试验,旨在评估单剂量替拉西明对乙酰胆碱受体结合抗体阳性重症肌无力患者的疗效、安全性和耐受性。

A Double-Blinded, Randomized, Placebo-Controlled Trial to Evaluate Efficacy, Safety, and Tolerability of Single Doses of Tirasemtiv in Patients with Acetylcholine Receptor-Binding Antibody-Positive Myasthenia Gravis.

作者信息

Sanders Donald B, Rosenfeld Jeffrey, Dimachkie Mazen M, Meng Lisa, Malik Fady I

机构信息

Duke University Medical Center, Durham, NC, 27710, USA,

出版信息

Neurotherapeutics. 2015 Apr;12(2):455-60. doi: 10.1007/s13311-015-0345-y.

Abstract

Tirasemtiv is a fast skeletal troponin activator that sensitizes the sarcomere to calcium and increases muscle force following subtetanic nerve input. In an animal model of myasthenia gravis (MG), single oral doses of tirasemtiv improved muscle force and reduced fatigability. The purpose of this study was to determine the effect of single doses of tirasemtiv on skeletal muscle function and fatigability in patients with generalized MG. Thirty-two patients with acetylcholine receptor-antibody positive MG and muscle weakness received single doses of tirasemtiv (250 mg or 500 mg) or placebo in a double-blind, randomized treatment sequence with each treatment separated by at least 1 week. Outcome measures included the Quantitative MG Score (QMG), MG Composite, Manual Muscle Testing, and forced vital capacity. At 6 h after dosing, tirasemtiv produced dose-related improvements from baseline in the QMG score (slope: -0.49 QMG point per 250 mg; p = 0.02) and in percent predicted forced vital capacity (slope: 2.2% per 250 mg; p = 0.04). QMG improved >3 points in twice as many patients after 500 mg tirasemtiv than after placebo. Both doses of tirasemtiv were well tolerated; there were no premature terminations or serious adverse events. The results of this study suggest that tirasemtiv may improve muscle function in MG and will be used to support further development of tirasemtiv in neuromuscular diseases.

摘要

替拉西明是一种快速作用的骨骼肌肌钙蛋白激活剂,可使肌节对钙敏感,并在亚强直神经输入后增加肌肉力量。在重症肌无力(MG)动物模型中,单次口服替拉西明可改善肌肉力量并减轻疲劳。本研究的目的是确定单次剂量的替拉西明对全身型MG患者骨骼肌功能和疲劳的影响。32例乙酰胆碱受体抗体阳性且有肌无力的MG患者,以双盲、随机治疗顺序接受单次剂量的替拉西明(250mg或500mg)或安慰剂治疗,每次治疗间隔至少1周。观察指标包括重症肌无力定量评分(QMG)、MG综合评分、徒手肌力测试和用力肺活量。给药后6小时,替拉西明使QMG评分较基线有剂量相关的改善(斜率:每250mg -0.49个QMG点;p = 0.02),以及预计用力肺活量百分比有改善(斜率:每250mg 2.2%;p = 0.04)。服用500mg替拉西明后QMG改善超过3分的患者数量是服用安慰剂后的两倍。两种剂量的替拉西明耐受性均良好;没有提前终止治疗或严重不良事件。本研究结果表明,替拉西明可能改善MG患者的肌肉功能,并将用于支持替拉西明在神经肌肉疾病中的进一步研发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff0/4404445/9972f707f887/13311_2015_345_Fig1_HTML.jpg

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