同样纠的第81号:皮里多斯提格 (mestinon®)
Nadia Mansoor1, Terry Heiman-Patterson1, Eva L Feldman2,3
1Neurology Department, Temple University, Philadelphia, PA, USA.
皮里多斯提格不会减缓肌缩侧面硬化症 (ALS) 的进展. 这种增强神经肌肉传播的药物缺乏修改ALS病理生理学的明确机制,并且在ALS患者的临床试验中没有显示出有效性.
科学领域:
- 神经学 神经学
- 神经科学是一个神经科学.
- 药理学 药理学是指药理学的学科.
背景情况:
- 神经肌肉结位功能障碍是肌缩侧面硬化症 (ALS) 的早期特征.
- 皮里多斯提格明可以增强乙胆的可用性,从而有可能改善ALS的神经肌肉传播.
- 改变神经肌肉传播在ALS进展中的作用仍然不确定.
研究的目的:
- 评估皮里多斯提格在减缓ALS进展方面的潜力.
- 评估pyridostigmine在ALS中的疗效的机理性可信性.
- 审查针对ALS治疗抗胆化酶剂的现有临床证据.
主要方法:
- 关于ALS中神经肌肉结位功能障碍的临床前发现的综述.
- 分析了pyridostigmine在ALS中提出的作用机制.
- 对ALS患者的pyridostigmine和类似药物的临床试验数据的检查.
主要成果:
- 皮里多斯提格缺乏合理的机制来修改ALS病理生理学,而不仅仅是暂时的神经肌肉传输增强.
- 阳性乙胆受体自身抗体的ALS (PALS) 患者没有严重骨髓灰质炎症状,不太可能受益.
- 涉及类似抗胆酶剂的临床试验没有证明ALS进展的减缓.
结论:
- 由于缺乏机理学依据和已证明的疗效,皮里多斯蒂格明不支持用于减缓ALS进展.
- 常见的副作用包括肌肉性胆固醇症状,特别是胃肠道问题.
- 根据当前的证据,对ALS的pyridostigmine进行进一步的临床研究是不必要的.
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