关于α2δ钙通道韧带药物治疗无腿症的 ADMET 考虑因素的综合更新。

Gaia Pellitteri, Salvatore Versace, Giovanni Merlino, Annacarmen Nilo, Gian Luigi Gigli, Mariarosaria Valente
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引用次数: 0

摘要

简介多动腿综合征/Willis-Ekbom 病(RLS/WED)是一种与睡眠相关的感觉-运动障碍,与睡眠质量差和日常功能受损有关。对于慢性 RLS/WED 患者,建议采用药物治疗。国际指南建议,在大多数情况下,除非有禁忌症,否则应从α2δ钙通道配体开始治疗:本综述基于 1986 年至 2024 年期间在互联网和 PubMed 上的广泛搜索。我们的目的是描述α2δ配体的吸收、分布、代谢和毒理学(ADMET),并共同考虑治疗类别、不同化合物的特异性、与其他治疗方案相关的疗效和安全性。专家观点:α2δ配体的ADMET特征十分相似,共享大多数药代动力学和潜在的不良反应。然而,我们强调的是,加巴喷丁恩阿卡波利和普瑞巴林的线性药代动力学与加巴喷丁不同。合并失眠、慢性疼痛综合征、冲动控制障碍和合并焦虑症的患者可获得额外的疗效。α2δ配体的使用与不良的增强风险有关。我们仍然需要新的长期安全有效的治疗方法,这些方法可以随着我们对 RLS/WED 病理生理学的了解而不断发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A comprehensive update on the ADMET considerations for α2δ calcium channel ligand medications for treating restless legs syndrome.

Introduction: Restless legs syndrome/Willis-Ekbom disease (RLS/WED) is a sleep-related sensory-motor disorder associated with poor sleep quality and impaired daily functioning. In patients affected by chronic RLS/WED, a pharmacological therapy is recommended. International guidelines suggest to start the treatment with a α2δ calcium channel ligand in most cases, unless contraindicated.

Areas covered: The present review is based on an extensive Internet and PubMed search from 1986 to 2024. Our purpose is to describe the absorption, distribution, metabolism, and toxicology (ADMET) of the α2δ ligands, with common consideration for the therapeutic class, specificities of different compounds, efficacy, and safety in relation to other treatment options.

Expert opinion: α2δ ligands are quite similar in their ADMET profiles, sharing most of the pharmacokinetics and potential adverse effects. However, we highlight the linear kinetic of gabapentin enacarbil and pregabalin, differently from gabapentin. α2δ ligands are safe and effective for the treatment of RLS/WED. Additional benefits can be obtained in comorbid insomnia, chronic pain syndromes, history of impulse control disorder, and comorbid anxiety. The use of α2δ ligands is associated with poor risk of augmentation. We still need new long-term safe and effective treatments, which could be developed along with our knowledge of RLS/WED pathophysiology.

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