Griffin Emily, Brown Jamie N
Durham VA Medical Center, NC, USA
Durham VA Medical Center, NC, USA.
Ann Pharmacother. 2016 Jul;50(7):586-91. doi: 10.1177/1060028016643097. Epub 2016 Apr 18.
To evaluate the efficacy and safety of pregabalin for the treatment of restless legs syndrome (RLS).
A search of the MEDLINE database (1956-February 2016) and EMBASE (1957-February 2016) was conducted, using the terms pregabalin and restless legs syndrome In addition, a manual review of the references cited in each publication identified from the database search was conducted to identify relevant articles.
All English-language, peer-reviewed publications were evaluated for relevance. From an initial review of 285 articles, 5 clinical trials were included in the final analysis.
Pregabalin is an analog of γ-aminobutyric acid that exhibits antinociceptive and anticonvulsant activity by binding to voltage-gated calcium channels in the central nervous system. Studies of pregabalin have demonstrated efficacy through significant reductions in mean International RLS Scale scores and wake after sleep onset scores, and it had a lower rate of augmentation than pramipexole treatment. Study durations ranged from 6 to 52 weeks, with doses ranging from 150 to 600 mg daily. The most common adverse effects associated with pregabalin use in all studies included dizziness and somnolence.
Clinical evidence suggests that pregabalin may improve symptoms of RLS and reduce disturbances in sleep, resulting in improvements in quality of life for patients affected by the disease. Pregabalin is considered to be relatively safe and poses a minimal risk of augmentation unlike current recommended first-line treatments for RLS. Thus, evidence suggests that pregabalin is a reasonable therapeutic option for the treatment of RLS.
评估普瑞巴林治疗不宁腿综合征(RLS)的疗效和安全性。
检索MEDLINE数据库(1956年 - 2016年2月)和EMBASE数据库(1957年 - 2016年2月),检索词为普瑞巴林和不宁腿综合征。此外,对数据库检索出的各出版物中引用的参考文献进行人工查阅以确定相关文章。
评估所有英文、经同行评审的出版物的相关性。在对285篇文章进行初步评审后,最终分析纳入了5项临床试验。
普瑞巴林是γ-氨基丁酸的类似物,通过与中枢神经系统中的电压门控钙通道结合发挥抗伤害感受和抗惊厥活性。对普瑞巴林的研究表明,其可通过显著降低国际不宁腿综合征量表平均得分和睡眠起始后觉醒得分来显示疗效,且与普拉克索治疗相比,其症状加重率更低。研究持续时间为6至52周,剂量范围为每日150至600毫克。在所有研究中,与使用普瑞巴林相关的最常见不良反应包括头晕和嗜睡。
临床证据表明,普瑞巴林可能改善不宁腿综合征症状并减少睡眠障碍,从而改善该病患者的生活质量。与目前推荐的不宁腿综合征一线治疗方法不同,普瑞巴林被认为相对安全,且症状加重风险最小。因此,有证据表明普瑞巴林是治疗不宁腿综合征的合理治疗选择。