Badillo Stephanie Patricia J, Jamora Roland Dominic G
Department of Clinical Neurosciences, University of the East Ramon Magsaysay Memorial Medical Center, Quezon City, Philippines.
Section of Neurology, Department of Internal Medicine, Cardinal Santos Medical Center, San Juan City, Philippines.
Front Neurol. 2019 Jul 17;10:779. doi: 10.3389/fneur.2019.00779. eCollection 2019.
There are recent reports of zolpidem being effective for the treatment of a variety of movement disorders, due to its action on the gamma-aminobutyric acid A receptors in the thalamus, subthalamic nucleus, and globus pallidus, hence facilitating inhibitory pathways in the basal ganglia motor loop. Its beneficial effects have been described for Parkinson's disease and other related disorders. The objective of this study was to assess the therapeutic effects of zolpidem for various types of dystonia. We conducted a literature search using MEDLINE via PubMed, Cochrane Library, EMBASE, Scopus, and Google Scholar. There were no randomized controlled trials. The literature included 6 case reports, 4 case series, and 1 non-randomized, non-controlled interventional trial. Overall, 49 adult participants (range 1-34 participants) with a mean age of 49.5 years were treated. Regardless of the dystonia subtype, a single dose of zolpidem at 10 mg causes improvement of symptoms for a mean duration of 3.4 h until patient returns to baseline. The main adverse effect noted was drowsiness, which was dose-dependent. While the current available literature suggests that zolpidem may be an effective pharmacologic option for treating dystonia, however the quality of evidence remains limited. Larger sample size, methodological consistency, and randomized controlled trials with long-term patient follow-ups are necessary to come up with definitive conclusion.
最近有报道称唑吡坦对多种运动障碍有效,这是由于其作用于丘脑、丘脑底核和苍白球中的γ-氨基丁酸A受体,从而促进基底神经节运动环路中的抑制性通路。其对帕金森病和其他相关疾病的有益作用已得到描述。本研究的目的是评估唑吡坦对各种类型肌张力障碍的治疗效果。我们通过PubMed、Cochrane图书馆、EMBASE、Scopus和谷歌学术搜索MEDLINE进行文献检索。没有随机对照试验。文献包括6例病例报告、4例病例系列和1项非随机、非对照干预试验。总体而言,治疗了49名成年参与者(范围为1至34名参与者),平均年龄为49.5岁。无论肌张力障碍亚型如何,单次服用10 mg唑吡坦可使症状改善,平均持续3.4小时,直至患者恢复至基线水平。观察到的主要不良反应是嗜睡,且呈剂量依赖性。虽然目前的现有文献表明唑吡坦可能是治疗肌张力障碍的一种有效药物选择,然而证据质量仍然有限。需要更大的样本量、方法学一致性以及对患者进行长期随访的随机对照试验才能得出明确结论。