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甘丙肽-B 标准化提取物与阿普唑仑治疗广泛性焦虑障碍的对照研究:一项为期十周的双盲、随机临床试验。

Galphimine-B Standardized Extract versus Alprazolam in Patients with Generalized Anxiety Disorder: A Ten-Week, Double-Blind, Randomized Clinical Trial.

机构信息

Centro de Investigación Biomédica del Sur, Instituto Mexicano del Seguro Social (CIBIS-IMSS), Xochitepec, Morelos, Mexico.

Facultad de Medicina de la Universidad Autónoma del Estado de Morelos, Cuernavaca, Morelos, Mexico.

出版信息

Biomed Res Int. 2019 Jan 30;2019:1037036. doi: 10.1155/2019/1037036. eCollection 2019.

Abstract

Galphimine-B (G-B), a compound isolated from , has been shown to possess important anxiolytic activity. In this study, we evaluated the effectiveness and tolerability of a G-B standardized extract (experimental treatment) that was administered daily for 10 weeks in patients with moderate or severe Generalized Anxiety Disorder (GAD). Alprazolam was used as control treatment and administered under the same conditions. A total of 167 patients were included. At the start of the study, the severe anxiety condition prevailed, with an average on the Hamilton Anxiety Scale of 35.1 ± 8.8 and 35.8 ± 8.1 points in the control and experimental groups, respectively. After the 10 weeks of administration, the average was reduced in the control group to 4.6 ± 6.5 points and in the experimental group to 3.5 ± 5.5 points. Therapeutic success in the control group was 85.7% and in the experimental group, 92.0%. A high proportion of patients (22.2%) treated with Alprazolam manifested daytime sleepiness, while in the group treated with the G-B standardized extract, daytime sleepiness was found in 4.7%. In conclusion, a G-B standardized extract demonstrated therapeutic effectiveness in patients with GAD, without exhibiting significant difference with Alprazolam, but showing fewer cases of daytime sleepiness. The trial was registered at http://clinicaltrials.gov by identifier: NCT03702803.

摘要

Galphimine-B (G-B),一种从 中分离出来的化合物,已被证明具有重要的抗焦虑活性。在这项研究中,我们评估了一种 G-B 标准化提取物(实验性治疗)的有效性和耐受性,该提取物每天给药 10 周,用于治疗中度或重度广泛性焦虑症(GAD)患者。阿普唑仑作为对照治疗,在相同条件下给药。共有 167 名患者入组。在研究开始时,严重焦虑状态占主导地位,汉密尔顿焦虑量表的平均得分为 35.1 ± 8.8 和 35.8 ± 8.1 分,分别在对照组和实验组。经过 10 周的治疗后,对照组的平均分数降至 4.6 ± 6.5 分,实验组降至 3.5 ± 5.5 分。对照组的治疗成功率为 85.7%,实验组为 92.0%。接受阿普唑仑治疗的患者中有 22.2%表现出白天嗜睡,而接受 G-B 标准化提取物治疗的患者中,有 4.7%出现白天嗜睡。总之,G-B 标准化提取物在 GAD 患者中表现出治疗效果,与阿普唑仑无显著差异,但白天嗜睡的病例较少。该试验在 http://clinicaltrials.gov 上注册,标识符为:NCT03702803。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/504b/6374797/9d5601a39405/BMRI2019-1037036.001.jpg

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