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双盲、随机、安慰剂对照的磷酸二酯酶-3 抑制剂西洛他唑作为抗抑郁药辅助治疗重性抑郁障碍患者的初步研究。

Double-blind, randomized, placebo-controlled pilot study of the phosphodiesterase-3 inhibitor cilostazol as an adjunctive to antidepressants in patients with major depressive disorder.

机构信息

Department of Clinical Pharmacy, Faculty of Pharmacy, University of Sadat City, Sadat City, Egypt.

Department of Neuropsychiatry, Faculty of Medicine, Menoufia University, Shebin El-Kom, Egypt.

出版信息

CNS Neurosci Ther. 2021 Dec;27(12):1540-1548. doi: 10.1111/cns.13731. Epub 2021 Sep 21.

DOI:10.1111/cns.13731
PMID:34545997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8611782/
Abstract

AIMS

Cilostazol (CLS) has shown antidepressant effect in cardiovascular patients, post-stroke depression, and animal models through its neurotrophic and antiinflammatory activities. Consequently, we aimed to investigate its safety and efficacy in patients with MDD by conducting double-blind, randomized, placebo-controlled pilot study.

METHODS

80 participants with MDD (DSM-IV criteria) and Hamilton Depression Rating Scale (HDRS) score >20 were treated with CLS 50 mg or placebo twice daily plus escitalopram (ESC) 20 mg once daily for six weeks. Patients were evaluated by HDRS scores (weeks 0, 2, 4, and 6). Serum levels of CREB1, BDNF, 5-HT, TNF-α, NF- κB, and FAM19A5 were assessed pre- and post-treatment.

RESULTS

Co-administration of CLS had markedly decreased HDRS score at all-time points compared to the placebo group (p < 0.001). Early improvement, response, and remission rates after 6 weeks were significantly higher in the CLS group (90%, 90%, 80%, respectively) than in the placebo group (25%, 65%, 50% respectively) (p < 0.001). Moreover, the CLS group was superior to the placebo group in modulation of the measured neurotrophic and inflammatory biomarkers.

CONCLUSION

CLS is safe and effective short-term adjunctive therapy in patients with MDD with no other comorbid conditions. Trial registration ID:NCT04069819.

摘要

目的

西洛他唑(CLS)通过其神经营养和抗炎活性,已显示出在心血管病患者、中风后抑郁和动物模型中具有抗抑郁作用。因此,我们旨在通过进行双盲、随机、安慰剂对照的初步研究,来研究其在 MDD 患者中的安全性和疗效。

方法

80 名 MDD 患者(DSM-IV 标准)和汉密尔顿抑郁评定量表(HDRS)评分>20 分的患者接受 CLS 50mg 或安慰剂每日两次联合艾司西酞普兰(ESC)20mg 每日一次治疗,共 6 周。患者在第 0、2、4 和 6 周进行 HDRS 评分评估。在治疗前后评估血清 CREB1、BDNF、5-HT、TNF-α、NF- κB 和 FAM19A5 水平。

结果

与安慰剂组相比,CLS 联合用药在所有时间点的 HDRS 评分均显著降低(p<0.001)。CLS 组在 6 周后早期改善、应答和缓解率明显高于安慰剂组(分别为 90%、90%和 80%)(p<0.001)。此外,CLS 组在调节所测量的神经营养和炎症生物标志物方面优于安慰剂组。

结论

在没有其他合并症的 MDD 患者中,CLS 是一种安全有效的短期辅助治疗方法。试验注册号:NCT04069819。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85d4/8611782/1e91b11fc44a/CNS-27-1540-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85d4/8611782/aac3eda6dd5e/CNS-27-1540-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85d4/8611782/1e91b11fc44a/CNS-27-1540-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85d4/8611782/aac3eda6dd5e/CNS-27-1540-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85d4/8611782/1e91b11fc44a/CNS-27-1540-g003.jpg

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