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

被引:14
|
作者
Abdallah, Mahmoud S. [1 ]
Ramadan, Ahmed N. [2 ]
Omara-Reda, Hend [2 ]
Mansour, Noha O. [3 ]
Elsokary, Mohamed A. [4 ]
Elsawah, Hozaifa K. [4 ]
Zaki, Shimaa Abdelsattar [5 ]
Abo Mansour, Hend E. [6 ]
Mosalam, Esraa M. [6 ]
机构
[1] Univ Sadat City, Fac Pharm, Dept Clin Pharm, Sadat City, Egypt
[2] Menoufia Univ, Fac Med, Dept Neuropsychiat, Shibin Al Kawm, Egypt
[3] Mansoura Univ, Fac Pharm, Clin Pharm & Pharm Practice Dept, Mansoura, Egypt
[4] Alexandria Univ, High Inst Publ Hlth, Dept Biostat, Alexandria, Egypt
[5] Menoufia Univ, Natl Liver Inst, Dept Clin Biochem & Mol Diagnost, Shibin Al Kawm, Egypt
[6] Menoufia Univ, Fac Pharm, Dept Biochem, Shibin Al Kawm, Egypt
关键词
adjunctive therapy; cilostazol; CREB; BDNF; inflammatory markers; major depressive disorder; NEUROTROPHIC FACTOR BDNF; BRAIN; ESCITALOPRAM; BIOMARKER; THERAPY; INJURY;
D O I
10.1111/cns.13731
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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-alpha, NF- kappa B, 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.
引用
收藏
页码:1540 / 1548
页数:9
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