Efficacy and safety of celecoxib monotherapy for treatment of moderate depressive symptoms following COVID-19 infection: A randomized, double-blind, placebo-controlled trial

被引:4
作者
Ansari, Sahar [1 ]
Moghaddam, Hossein Sanjari [2 ]
Basti, Fatemeh A. [3 ]
Salehi, Mohammadreza [4 ]
Akhondzadeh, Shahin [2 ,5 ]
机构
[1] Univ Tehran Med Sci, Imam Hosp, Psychosomat Med Res Ctr, Tehran, Iran
[2] Univ Tehran Med Sci, Roozbeh Hosp, Psychiat Res Ctr, Tehran, Iran
[3] Islamic Azad Univ, Tehran Med Branch, Tehran, Iran
[4] Univ Tehran Med Sci, Imam Hosp, Res Ctr Antibiot Stewardship & Antimicrobial Resis, Infect Dis Dept, Tehran, Iran
[5] Univ Tehran Med Sci, Roozbeh Psychiat Hosp, Psychiat Res Ctr, South Kargar St, Tehran 13337, Iran
关键词
Celecoxib; Post-COVID-19 depressive symptoms; COVID-19; Depressive symptoms; BIPOLAR DEPRESSION; CORONAVIRUS; DISORDERS; ANXIETY;
D O I
10.1016/j.jpsychores.2023.111471
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Celecoxib, a nonsteroidal anti-inflammatory agent, was found to be an effective add-on treatment for unipolar and bipolar depression. We investigated the potential beneficial effect of celecoxib monotherapy on depressive symptoms after Coronavirus disease (COVID-19).Methods: This was a randomized, double-blind, placebo-controlled clinical trial investigating the therapeutic effects of celecoxib monotherapy in patients with moderate depressive symptoms following COVID-19 infection.Patients were randomized to receive either a celecoxib capsule (100 mg) twice daily or a placebo capsule twice daily for 6 weeks. Participants were assessed with the Hamilton Depression Rating Scale (HDRS) and the side effect checklist at baseline and weeks 3 and 6.Results: A total of 62 patients were included. GLM repeated-measures showed a significant effect of time x treatment (F = 12.95, df = 1.98, p < 0.001) for celecoxib, suggesting superior improvement of depressive symptoms in celecoxib compared to placebo from baseline to the study endpoint. HDRS scores in the celecoxib group showed a greater decline from baseline to both week 3 (t = 4.12, p < 0.001, Cohen's d = 1.10) and week 6 (t = 4.76, p < 0.001, Cohen's d = 1.27), compared to the placebo group. Rate of response to treatment (70% vs 9%, p < 0.001) and remission (67% vs 0%, p < 0.001) was significantly higher in celecoxib compared to the placebo group at week 6. Adverse event frequencies were not significantly different between the two groups.Conclusion: We demonstrated that treatment with celecoxib significantly improved depression scores of patients with depressive symptoms following COVID-19 infection. Further trials with larger sample sizes and longer study periods should assess our findings before any suggestion for clinical use.The trial was prospectively registered at the Iranian registry of clinical trials (www.irct.ir; registration number: IRCT20090117001556N142).
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页数:7
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共 49 条
[41]   Bidirectional associations between COVID-19 and psychiatric disorder: retrospective cohort studies of 62 354 COVID-19 cases in the USA [J].
Taquet, Maxime ;
Luciano, Sierra ;
Geddes, John R. ;
Harrison, Paul J. .
LANCET PSYCHIATRY, 2021, 8 (02) :130-140
[42]   Neuroinflammation and depression: A review [J].
Troubat, Romain ;
Barone, Pascal ;
Leman, Samuel ;
Desmidt, Thomas ;
Cressant, Arnaud ;
Atanasova, Boriana ;
Brizard, Bruno ;
El Hage, Wissam ;
Surget, Alexandre ;
Belzung, Catherine ;
Camus, Vincent .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2021, 53 (01) :151-171
[43]   Are we facing a crashing wave of neuropsychiatric sequelae of COVID-19? Neuropsychiatric symptoms and potential immunologic mechanisms [J].
Troyer, Emily A. ;
Kohn, Jordan N. ;
Hong, Suzi .
BRAIN BEHAVIOR AND IMMUNITY, 2020, 87 :34-39
[44]   Mental disorders and risk of COVID-19-related mortality, hospitalisation, and intensive care unit admission: a systematic review and meta-analysis [J].
Vai, Benedetta ;
Mazza, Mario Gennaro ;
Colli, Claudia Delli ;
Foiselle, Marianne ;
Allen, Bennett ;
Benedetti, Francesco ;
Borsini, Alessandra ;
Dias, Marisa Casanova ;
Tamouza, Ryad ;
Leboyer, Marion ;
Benros, Michael E. ;
Branchi, Igor ;
Fusar-Poli, Paolo ;
De Picker, Livia J. .
LANCET PSYCHIATRY, 2021, 8 (09) :797-812
[45]   Effect of celecoxib on improving depression: A systematic review and meta-analysis [J].
Wang, Zhi ;
Wu, Qiao ;
Wang, Qing .
WORLD JOURNAL OF CLINICAL CASES, 2022, 10 (22) :7872-7882
[46]   Integrating neuroimmune systems in the neurobiology of depression [J].
Wohleb, Eric S. ;
Franklin, Tina ;
Iwata, Masaaki ;
Duman, Ronald S. .
NATURE REVIEWS NEUROSCIENCE, 2016, 17 (08) :497-511
[47]   Correlation between anxiety-depression symptoms and immune characteristics in inpatients with 2019 novel coronavirus in Wuhan, China [J].
Wu, Congchong ;
Zhou, Zhiying ;
Ni, Li ;
Cao, Jiang ;
Tan, Meifang ;
Wu, Xiu ;
Xu, Yi ;
Hu, Jianbo .
JOURNAL OF PSYCHIATRIC RESEARCH, 2021, 141 :378-384
[48]   Endotoxin produces a depressive-like episode in rats [J].
Yirmiya, R .
BRAIN RESEARCH, 1996, 711 (1-2) :163-174
[49]   Correlation between immune response and self-reported depression during convalescence from COVID-19 [J].
Yuan, Bo ;
Li, Weixin ;
Liu, Hanqing ;
Cai, Xin ;
Song, Shuo ;
Zhao, Jia ;
Hu, Xiaopeng ;
Li, Zhiwen ;
Chen, Yongxin ;
Zhang, Kai ;
Liu, Zhiyong ;
Peng, Jing ;
Wang, Cheng ;
Wang, Jianchun ;
An, Yawen .
BRAIN BEHAVIOR AND IMMUNITY, 2020, 88 :39-43