Comparative Efficacy and Acceptability of Anti-inflammatory Agents on Major Depressive Disorder: A Network Meta-Analysis
- PMID: 34276378
- PMCID: PMC8281269
- DOI: 10.3389/fphar.2021.691200
Comparative Efficacy and Acceptability of Anti-inflammatory Agents on Major Depressive Disorder: A Network Meta-Analysis
Abstract
Background: With the growing importance of research about the association between neuroinflammation and major depressive disorder (MDD), anti-inflammatory agents have been used as a new antidepressant therapy in clinical practice. We conducted a network meta-analysis (NMA) with up-to-date evidence to compare different anti-inflammatory agents for improving the treatment of MDD patients. Methods: To identify eligible randomized clinical trials, four databases (i.e, the Cochrane Library, Web of Science, PubMed and Embase) were searched from inception date to May 31, 2020. Anti-inflammatory agents were defined as non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids, cytokine inhibitors, statins, pioglitazone, minocycline, N-acetylcysteine (NAC) and omega-3 fatty acid (Omega-3 FA). The main outcomes of this NMA were efficacy, acceptability and remission rate. Risk ratio (RR) was adopted for dichotomous outcomes, and the confidence interval (CI) was set at 95%. STATA 14.0 and R 3.6.3 were used to conduct the NMA. The study protocol was registered with PROSPERO (CRD42020182531). Results: A total of 39 studies, involving 2871 participants, were included in quantitative data synthesis. For efficacy, NSAIDs (RR=0.50, 95%CI: 0.26-0.73) and pioglitazone (RR=0.45, 95%CI: 0.20-0.84) were more favorable than placebo. With respect to acceptability, NSAIDs were more acceptable than placebo (RR=0.89, 95%CI: 0.77-0.99) and minocycline (RR=1.22, 95%CI: 1.03-1.49). For remission, NSAIDs were more superior than placebo (RR=0.48, 95%CI: 0.27-0.79) and Omega-3 FA (RR=2.01, 95%CI: 1.09-3.90), while NACs were more favorable than placebo (RR=0.39, 95%CI: 0.13-0.99). Based on the surface under the cumulative ranking curve (SUCRA) value, corticosteroids (0.86) were the best anti-inflammatory agent for MDD patients in terms of efficacy, but the head-to-head comparisons for the efficacy of glucocorticoids and other agents were not statistically significant. As for acceptability, NSAIDs (0.81) were much better than other anti-inflammatory agents. Besides, NAC (0.80) was the best anti-inflammatory agent in the terms of remission. Conclusions: In summary, we found that corticosteroids were more superior than other agents in terms of efficacy according to the SUCRA value. However, this result must be interpreted with caution because the head-to-head comparisons for the efficacy of glucocorticoids and other agents did not reach statistical significance. NSAIDs were recommended for acceptability and NAC for remission rate.
Keywords: acceptability; anti-inflammatory; efficacy; major depressive disorder; network meta-analysis.
Copyright © 2021 Hang, Zhang, Li, Li, Zhang, Ye, Tang and Sun.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Figures
Similar articles
-
Comparative efficacy, acceptability, and tolerability of adjunctive anti-inflammatory agents on bipolar disorder: A systemic review and network meta-analysis.Asian J Psychiatr. 2023 Feb;80:103394. doi: 10.1016/j.ajp.2022.103394. Epub 2022 Dec 5. Asian J Psychiatr. 2023. PMID: 36525766 Review.
-
Efficacy of anti-inflammatory treatment on major depressive disorder or depressive symptoms: meta-analysis of clinical trials.Acta Psychiatr Scand. 2019 May;139(5):404-419. doi: 10.1111/acps.13016. Epub 2019 Mar 28. Acta Psychiatr Scand. 2019. PMID: 30834514
-
Comparative efficacy and acceptability of 21 antidepressant drugs for the acute treatment of adults with major depressive disorder: a systematic review and network meta-analysis.Lancet. 2018 Apr 7;391(10128):1357-1366. doi: 10.1016/S0140-6736(17)32802-7. Epub 2018 Feb 21. Lancet. 2018. PMID: 29477251 Free PMC article. Review.
-
TNF-alpha inhibitors for ankylosing spondylitis.Cochrane Database Syst Rev. 2015 Apr 18;(4):CD005468. doi: 10.1002/14651858.CD005468.pub2. Cochrane Database Syst Rev. 2015. PMID: 25887212 Review.
-
Nonsteroidal anti-inflammatory drugs (NSAIDs) and non-opioids for acute renal colic.Cochrane Database Syst Rev. 2015 Jun 29;(6):CD006027. doi: 10.1002/14651858.CD006027.pub2. Cochrane Database Syst Rev. 2015. PMID: 26120804 Review.
Cited by
-
Exploring the Roles of Vitamins C and D and Etifoxine in Combination with Citalopram in Depression/Anxiety Model: A Focus on ICAM-1, SIRT1 and Nitric Oxide.Int J Mol Sci. 2024 Feb 6;25(4):1960. doi: 10.3390/ijms25041960. Int J Mol Sci. 2024. PMID: 38396638 Free PMC article.
-
Chronic Treatment with Nigella sativa Oil Exerts Antimanic Properties and Reduces Brain Inflammation in Rats.Int J Mol Sci. 2024 Feb 2;25(3):1823. doi: 10.3390/ijms25031823. Int J Mol Sci. 2024. PMID: 38339101 Free PMC article.
-
The pharmacological bases for repurposing statins in depression: a review of mechanistic studies.Transl Psychiatry. 2023 Jul 12;13(1):253. doi: 10.1038/s41398-023-02533-z. Transl Psychiatry. 2023. PMID: 37438361 Free PMC article. Review.
-
Celecoxib for Mood Disorders: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.J Clin Med. 2023 May 16;12(10):3497. doi: 10.3390/jcm12103497. J Clin Med. 2023. PMID: 37240605 Free PMC article. Review.
-
Nanomedicines: intervention in inflammatory pathways of cancer.Inflammopharmacology. 2023 Jun;31(3):1199-1221. doi: 10.1007/s10787-023-01217-w. Epub 2023 Apr 15. Inflammopharmacology. 2023. PMID: 37060398 Free PMC article. Review.
References
-
- Abbasi S. H., Hosseini F., Modabbernia A., Ashrafi M., Akhondzadeh S. (2012). Effect of Celecoxib Add-On Treatment on Symptoms and Serum IL-6 Concentrations in Patients with Major Depressive Disorder: Randomized Double-Blind Placebo-Controlled Study. J. Affect Disord., 141(null), 308–314. 10.1016/j.jad.2012.03.033 - DOI - PubMed
LinkOut - more resources
Full Text Sources
Research Materials
