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Sertraline as an Antidepressant and Inflammatory Cytokines in Depressive Disorders: A Systematic Review and Meta-Analysis of Randomized Double-Blind Placebo-Controlled Trials

Journal
Medical sciences (Basel, Switzerland) (Q1)
Published
6 August 2026
Study design
Systematic review / meta-analysis of RCTs
Evidence level
Level 1, High (CEBM 1a)
Authors
Rafaela F Rossetto, Julia S Pissocaro, Davi A Cavalheri, Rodrigo D Raimundo, Sandra Maria Barbalho, Andrey A Porto, et al.
PMID
42646594
DOI
10.3390/medsci14040460

Why clinicians should know about it

  • Picked for Biochemistry (medical) (top studies of the week, 30 August 2026): Sertraline effect on inflammatory cytokines meta‑analysis

Abstract

Background: Sertraline, a selective serotonin reuptake inhibitor widely prescribed for depressive disorders, has been proposed to exert immunomodulatory effects through modulation of inflammatory pathways; however, clinical evidence regarding its effects on circulating cytokines remains inconsistent. This systematic review and meta-analysis evaluated the effects of sertraline on inflammatory cytokines in adults. Methods: Searches were conducted in LILACS, CINAHL, MEDLINE/PubMed, Cochrane Library, Scopus, and Web of Science to identify randomized single- or double-blind placebo-controlled trials assessing sertraline and inflammatory biomarkers. Ten studies met the eligibility criteria. Random-effects meta-analyses were performed for interleukin-6 (IL-6), interleukin-10 (IL-10), and tumor necrosis factor-α (TNF-α). Results: Sertraline did not significantly reduce circulating IL-6 (MD -1.06, 95% CI -2.32 to 0.19; I2 = 86%; p = 0.10), IL-10 (MD < 0.01, 95% CI -0.23 to 0.23; I2 = 72%; p = 0.98), or TNF-α levels (MD -0.84, 95% CI -4.04 to 2.37; I2 = 72%; p = 0.61). Heterogeneity was substantial, all studies showed high overall risk of bias, and the certainty of evidence was very low for all outcomes. Conclusions: Current evidence does not support a significant or reliable anti-inflammatory effect of sertraline on circulating cytokines, and further well-designed trials using standardized inflammatory assessments are warranted.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.