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Published on: September 15, 2017
Effect of resveratrol on inflammatory cytokines: A meta-analysis of randomized controlled trials
Melodi Omraninava1, Bahman Razi2, Saeed Aslani3
1Department of Infectious Disease, Faculty of Medical Sciences, Sari Branch, Islamic Azad University, Sari, Iran.
Abstract:
The aim of the current study was to perform a meta-analysis of randomized clinical trials regarding the effect of resveratrol in decreasing the levels of inflammatory cytokines, including interleukin (IL)-1, IL-6, IL-8, and tumor necrosis factor (TNF)-α in a combination of inflammatory diseases. Literature search was carried out in Scopus, ISI web of science, Medline, and Cochrane Library databases by up to September 2020. The pooled effect size was determined through measuring the weighted mean differences (WMD) and their corresponding 95% confidence intervals (CI) for the difference between the resveratrol-receiving and control groups. Finally, 33 publications, including 3 studies on IL-1, 26 studies on IL-6, 4 studies on IL-8, and 21 studies on TNF-α met our final inclusion criteria and included in the quantitative analysis. Analysis in the overall population showed a significant effect of resveratrol consumption in reducing serum TNF-α levels (WMD = -0.66 pg/ml, 95% CI = -1.05 to -0.27, P = 0.001). A significant reduction of IL-6 concentration was observed only in the patients receiving ≥500 mg/day dose of resveratrol (WMD = -1.89 pg/ml, 95% CI = -3.73 to -0.05, P = 0.04) with inter-study heterogeneity (I2 = 94.4%, P < 0.001). Nonetheless, no significant alteration was observed in IL-1 (WMD = -0.14 pg/ml, 95% CI = -0.31 to 0.03, P = 0.10) and IL-8 (WMD = 0.18 pg/ml, 95% CI = -1.04 to 1.40, P = 0.73) levels following resveratrol consumption. Based on the present findings, resveratrol is able to decrease TNF-α and IL-6 (in ≥500 mg/day dose) levels but not IL-1 and IL-8 levels.
Insights
Resveratrol effectively reduces levels of tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) in inflammatory conditions, particularly at higher doses. However, it does not significantly impact interleukin-1 (IL-1) or interleukin-8 (IL-8) levels.
Area of Science:
- Biochemistry
- Immunology
- Pharmacology
Background:
- Inflammatory cytokines like IL-1, IL-6, IL-8, and TNF-α play critical roles in various inflammatory diseases.
- Resveratrol, a natural polyphenol, has demonstrated anti-inflammatory properties in preclinical studies.
- Understanding the precise impact of resveratrol on specific inflammatory markers is crucial for therapeutic applications.
Purpose of the Study:
- To conduct a meta-analysis of randomized clinical trials evaluating resveratrol's efficacy in reducing serum levels of IL-1, IL-6, IL-8, and TNF-α.
- To synthesize existing evidence on resveratrol's anti-inflammatory effects across a spectrum of inflammatory conditions.
- To determine the dose-dependent effects of resveratrol on inflammatory cytokine levels.
Main Methods:
- A comprehensive literature search was performed across major scientific databases (Scopus, Web of Science, Medline, Cochrane Library) up to September 2020.
- Meta-analysis of 33 selected randomized clinical trials was conducted using weighted mean differences (WMD) and 95% confidence intervals (CI).
- Quantitative analysis focused on changes in IL-1, IL-6, IL-8, and TNF-α levels between resveratrol and control groups.
Main Results:
- Resveratrol consumption significantly reduced serum TNF-α levels (WMD = -0.66 pg/ml, P = 0.001).
- A significant reduction in IL-6 was observed only with doses of ≥500 mg/day (WMD = -1.89 pg/ml, P = 0.04), with high heterogeneity.
- No significant alterations were found in IL-1 (WMD = -0.14 pg/ml, P = 0.10) or IL-8 (WMD = 0.18 pg/ml, P = 0.73) levels.
Conclusions:
- Resveratrol demonstrates a significant capacity to lower TNF-α levels in patients with inflammatory diseases.
- Higher doses of resveratrol (≥500 mg/day) are associated with a significant reduction in IL-6 levels.
- Resveratrol does not appear to significantly affect IL-1 or IL-8 levels, suggesting a targeted anti-inflammatory action on specific cytokines.
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