The effects of silymarin consumption on inflammation and oxidative stress in adults: a systematic review and meta-analysis

Background Owing to the rich phytochemical content of Silymarin, it may effectively manage inflammation and oxidative stress. We, therefore, aimed to examine the existing evidence on the effect of Silymarin consumption on inflammation and oxidative stress factors by conducting a systematic review an...

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Veröffentlicht in:Inflammopharmacology 2024-04, Vol.32 (2), p.949-963
Hauptverfasser: Bahari, Hossein, Shahraki Jazinaki, Mostafa, Rashidmayvan, Mohammad, Taheri, Shaghayegh, Amini, Mohammad Reza, Malekahmadi, Mahsa
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Sprache:eng
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Zusammenfassung:Background Owing to the rich phytochemical content of Silymarin, it may effectively manage inflammation and oxidative stress. We, therefore, aimed to examine the existing evidence on the effect of Silymarin consumption on inflammation and oxidative stress factors by conducting a systematic review and meta-analysis of randomized controlled trials. Methods A systematic literature search up to September 2023 was completed in PubMed/Medline, Scopus, and Web of Science, to identify eligible RCTs. Heterogeneity tests of the selected trials were performed using the I 2 statistic. Random effects models were assessed based on the heterogeneity tests, and pooled data were determined as weighted mean differences with a 95% confidence interval. Results Fifteen RCTs were included in this meta-analysis. Our findings showed that Silymarin consumption significantly decreased CRP (WMD, − 0.50 mg/L; 95% CI, (− 0.95 to − 0.04); p  = 0.03), MDA (WMD, − 1.19 nmol/mL; 95% CI, (− 1.99 to − 0.38); p  = 0.004), and IL-6 (WMD, − 0.44 pg/ml; 95% CI, (− 0.75 to − 0.12); p  = 0.006). Silymarin consumption had no significant effects on IL-10, TAC, and GSH. A significant non-linear relationship was observed between the duration of the intervention and MDA changes. Conclusions Silymarin can help reduce inflammation in patients with diabetes and thalassemia by reducing MDA as an oxidative stress marker and CRP and IL-6 as inflammatory markers.
ISSN:0925-4692
1568-5608
DOI:10.1007/s10787-023-01423-6