Mohammadi, Shooka and Asbaghi, Omid and Afrisham, Reza and Farrokhi, Vida and Jadidi, Yasaman and Mofidi, Fatemeh and Ashtary-Larky, Damoon (2024) Impacts of Supplementation with Silymarin on Cardiovascular Risk Factors: A Systematic Review and Dose-Response Meta-Analysis. Antioxidants, 13 (4). p. 390. ISSN 2076-3921, DOI https://doi.org/10.3390/antiox13040390.
Full text not available from this repository.Abstract
It has been suggested that silymarin (SIL) supplementation has positive effects on cardiovascular health and reduces the risk of cardiometabolic syndrome (CMS). This systematic review and dose-response meta-analysis assessed the impacts of SIL administration on cardiovascular risk factors. A systematic search of multiple databases was performed to identify eligible controlled trials published up to January 2023. The analysis used a random-effects model and included 33 trials with 1943 participants. It was revealed that SIL supplementation led to a notable reduction in serum levels of fasting blood glucose (FBG) (weighted mean difference (WMD): -21.68 mg/dL, 95% CI: -31.37, -11.99; p < 0.001), diastolic blood pressure (DBP) (WMD: -1.25 mmHg; 95% CI: -2.25, -0.26; p = 0.013), total cholesterol (TC) (WMD: -13.97 mg/dL, 95% CI: -23.09, -4.85; p = 0.003), triglycerides (TG) (WMD: -26.22 mg/dL, 95% CI: -40.32, -12.12; p < 0.001), fasting insulin (WMD: -3.76 mU/mL, 95% CI: -4.80, -2.72; p < 0.001), low-density lipoprotein (LDL) (WMD: -17.13 mg/dL, 95% CI: -25.63, -8.63; p < 0.001), and hemoglobin A1C (HbA1c) (WMD: -0.85%, 95% CI: -1.27, -0.43; p < 0.001) in the SIL-treated groups compared to their untreated counterparts. In addition, there were no substantial differences in body mass index (BMI), systolic blood pressure (SBP), C-reactive protein (CRP), body weight, and high-density lipoprotein (HDL) between the two groups. These outcomes suggest that SIL consumption reduces certain CMS risk factors and has favorable impacts on lipid and glycemic profiles with potential hypotensive effects. These findings should be supported by additional trials with larger sample sizes and longer durations.
Item Type: | Article |
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Funders: | UNSPECIFIED |
Uncontrolled Keywords: | silymarin; cardiometabolic syndrome (CMS); blood pressure (BP); glycemic parameters; lipid profile |
Subjects: | R Medicine |
Divisions: | Faculty of Medicine > Social & Preventive Medicine |
Depositing User: | Ms. Juhaida Abd Rahim |
Date Deposited: | 15 Oct 2024 02:16 |
Last Modified: | 15 Oct 2024 02:16 |
URI: | http://eprints.um.edu.my/id/eprint/45370 |
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