Molecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Cardiovascular Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Inflammopharmacology. 2023 Oct;31(5):2421-2430. doi: 10.1007/s10787-023-01328-4. Epub 2023 Sep 4.
To evaluate the effect of oral magnesium sulfate (MgSO) on the gene expression and serum levels of inflammatory cytokines including TNF-α, IL-18, IL-1β, IL-6, and IFN-γ in patients with moderate coronary artery disease (CAD).
60 CAD patients were selected based on angiography findings and were randomly divided into two groups that received 300 mg/day MgSO (n = 30) or placebo (n = 30) for 3 months. Gene expression and serum levels of inflammatory cytokines were assessed.
After 3 months of intervention, gene expression and serum levels of IL-18 and TNF-α in the MgSOgroup were significantly less than the placebo group (P < 0.05). However, no significant difference in gene expression and serum levels of IL-1β, IL-6, and IFN-γ was observed between the two groups (P > 0.05). In addition, within group analysis demonstrate that Mg-treatment significantly decrease serum level of TNF-α and IL-18 as compared to pretreatment.
The results of our study demonstrate that 3-month magnesium sulfate administration (300 mg/day) to CAD patients could significantly decrease serum concentration and gene expression levels of IL-18 and TNF-α. Our findings support the potential beneficial effect of magnesium supplementation on alleviating CAD complications through modulating inflammatory cytokines.
评估口服硫酸镁(MgSO)对中度冠状动脉疾病(CAD)患者的基因表达和血清炎症细胞因子水平(包括 TNF-α、IL-18、IL-1β、IL-6 和 IFN-γ)的影响。
根据血管造影结果选择 60 名 CAD 患者,并将其随机分为两组,分别给予 300mg/天 MgSO(n = 30)或安慰剂(n = 30),为期 3 个月。评估基因表达和血清炎症细胞因子水平。
干预 3 个月后,MgSO 组的 IL-18 和 TNF-α 的基因表达和血清水平明显低于安慰剂组(P < 0.05)。然而,两组间的 IL-1β、IL-6 和 IFN-γ 的基因表达和血清水平无显著差异(P > 0.05)。此外,组内分析表明,与治疗前相比,Mg 治疗可显著降低 TNF-α 和 IL-18 的血清水平。
我们的研究结果表明,3 个月的 MgSO(300mg/天)治疗 CAD 患者可显著降低血清中 IL-18 和 TNF-α 的浓度和基因表达水平。我们的研究结果支持镁补充剂通过调节炎症细胞因子减轻 CAD 并发症的潜在有益作用。