绿咖啡对肥胖者体内 miR-133a、miR-155 和炎症生物标志物的影响

IF 3.4 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM Diabetology & Metabolic Syndrome Pub Date : 2024-10-28 DOI:10.1186/s13098-024-01478-7
Naglaa F Khedr, Enas S Zahran, Abla M Ebeid, Samuel T Melek, Rehab H Werida
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引用次数: 0

摘要

目的:代谢综合征是增加动脉粥样硬化性心血管疾病风险的一组病症。本研究是一项随机、双盲、安慰剂对照研究,旨在通过分析 miRNA-155、miRNA-133a 和炎症生物标志物,如抵抗素、TNF-α、总硅酸、同型半胱氨酸、高敏 C 反应蛋白(hs-CRP)以及抗炎细胞因子--脂肪连通素,确定绿咖啡(GC)对代谢综合征肥胖患者的影响:166 名肥胖症患者每天随机服用 GC 胶囊(800 毫克)或安慰剂,为期 6 个月。两组患者均被建议均衡饮食。在基线和补充剂服用 6 个月后采集血液样本:与安慰剂相比,连续 6 个月补充 GC 可降低体重指数(p = 0.002)、腰围(p = 0.038)、血糖(p = 0.002)、HbA1c%(p = 0.000)、胰岛素(p = 0.000)、收缩压(p = 0.005)和舒张压(p = 0.001)。与安慰剂组相比,GC 能明显降低总胆固醇(TC,p = 0.000)、低密度脂蛋白胆固醇(LDL-C,p = 0.001)、甘油三酯(TG,p = 0.002),增加高密度脂蛋白胆固醇(HDL-C,p = 0.008)。此外,与安慰剂组相比,GC 能明显(p ≤ 0.005)减少总硅酸、同型半胱氨酸、抵抗素、TNF-α、hs-CRP 和氧化应激标志物丙二醛(MDA),但能增加血清脂肪连蛋白(p = 0.000)。与基线水平和对照安慰剂组相比(p = 0.001),6 个月后 GC 组 miR-133a 的基因表达明显减少(p = 0.000):结论:服用 GC 可降低构成心血管疾病风险因素的 BMI、高血压、血糖、血脂异常、miRNA-133a 和炎症生物标志物,从而调节代谢综合征。
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Effect of green coffee on miR-133a, miR-155 and inflammatory biomarkers in obese individuals.

Objectives: Metabolic syndrome is a cluster of conditions that increases the risk of atherosclerotic cardiovascular diseases. The current study was a randomized, double blind, placebo-controlled study that aimed to determine the impact of green coffee (GC) in obese patients with metabolic syndrome through analysis of miRNA-155, miRNA-133a and the inflammatory biomarkers such as resistin, TNF-α, total sialic acid, homocysteine, high sensitivity C-reactive protein (hs-CRP), and the anti-inflammatory cytokine, adiponectin.

Methods: One hundred-sixty obese patients were randomly supplemented either with GC capsules (800 mg) or placebo daily for six months. Both groups were advised to take a balanced diet. Blood samples were collected at baseline and after six months of supplementation.

Results: GC supplementation for 6 months reduced BMI (p = 0.002), waist circumference (p = 0.038), blood glucose (p = 0.002), HbA1c% (p = 0.000), Insulin (p = 0.000), systolic blood pressure (p = 0.005), diastolic BP (p = 0.001) compared with placebo. GC significantly decreased total cholesterol (TC, p = 0.000), LDL-C (p = 0.001), triglycerides (TG, p = 0.002) and increased HDL-C (p = 0.008) compared with placebo group. In addition, GC significantly (p ≤ 0.005) reduced total sialic acid, homocysteine, resistin, TNF-α, hs-CRP and the oxidative stress marker malondialdehyde (MDA), but increased serum adiponectin (p = 0.000) compared to placebo group. There was a significant reduction in the gene expression of miR-133a (p = 0.000) in GC group as compared with baseline levels and with the control placebo group (p = 0.001) after 6 months.

Conclusion: GC administration modulated metabolic syndrome by decreasing BMI, high BP, blood glucose, dyslipidemia, miRNA-133a and inflammatory biomarkers that constitute risk factors for cardiovascular diseases.

Clinicaltrials: gov registration No. is NCT05688917.

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来源期刊
Diabetology & Metabolic Syndrome
Diabetology & Metabolic Syndrome ENDOCRINOLOGY & METABOLISM-
CiteScore
6.20
自引率
0.00%
发文量
170
审稿时长
7.5 months
期刊介绍: Diabetology & Metabolic Syndrome publishes articles on all aspects of the pathophysiology of diabetes and metabolic syndrome. By publishing original material exploring any area of laboratory, animal or clinical research into diabetes and metabolic syndrome, the journal offers a high-visibility forum for new insights and discussions into the issues of importance to the relevant community.
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