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非诺贝特可改善代谢综合征患者的胰岛素抵抗、高血压和新型氧化应激标志物。

Fenofibrate ameliorates insulin resistance, hypertension and novel oxidative stress markers in patients with metabolic syndrome.

机构信息

Division of Neurology, Respirology, Endocrinology and Metabolism, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, 5200, Kiyotake, Miyazaki 889-1692, Japan.

Division of Neurology, Respirology, Endocrinology and Metabolism, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, 5200, Kiyotake, Miyazaki 889-1692, Japan.

出版信息

Obes Res Clin Pract. 2011 Oct-Dec;5(4):e267-360. doi: 10.1016/j.orcp.2011.03.012.

Abstract

OBJECTIVE

The benefits of fenofibrate, a peroxisome proliferator-activated receptor α agonist, against cardiovascular risk factors have been established. To clarify the underlying mechanisms of these benefits, we examined the effects of fenofibrate on insulin resistance, hypertension, inflammation, oxidative stress and coagulation markers in patients with metabolic syndrome.

METHODS

Eleven Japanese patients with metabolic syndrome underwent physical examinations and blood tests before and after treatment with fenofibrate 200 mg daily for 8 weeks.

RESULTS

Fenofibrate significantly decreased systolic blood pressure, pulse wave velocity, serum insulin, insulin resistance (calculated from the homeostasis model assessment), total cholesterol, triglyceride, remnant-like particles cholesterol, uric acid, D-dimer, fibrinogen, serum amyloid A/low-density lipoprotein (LDL) and apoA1/LDL levels. It also significantly increased levels of high molecular weight adiponectin, thrombomodulin and high-density lipoprotein cholesterol in these patients. Plasminogen activator inhibitor-1, C-reactive protein, fasting plasma glucose and thrombin-antithrombin complex levels did not change.

LIMITATION

Small sample size.

CONCLUSION

Short-term fenofibrate administration not only improved lipid profiles, but also ameliorated insulin resistance, hypertension and oxidative stress markers in patients with metabolic syndrome, suggesting that fenofibrate can decrease the risk of arteriosclerosis through various pathways.

摘要

目的

已证实贝特类药物(过氧化物酶体增殖物激活受体α激动剂)可降低心血管风险因素。为阐明这些益处的潜在机制,我们研究了贝特类药物对代谢综合征患者胰岛素抵抗、高血压、炎症、氧化应激和凝血标志物的影响。

方法

11 例日本代谢综合征患者接受贝特 200mg/d 治疗 8 周前后的体格检查和血液检查。

结果

贝特显著降低了收缩压、脉搏波速度、血清胰岛素、胰岛素抵抗(稳态模型评估计算)、总胆固醇、甘油三酯、残粒样颗粒胆固醇、尿酸、D-二聚体、纤维蛋白原、血清淀粉样蛋白 A/低密度脂蛋白(LDL)和载脂蛋白 A1/LDL 水平。还显著增加了这些患者的高分子量脂联素、血栓调节蛋白和高密度脂蛋白胆固醇水平。纤溶酶原激活物抑制剂-1、C 反应蛋白、空腹血糖和凝血酶-抗凝血酶复合物水平没有变化。

局限性

样本量小。

结论

短期贝特类药物治疗不仅改善了血脂谱,还改善了代谢综合征患者的胰岛素抵抗、高血压和氧化应激标志物,提示贝特类药物可通过多种途径降低动脉硬化风险。

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