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The Effect of a Persian Herbal Medicine Compound on the Lipid Profiles of Patients with Dyslipidemia: A Randomized Double-Blind Placebo-Controlled Clinical Trial

机译:波斯草药化合物对血脂血症患者脂质谱的影响:随机双盲安慰剂对照临床试验

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Introduction . It has been well established in the world that lipid disorders promote the development of atherosclerosis and its clinical consequences. This study aimed to assess the impacts of a Persian medicinal (PM) compound on lipid profile. Materials and Methods . From June 21 to October 21, 2020, a randomized double-blind controlled clinical trial was conducted with 74 dyslipidemic patients, who were randomly divided into two equally populated groups: one prescribed with a Persian medicinal herbal compound ( n ?=?37) and a placebo group ( n ?=?37). A Persian herbal medicine including fenugreek, sumac, and purslane is introduced. Biochemical parameters including 12-hour fasting serum levels of total cholesterol, low-density lipoprotein (LDL), high-density lipoprotein (HDL), very-low-density lipoprotein (VLDL), and triglyceride (TG) were measured before the initiation and after the completion of study protocol. Results . Percent changes of biochemical parameters include the following: intervention group?=?cholesterol: 35.22, Tg: 45.91, LDL: 24.81, HDL: 2.05, VLDL: 8.94 and placebo group?=?cholesterol: 6.94, Tg: ?7.3, LDL: 7.37, HDL: 2.88, VLDL: ?0.14. The serum levels of total cholesterol ( ) and LDL ( ) significantly decreased and no increase was recorded in HDL ( ) levels over time in the intervention group. Furthermore, between-group analysis showed a statistically significant difference between the intervention and placebo groups in this regard. VLDL ( ) and TG ( ) levels also decreased, however not significantly. Conclusion . This study showed that a Persian medicinal herbal compound could be safe and beneficial to decrease the levels of serum cholesterol and LDL in dyslipidemic patients. However, larger long-term studies are recommended to clarify this effect.
机译:介绍 。它在世界范围内已经成熟,脂质疾病促进动脉粥样硬化的发展及其临床后果。本研究旨在评估波斯药物(PM)化合物对脂质谱的影响。材料和方法 。从6月21日至10月21日,随机分为74例随机分为两种平等人群的患者:用波斯药草化合物(n?= 37)和安慰剂组(n?=?37)。介绍了一个波斯草药,包括葫芦巴,舒适和追踪。在起始之前测量,在发起之前测量包括总胆固醇,低密度脂蛋白(LDL),高密度脂蛋白(LDL),非常低密度脂蛋白(VLDL),非常低密度脂蛋白(VLDL)和甘油三酯(TG)的12小时禁食血清水平的生物化学参数。研究协议完成后。结果 。生化参数的百分比包括以下内容:干预组?=?胆固醇:35.22,Tg:45.91,LDL:24.81,HDL:2.05,VLDL:8.94和安慰剂组?=胆固醇:6.94,TG:?7.3,LDL: 7.37,HDL:2.88,VLDL:?0.14。总胆固醇()和LDL()的血清水平显着降低,在干预组中,在HDL()水平中没有增加。此外,组分析在这方面的干预和安慰剂组之间显示了统计学上的差异。 VLDL()和TG()水平也降低,但没有显着。结论 。这项研究表明,波斯药草化合物可以安全且有益,可降低血液血清患者的血清胆固醇和LDL的水平。但是,建议更大的长期研究来澄清这种效果。

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