Effect of adding fenofibrate versus curcumin to glimepiride in patients with type 2 diabetes: a randomized controlled trial.

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Eman M Nada, Nashwa M El-Gharbawy, Haidy Abbas, Rehab H Werida
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引用次数: 0

Abstract

Background: Type 2 diabetes is a recognized risk factor for the development of cardiovascular disease. Fenofibrate and curcumin were found to be effective in improving hyperlipidemia in patients with diabetes. This study aimed to evaluate the effect of adding fenofibrate versus curcumin on weight, glycemic status, lipids profile, high-sensitivity C-reactive protein (hs-CRP), fetuin-A, and sirtuin 1 in patients with type 2 diabetes treated with glimepiride.

Method: In a double-blind, randomized control trial, 60 patients with type 2 diabetes mellitus were randomly assigned into three groups: Group I was given placebo; Group II curcumin 1100 mg; Group III fenofibrate 160 mg (each administered orally once daily) to ongoing glimepiride 4 mg therapy administered orally once daily for three months. Inclusion criteria were as follows: patients aged 35-70 years, those with uncontrolled type 2 diabetes, hyperlipidemia, and those treated with glimepiride 4 mg. Exclusion criteria were as follows: other types of diabetes, pregnancy, abnormal liver or kidney function tests, using other anti-diabetes medications, and non-adherence to medications. At baseline and after three months of intervention, anthropometric measurements were measured, and blood samples were collected for biochemical analysis of blood glucose, glycated hemoglobin (HbA1c), lipid profile, hs-CRP, fetuin-A, and sirtuin 1. Paired t-test and one-way ANOVA were used for normally distributed data. However, the Wilcoxon signed-rank and the Kruskal-Wallis tests were used to analyze non-normally distributed data.

Results: Three months after the intervention, when the three groups were compared, no significant differences were found regarding weight, body mass index, fasting blood glucose, two-hour postprandial glucose (2 h-PPG), and HbA1c (p > 0.05). Compared to placebo, significant decreases were observed in total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), non-high-density lipoprotein cholesterol (non-HDL-C), very-low-density lipoprotein cholesterol (VLDL-C), coronary risk index (CRI), atherogenic index (AI), and hs-CRP and increasing sirtuin 1 in the fenofibrate (p < 0.001) and curcumin (p < 0.05) groups. High-density lipoprotein cholesterol (HDL-C) levels in the fenofibrate group were found to be significantly higher than in the placebo group (p < 0.001). Furthermore, when compared to curcumin, fenofibrate significantly reduced waist circumferences and fetuin-A and increased sirtuin 1 (p < 0.05).

Conclusion: Both fenofibrate and curcumin are effective at decreasing lipid profiles and improving inflammatory markers in patients with type 2 diabetes. Fenofibrate might have a superior effect in reducing waist circumference, decreasing fetuin-A, and increasing sirtuin 1.

Trial registration: This trial was registered (August 27, 2020) on clinical trial.gov with an identification code NCT04528212. https://www.

Clinicaltrials: gov/study/NCT04528212 .

在格列美脲中加入非诺贝特与姜黄素对2型糖尿病患者的影响:一项随机对照试验。
背景:2型糖尿病是公认的心血管疾病发展的危险因素。发现非诺贝特和姜黄素对改善糖尿病患者的高脂血症有效。本研究旨在评估非诺贝特与姜黄素对格列美脲治疗2型糖尿病患者体重、血糖状态、血脂、高敏c反应蛋白(hs-CRP)、胎儿蛋白a和sirtuin 1的影响。方法:采用双盲、随机对照试验,将60例2型糖尿病患者随机分为3组:1组给予安慰剂;II组姜黄素1100毫克;III组非诺贝特160毫克(每天口服一次)到持续的格列美脲4毫克治疗,每天口服一次,持续三个月。纳入标准如下:年龄35-70岁、2型糖尿病、高脂血症未控制、格列美脲4mg治疗的患者。排除标准如下:其他类型糖尿病、妊娠、肝肾功能检查异常、使用其他抗糖尿病药物、不遵医嘱。在基线和干预3个月后,测量人体测量值,并采集血样进行血糖、糖化血红蛋白(HbA1c)、血脂、hs-CRP、胎蛋白a和sirtuin 1的生化分析。正态分布数据采用配对t检验和单因素方差分析。然而,使用Wilcoxon有符号秩检验和Kruskal-Wallis检验来分析非正态分布的数据。结果:干预3个月后,三组比较体重、体质指数、空腹血糖、餐后2小时血糖(2 h-PPG)、糖化血红蛋白(HbA1c)均无显著差异(p < 0.05)。与安慰剂相比,非诺贝特组总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)、非高密度脂蛋白胆固醇(non-HDL-C)、极低密度脂蛋白胆固醇(VLDL-C)、冠状动脉危险指数(CRI)、动脉粥样硬化指数(AI)、hs-CRP显著降低,sirtuin 1升高(p)。非诺贝特和姜黄素都能有效降低2型糖尿病患者的脂质谱和改善炎症标志物。非诺贝特在减小腰围、降低胎儿素a和增加sirtuin 1方面可能有较好的效果。试验注册:该试验于2020年8月27日在clinical Trial .gov上注册,识别码为NCT04528212。https://www.Clinicaltrials: gov/study/NCT04528212。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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