Balleza Alejandri Luis Ricardo, Grover Páez Fernando, González Campos Erick, Ramos Becerra Carlos G, Cardona Muñóz Ernesto Germán, Pascoe González Sara, Ramos Zavala María Guadalupe, Reynoso Roa Africa Samantha, Suárez Rico Daniel Osmar, Beltrán Ramírez Alberto, García Galindo Jesús Jonathan, Cardona Müller David, Galán Ruíz Claudia Yanette
Department of Physiology, University Health Sciences Center, Universidad de Guadalajara, Guadalajara 44340, Mexico.
Arterial Stiffness Laboratory, Department of Physiology, Experimental and Clinical Therapeutics Institute, University Health Sciences Center, Universidad de Guadalajara, Guadalajara 44340, Mexico.
J Cardiovasc Dev Dis. 2024 Jun 15;11(6):182. doi: 10.3390/jcdd11060182.
To assess the acute effect of empagliflozin versus dapagliflozin administration on flow-mediated vasodilation in patients with type 2 diabetes mellitus.
A double-blind clinical trial, at the Experimental and Clinical Therapeutics Institute, University Health Sciences Center, at the Universidad de Guadalajara, in inpatients with T2D according to the 2023 ADA criteria.
Thirty patients (15 males and 15 females), aged between 35 and 65 years, were included in this study, according to the 2023 ADA criteria. The eligible patients were randomly assigned to three groups: empagliflozin 25 mg once daily, dapagliflozin 10 mg once daily, or placebo once daily. Anthropometric parameters were taken using validated techniques. FMD was measured using a high-resolution semiautomatic ultrasound UNEX-EF 38G (UNEX Co., Ltd., Nagoya, Japan). Arterial tension was determined with the OMRON electronic digital sphygmomanometer (HEM 907 XL, Kyoto, Japan).
The group of patients who received empagliflozin had a significantly lower baseline flow-mediated dilation (FMD) compared to the group receiving dapagliflozin ( = 0.017); at the end of this study, the empagliflozin group achieved a comparable FMD to the dapagliflozin group ( = 0.88).
After the treatment period, the empagliflozin and dapagliflozin groups achieved similar FMD, suggesting a class effect.
评估恩格列净与达格列净给药对2型糖尿病患者血流介导的血管舒张的急性影响。
一项双盲临床试验,在瓜达拉哈拉大学健康科学中心实验与临床治疗研究所,针对符合2023年美国糖尿病协会(ADA)标准的2型糖尿病住院患者进行。
根据2023年ADA标准,本研究纳入了30名年龄在35至65岁之间的患者(15名男性和15名女性)。符合条件的患者被随机分为三组:恩格列净25毫克每日一次、达格列净10毫克每日一次或安慰剂每日一次。使用经过验证的技术测量人体测量参数。使用高分辨率半自动超声UNEX-EF 38G(日本名古屋UNEX有限公司)测量血流介导的血管舒张(FMD)。用欧姆龙电子数字血压计(日本京都HEM 907 XL)测定动脉血压。
与接受达格列净的组相比,接受恩格列净的患者组基线血流介导的血管舒张(FMD)显著更低(P = 0.017);在本研究结束时,恩格列净组的FMD与达格列净组相当(P = 0.88)。
在治疗期后,恩格列净组和达格列净组的FMD相似,提示有类效应。