Empagliflozin Ameliorates the Oxidative Stress Profile in Type 2 Diabetic Patients with Heart Failure and Reduced Ejection Fraction: Results of a Randomized, Double-blind, Placebo-controlled Study.

IF 1.4 Q4 PHARMACOLOGY & PHARMACY
Azadeh Eshraghi, Somayeh Khalesi, Kiumarth Amini, Fahmi Hassan Salleh, Mahdis Sharifikia, Minoo Sadat Hajmiri, Maryam Zamanirafe, Amirhossein Yazdi, Maryam Mehrpooya
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引用次数: 0

Abstract

Introduction: In the present study, we evaluated the impact of empagliflozin on serum levels of oxidative stress parameters in individuals with type 2 diabetes (T2DM) who also suffer from heart failure with Reduced Ejection Fraction (HFrEF).

Methods: In this prospective, single-center clinical trial, 80 patients with T2DM and HFrEF, stabilized on guideline-directed heart failure therapy and classified as New York Heart Association functional (NYHA) functional classes II or III, were randomized to receive either empagliflozin (10 mg/daily) or a matching placebo for a duration of 12 weeks. Serum levels of malondialdehyde (MDA), along with the activity of superoxide dismutase (SOD) and glutathione peroxidase (GPx), were measured at baseline and after the 12-week treatment period.

Results: The baseline demographic and clinical characteristics of the randomized patients were comparable across the study groups. As anticipated, empagliflozin demonstrated a significant reduction in fasting blood glucose (FBG) and glycated hemoglobin (HbA1c) compared to the placebo after 12 weeks of treatment. Additionally, in comparison to the placebo, empagliflozin significantly increased the antioxidant capacity by elevating serum activity of SOD and GPx, while reducing oxidative damage, as evidenced by diminished MDA levels. Empagliflozin-treated patients also experienced greater improvement in their NYHA functional classes by week 12, though no significant changes in Left Ventricular Ejection Fraction (LVEF) were observed.

Conclusion: The findings of this study shed light on the potential mechanisms through which SGLT2 inhibitors exert their beneficial effects on clinical outcomes in diabetic patients with HFrEF. This provides compelling evidence supporting the cardio-protective of SGLT2 inhibitors in this patient population.

Clinical trial registration number: The trial was registered at the Iranian Registry of Clinical Trials (https://irct.behdasht.gov.ir/trial/72825, identifier code: IRCT20120215009014N484). Registration date: 2022-09-30.

恩格列净改善2型糖尿病心力衰竭和射血分数降低患者的氧化应激状况:一项随机、双盲、安慰剂对照研究的结果
在本研究中,我们评估了恩格列净对伴有心力衰竭并射血分数降低(HFrEF)的2型糖尿病(T2DM)患者血清氧化应激参数水平的影响。方法:在这项前瞻性的单中心临床试验中,80例T2DM和HFrEF患者,在指南指导的心力衰竭治疗中稳定,被划分为纽约心脏协会功能(NYHA) II级或III级,随机接受恩帕列嗪(10mg /天)或匹配的安慰剂,持续12周。在基线和12周治疗期后测定血清丙二醛(MDA)水平、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx)活性。结果:随机分组患者的基线人口学和临床特征在各研究组之间具有可比性。正如预期的那样,经过12周的治疗,与安慰剂相比,恩格列净显示出空腹血糖(FBG)和糖化血红蛋白(HbA1c)的显著降低。此外,与安慰剂相比,恩格列净通过提高血清SOD和GPx的活性显著提高抗氧化能力,同时减少氧化损伤,MDA水平降低。恩帕列净治疗的患者在第12周的NYHA功能等级也有更大的改善,尽管左心室射血分数(LVEF)没有明显变化。结论:本研究的发现揭示了SGLT2抑制剂对糖尿病合并HFrEF患者的临床结果发挥有益作用的潜在机制。这提供了令人信服的证据,支持SGLT2抑制剂在该患者群体中的心脏保护作用。临床试验注册号:该试验在伊朗临床试验注册中心注册(https://irct.behdasht.gov.ir/trial/72825,识别码:IRCT20120215009014N484)。报名日期:2022-09-30。
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
Reviews on recent clinical trials
Reviews on recent clinical trials PHARMACOLOGY & PHARMACY-
CiteScore
3.10
自引率
5.30%
发文量
44
期刊介绍: Reviews on Recent Clinical Trials publishes frontier reviews on recent clinical trials of major importance. The journal"s aim is to publish the highest quality review articles in the field. Topics covered include: important Phase I – IV clinical trial studies, clinical investigations at all stages of development and therapeutics. The journal is essential reading for all researchers and clinicians involved in drug therapy and clinical trials.
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