二甲双胍对非糖尿病性心力衰竭患者氧化应激和左心室几何结构的影响:一项随机对照试验。

IF 1.3 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Metabolic syndrome and related disorders Pub Date : 2024-02-01 Epub Date: 2023-10-10 DOI:10.1089/met.2023.0164
Ahmed M Kamel, Batool Ismail, Gamal Abdel Hafiz, Nirmeen Sabry, Samar Farid
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引用次数: 0

摘要

引言:人们对二甲双胍在心血管疾病中的应用及其潜在的新作用越来越感兴趣。只有两项随机对照试验研究了二甲双胍对非糖尿病性心力衰竭(HF)患者的影响。然而,这些研究都没有评估二甲双胍在减少氧化应激中的作用。我们假设二甲双胍可能改善射血分数降低的非糖尿病HF患者的氧化应激和左心室重构。方法和方法:70例HFrEF患者(EF 37% ± 8%;中位年龄66岁)随机接受二甲双胍治疗(n = 35)或HF(n)的护理标准(SOC) = 35)治疗6个月。结果包括总抗氧化能力(TAC)和丙二醛(MDA)的变化(Δ)的差异,这两种变化都是通过色度法评估的,左心室质量指数(LVMI)是通过经胸超声心动图评估的。结果:与SOC相比,二甲双胍治疗增加了TAC[Δ = 0.12 mmol/L,置信区间(95%CI):0.03-0.21;P = 0.007]。TAC仅在二甲双胍组中显著增加(0.90 ± 0.08 基线时mmol/L与1.04 ± 0.99 6个月时mmol/L,P 2、95%可信区间:-42.91~-4.92;P = 0.014)和降低的空腹血糖(Δ = -6.16,95%可信区间:-12.31至-0.02,P = 0.047)。调整基线值后,结果没有变化。MDA左心室射血分数(LVEF)和血压的变化在各组之间没有显著差异。结论:与SOC相比,二甲双胍治疗LVEF降低的HF患者可改善TAC,防止LVMI增加。二甲双胍的这些作用值得在无糖尿病的HF患者中进行进一步研究,以探索二甲双胍的潜在益处。试验注册号:本方案在ClinicalTrials.gov上注册,编号为NCT05177588。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Metformin on Oxidative Stress and Left Ventricular Geometry in Nondiabetic Heart Failure Patients: A Randomized Controlled Trial.

Introduction: There is an increasing interest in using metformin in cardiovascular diseases and its potential new roles. Only two randomized controlled trials investigated the effect of metformin in nondiabetic heart failure (HF) patients. However, none of these studies assess the role of metformin in reducing oxidative stress. We hypothesized that metformin might improve oxidative stress and left ventricular remodeling in nondiabetic HF patients with reduced ejection fraction (HFrEF). Methods and Methods: Seventy HFrEF patients (EF 37% ± 8%; median age 66 years) were randomized to metformin (n = 35) or standard of care (SOC) for HF (n = 35) for 6 months in addition to standard therapy. Outcomes included the difference in the change (Δ) in total antioxidant capacity (TAC) and malondialdehyde (MDA), both assessed colorimetrically and left ventricular mass index (LVMI) assessed through transthoracic echocardiography. Results: Compared with the SOC, metformin treatment increased TAC [Δ = 0.12 mmol/L, confidence intervals (95% CIs): 0.03-0.21; P = 0.007]. TAC increased significantly only in the metformin group (0.90 ± 0.08 mmol/L at baseline vs. 1.04 ± 0.99 mmol/L at 6 months, P < 0.05). Metformin therapy preserved LVMI (Δ = -23 g/m2, 95% CI: -42.91 to -4.92; P = 0.014) and reduced fasting plasma glucose (Δ = -6.16, 95% CI: -12.31 to -0.02, P = 0.047) compared with the SOC. Results did not change after adjusting for baseline values. Changes in MDA left ventricular ejection fraction (LVEF) and blood pressure were not significantly different between groups. Conclusion: Metformin treatment in HF patients with reduced LVEF improved TAC and prevented the increase in LVMI compared with the SOC. These effects of metformin warrant further research in HF patients without diabetes to explore the potential benefits of metformin. Trial Registration Number: This protocol was registered in ClinicalTrials.gov under the number NCT05177588.

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来源期刊
Metabolic syndrome and related disorders
Metabolic syndrome and related disorders MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.40
自引率
0.00%
发文量
74
审稿时长
6-12 weeks
期刊介绍: Metabolic Syndrome and Related Disorders is the only peer-reviewed journal focusing solely on the pathophysiology, recognition, and treatment of this major health condition. The Journal meets the imperative for comprehensive research, data, and commentary on metabolic disorder as a suspected precursor to a wide range of diseases, including type 2 diabetes, cardiovascular disease, stroke, cancer, polycystic ovary syndrome, gout, and asthma. Metabolic Syndrome and Related Disorders coverage includes: -Insulin resistance- Central obesity- Glucose intolerance- Dyslipidemia with elevated triglycerides- Low HDL-cholesterol- Microalbuminuria- Predominance of small dense LDL-cholesterol particles- Hypertension- Endothelial dysfunction- Oxidative stress- Inflammation- Related disorders of polycystic ovarian syndrome, fatty liver disease (NASH), and gout
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