A randomized controlled trial of metformin on left ventricular hypertrophy in patients with coronary artery disease without diabetes: the MET-REMODEL trial

被引:111
作者
Mohan, Mohapradeep [1 ]
Al-Talabany, Shaween [1 ]
McKinnie, Angela [2 ]
Mordi, Ify R. [1 ]
Singh, Jagdeep S. S. [1 ]
Gandy, Stephen J. [3 ]
Baig, Fatima [1 ]
Hussain, Muhammad S. [1 ]
Bhalraam, U. [1 ]
Khan, Faisel [1 ]
Choy, Anna-Maria [1 ]
Matthew, Shona [1 ]
Houston, John Graeme [1 ]
Struthers, Allan D. [1 ]
George, Jacob [1 ]
Lang, Chim C. [1 ]
机构
[1] Univ Dundee, Ninewells Hosp & Med Sch, Sch Med, Div Mol & Clin Med, Dundee DD1 9SY, Scotland
[2] Ninewells Hosp & Med Sch, NHS Tayside Clin Radiol, Dundee DD1 9SY, Scotland
[3] Ninewells Hosp & Med Sch, Dept Med Phys, NHS Tayside, Dundee DD1 9SY, Scotland
关键词
Coronary artery disease; Left ventricular mass; Metformin; Pre-diabetes; Insulin resistance; Oxidative stress; NONDIABETIC PATIENTS; INSULIN-RESISTANCE; CARDIOVASCULAR-DISEASE; ENDOTHELIAL FUNCTION; OXIDATIVE STRESS; HIGHLY PREVALENT; HEART-DISEASE; REDUCTION; IMPACT; RISK;
D O I
10.1093/eurheartj/ehz203
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim We tested the hypothesis that metformin may regress left ventricular hypertrophy (LVH) in patients who have coronary artery disease (CAD), with insulin resistance (IR) and/or pre-diabetes. Methods and results We randomly assigned 68 patients (mean age 65 +/- 8 years) without diabetes who have CAD with IR and/or prediabetes to receive either metformin XL (2000 mg daily dose) or placebo for 12 months. Primary endpoint was change in left ventricular mass indexed to height(1.7) (LVMI), assessed by magnetic resonance imaging. In the modified intention-to-treat analysis (n = 63), metformin treatment significantly reduced LVMI compared with placebo group (absolute mean difference -1.37 (95% confidence interval: -2.63 to -0.12, P = 0.033). Metformin also significantly reduced other secondary study endpoints such as: LVM (P = 0.032), body weight (P = 0.001), subcutaneous adipose tissue (P = 0.024), office systolic blood pressure (BP, P = 0.022) and concentration of thiobarbituric acid reactive substances, a biomarker for oxidative stress (P = 0.04). The glycated haemoglobin A1C concentration and fasting IR index did not differ between study groups at the end of the study. Conclusion Metformin treatment significantly reduced LVMI, LVM, office systolic BP, body weight, and oxidative stress. Although LVH is a good surrogate marker of cardiovascular (CV) outcome, conclusive evidence for the cardioprotective role of metformin is required from large CV outcomes trials.
引用
收藏
页码:3409 / 3417
页数:9
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