Metformin in the Diastolic Dysfunction of Metabolic Syndrome: MET-DIME Trial
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 54
- 试验地点
- 1
- 主要终点
- Change in mean early diastolic mitral annular velocity (cm/s)
研究概览
简要总结
Metabolic syndrome (MS) is a cluster of risk factors for cardiovascular disease with increasing prevalence worldwide and insulin resistance is central to its pathophysiology and multi-organ deleterious effects. One of the most affected organs, the heart, undergoes a remodeling process with an increase in fibrous tissue that impairs global cardiac function. Considering that myocardial fibrosis increases myocardial stiffness, one important determinant of diastolic function, it probably contributes decisively to subclinical left ventricular diastolic dysfunction (DD) and heart failure with preserved ejection fraction in patients with MS.
Since insulin resistance is a dominant player in the pathophysiology of MS, improvement of the metabolic profile of these patients with metformin might be associated with favorable remodeling of myocardial structure and an improvement in myocardial function. Metformin is a widely used drug to treat type 2 diabetes mellitus and is considered an option in the treatment of high-risk non-diabetic patients with MS, in addition to lifestyle counseling including a healthy diet and physical activity.
In this way, we aim to: i) assess if treating non-diabetic patients with MS and DD with metformin in addition to lifestyle counseling decreases cardiac fibrosis and improves diastolic function and assess its impact in functional capacity and health-related quality of life (HRQoL); ii) evaluate if biomarkers of cardiac remodeling and inflammation are predictive factors of response to metformin treatment in these patients.
This is a prospective, randomized, open-label, blinded-endpoint (PROBE) trial (scheduled follow-up of 24 months) with 2 arms: lifestyle counseling only and lifestyle counseling plus metformin (maximum dose of 1000mg twice daily).
The primary endpoint will be change in change in mean of septal and lateral early diastolic mitral annular velocities (E') (at the end of the 24 months of follow-up).
The secondary endpoints will include a composite of major cardiovascular events; diastolic function parameters at rest; plasma levels of insulin, glucose, insulin resistance index, NTproBNP, high-sensitivity C-reactive protein, tumor necrosis factor-α (TNFα), tissue inhibitor of matrix metalloproteinase type 1 (TIMP1) and growth differentiation factor-15 (GDF-15); functional capacity; epicardial, pericardial and abdominal adipose tissue volumes, and coronary calcium score; HRQoL.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 40 Years 至 64 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Non-diabetic adults aged between 40 and 64 years fulfilling the American Heart Association/National Heart, Lung and Blood Institute diagnostic criteria of metabolic syndrome (at least 3 of the following: waist circumference ≥102 cm (males) or ≥88 cm (females); fasting triglycerides≥150 mg/dL or on drug therapy for decreasing triglycerides; fasting HDL-cholesterol ˂40 mg/dL (males) or ˂50 mg/dL (females) or on drug therapy for increase HDL-c; systolic blood pressure ≥130 mmHg or diastolic blood pressure ≥85 mmHg or on antihypertensive drug therapy; fasting glycemia≥100 mg/dL
- •Echocardiographic evidence of left ventricle diastolic dysfunction at rest (mean E'˂10,2 cm/s if 40-59 years and ˂7,2 cm/s if 60-64 years).
排除标准
- •diagnosis of diabetes mellitus according to the American Diabetes Association criteria;
- •previous diagnosis of ischemic heart disease;
- •moderate or severe cardiac valvular disease;
- •left ventricle ejection fraction lower than 50%
- •pericardial disease;
- •uncontrolled atrial or ventricular tachyarrhythmias;
- •chronic kidney disease (estimated creatinine clearance lower than 60 mL/min);
- •significant liver disease (aspartate aminotransferase or alanine aminotransferase equal or above 2.5 times the upper limit of normal);
- •females who are pregnant, planning to become pregnant or who admit sexual activity without appropriate contraception;
- •lactation;
- •unable to perform cardiopulmonary exercise test;
- •recent (less than 1 month) change in drug therapy.
研究组 & 干预措施
Lifestyle Counseling
Written and individualized information during the interview in all clinic visits, emphasizing the importance of regular moderate-intensity physical activity and healthy diet.
干预措施: Lifestyle Counseling (Behavioral)
Metformin + Lifestyle Counseling
Metformin: maximum dose of 1000mg twice daily. Lifestyle counseling: Written and individualized information during the interview in all clinic visits, emphasizing the importance of regular moderate-intensity physical activity and healthy diet.
干预措施: Lifestyle Counseling (Behavioral)
Metformin + Lifestyle Counseling
Metformin: maximum dose of 1000mg twice daily. Lifestyle counseling: Written and individualized information during the interview in all clinic visits, emphasizing the importance of regular moderate-intensity physical activity and healthy diet.
干预措施: Metformin (Drug)
结局指标
主要结局
Change in mean early diastolic mitral annular velocity (cm/s)
时间窗: Baseline, 6,12 and 24 months
Change in mean of septal and lateral early diastolic mitral annular velocities (E'), assessed by tissue doppler echocardiography
次要结局
- Functional capacity during cardiopulmonary exercise test(Baseline, 12, 24 months)
- Epicardial, pericardial and abdominal adipose tissue volumes(Baseline, 24 months)
- Healthcare related quality of life(Baseline, 12, 24 months)
- Major adverse cardiovascular events(12 and 24 months)
- Diastolic echocardiographic parameters(Baseline, 6, 12, 24 months)
- Plasma levels of inflammatory and metabolic biomarkers(Baseline, 6, 12, 24 months)
- Coronary artery calcium quantification(Baseline, 24 months)
研究者
Ricardo Ladeiras-Lopes
Dr. Ricardo Ladeiras-Lopes
Universidade do Porto