There is an increasing interest in the use of metformin in CV diseases and there is an increasing interest in studying its potential new roles in heart failure patients. There were some concerns related to the safety of metformin in such diabetic patients due to the risk of lactic acidosis. However, recent studies showed that metformin was safe or even beneficial in HF patients. We hypothesized that metformin might improve morbidity, mortality, cardiac function, and HR-QoL in non-diabetic patients with HFrEF.
Metformin is an anti-diabetic drug that is known improve insulin sensitivity and reduce insulin resistance. A published meta-analysis of randomized controlled trials (RCTs) reported a reduction of weight and insulin resistance in metformin users. Animal models also showed that metformin reduces cardiac hypertrophy. Observational studies showed a beneficial effect for metformin in patients with type 2 diabetes mellitus (T2DM) and heart failure. A recent study found that metformin reduced oxidative stress in non-diabetic patients with CAD. Metformin has multiple modes of actions involving both AMP-activated protein kinase (AMPK) dependent and AMPK-independent mechanisms that may be implicated in cardiac hypertrophy. At the systemic level, a review of clinical and experimental data showed that metformin improves endothelial function, protects from oxidative stress and inflammation, as well as the negative effects of angiotensin II. Observational studies also reported cardiovascular benefits in metformin users especially in patients with type 2 diabetes mellitus (T2DM) and heart failure. Metformin has also been shown to exert a cardio protective effect and it has been shown to reduce oxidative stress which is a common finding in heart failure patients. For these reasons, there is an increasing interest in the use of metformin in CV diseases and there is an increasing interest in studying its potential new roles in this aspect. We hypothesized that metformin might improve morbidity, mortality, cardiac function, and HR-QoL in non-diabetic patients with HFrEF.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
70
Metformin 2000 mg/day
Agouza Hospital
Giza, Egypt
Change in total antioxidant capacity (relative and absolute)
Change Total antioxidant capacity as assessed by colorimetric assay
Time frame: 6 months
Change in Malondialdehyde (MDA)
Change in Malondialdehyde (MDA) as assessed by colorimetric assay
Time frame: 6 months
Chagne in left ventricular mass index
Chagne in left ventricular mass index as assessed by Echocardiography
Time frame: 6 months
Chagne in Ejection Fraction
Ejection fraction as assessed by echocardiography
Time frame: 6 months
New York Heart Association functional classification (NYHA):
The NYHA classifies patients in one of four possible categories based on the physical activity limitations; the limitations/symptoms are in regards to normal breathing andvarying degrees in shortness of breath and or angina pain
Time frame: 6 months
TAC
Total antioxidant capacity as assessed by colorimetric assay
Time frame: 6 months
MDA
MDA as assessed by colorimetric assay
Time frame: 6 months
Adverse reactions of metformin
Incidence of lactic acidosis
Time frame: 6 months
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Change in fasting blood glucose (FBG)
Change in FBG from baseline
Time frame: 6 months