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Published on: November 29, 2024
Glimepiride Use is Associated with Reduced Cardiovascular Mortality in Patients with Type 2 Diabetes and Chronic
1Division of Cardiology, Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology; Hubei Key Laboratory of Genetics and Molecular Mechanisms of Cardiological Disorders, Wuhan 430030, China.
Insights
Glimepiride use in type 2 diabetes patients with chronic heart failure significantly reduces mortality and hospitalizations. High-dose glimepiride offers greater cardiovascular protection, potentially via increased epoxyeicosatrienoic acid levels.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Glimepiride demonstrates favorable cardiovascular safety.
- Clinical benefits of glimepiride on cardiovascular outcomes in patients with type 2 diabetes and chronic heart failure remain unclear.
Purpose of the Study:
- To investigate the association between glimepiride use and clinical cardiovascular outcomes in patients with type 2 diabetes (T2D) and chronic heart failure (CHF).
Main Methods:
- Analysis of 21,451 inpatients with T2D and CHF, comparing 638 glimepiride users to 20,813 non-users.
- Propensity score matching created 509 pairs for analysis.
- Kaplan-Meier and Cox regression analyses assessed mortality, heart failure events, myocardial infarction, and stroke.
Main Results:
- Glimepiride use was linked to significantly lower all-cause mortality (aHR, 0.47), cardiovascular mortality (aHR, 0.34), heart failure events (aHR, 0.42), and acute myocardial infarction/stroke hospitalizations (aHR, 0.53).
- High-dose glimepiride (2-4 mg/day) showed greater cardiovascular protection than low-dose (1 mg/day).
- Glimepiride demonstrated molecular docking with soluble epoxide hydrolase (sEH) and increased epoxyeicosatrienoic acid (EET) levels.
Conclusions:
- Long-term glimepiride use improves survival and reduces cardiovascular events in T2D patients with CHF.
- Higher glimepiride doses provide enhanced cardiovascular benefits.
- The cardioprotective effects may involve increased EET levels via sEH inhibition.
Background:
Glimepiride has good cardiovascular safety. However, whether glimepiride benefits clinical cardiovascular outcomes is unclear.
Methods:
A total of 21,451 inpatients with type 2 diabetes (T2D) and chronic heart failure (CHF) were analyzed, including 638 who received glimepiride treatment and 20,813 who did not. Propensity score matching yielded 509 pairs (glimepiride and non-glimepiride groups), and both groups were followed up. Kaplan-Meier and Cox regression analyses were used to compare all-cause mortality, cardiovascular mortality, hospitalizations and emergency visits for heart failure, and hospitalizations for acute myocardial infarction or stroke.
Results:
During follow-up, the all-cause mortality (adjusted hazard ratio [HR], 0.47; 95% confidence interval [CI], 0.35-0.63; P < 0.001), cardiovascular mortality (adjusted HR, 0.34; 95% CI, 0.24-0.48; P < 0.001), and number of hospitalizations and emergency visits for heart failure (adjusted HR, 0.42; 95% CI, 0.36-0.50; P < 0.001) and hospitalizations for acute myocardial infarction or stroke (adjusted HR, 0.53; 95% CI, 0.38-0.73; P < 0.001) were significantly lower in the glimepiride group; the conclusion remained similar in all subgroups. Furthermore, high-dose glimepiride use (2-4 mg/day) was associated with lower cardiovascular mortality than low-dose (1 mg/day) (adjusted HR, 0.55; 95% CI, 0.31-0.99; P = 0.047). Glimepiride exhibited good molecular docking with soluble epoxide hydrolase (sEH) and increased the level epoxyeicosatrienoic acid (EET).
Conclusions:
Long-term continuous glimepiride use is associated with better survival, fewer hospitalizations and emergency visits for heart failure, and fewer hospitalizations for acute myocardial infarction or stroke in patients with T2D and CHF. High-dose glimepiride has greater cardiovascular protective advantages than low-dose glimepiride. The cardiovascular protective effect of glimepiride may be related to the EET level increase through sEH inhibition.
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