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Lercanidipine and losartan effects on blood pressure and fibrinolytic parameters
Tsung-Hsien Lin1, Wen-Chol Voon, Hsueh-Wei Yen
1Division of Cardiology, Department of Internal Medicine, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Insights
Lercanidipine and losartan effectively lower blood pressure in patients with essential hypertension. Lercanidipine also significantly reduced plasminogen activator inhibitor-1 (PAI-1), suggesting a potential benefit in modulating fibrinolysis.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Antihypertensive agents can influence blood pressure and fibrinolysis.
- Essential hypertension is a common condition requiring effective treatment.
Purpose of the Study:
- To compare the effects of lercanidipine and losartan on blood pressure and fibrinolytic parameters.
- To assess the impact on plasminogen activator inhibitor-1 (PAI-1), D-dimer, and fibrinogen.
Main Methods:
- Randomized trial with 26 essential hypertension patients.
- Placebo run-in followed by 8 weeks of lercanidipine (10-20 mg/day) or losartan (50-100 mg/day).
- Measured blood pressure (BP), PAI-1, D-dimer, and fibrinogen levels.
Main Results:
- Both lercanidipine and losartan significantly reduced systolic and diastolic blood pressure.
- Lercanidipine treatment led to a significant reduction in PAI-1 levels (p = 0.047).
- No significant changes in D-dimer or fibrinogen were observed in either group.
Conclusions:
- Lercanidipine and losartan are effective antihypertensive treatments for essential hypertension.
- Lercanidipine may offer an additional therapeutic advantage by improving fibrinolysis through PAI-1 reduction.
Abstract:
Antihypertensive agents may modulate fibrinolysis in addition to reducing blood pressure. We conducted a randomized trial to assess the effects of lercanidipine and losartan on blood pressure (BP) lowering and three fibrinolytic parameters: plasminogen activator inhibitor-1 (PAI-1), D-dimer, and fibrinogen. All patients enrolled had essential hypertension and underwent a placebo run-in period of 2 weeks before randomization to either lercanidipine tablets 10-20 mg once daily or losartan tablets 50-100 mg once daily. Twenty-six patients completed this study. After 8 weeks of treatment, both groups of patients had significantly reduced systolic (SBP) and diastolic BP (DBP) (SBP, p = 0.034 and 0.050, respectively; DBP, p = 0.018 and 0.034 for lercanidipine and losartan, respectively). Both drugs were well tolerated. Only in the group treated with lercanidipine was PAI-1 concentration significantly reduced (57.1 +/- 4.7 to 43.1 +/- 4.8 ng/mL, p = 0.047). No difference was found with D-dimer and fibrinogen in either group. This study shows that both lercanidipine and losartan are effective antihypertensive drugs in patients with essential hypertension. Lercanidipine may provide additional benefit in fibrinolysis.
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