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Calcium antagonists and atherosclerosis protection in hypertension
Rafael Hernández Hernández1, María José Armas-Hernández, Manuel Velasco
1Clinical Pharmacology Unit, School of Medicine, Universidad Centroccidental Lisandro Alvarado, Barquisimeto, Venezuela. rhernan@cantv.net
Insights
Calcium antagonists are effective for hypertension and show potential antiatherosclerotic effects. Studies indicate these drugs can reduce cardiovascular events and slow atherosclerosis progression in patients.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Atherosclerosis Research
Background:
- Calcium antagonists are established antihypertensive agents effective across diverse patient groups.
- Emerging evidence suggests these drugs possess properties beyond blood pressure reduction, including antioxidant and antiatherosclerotic effects.
- The role of calcium antagonists in modifying atherosclerosis progression requires further investigation.
Purpose of the Study:
- To evaluate the efficacy of calcium antagonists in reducing cardiovascular morbidity and mortality.
- To assess the impact of calcium antagonists on the progression of atherosclerosis in hypertensive patients.
- To explore the antiatherosclerotic mechanisms of specific calcium antagonists, such as their antioxidant properties.
Main Methods:
- Analysis of prospective studies and long-term clinical trials evaluating calcium antagonists (e.g., nifedipine GITS, nitrendipine, amlodipine, lacidipine, nisoldipine, verapamil).
- Assessment of cardiovascular event rates, atherosclerosis progression markers (e.g., intima-media thickness), and LDL oxidation.
- Comparison of calcium antagonists with other antihypertensive agents (e.g., diuretics, chlorthalidone, atenolol) and combination therapies.
Main Results:
- Calcium antagonists effectively reduce cardiovascular morbidity and mortality, comparable to diuretics.
- Specific agents like amlodipine, lacidipine, and nisoldipine exhibit antioxidant properties, reducing LDL oxidation and atherosclerotic lesions in animal models.
- Clinical trials demonstrate that calcium antagonists can slow atherosclerosis progression, reduce new angiographic lesions, promote carotid lesion regression, and decrease intima-media thickness in hypertensive and coronary heart disease patients.
Conclusions:
- Calcium antagonists are effective antihypertensive agents with demonstrated benefits in reducing cardiovascular events.
- These drugs exhibit antiatherosclerotic properties, potentially through antioxidant mechanisms and direct effects on vascular wall processes.
- Selective calcium antagonists represent a promising therapeutic option for managing atherosclerosis progression in hypertensive patients.
Abstract:
Calcium antagonists are effective in hypertensive patients of all ethnic groups, irrespective of age, dietary salt intake, salt-sensitivity status or plasma renin activity profile. Some prospective studies show that the calcium antagonists, nifedipine GITS and nitrendipine, reduce cardiovascular morbidity and mortality at least to the same extent as the diuretics. Other prospective studies are in progress to evaluate the effect of calcium antagonists on cardiovascular morbidity and mortality, and the progression of atherosclerosis in hypertensive patients. Calcium antagonists, especially the highly lipophilic amlodipine, lacidipine and nisoldipine, are shown to possess antioxidant properties. These drugs reduce the oxidation of LDL and its influx into the arterial wall, and reduce atherosclerotic lesions in animals. Platelet production of malondialdehyde, a marker of oxygen free radical formation, is suppressed by amlodipine, lacidipine or nifedipine in hypertensive patients. New evidence from long-term clinical trials of calcium antagonists indicates that these drugs can reduce the rate of progression of atherosclerosis in hypertensive and coronary heart disease patients. In the Regression Growth Evaluation Statin Study (REGRESS), co-administration of calcium antagonist, amlodipine or nifedipine with pravasatin caused a significant reduction in the appearance of new angiographic lesions. In the Verapamil in Hypertension and Atherosclerosis Study (VHAS), verapamil was more effective than chlorthalidone in promoting regression of thicker carotid lesions in parallel with a reduction in the incidence of cardiovascular events. In the Prospective Randomized Evaluation of the Vascular Effects of Norvasc Trial (PREVENT), amlodipine slowed the progression of early coronary atherosclerosis in patients with coronary artery disease. In a subprotocol of the Intervention as a Goal in the Hypertension Treatment (INSIGHT) study, nifedipine GITS significantly decreased intima-media thickness as compared to co-amilozide (hydrochlorothiazide + amiloride). Preliminary results of the European Lacidipine Study on Atherosclerosis (ELSA) show that lacidipine reduced the intima-media thickness progression rate as compared to atenolol. Thus, selective calcium antagonists are potential antiatherosclerotic agents.
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