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Published on: June 9, 2021
Morbidity and mortality with dihydropyridines
1Department of Geriatrics, Clinical Hypertension Research, University of Uppsala, Sweden.
Insights
Dihydropyridine calcium antagonists effectively lower blood pressure and reduce cardiovascular disease. Long-term trials confirm their benefit in hypertension treatment, refuting earlier safety concerns.
Area of Science:
- Cardiology
- Pharmacology
- Hypertension Management
Background:
- Dihydropyridine calcium antagonists (CaAs) are widely prescribed for hypertension.
- Their efficacy in lowering blood pressure and tolerability are well-established.
- Emerging trial data investigate their impact on cardiovascular morbidity.
Purpose of the Study:
- To review the evidence for the cardiovascular benefits of dihydropyridine CaAs in hypertension.
- To address concerns regarding potential adverse effects on morbidity and mortality.
- To compare CaA-based therapy with conventional treatments.
Main Methods:
- Review of data from landmark intervention trials, including STONE and Syst-Eur.
- Inclusion of ongoing studies like HOT and STOP-2.
- Consideration of analyses by the World Health Organization and International Society of Hypertension.
Main Results:
- Trials like Syst-Eur demonstrated significant cardiovascular disease prevention with CaA treatment.
- Ongoing studies suggest a positive effect on cardiovascular morbidity.
- Expert reviews have refuted claims of increased morbidity and mortality associated with CaAs.
Conclusions:
- Available evidence supports a beneficial effect of dihydropyridine CaAs on cardiovascular morbidity in hypertensive patients.
- Further results from STOP-2 will clarify if CaA benefits exceed those of diuretics or beta-blockers.
Abstract:
Calcium antagonists (CaAs) of the dihydropyridine type are widely used in the treatment of hypertension and other cardiovascular disorders. They are markedly effective in lowering elevated arterial pressure, and are well tolerated. Data from long-term intervention trials are emerging, which also show a beneficial effect on cardiovascular morbidity with the use of CaAs in the treatment of hypertension. The first such evidence was from the Shanghai Trial of Nifedipine in the Elderly (STONE), and, in February 1997, the Systolic Hypertension in Europe (Syst-Eur) trial was stopped prematurely because the active treatment, based on a CaA, was found to be significantly better than placebo in preventing cardiovascular disease. In addition, ongoing trials with dihydropyridine CaAs (e.g. the Hypertension Optimal Treatment [HOT] Study and the Swedish Trial in Old Patients with Hypertension-2 [STOP-2]) are close to termination. Final results are not yet available, but cardiovascular morbidity appears to be lower than expected in the HOT Study, suggesting a positive effect of the CaA-based therapeutic regimen. Claims of increased morbidity and mortality from the use of CaAs have been clearly refuted by the thorough scrutiny of all available data by a committee formed by the World Health Organization and the International Society of Hypertension. It can therefore be concluded that the available evidence on the use of dihydropyridine CaAs shows that these agents have a beneficial effect on morbidity. Whether this effect of CaAs is greater than that obtained with conventional therapies, such as diuretics and/or beta-blockers, will be shown by the STOP-2 Study, which is expected to be completed in 1998.
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