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Published on: September 17, 2015
Differential effects of antihypertensive drug therapy on arterial compliance
Lawrence M Resnick1, Melvin H Lester
1Hypertension Center, New York Presbyterian Hospital-Cornell University Medical Center, New York, New York 10021, USA. lmresnick@aol.com
Insights
Antihypertensive drugs differentially improve vascular compliance, independent of blood pressure reduction. Some medications, like calcium channel blockers, angiotensin receptor blockers, and ACE inhibitors, enhance arterial compliance, while beta-blockers do not.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Hypertension Research
Background:
- Vascular compliance is abnormal in essential hypertension and can be improved by antihypertensive therapy.
- It remains unclear if drug-induced changes in vascular compliance are solely due to reduced blood pressure or if specific drug classes have differential effects.
Purpose of the Study:
- To investigate whether different classes of antihypertensive drugs, despite similar blood pressure-lowering efficacy, differentially affect arterial compliance.
- To determine if improvements in arterial compliance are drug-class specific or solely a consequence of blood pressure reduction.
Main Methods:
- Computerized arterial pulse waveform analysis (CAPWA) was used to measure capacitive (C1) and oscillatory (C2) components of arterial compliance.
- 39 essential hypertensive subjects were studied before and after 1-3 months of treatment with dihydropyridine calcium channel antagonists (CaBl), converting enzyme inhibitors (CEI), angiotensin receptor blockers (ARB), or beta-blockers (BBl) to achieve normotensive blood pressure.
Main Results:
- All drug classes achieved equivalent reductions in blood pressure.
- CaBl, CEI, and ARB significantly increased both capacitive (C1) and oscillatory (C2) components of arterial compliance.
- Beta-blockers (BBl) did not significantly alter arterial compliance compared to baseline, despite equivalent blood pressure reduction.
Conclusions:
- Arterial compliance improves with antihypertensive therapy in a drug-class-dependent manner, beyond the effects of blood pressure reduction.
- Drugs such as CaBl, CEI, and ARB enhance arterial compliance, whereas BBl do not.
- Preferential use of antihypertensive drugs that also improve arterial compliance may lead to greater clinical benefit in managing hypertension.
Abstract:
Although vascular compliance, deltaV/deltaP, is abnormal in essential hypertension and can be improved by antihypertensive drug therapy, it is not clear whether drug-induced changes in compliance are attributable solely to lower achieved blood pressure (BP), and thus equally likely with different drugs possessing similar antihypertensive efficacy. Therefore, we used computerized arterial pulse waveform analysis (CAPWA) to measure capacitive (C1) and oscillatory (C2) components of arterial compliance in essential hypertensive subjects (n = 39) before, and 1 and 3 months after achieving normotensive BP values with administration of either dihydropyridine calcium channel antagonists (CaBl, n = 11), converting enzyme inhibitors (CEI, n = 9), angiotensin receptor blockers (ARB, n = 9), or beta-blockers (BBl, n = 10). Despite equivalent effects on BP (CABL: -19 +/- 4/-15 +/- 2 mm Hg; CEI: -12 +/- 3/-13 +/- 2 mm Hg; ARB: -10 +/- 3/-12 +/- 2 mm Hg; and BBl: -14 +/- 3/-12 +/- 2 mm Hg; P <.005 for each drug v pretreatment), CaBl, CEI, and ARB significantly increased arterial compliance (CaBl: %deltaC1 = 30.0 +/- 5.8, %Delta C2 = 43.7 +/- 23.3; CEI: %deltaC1 = 32.7 +/- 5.4, %deltaC2 = 26.7 +/- 7.1; ARB: %deltaC1 = 36.3 +/- 11.8, %deltaC2 = 43.6 +/- 23.1; P <.01 for CaBl, CEI, and ARB v pretreatment), but BBl did not (%deltaC1 = -3.9 +/- 7.6, %deltaC2 = -7.0 +/- 11.5, P = not significant v pretreatment, sig = 0.01 v other drugs). We conclude that for an equivalent effect on BP, arterial compliance improves after therapy with some, but not all antihypertensive drugs. We hypothesize that a greater clinical benefit may result from the preferential use of drugs that concomitantly improve arterial compliance.
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