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Effect of perindopril on pulse-wave velocity and endothelin-1 in black hypertensive patients
Elzbieta Osuch1, Willem J Du Plooy, Sandra H Du Plooy
1Department of Pharmacology and Therapeutics, School of Medicine, MEDUNSA Campus, University of Limpopo, South Africa.
Insights
Perindopril therapy significantly improved arterial elasticity in black hypertensive patients, as shown by reduced pulse-wave velocity (PWV). Endothelin-1 levels were not correlated with these improvements.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
Background:
- Investigated perindopril's impact on arterial elasticity and endothelin-1 (ET-1) in black hypertensive patients.
- Arterial elasticity assessed via pulse-wave velocity (PWV).
Purpose of the Study:
- To evaluate the effect of perindopril on arterial elasticity and ET-1 levels.
- To determine if perindopril improves vascular function in hypertensive individuals.
Main Methods:
- Forty-four newly diagnosed hypertensive patients received 4 mg perindopril daily for nine months.
- Noninvasive PWV measurements were taken along carotid-femoral and brachial-ulnar segments.
- ET-1 levels were monitored throughout the study.
Main Results:
- Significant improvement in arterial elasticity observed, indicated by a decrease in carotid-femoral PWV from 11.6 to 7.5 m/s.
- Treatment group's final PWV (7.5 m/s) was lower than healthy volunteers (8.2 m/s), though not statistically significant.
- No significant correlation found between ET-1 levels and PWV changes.
Conclusions:
- Perindopril enhances arterial elasticity in hypertensive patients, beyond its blood pressure-lowering effects.
- The observed improvement in vascular function is not associated with changes in ET-1 levels.
Introduction:
We investigated the effect of perindopril on pulse-wave velocity (as indicator of arterial elasticity) and endothelin-1 (ET-1) levels in black hypertensive patients.
Methods:
Forty-four newly diagnosed hypertensive patients who received 4 mg perindopril daily were monitored for nine months. Pulse-wave velocity (PWV) was measured noninvasively along the carotid-femoral arterial segment (high elastic content) and the brachial-ulnar segment (low elastic content).
Results:
There was a significant increase in arterial elasticity, as indicated by a slower PWV in the carotid-femoral segment of the treatment group, from 11.6 to 7.5 m/s after nine months. The PWV of the treatment group (7.5 m/s) after nine months was lower than that of the healthy volunteer group (8.2 m/s) but it was not statistically significant. No correlation between ET-1 and PWV could be found.
Conclusion:
In addition to its blood pressure-lowering effect, our study confirmed the improvement in arterial elasticity in patients on perindopril therapy, without involvement of ET-1.
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