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Published on: May 26, 2022
Irbesartan reduces QT dispersion in hypertensive individuals
1Hypertension Research Centre, Department of Clinical Pharmacology and Therapeutics, University of Dundee, Ninewells Hospital and Medical School, Dundee, UK. pitt@clinpharm.dundee.ac.uk
Insights
Irbesartan significantly reduced QT dispersion in hypertensive patients, potentially lowering the risk of sudden cardiac death. Amlodipine showed a trend towards improvement but did not reach statistical significance.
Area of Science:
- Cardiology
- Pharmacology
- Hypertension Research
Background:
- Angiotensin type 1 receptor antagonists influence the autonomic nervous system and myocardium.
- QT dispersion is a marker of cardiac electrical instability.
Purpose of the Study:
- To compare the effects of irbesartan and amlodipine on QT dispersion in elderly hypertensive patients.
- To test the hypothesis that irbesartan reduces QT dispersion more than amlodipine.
Main Methods:
- A multinational, randomized, double-blind study comparing irbesartan and amlodipine over 6 months.
- Electrocardiograms (ECGs) were collected at baseline and 6 months.
- 104 subjects with complete ECG data were analyzed.
Main Results:
- Irbesartan significantly reduced QT dispersion (mean -11.4 ms, P=0.02) and QTc max ( -12.8 ms, P=0.01).
- Amlodipine showed a non-significant trend towards reduced QT indexes (QTc dispersion -9.7 ms, P=0.06).
- QTc dispersion changes did not correlate with blood pressure changes for irbesartan, but did for amlodipine.
Conclusions:
- Irbesartan effectively improved QT dispersion in hypertensive patients.
- This improvement may contribute to preventing sudden cardiac death in at-risk individuals.
- Further research is warranted to confirm these findings and their clinical implications.
Abstract:
Angiotensin type 1 receptor antagonists have direct effects on the autonomic nervous system and myocardium. Because of this, we hypothesized that irbesartan would reduce QT dispersion to a greater degree than amlodipine, a highly selective vasodilator. To test this, we gathered electrocardiographic (ECG) data from a multinational, multicenter, randomized, double-blind parallel group study that compared the antihypertensive efficacy of irbesartan and amlodipine in elderly subjects with mild to moderate hypertension. Subjects were treated for 6 months with either drug. Hydrochlorothiazide and atenolol were added after 12 weeks if blood pressure (BP) remained uncontrolled. ECGs were obtained before randomization and at 6 months. A total of 188 subjects (118 with baseline ECGs) were randomized. We analyzed 104 subjects who had complete ECGs at baseline and after 6 months of treatment. Baseline characteristics between treatments were similar, apart from a slight imbalance in diastolic BP (irbesartan [n=53] versus amlodipine [n=51], 99.2 [SD 3. 6] versus 100.8 [3.8] mm Hg; P=0.03). There were no significant differences in BP normalization (diastolic BP <90 mm Hg) between treatments at 6 months (irbesartan versus amlodipine, 80% versus 88%; P=0.378). We found a significant reduction in QT indexes in the irbesartan group (QTc dispersion mean, -11.4 [34.5] milliseconds, P=0.02; QTc max, -12.8 [35.5] milliseconds, P=0.01), and QTc dispersion did not correlate with the change in BP. The reduction in QT indexes with amlodipine (QTc dispersion, -9.7 [35.4] milliseconds, P=0.06; QTc max, -8.6 [33.2] milliseconds, P=0.07) did not quite reach statistical significance, but there was a correlation between the change in QT indexes and changes in systolic BP. In conclusion, irbesartan improved QT dispersion, and this effect may be important in preventing sudden cardiac death in at-risk hypertensive subjects.
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