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Antiarrhythmic drug, cibenzoline, can directly improve the left ventricular diastolic function in patients with
M Hamada1, Y Shigematsu, Y Hara
1The Second Department of Internal Medicine, Ehime University School of Medicine, Onsen-gun, Japan.
Insights
Cibenzoline improves diastolic function in hypertrophic cardiomyopathy (HCM) patients by enhancing E-wave velocity and reducing A-wave velocity. While it suppresses systolic function, its direct action markedly improves left ventricular diastolic dysfunction.
Area of Science:
- Cardiology
- Pharmacology
- Medical Research
Background:
- Hypertrophic cardiomyopathy (HCM) is a complex heart condition affecting left ventricular function.
- Diastolic dysfunction is a key feature of HCM, impacting cardiac filling and relaxation.
- Understanding drug effects on HCM is crucial for patient management.
Purpose of the Study:
- To investigate the effects of cibenzoline on left ventricular diastolic function in patients with hypertrophic cardiomyopathy (HCM).
- To assess changes in systolic and diastolic parameters following oral administration of cibenzoline.
Main Methods:
- Echocardiography, apexcardiography, and gated radionuclide angiography were used.
- Measurements were taken before and 2 hours after oral administration of 200 mg cibenzoline.
- The study included patients with hypertrophic obstructive cardiomyopathy (HOCM) and hypertrophic nonobstructive cardiomyopathy (HNCM).
Main Results:
- Cibenzoline significantly reduced the left ventricular pressure gradient in HOCM patients.
- Fractional shortening decreased, indicating suppressed systolic function in both HOCM and HNCM groups.
- E-wave velocity increased, A-wave velocity decreased, and filling times shortened, demonstrating improved diastolic function.
Conclusions:
- Cibenzoline demonstrates a dual effect in HCM patients: suppressing systolic function while significantly improving left ventricular diastolic dysfunction.
- The drug's direct action appears to be beneficial for diastolic abnormalities in HCM.
- Further research may explore cibenzoline's therapeutic potential in managing HCM-related diastolic dysfunction.
Abstract:
The effect of cibenzoline on left ventricular diastolic function was investigated in patients with hypertrophic cardiomyopathy (HCM). Before and 2 h after an oral administration of 200 mg of cibenzoline, echocardiographic, apexcardiographic and gated radionuclide angiographic studies were performed in 12 patients with hypertrophic obstructive cardiomyopathy (HOCM) and 7 with hypertrophic nonobstructive cardiomyopathy (HNCM). After administration of cibenzoline, the left ventricular pressure gradient decreased from 96+/-33 mmHg to 29+/-22 mmHg (<0.0001). Fractional shortening decreased from 53.3+/-7.5 to 45.4+/-6.2% (p=0.0008) in patients with HOCM and from 49.9+/-8.7 to 40.9+/-7.5% (p=0.0039) in patients with HNCM. On the other hand, E-wave velocity increased and A-wave velocity decreased in both groups. The time between the second heart sound and O point was shortened from 253+/-53 to 176+/-21 ms (p<0.0001) in patients with HOCM and from 245+/-54 to 185+/-44 ms (p=0.0050) in patients with HNCM. The time to peak filling rate was shortened from 248+/-79 to 190+/-40 ms (p=0.0072) in patients with HOCM and from 218+/-33 to 163+/-26 ms (p=0.0052) in patients with HNCM. These results indicate that in patients with HCM, cibenzoline suppresses left ventricular systolic function, but can markedly improve left ventricular diastolic dysfunction through its direct action.
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