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Effects of Sulfonylurea Hypoglycemic Agents and Adenosine Triphosphate Dependent Potassium Channel Antagonists on Ventricular Arrhythmias in Patients with Decompensated Heart Failure
Author(s) -
ARONSON DORON,
MITTLEMAN MURRAY A.,
BURGER ANDREW J.
Publication year - 2003
Publication title -
pacing and clinical electrophysiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.686
H-Index - 101
eISSN - 1540-8159
pISSN - 0147-8389
DOI - 10.1046/j.1460-9592.2003.t01-1-00177.x
Subject(s) - medicine , cardiology , sulfonylurea , ventricular tachycardia , diabetes mellitus , population , heart failure , anesthesia , endocrinology , insulin , environmental health
Hypoglycemic sulfonylureas block cardiac ATP‐sensitive potassium channels (K ATP ). The opening of these channels in cardiomyocytes can induce arrhythmias. In animal studies, sulfonylureas exert an antiarrhythmic effect on the ischemic myocardium, but data on human arrhythmic events are lacking. The study population included 207 patients (age 61 ± 14 years) admitted for decompensated CHF. The severity of ventricular arrhythmias was assessed by 24‐hour Holter monitoring. None of the patients were on parenteral vasoactive therapy or antiarrhythmics during Holter recording. Diabetic patients comprised 48% of the study population, and 34% of diabetic patients were prescribed sulfonylureas. The mean hourly ventricular pairs (3.6 ± 0.5vs1.8 ± 0.3, P = 0.03), the mean hourly repetitive ventricular beats (5.7 ± 1.0vs2.6 ± 0.1, P = 0.03), and the frequency of ventricular tachycardia episodes per 24 hours (4.7 ± 0.8vs2.2 ± 0.4, P = 0.03) were significantly lower in patients with diabetes who were receiving sulfonylureas compared with nondiabetics. No significant difference occurred between patients with diabetes who were not receiving sulfonylureas and nondiabetic patients. Multivariate regression revealed a negative independent relationship between sulfonylurea therapy and hourly ventricular pairs(P = 0.03),the mean hourly repetitive ventricular beats(P = 0.03),and ventricular tachycardia episodes(P = 0.04). In a multiple logistic regression, sulfonylurea therapy was a negative predictor of repetitive ventricular beats ( P = 0.01, adjusted OR, 0.31; 95% CI, 0.12–0.78). Concomitant sulfonylurea therapy may reduce the occurrence of complex ventricular ectopy in the setting of severe CHF. These results suggest that cardiac K ATP channel activation may be involved in the genesis of ventricular arrhythmias in CHF. (PACE 2003; 26:1254–1261)