Why the study?
Higher progesterone concentrations protect against drug-induced prolongation of ventricular repolarization, but whether progesterone pretreatment reduces drug-induced torsades de pointes was unconfirmed.
Does progesterone pretreatment reduce the incidence of drug-induced torsades de pointes in an isolated perfused rabbit heart model?
Does progesterone pretreatment reduce the incidence of drug-induced torsades de pointes in an isolated perfused rabbit heart model?
Progesterone pretreatment significantly reduces the incidence of dofetilide-induced torsades de pointes and other ventricular arrhythmias in an isolated AV node-ablated rabbit heart model.
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Findings in this rabbit model should not yet change clinical practice; leaves open whether progesterone protects against drug-induced TdP in humans.
Introduction Higher progesterone concentrations are protective against drug‐induced prolongation of ventricular repolarization. We tested the hypothesis that pretreatment with progesterone reduces the incidence of drug‐induced torsades de pointes (TdP). Methods and Results Female New Zealand white rabbits (2.5‐3.2 kg) underwent ovariectomy and were randomized to undergo implantation with subcutaneous 21‐day sustained release pellets containing progesterone 50 mg (n = 22) or placebo (n = 23). After 20 days, hearts were excised, mounted, and perfused with modified Krebs‐Henseleit solution. The atrioventricular (AV) node was destroyed manually. Following a 15‐minute equilibration period, hearts were perfused with dofetilide 100 nM for 30 minutes, during which the electrocardiogram was recorded continuously. Incidences of spontaneous TdP, other ventricular arrhythmias and mean QT c intervals were compared. Median serum progesterone concentrations were higher in progesterone vs placebo‐treated rabbits (3.8 [range, 2.8‐5.1] vs 0.7 [0.4‐1.7] ng/mL, P < 0.0001). Median serum estradiol concentrations were similar (58 [22‐72] vs 53 [34‐62] pg/mL), P = 0.79). The incidence of TdP was lower in hearts from progesterone‐treated rabbits (27% vs 61%, P = 0.049). The incidences of bigeminy (36% vs 74%, P = 0.03) and trigeminy (18% vs 57%, P = 0.01) were also lower in hearts from progesterone‐treated rabbits. There was no significant difference between groups in incidence of couplets (59% vs 74%, P = 0.54) or monomorphic ventricular tachycardia (14% vs 30%, P = 0.28). Maximum QT c interval and short‐term beat‐to‐beat QT interval variability during dofetilide perfusion were significantly shorter in hearts from progesterone‐treated rabbits. Conclusions Pretreatment with progesterone reduces the incidence of drug‐induced TdP, bigeminy, and trigeminy in isolated perfused AV node‐ablated rabbit hearts.
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Tisdale et al. (2019) studied this question.
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