Prospective study identifies significant QTc shortening after testosterone in AFAB adults, suggesting rapid cardiac adaptation.
Testosterone modulates ventricular repolarization, yet the early time course of its effects in humans remains unclear. We conducted a prospective, single-centre study in ten healthy adults assigned female at birth initiating gender-affirming hormone therapy with daily transdermal testosterone gel. Standard 12-lead ECGs at baseline and 3 months showed no change in uncorrected QT, but significant QTc shortening by Bazett (−32 ms; p=0.002) and Fridericia (−14 ms; p=0.010) formulas, despite a concurrent heart rate reduction and with no association to changes in serum testosterone. These findings demonstrate rapid ventricular repolarization remodeling after testosterone initiation, with a magnitude comparable to the sex-based QTc gap. This study contributes to the characterization of early electrophysiologic adaptation to androgens in a standardized clinical model, and may inform cardiovascular monitoring strategies during abrupt hormonal transitions.
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Tienforti et al. (2025) studied this question.
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