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Updated: Jul 5, 2026

Establishment of Rat Models Mimicking Gender-affirming Hormone Therapies
Published on: January 10, 2025
Drugs for men and women - how important is gender as a risk factor for TdP?
1Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow G4 0NR, United Kingdom. susan.coker@strath.ac.uk
Abstract:
The cardiac arrhythmia known as torsade de pointes (TdP), which is a very rare but potentially lethal side effect of a variety of drugs, occurs approximately twice as often in women as it does in men. Most drugs that have this adverse effect prolong the repolarization phase of the cardiac action potential which can be detected by a lengthening of the QT interval on the ECG. The gender difference in susceptibility to TdP only appears after puberty suggesting that sex hormones are contributory factors. Studies in patients indicate that testosterone-induced shortening of action potential duration may account for the shorter rate-corrected QT interval in men rather than any effect of estradiol in women, whereas drug-induced QT prolongation can be potentiated by estradiol. Experimental investigations suggest that sex hormones may alter either Ca2+ currents, K+ currents, or both and that actions on these ionic currents may account for the gender differences in cardiac repolarization. Although estradiol exacerbated drug-induced TdP in an in vivo model, no similar information is available for progesterone or testosterone. Further studies are required to clarify the influence of these sex hormones and to investigate the importance of the balance between sex hormones in both genders. Such information would assist in risk:benefit analysis and may allow the development of "drugs for men" and "drugs for women".
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