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Transdermal Testosterone Attenuates Drug-Induced Lengthening of Both Early and Late Ventricular Repolarization in Older Men.

Authors :
Tomaselli Muensterman E
Jaynes HA
Sowinski KM
Overholser BR
Shen C
Kovacs RJ
Tisdale JE
Source :
Clinical pharmacology and therapeutics [Clin Pharmacol Ther] 2021 Jun; Vol. 109 (6), pp. 1499-1504. Date of Electronic Publication: 2020 Nov 15.
Publication Year :
2021

Abstract

We have previously reported that transdermal testosterone attenuates drug-induced QT interval lengthening in older men. However, it is unknown whether this is due to modulation of early ventricular repolarization, late repolarization, or both. In a secondary analysis of a prospective, randomized, double-blind, placebo-controlled three-way crossover study, we determined if transdermal testosterone and oral progesterone attenuate drug-induced lengthening of early and late ventricular repolarization, represented by the electrocardiographic measurements J-T <subscript>peak</subscript> c and T <subscript>peak</subscript> -T <subscript>end</subscript> , respectively, as well as T <subscript>peak</subscript> -T <subscript>end</subscript> /QT, a measure of transmural dispersion of repolarization. Male volunteers ≥ 65 years of age (n = 14) were randomized to receive transdermal testosterone 100 mg, oral progesterone 400 mg, or matching transdermal/oral placebo daily for 7 days. On the morning following the seventh day, subjects received intravenous ibutilide 0.003 mg/kg, after which electrocardiograms were performed serially. One subject was excluded due to difficulty in T-wave interpretation. Pre-ibutilide J-T <subscript>peak</subscript> c was lower during the testosterone phase than during progesterone and placebo (216 ± 23 vs. 227 ± 28 vs. 227 ± 21 ms, P = 0.002). Maximum post-ibutilide J-T <subscript>peak</subscript> c was also lower during the testosterone phase (233 ± 22 vs. 246 ± 29 vs. 248 ± 23 ms, P < 0.0001). Pre-ibutilide T <subscript>peak</subscript> -T <subscript>end</subscript> was not significantly different during the three phases, but maximum post-ibutilide T <subscript>peak</subscript> -T <subscript>end</subscript> was lower during the testosterone phase (80 ± 12 vs. 89 ± 18 vs. 86 ± 15 ms, P = 0.002). Maximum T <subscript>peak</subscript> -T <subscript>end</subscript> /QT was also lower during the testosterone phase (0.199 ± 0.023 vs. 0.216 ± 0.035 vs. 0.209 ± 0.031, P = 0.005). Progesterone exerted minimal effect on drug-induced lengthening of J-T <subscript>peak</subscript> c, and no effect on T <subscript>peak</subscript> -T <subscript>end</subscript> or T <subscript>peak</subscript> -T <subscript>end</subscript> /QT. Transdermal testosterone attenuates drug-induced lengthening of both early and late ventricular repolarization in older men.<br /> (© 2020 The Authors Clinical Pharmacology & Therapeutics © 2020 American Society for Clinical Pharmacology and Therapeutics.)

Details

Language :
English
ISSN :
1532-6535
Volume :
109
Issue :
6
Database :
MEDLINE
Journal :
Clinical pharmacology and therapeutics
Publication Type :
Academic Journal
Accession number :
33020898
Full Text :
https://doi.org/10.1002/cpt.2072