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Acute anti-ischemic effect of testosterone in men with coronary artery disease
G M Rosano1, F Leonardo, P Pagnotta
1Department of Cardiology, Istituto H. San Raffaele, Roma and Milano, Italy. rosanog@roma.hsr.it
Insights
Short-term testosterone administration improved exercise-induced myocardial ischemia in men with coronary artery disease. This hormone may offer a direct coronary-relaxing effect, benefiting heart health.
Area of Science:
- Cardiology
- Endocrinology
- Exercise Physiology
Background:
- The role of testosterone in male coronary artery disease (CAD) is debated.
- Higher CAD incidence in men suggests a testosterone link, yet it may improve coronary artery function.
- This study investigated acute testosterone's impact on exercise-induced myocardial ischemia.
Purpose of the Study:
- To evaluate the effect of acute testosterone administration on exercise-induced myocardial ischemia in men with coronary artery disease.
- To determine if testosterone influences the physiological responses to exercise stress in these patients.
Main Methods:
- 14 men with CAD underwent three randomized exercise tests (baseline, testosterone, placebo) after antianginal therapy withdrawal.
- Tests followed a modified Bruce protocol, with testosterone (2.5 mg IV) or placebo administered 30 minutes prior.
- Outcomes included ST-segment depression, chest pain, exercise duration, heart rate, and rate-pressure product.
Main Results:
- Testosterone reduced the incidence of positive exercise tests (ST-segment depression) and reported chest pain compared to placebo.
- Testosterone significantly increased time to ST-segment depression and total exercise duration.
- The hormone elevated heart rate and rate-pressure product at ST-segment onset and peak exercise.
Conclusions:
- Acute testosterone administration demonstrated a beneficial effect on exercise-induced myocardial ischemia in men with CAD.
- The findings suggest a potential direct coronary-relaxing effect of testosterone.
- Testosterone may be a therapeutic option for managing myocardial ischemia in specific male populations.
Background:
The role of testosterone on the development of coronary artery disease in men is controversial. The evidence that men have a greater incidence of coronary artery disease than women of a similar age suggests a possible causal role of testosterone. Conversely, recent studies have shown that the hormone improves endothelium-dependent relaxation of coronary arteries in men. Accordingly, the aim of the present study was to evaluate the effect of acute administration of testosterone on exercise-induced myocardial ischemia in men.
Methods And Results:
After withdrawal of antianginal therapy, 14 men (mean age, 58+/-4 years) with coronary artery disease underwent 3 exercise tests according to the modified Bruce protocol on 3 different days (baseline and either testosterone or placebo given in a random order). The exercise tests were performed 30 minutes after administration of testosterone (2.5 mg IV in 5 minutes) or placebo. All patients showed at least 1-mm ST-segment depression during the baseline exercise test and after placebo, whereas only 10 patients had a positive exercise test after testosterone. Chest pain during exercise was reported by 12 patients during baseline and placebo exercise tests and by 8 patients after testosterone. Compared with placebo, testosterone increased time to 1-mm ST-segment depression (579+/-204 versus 471+/-210 seconds; P<0. 01) and total exercise time (631+/-180 versus 541+/-204 seconds; P<0. 01). Testosterone significantly increased heart rate at the onset of 1-mm ST-segment depression (135+/-12 versus 123+/-14 bpm; P<0.01) and at peak exercise (140+/-12 versus 132+/-12 bpm; P<0.01) and the rate-pressure product at the onset of 1-mm ST-segment depression (24 213+/-3750 versus 21 619+/-3542 mm Hgxbpm; P<0.05) and at peak exercise (26 746+/-3109 versus 22 527+/-5443 mm Hgxbpm; P<0.05).
Conclusions:
Short-term administration of testosterone induces a beneficial effect on exercise-induced myocardial ischemia in men with coronary artery disease. This effect may be related to a direct coronary-relaxing effect.
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