Men with low or low-normal testosterone levels who received testosterone replacement therapy for 3 years as part of a study experienced no significant change in subclinical atherosclerosis progression. They also had no significant improvement in overall sexual function or health-related quality of life (QOL).
Researchers led by Shalender Bhasin, MBBS, of Harvard Medical School in Boston, randomized 156 men to receive 7.5 g of 1% testosterone gel and 152 to receive placebo gel packets daily for 3 years. Patients had a mean age of 67.6 years. To be included in the study, men had to have testosterone levels of 100–400 ng/dL or free testosterone levels less than 50 pg/mL. The co-primary outcomes were the rate of change in distal right common carotid intima-media thickness and coronary artery calcium.
The rate of change in carotid artery intima-media thickness was 0.010 mm per year in the placebo group and 0.012 mm per year in the testosterone group, Dr. Bhasin’s group reported in the Journal of the American Medical Association (2015314:570-581). The rate of change in the coronary artery calcium score was 41.4 Agatston units per year in the placebo group and 31.4 Agatston units per year in the testosterone group. None of these between-group differences were statistically significant.
The researchers assessed sexual function using the International Index of Erectile Function, a validated 15-item questionnaire that assesses 5 domains of sexual function (erectile function, orgasmic function, sexual desire, intercourse satisfaction, and overall sexual satisfaction). They used the Medical Outcomes Study 36-item short form health survey (SF-36) to assess health-related QOL.
Dr. Bhasin and his colleagues found that testosterone administration did not significantly improve erectile or ejaculatory function, sexual desire, partner intimacy, health-related QOL. Intercourse satisfaction showed statistically significant improvements, but these “were of small magnitude and could be due to chance alone, in light of the lack of improvements in other domains of sexual function.”
“Because this trial was only powered to evaluated atherosclerosis progression and not cardiovascular events, these findings should not be interpreted as establishing cardiovascular safety of testosterone use in older men such as those enrolled in this trial,” the authors cautioned.