Abstract
Introduction: Reduced testosterone levels are frequently observed in obese men. Increased aromatase activity may be an etiological factor. Objective: In this study, we evaluate the clinical effects of aromatase inhibition in obesity-related hypogonadotropic hypotestosteronemia (OrHH). Methods: Double-blind, placebo-controlled, 6-month trial in 42 obese men with a BMI >35 kg/m2, and a serum total testosterone <10 nmol/l. All patients started on one tablet of 2.5 mg/week, with subsequent dose escalation every month until a serum total testosterone of 20 nmol/l was reached. Endpoints: Psychological function, body composition, exercise capacity, and glucose, lipid, and bone metabolism. Results: Thirty-nine patients completed the study according to protocol. Letrozole decreased serum estradiol from 119.1±10.1 to 59.2±6.1 pmol/l (P>0.001), and increased serum LH from 3.3±0.3 to 8.8±0.9 U/l (P>0.0001) and serum total testosterone from 8.6±0.7 to 21.5±1.3 nmol/l (P>0.0001). Significant effects on the predefined endpoints were not observed. Conclusion: Despite a marked rise in serum testosterone, low-dose aromatase inhibition had no somatic or psychological effects in men with OrHH. © 2013 European Society of Endocrinology.
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CITATION STYLE
Loves, S., De Jong, J., Van Sorge, A., Telting, D., Tack, C. J., Hermus, A., … De Boer, H. (2013). Somatic and psychological effects of low-dose aromatase inhibition in men with obesity-related hypogonadotropic hypotestosteronemia. European Journal of Endocrinology, 169(5), 705–714. https://doi.org/10.1530/EJE-13-0190
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