Circulating Testosterone as the Hormonal Basis of Sex Differences in Athletic Performance

• Published in: Endocrine reviews Vol. 39; no. 5; pp. 803 - 829
• Main Authors: Handelsman, David J, Hirschberg, Angelica L, Bermon, Stephane
• Format: Journal Article
• Language: English
• Published: Washington, DC Endocrine Society 01.10.2018; Copyright Oxford University Press; Oxford University Press
• Subjects: Athletes; Athletic Performance - physiology; Development and progression; Dichotomies; Female; Gender aspects; Gender differences; Hemoglobin; Humans; Liquid chromatography; Male; Mass spectrometry; Mass spectroscopy; Medicin och hälsovetenskap; Men; Muscles; Polycystic ovary syndrome; Puberty; Reviews; Sex; Sex Characteristics; Sex differences; Sports; Stein-Leventhal syndrome; Testosterone; Testosterone - blood; Transgender persons; Women
• ISSN: 0163-769X; 1945-7189; 1945-7189
• DOI: 10.1210/er.2018-00020

Abstract Elite athletic competitions have separate male and female events due to men's physical advantages in strength, speed, and endurance so that a protected female category with objective entry criteria is required. Prior to puberty, there is no sex difference in circulating testosterone concentrations or athletic performance, but from puberty onward a clear sex difference in athletic performance emerges as circulating testosterone concentrations rise in men because testes produce 30 times more testosterone than before puberty with circulating testosterone exceeding 15-fold that of women at any age. There is a wide sex difference in circulating testosterone concentrations and a reproducible dose-response relationship between circulating testosterone and muscle mass and strength as well as circulating hemoglobin in both men and women. These dichotomies largely account for the sex differences in muscle mass and strength and circulating hemoglobin levels that result in at least an 8% to 12% ergogenic advantage in men. Suppression of elevated circulating testosterone of hyperandrogenic athletes results in negative effects on performance, which are reversed when suppression ceases. Based on the nonoverlapping, bimodal distribution of circulating testosterone concentration (measured by liquid chromatography-mass spectrometry)-and making an allowance for women with mild hyperandrogenism, notably women with polycystic ovary syndrome (who are overrepresented in elite athletics)-the appropriate eligibility criterion for female athletic events should be a circulating testosterone of <5.0 nmol/L. This would include all women other than those with untreated hyperandrogenic disorders of sexual development and noncompliant male-to-female transgender as well as testosterone-treated female-to-male transgender or androgen dopers.