Abstract
Context: Studies have found a variable incidence of erythrocytosis among people using testosterone as part of gender-affirming hormone therapy (GAHT). Objective: To examine the effect of using exogenous testosterone as GAHT on hematocrit in a large North American cohort. Methods: We conducted a cross-sectional analysis of testosterone and hematocrit laboratory values in 6670 patients who were prescribed testosterone through Plume, a national provider of GAHT. The prevalence of erythrocytosis, the mean hematocrit at predetermined testosterone thresholds and with varying routes of testosterone administration were assessed. Results: Among 6670 individuals, 560 (8.4%) had a hematocrit ≥50%, 182 ≥ 52% (2.7%), and 60 ≥ 54% (0.9%). There was significant variation (P < 50 vs T 50-299 vs T 300-999 vs T ≥ 1000 ng/dL) and when comparing serum testosterone in increments of 50 ng/dL within the target range for males (300-1000 ng/dL) (P < 50 ng/dL) to 45.68% (T 900-949 ng/dL). Patients on intramuscular testosterone had a higher mean hematocrit than those on transdermal testosterone (44.96% vs 43.41%, P
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Krishnamurthy, N., Slack, D. J., Kyweluk, M., Cullen, O., Kirkley, J., & Safer, J. D. (2024). Erythrocytosis Is Rare With Exogenous Testosterone in Gender-Affirming Hormone Therapy. Journal of Clinical Endocrinology and Metabolism, 109(5), 1285–1290. https://doi.org/10.1210/clinem/dgad651
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