3.8 Article

Reproductive Endocrinology Reference Intervals for Transgender Women on Stable Hormone Therapy

Journal

JOURNAL OF APPLIED LABORATORY MEDICINE
Volume 6, Issue 1, Pages 15-26

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/jalm/jfaa028

Keywords

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Funding

  1. University of Washington, Department of Laboratory Medicine
  2. University of Iowa, Department of Pathology

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This study aimed to establish reference intervals for commonly measured analytes related to reproductive endocrinology in transgender women. The use of spironolactone was associated with changes in the result distribution of some tests. Immunoassay was found to be sufficient for measuring estradiol and total testosterone in most cases.
Background: Transgender women and nonbinary people seeking feminizing therapy are often prescribed estrogen as a gender-affirming hormone, which will alter their reproductive hormone axis. Testosterone, estradiol, and other reproductive hormones are commonly evaluated to assess therapy, but reference intervals specific to transgender women have not been established. The objective of this study was to derive reference intervals for commonly measured analytes related to reproductive endocrinology in a cohort of healthy gender nonconforming individuals on stable feminizing hormone therapy. Methods: Healthy transgender individuals who had been prescribed estrogen (n = 93) for at least a year were recruited from internal medicine and primary care clinics that specialize in transgender medical care. Total testosterone and estradiol were measured using immunoassay and mass spectrometry; LH, FSH, sex hormone binding globulin, prolactin, progesterone, anti-mullerian hormone (AMH), and dehydroepiandrosterone sulfate (DHEAS) were measured using immunoassay; free testosterone was calculated. Reference intervals (central 95%) were calculated according to Clinical Laboratory Standards Institute guidelines. Results: The distribution of results for transgender women was different than what would be expected from cis-gender men or women across all measurements. Use of spironolactone was associated with changes in the result distribution of AMH, FSH, LH, and progesterone. Compared to liquid chromatography coupled to tandem mass spectrometry (LC/MS/MS), immunoassay was sufficient for the majority of estradiol and total testosterone measurements; free testosterone added little clinical value beyond total testosterone. Conclusion: Reference intervals specific to transgender women should be applied when evaluating reproductive endocrine analytes. Spironolactone is a significant variable for result interpretation of some tests.

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