Laboratory Monitoring in Transgender and Gender-Diverse Individuals

被引:0
|
作者
Nolan, Brendan J. [1 ,2 ]
Cheung, Ada S. [2 ,3 ,4 ]
机构
[1] Princess Alexandra Hosp, Dept Diabet & Endocrinol, Woolloongabba, Qld, Australia
[2] Univ Melbourne, Austin Hlth, Dept Med, Trans Hlth Res Grp, Heidelberg, Vic, Australia
[3] Thorne Harbour Hlth, Equinox Gender Diverse Clin, Abbotsford, Vic, Australia
[4] Austin Hlth, Dept Endocrinol, Heidelberg, Vic, Australia
基金
英国医学研究理事会;
关键词
SEX HORMONE-THERAPY; BONE-MINERAL DENSITY; TERM-FOLLOW-UP; CYPROTERONE-ACETATE; ANDROGEN DEPRIVATION; LEUPROLIDE ACETATE; PROSTATE-CANCER; TESTOSTERONE; ESTRADIOL; COHORT;
D O I
10.1093/clinchem/hvaf001
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background Increasing numbers of transgender and gender-diverse individuals are seeking initiation of gender-affirming hormone therapy. This aligns an individual's physical characteristics with their gender identity and improves psychological outcomes. Physical changes, including changes to muscle mass and body fat redistribution, can alter sex-specific laboratory reference ranges.Content We review the impact of gender-affirming hormone therapy on laboratory parameters with sex-specific reference ranges, with a focus on hemoglobin/hematocrit, renal function, cardiac biomarkers, and prostate-specific antigen.Summary Gender-affirming hormone therapy results in changes in laboratory parameters with sex-specific reference ranges. For individuals established on gender-affirming hormone therapy, reference ranges that align with an individual's gender identity should be used for hemoglobin/hematocrit, serum creatinine, and high-sensitivity cardiac troponin and N-terminal brain natriuretic peptide. Clinicians should interpret these biomarkers according to the reference range that aligns with one's affirmed gender.
引用
收藏
页码:358 / 377
页数:20
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