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Comparison of the Subcutaneous and Intramuscular Estradiol Regimens as Part of Gender-Affirming Hormone Therapy
Institution:1. Mayo Clinic Department of Medicine, Division of Endocrinology, Diabetes, Nutrition Rochester, Minnesota;2. Midwest Endocrinology, Crystal Lake, Illinois;3. Mayo Clinic Department of Medicine, Division of Endocrinology, Diabetes and Metabolism, Jacksonville, Florida;1. The Department of General Surgery, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China;2. Department of Ultrasonography, Yuhang Third People’s Hospital, Hangzhou, China;3. Department of Ultrasonography, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, China;1. Department of Pathology, Houston Methodist Hospital, Houston, Texas;2. Department of Pathology, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, Ohio;3. Department of Pathology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois;4. Endocrinology and Metabolism Institute, Cleveland Clinic Foundation, Cleveland, Ohio;1. Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran;2. Department of Endocrinology, Royal Victoria Infirmary, Newcastle Upon Tyne, United Kingdom;1. Department of Biostatistics, School of Public Health, University of Washington, Seattle, WA;2. Department of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA;3. Geriatric Research Education and Clinical Center, VA Health Care System, Minneapolis, MN;4. Department of Medicine, University of California, Irvine, CA;5. Department of Medicine, Beth Israel Deaconess Medical Center, Brookline, MA;6. Division of Endocrinology, Kaiser Permanente of Georgia, and Department of Endocrinology, Emory University School of Medicine, Atlanta, GA;1. Department of Surgery, University of Maryland, Baltimore, Baltimore, Maryland;2. Department of Practice, Sciences, and Health Outcomes Research, University of Maryland School of Pharmacy, Baltimore, Maryland;3. Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland;4. Department of Family Medicine, University of Maryland Baltimore, Baltimore, Maryland;1. Division of Endocrinology, Diabetes, and Metabolism, Department of Medicine, Houston Methodist Hospital, Weill Cornell Medicine, Houston, Texas;2. Center for Health Data Science and Analytics, Houston Methodist Hospital Research Institute and Weill Cornell Medicine, Houston, Texas
Abstract:ObjectiveGender-affirming hormone therapy guidelines describe the estradiol (E2) doses for intramuscular (IM), but not subcutaneous (SC), routes. The objective was to compare the SC and IM E2 doses and hormone levels in transgender and gender diverse individuals.MethodsThis is a retrospective cohort study at a single-site tertiary care referral center. Patients were transgender and gender diverse individuals who received injectable E2 with at least 2 E2 measurements. The main outcomes were the dose and serum hormone levels between the SC and IM routes.ResultsThere were no statistically significant differences in age, body mass index, or antiandrogen use between patients on SC (n = 74) and those on IM (n = 56). The weekly doses of SC E2, 3.75 mg (IQR, 3-4 mg), were statistically significantly lower than those of IM E2, 4 mg (IQR, 3-5.15 mg) (P =.005); however, the E2 levels achieved were not significantly different (P =.69), and the testosterone levels were in the cisgender female range and not significantly different between routes (P =.92). Subgroup analysis demonstrated significantly higher doses in the IM group when the E2 and testosterone levels were >100 pg/mL and <50 ng/dL, respectively, with the presence of the gonads or use of antiandrogens. Multiple regression analysis demonstrated that the dose was significantly associated with the E2 levels after adjusting for injection route, body mass index, antiandrogen use, and gonadectomy status.ConclusionBoth the SC and IM E2 achieve therapeutic E2 levels without a significant difference in the dose (3.75 vs 4 mg). SC may achieve therapeutic levels at lower doses than IM .
Keywords:transgender women  transfeminine  estrogen  GAHT  parenteral administration  BMI"}  {"#name":"keyword"  "$":{"id":"kwrd0040"}  "$$":[{"#name":"text"  "_":"body mass index  E2"}  {"#name":"keyword"  "$":{"id":"kwrd0050"}  "$$":[{"#name":"text"  "_":"estradiol  GAHT"}  {"#name":"keyword"  "$":{"id":"kwrd0060"}  "$$":[{"#name":"text"  "_":"gender-affirming hormone therapy  IM"}  {"#name":"keyword"  "$":{"id":"kwrd0070"}  "$$":[{"#name":"text"  "_":"intramuscular  SC"}  {"#name":"keyword"  "$":{"id":"kwrd0080"}  "$$":[{"#name":"text"  "_":"subcutaneous  TGD"}  {"#name":"keyword"  "$":{"id":"kwrd0090"}  "$$":[{"#name":"text"  "_":"transgender and gender diverse
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