Current Recommended Estrogen Dosing for Pubertal Induction in Turner Syndrome Results in Normal Uterine Growth

Author:

Lindsay Mart Faith12ORCID,Gutmark-Little Iris12ORCID,Streich-Tilles Tara34,Trout Andrew T25ORCID,Khoury Jane26ORCID,Bowers Katherine26,Casnellie Lori1ORCID,Backeljauw Philippe12ORCID

Affiliation:

1. Division of Endocrinology, Cincinnati Children's Hospital Medical Center , Cincinnati, OH 45229-3026 , USA

2. Department of Pediatrics, University of Cincinnati College of Medicine , Cincinnati, OH 45267 , USA

3. Division of Pediatric and Adolescent Gynecology, Cincinnati Children's Hospital Medical Center , Cincinnati, OH 45229-3026 , USA

4. Department of Surgery, University of Cincinnati College of Medicine , Cincinnati, OH 45267 , USA

5. Department of Radiology, Cincinnati Children's Hospital Medical Center , Cincinnati, OH 45229-3026 , USA

6. Division of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center , Cincinnati, OH 45229-3026 , USA

Abstract

Abstract Context Most individuals with Turner syndrome (TS) require estrogen for pubertal induction. Current estrogen dosing guidelines are based on expert consensus opinion. Objective Evaluate whether current international guidelines for estrogen dosing during pubertal induction of individuals with TS result in normal uterine growth. We hypothesized that uterine size in individuals with TS who reached adult estrogen dosing is smaller than in mature females without TS. Methods Cross-sectional study of patients with TS at the Cincinnati Center for Pediatric and Adult Turner Syndrome Care. Twenty-nine individuals (age 15-26 years) with primary ovarian insufficiency who reached adult estrogen dosing (100 µg of transdermal or 2 mg of oral 17β-estradiol) were included. Comparison of uterine measurements with a published sample of 292 age-appropriate (age 15-20 years) controls without TS. Uterine length, volume, and fundal–cervical ratio (FCR) were measured. Clinical information (karyotype, Tanner staging for breast development, laboratory data) was extracted from an existing institutional patient registry. Results There was no evidence of compromise of the uterine size/configuration in the TS cohort compared with the controls; in fact, uterine length, mean 7.7 cm (±1.3) vs 7.2 cm (±1.0) (P = .03), and volume, mean 60.6 cm3 (±26.6) vs 50.5 cm3 (±20.5) (P = .02), were both larger in individuals with TS. Conclusion Current international guidelines for hormone replacement using 17β-estradiol in individuals with TS appear adequate to allow for normal uterine growth by the end of pubertal induction.

Funder

Endocrine Fellows Foundation

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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