Effects of low-dose estrogen replacement during childhood on pubertal development and gonadotropin concentrations in patients with Turner syndrome: results of a randomized, double-blind, placebo-controlled clinical trial

dc.contributor.authorQuigley, Charmian A.
dc.contributor.authorWan, Xiaohai
dc.contributor.authorGarg, Sipi
dc.contributor.authorKowal, Karen
dc.contributor.authorCutler, Gordon B. Jr.
dc.contributor.authorRoss, Judith L.
dc.contributor.departmentDepartment of Medicine, IU School of Medicineen_US
dc.date.accessioned2016-06-14T13:41:18Z
dc.date.available2016-06-14T13:41:18Z
dc.date.issued2014-09
dc.description.abstractCONTEXT: The optimal approach to estrogen replacement in girls with Turner syndrome has not been determined. OBJECTIVE: The aim of the study was to assess the effects of an individualized regimen of low-dose ethinyl estradiol (EE2) during childhood from as early as age 5, followed by a pubertal induction regimen starting after age 12 and escalating to full replacement over 4 years. DESIGN: This study was a prospective, randomized, double-blind, placebo-controlled clinical trial. SETTING: The study was conducted at two US pediatric endocrine centers. SUBJECTS: Girls with Turner syndrome (n = 149), aged 5.0-12.5 years, were enrolled; data from 123 girls were analyzable for pubertal onset. INTERVENTION(S): Interventions comprised placebo or recombinant GH injections three times a week, with daily oral placebo or oral EE2 during childhood (25 ng/kg/d, ages 5-8 y; 50 ng/kg/d, ages >8-12 y); after age 12, all patients received escalating EE2 starting at a nominal dosage of 100 ng/kg/d. Placebo/EE2 dosages were reduced by 50% for breast development before age 12 years, vaginal bleeding before age 14 years, or undue advance in bone age. MAIN OUTCOME MEASURES: The main outcome measures for this report were median ages at Tanner breast stage ≥2, median age at menarche, and tempo of puberty (Tanner 2 to menarche). Patterns of gonadotropin secretion and impact of childhood EE2 on gonadotropins also were assessed. RESULTS: Compared with recipients of oral placebo (n = 62), girls who received childhood low-dose EE2 (n = 61) had significantly earlier thelarche (median, 11.6 vs 12.6 y, P < 0.001) and slower tempo of puberty (median, 3.3 vs 2.2 y, P = 0.003); both groups had delayed menarche (median, 15.0 y). Among childhood placebo recipients, girls who had spontaneous breast development before estrogen exposure had significantly lower median FSH values than girls who did not. CONCLUSIONS: In addition to previously reported effects on cognitive measures and GH-mediated height gain, childhood estrogen replacement significantly normalized the onset and tempo of puberty. Childhood low-dose estrogen replacement should be considered for girls with Turner syndrome.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationQuigley, C. A., Wan, X., Garg, S., Kowal, K., Cutler, G. B., & Ross, J. L. (2014). Effects of Low-Dose Estrogen Replacement During Childhood on Pubertal Development and Gonadotropin Concentrations in Patients With Turner Syndrome: Results of a Randomized, Double-Blind, Placebo-Controlled Clinical Trial. The Journal of Clinical Endocrinology and Metabolism, 99(9), E1754–E1764. http://doi.org/10.1210/jc.2013-4518en_US
dc.identifier.urihttps://hdl.handle.net/1805/9936
dc.language.isoen_USen_US
dc.publisherThe Endocrine Societyen_US
dc.relation.isversionof10.1210/jc.2013-4518en_US
dc.relation.journalThe Journal of Clinical Endocrinology and Metabolismen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectAdolescenten_US
dc.subjectBody height -- Drug effectsen_US
dc.subjectBreast -- Growth & developmenten_US
dc.subjectEstrogensen_US
dc.subjectEthinyl estradiolen_US
dc.subjectGonadotropinsen_US
dc.subjectHormone replacement therapyen_US
dc.subjectKaplan-Meier estimateen_US
dc.subjectTurner Syndromeen_US
dc.titleEffects of low-dose estrogen replacement during childhood on pubertal development and gonadotropin concentrations in patients with Turner syndrome: results of a randomized, double-blind, placebo-controlled clinical trialen_US
dc.typeArticleen_US
ul.alternative.fulltexthttp://pubmed.gov/24762109en_US
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