Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome

Background: We have previously shown that adult height (AH) in males with Silver-Russell syndrome (SRS) correlated negatively with prepubertal estradiol concentrations. We aimed to identify the source of estradiol by analyzing androgen secretion profiles and measuring anti-Müllerian hormone (AMH) an...

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Main Authors: Kjersti Kvernebo Sunnergren, Carina Ankarberg-Lindgren, Jovanna Dahlgren
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-12-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fendo.2019.00829/full
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spelling doaj-6152c3d1816e4378b119cbd70645598b2020-11-24T21:17:52ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922019-12-011010.3389/fendo.2019.00829462447Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell SyndromeKjersti Kvernebo Sunnergren0Kjersti Kvernebo Sunnergren1Carina Ankarberg-Lindgren2Jovanna Dahlgren3Jovanna Dahlgren4Göteborg Pediatric Growth Research Center (GP-GRC), Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, SwedenDepartment of Pediatrics, Ryhov County Hospital, Jönköping, SwedenGöteborg Pediatric Growth Research Center (GP-GRC), Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, SwedenGöteborg Pediatric Growth Research Center (GP-GRC), Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, SwedenDepartment of Endocrinology, Sahlgrenska University Hospital, Queen Silva Hospital, Gothenburg, SwedenBackground: We have previously shown that adult height (AH) in males with Silver-Russell syndrome (SRS) correlated negatively with prepubertal estradiol concentrations. We aimed to identify the source of estradiol by analyzing androgen secretion profiles and measuring anti-Müllerian hormone (AMH) and inhibin B concentrations during childhood and puberty in this group of patients.Methods: In a retrospective longitudinal single-center study, 13 males with SRS were classified as non-responders (NRs = 8) or responders (Rs = 5), depending on the AH outcome. From 6 years of age, androgens were determined by mass spectrometry, and AMH, inhibin B and sex hormone-binding globulin concentrations were analyzed by immunoassays.Results: AH outcome correlated negatively with dehydroepiandrosterone-sulfate (DHEAS) at 8 (r = −0.72), 10 (r = −0.79), and 12 years (r = −0.72); testosterone at 10 (r = −0.94), 12 (r = −0.70) and 14 years (r = −0.64); dihydrotestosterone (DHT) at 10 (r = −0.62) and 12 years; (r = −0.57) and AMH at 12 years (r = 0.62) of age. Compared with Rs, NRs had higher median concentrations of DHEAS (μmol/L) at 10 years (2.9 vs. 1.0); androstenedione (nmol/L) at 10 (1.1 vs. 0.6) and 12 years (1.7 vs. 0.8); testosterone (nmol/L) at 10 (0.3 vs. 0.1), 12 (7.8 vs. 0.2) and 14 years (15.6 vs. 10.4); and DHT (pmol/L) at 10 (122 vs. 28) and 12 years (652 vs. 59) of age. AMH (ng/mL) was lower in NRs than in Rs at 12 years of age (11 vs. 50). No significant differences were observed in the inhibin B concentrations at any age.Conclusions: The elevated androgen concentrations before and during puberty, originated from both adrenal and gonadal secretion and correlated negatively with AH outcomes in males with SRS.https://www.frontiersin.org/article/10.3389/fendo.2019.00829/fullsmall for gestation ageandrogenshypogonadismanti-Müllerian hormonemass spectrometrySilver-Russell syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Kjersti Kvernebo Sunnergren
Kjersti Kvernebo Sunnergren
Carina Ankarberg-Lindgren
Jovanna Dahlgren
Jovanna Dahlgren
spellingShingle Kjersti Kvernebo Sunnergren
Kjersti Kvernebo Sunnergren
Carina Ankarberg-Lindgren
Jovanna Dahlgren
Jovanna Dahlgren
Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
Frontiers in Endocrinology
small for gestation age
androgens
hypogonadism
anti-Müllerian hormone
mass spectrometry
Silver-Russell syndrome
author_facet Kjersti Kvernebo Sunnergren
Kjersti Kvernebo Sunnergren
Carina Ankarberg-Lindgren
Jovanna Dahlgren
Jovanna Dahlgren
author_sort Kjersti Kvernebo Sunnergren
title Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
title_short Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
title_full Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
title_fullStr Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
title_full_unstemmed Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
title_sort adrenal and gonadal activity, androgen concentrations, and adult height outcomes in boys with silver-russell syndrome
publisher Frontiers Media S.A.
series Frontiers in Endocrinology
issn 1664-2392
publishDate 2019-12-01
description Background: We have previously shown that adult height (AH) in males with Silver-Russell syndrome (SRS) correlated negatively with prepubertal estradiol concentrations. We aimed to identify the source of estradiol by analyzing androgen secretion profiles and measuring anti-Müllerian hormone (AMH) and inhibin B concentrations during childhood and puberty in this group of patients.Methods: In a retrospective longitudinal single-center study, 13 males with SRS were classified as non-responders (NRs = 8) or responders (Rs = 5), depending on the AH outcome. From 6 years of age, androgens were determined by mass spectrometry, and AMH, inhibin B and sex hormone-binding globulin concentrations were analyzed by immunoassays.Results: AH outcome correlated negatively with dehydroepiandrosterone-sulfate (DHEAS) at 8 (r = −0.72), 10 (r = −0.79), and 12 years (r = −0.72); testosterone at 10 (r = −0.94), 12 (r = −0.70) and 14 years (r = −0.64); dihydrotestosterone (DHT) at 10 (r = −0.62) and 12 years; (r = −0.57) and AMH at 12 years (r = 0.62) of age. Compared with Rs, NRs had higher median concentrations of DHEAS (μmol/L) at 10 years (2.9 vs. 1.0); androstenedione (nmol/L) at 10 (1.1 vs. 0.6) and 12 years (1.7 vs. 0.8); testosterone (nmol/L) at 10 (0.3 vs. 0.1), 12 (7.8 vs. 0.2) and 14 years (15.6 vs. 10.4); and DHT (pmol/L) at 10 (122 vs. 28) and 12 years (652 vs. 59) of age. AMH (ng/mL) was lower in NRs than in Rs at 12 years of age (11 vs. 50). No significant differences were observed in the inhibin B concentrations at any age.Conclusions: The elevated androgen concentrations before and during puberty, originated from both adrenal and gonadal secretion and correlated negatively with AH outcomes in males with SRS.
topic small for gestation age
androgens
hypogonadism
anti-Müllerian hormone
mass spectrometry
Silver-Russell syndrome
url https://www.frontiersin.org/article/10.3389/fendo.2019.00829/full
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