Literature DB >> 24051620

Adult height and epigenotype in children with Silver-Russell syndrome treated with GH.

G Binder1, M Liebl, J Woelfle, T Eggermann, G Blumenstock, R Schweizer.   

Abstract

AIMS: To compare adult heights of GH-treated and GH-untreated patients with Silver-Russell syndrome (SRS) who were epigenotyped.
METHODS: This was a nonrandomized retrospective study with matched controls at a single center. Molecular analysis of 32 out of 37 GH-treated patients (16 females) revealed IGF2-H19 epimutations in 12 and maternal uniparental disomy of chromosome 7 (matUPD7) in 5 patients; 15 were negative. At start of GH, mean age was 7.2 years and mean height -3.34 standard deviation score (SDS). Mean GH dose used was 51 µg/kg·day, mean duration of therapy was 5.6 years. Puberty was blocked by GnRH analogs in 16 patients. The untreated group comprised 13 individuals (5 females, mean age 6.8 years and mean height -3.34 SDS). End points were adult height and overall height gain.
RESULTS: GH-treated patients reached an adult height of -2.12 ± 0.98 SDS gaining 1.22 SDS in comparison to baseline. Adult height SDS of the untreated was -3.13 ± 1.37 SDS. The matched treated patients were significantly taller than their untreated counterparts. Outcome was dependent on height at start of GH and duration of therapy. Height gain was highest in the shortest patients.
CONCLUSIONS: GH improved adult height in SRS to a comparable degree as reported in nonsyndromic SGA children. A trend toward a better outcome in matUPD7 needs confirmation in larger cohorts.
Copyright © 2013 S. Karger AG, Basel.

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Year:  2013        PMID: 24051620     DOI: 10.1159/000354658

Source DB:  PubMed          Journal:  Horm Res Paediatr        ISSN: 1663-2818            Impact factor:   2.852


  12 in total

Review 1.  Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology.

Authors:  Katrin Õunap
Journal:  Mol Syndromol       Date:  2016-07-06

2.  Diagnosis and management of Silver-Russell syndrome: first international consensus statement.

Authors:  Emma L Wakeling; Frédéric Brioude; Oluwakemi Lokulo-Sodipe; Susan M O'Connell; Jennifer Salem; Jet Bliek; Ana P M Canton; Krystyna H Chrzanowska; Justin H Davies; Renuka P Dias; Béatrice Dubern; Miriam Elbracht; Eloise Giabicani; Adda Grimberg; Karen Grønskov; Anita C S Hokken-Koelega; Alexander A Jorge; Masayo Kagami; Agnes Linglart; Mohamad Maghnie; Klaus Mohnike; David Monk; Gudrun E Moore; Philip G Murray; Tsutomu Ogata; Isabelle Oliver Petit; Silvia Russo; Edith Said; Meropi Toumba; Zeynep Tümer; Gerhard Binder; Thomas Eggermann; Madeleine D Harbison; I Karen Temple; Deborah J G Mackay; Irène Netchine
Journal:  Nat Rev Endocrinol       Date:  2016-09-02       Impact factor: 43.330

3.  Components of IGF-axis in growth disorders: a systematic review and patent landscape report.

Authors:  Amit Singh; Ketan Pajni; Inusha Panigrahi; Navdeep Dhoat; Sabyasachi Senapati; Preeti Khetarpal
Journal:  Endocrine       Date:  2022-05-06       Impact factor: 3.925

4.  Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testing.

Authors:  Thomas Eggermann; Ann-Kathrin Heilsberg; Susanne Bens; Reiner Siebert; Jasmin Beygo; Karin Buiting; Matthias Begemann; Lukas Soellner
Journal:  J Mol Med (Berl)       Date:  2014-07       Impact factor: 4.599

5.  Isolated Hypomethylation of IGF2 Associated with Severe Hypoglycemia Responsive to Growth Hormone Treatment.

Authors:  Sarah C Grünert; Uta Matysiak; Franka Hodde; Gunda Ruzaike; Ekkehart Lausch; Anke Schumann; Natascha van der Werf-Grohmann; Ute Spiekerkoetter; Miriam Schmidts
Journal:  Diagnostics (Basel)       Date:  2021-04-22

6.  EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome.

Authors:  Katja Eggermann; Jet Bliek; Frédéric Brioude; Elizabeth Algar; Karin Buiting; Silvia Russo; Zeynep Tümer; David Monk; Gudrun Moore; Thalia Antoniadi; Fiona Macdonald; Irène Netchine; Paolo Lombardi; Lukas Soellner; Matthias Begemann; Dirk Prawitt; Eamonn R Maher; Marcel Mannens; Andrea Riccio; Rosanna Weksberg; Pablo Lapunzina; Karen Grønskov; Deborah Jg Mackay; Thomas Eggermann
Journal:  Eur J Hum Genet       Date:  2016-05-11       Impact factor: 4.246

7.  Novel mutation points to a hot spot in CDKN1C causing Silver-Russell syndrome.

Authors:  Gerhard Binder; Julian Ziegler; Roland Schweizer; Wisam Habhab; Tobias B Haack; Tilman Heinrich; Thomas Eggermann
Journal:  Clin Epigenetics       Date:  2020-10-19       Impact factor: 6.551

8.  Clinical Application of Sequential Epigenetic Analysis for Diagnosis of Silver-Russell Syndrome.

Authors:  Soo Yeon Kim; Chang Ho Shin; Young Ah Lee; Choong Ho Shin; Sei Won Yang; Tae-Joon Cho; Jung Min Ko
Journal:  Ann Lab Med       Date:  2021-07-01       Impact factor: 3.464

Review 9.  Should Skeletal Maturation Be Manipulated for Extra Height Gain?

Authors:  Jan M Wit
Journal:  Front Endocrinol (Lausanne)       Date:  2021-12-16       Impact factor: 5.555

10.  Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important.

Authors:  Thomas Eggermann; Johanna Brück; Cordula Knopp; György Fekete; Christian Kratz; Velibor Tasic; Ingo Kurth; Miriam Elbracht; Katja Eggermann; Matthias Begemann
Journal:  J Mol Med (Berl)       Date:  2020-08-24       Impact factor: 4.599

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