Back to Search Start Over

Is ghrelin a biomarker of early-onset scoliosis in children with Prader–Willi syndrome?

Authors :
Dibia Liz Pacoricona Alfaro
Gwenaelle Diene
Graziella Pinto
Jean-Pierre Salles
Isabelle Gennero
Sandy Faye
Catherine Molinas
Marion Valette
Catherine Arnaud
Maithé Tauber
Source :
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Publication Year :
2021
Publisher :
BMC, 2021.

Abstract

Abstract Background Adolescents with idiopathic scoliosis display high ghrelin levels. As hyperghrelinemia is found in patients with PWS and early-onset scoliosis (EOS) is highly prevalent in these patients, our aims were to explore (1) whether ghrelin levels differ between those with and without EOS and correlate with scoliosis severity, and (2) whether ghrelin levels in the first year of life are associated with the later development of EOS. Methods We used a case control study design for the first question and a longitudinal design for the second. Patients with PWS having plasma ghrelin measurements recorded between 2013 and 2018 in our database were selected and 30 children

Details

Language :
English
ISSN :
17501172
Volume :
16
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.85c4c50f7a6a445abadf58f6047bda63
Document Type :
article
Full Text :
https://doi.org/10.1186/s13023-021-01930-1