Urinary pyridinoline cross-links as biomarkers of osteogenesis imperfecta.

Détails

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Etat: Public
Version: Final published version
ID Serval
serval:BIB_3C9B6096429E
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Urinary pyridinoline cross-links as biomarkers of osteogenesis imperfecta.
Périodique
Orphanet Journal of Rare Diseases
Auteur⸱e⸱s
Lindert U., Kraenzlin M., Campos-Xavier A.B., Baumgartner M.R., Bonafé L., Giunta C., Rohrbach M.
ISSN
1750-1172 (Electronic)
ISSN-L
1750-1172
Statut éditorial
Publié
Date de publication
2015
Peer-reviewed
Oui
Volume
10
Numéro
1
Pages
104
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Résumé
Osteogenesis imperfecta (OI) is a group of genetic heterogeneous connective tissue disorders characterized by increased bone fragility and susceptibility to fractures. Laboratory diagnosis relies on time-consuming and cost-intensive biochemical and molecular genetics analyses. Therefore, it is desirable to identify and establish new diagnostic markers for OI that are reliable, cost-effective and easily accessible. In our study we have identified the ratio of the urinary pyridinoline cross-links lysyl-pyridinoline and hydroxylysyl-pyridinoline as a promising, time- and cost-effective biomarker for osteogenesis imperfecta, that could be used furthermore to investigate cases of suspected non-accidental injury in infants.
Mots-clé
Amino Acids/urine, Biomarkers/urine, Humans, Mutation, Osteogenesis Imperfecta/genetics, Osteogenesis Imperfecta/urine
Pubmed
Web of science
Open Access
Oui
Création de la notice
15/09/2015 17:27
Dernière modification de la notice
20/08/2019 14:32
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