Urinary pyridinoline cross-links as biomarkers of osteogenesis imperfecta.


Autoria(s): Lindert U.; Kraenzlin M.; Campos-Xavier A.B.; Baumgartner M.R.; Bonafé L.; Giunta C.; Rohrbach M.
Data(s)

2015

Resumo

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.

Identificador

https://serval.unil.ch/?id=serval:BIB_3C9B6096429E

isbn:1750-1172 (Electronic)

pmid:26306627

doi:10.1186/s13023-015-0315-9

isiid:000360039000001

Idioma(s)

en

Fonte

Orphanet Journal of Rare Diseases, vol. 10, no. 1, pp. 104

Palavras-Chave #Amino Acids/urine; Biomarkers/urine; Humans; Mutation; Osteogenesis Imperfecta/genetics; Osteogenesis Imperfecta/urine
Tipo

info:eu-repo/semantics/article

article