Orphanet Journal of Rare Diseases (Aug 2023)

Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification

  • Hongjie Yu,
  • Changrong Li,
  • Huixiao Wu,
  • Weibo Xia,
  • Yanzhou Wang,
  • Jiajun Zhao,
  • Chao Xu

DOI
https://doi.org/10.1186/s13023-023-02849-5
Journal volume & issue
Vol. 18, no. 1
pp. 1 – 9

Abstract

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Abstract Osteogenesis imperfecta (OI) is a connective tissue disorder affecting the skeleton and other organs, which has multiple genetic patterns, numerous causative genes, and complex pathogenic mechanisms. The previous classifications lack structure and scientific basis and have poor applicability. In this paper, we summarize and sort out the pathogenic mechanisms of OI, and analyze the molecular pathogenic mechanisms of OI from the perspectives of type I collagen defects(synthesis defects, processing defects, post-translational modification defects, folding and cross-linking defects), bone mineralization disorders, osteoblast differentiation and functional defects respectively, and also generalize several new untyped OI-causing genes and their pathogenic mechanisms, intending to provide the evidence of classification and a scientific basis for the precise diagnosis and treatment of OI.

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