Atypical Femoral Fracture in Osteoporosis Pseudoglioma Syndrome Associated With Two Novel Compound Heterozygous Mutations in LRP5

Nerea Alonso, Dinesh C Soares, Eugene McCloskey, Gregory D Summers, Stuart H Ralston, Celia L Gregson

Research output: Contribution to journalArticle (Academic Journal)peer-review

18 Citations (Scopus)

Abstract

Osteoporosis pseudoglioma syndrome (OPPG) is a rare autosomal recessive condition of congenital blindness and severe childhood osteoporosis with skeletal fragility, caused by loss-of-function mutations in the LRP5 (Low-density lipoprotein receptor-related protein 5) gene. We report the first case of atypical (subtrochanteric) femoral fracture (AFF) in OPPG, occurring in a 38 year old man within the context of relatively low bone turnover and trabecular osteoporosis on bone histology. We identify two novel LRP5 mutations: R752W is associated with low bone mass density (BMD), as demonstrated by the heterozygous carriage identified in his 57 year old mother; however, the combination of this R752W mutation with another novel W79R mutation, causes a severe case of compound heterozygous OPPG. We undertake three-dimensional homology modelling of the four extracellular YWTD β-propeller/EGF-like domains (E1-E4) of LRP5, and show that both novel mutations destabilise the β-propeller domains that are critical for protein and ligand binding to regulate Wnt signalling and osteoblast function. Whilst AFFs have been reported in other rare bone diseases, this is the first in a genetic condition of primary osteoblast dysfunction. The relatively low bone turnover observed, and knowledge of LRP5 function, implicates impaired bone remodelling in the pathogenesis of AFF. © 2014 American Society for Bone and Mineral Research.

Original languageEnglish
Pages (from-to)615-620
Number of pages6
JournalJournal of Bone and Mineral Research
Volume30
Issue number4
DOIs
Publication statusPublished - 10 Nov 2014

Keywords

  • ATYPICAL FEMORAL FRACTURE;COMPOUND HETEROZYGOTE;LRP5;OPPG;PROTEIN MODEL

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