Bone tissue homeostasis and risk of fractures in Costello syndrome: A 4-year follow-up study

Am J Med Genet A. 2022 Feb;188(2):422-430. doi: 10.1002/ajmg.a.62615. Epub 2021 Dec 15.

Abstract

Costello syndrome (CS) is a neurodevelopmental disorder with a distinctive musculoskeletal phenotype and reduced bone mineral density (BMD) caused by activating de novo mutations in the HRAS gene. Herein, we report the results of a prospective study evaluating the efficacy of a 4-year vitamin D supplementation on BMD and bone health. A cohort of 16 individuals ranging from pediatric to adult age with molecularly confirmed CS underwent dosages of bone metabolism biomarkers (serum/urine) and dual-energy X-ray absorptiometry (DXA) scans to assess bone and body composition parameters. Results were compared to age-matched control groups. At baseline evaluation, BMD was significantly reduced (p ≤ 0.05) compared to controls, as were the 25(OH)vitD levels. Following the 4-year time interval, despite vitamin D supplementation therapy at adequate dosages, no significant improvement in BMD was observed. The present data confirm that 25(OH)vitD and BMD parameters are reduced in CS, and vitamin D supplementation is not sufficient to restore proper BMD values. Based on this evidence, routine monitoring of bone homeostasis to prevent bone deterioration and possible fractures in adult patients with CS is highly recommended.

Keywords: Costello syndrome; RASopathies; bone metabolism biomarkers; bone mineral density; patient-centered care; personalized medicine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Absorptiometry, Photon
  • Bone Density
  • Bone and Bones
  • Child
  • Costello Syndrome* / complications
  • Costello Syndrome* / genetics
  • Follow-Up Studies
  • Homeostasis
  • Humans
  • Prospective Studies
  • Vitamin D / therapeutic use

Substances

  • Vitamin D