Low Vitamin D Levels in Children with Fractures: a Comparative Cohort Study Academic Article uri icon

Overview

MeSH Major

  • Age Determination by Skeleton
  • Bone and Bones
  • Hand

abstract

  • © 2015, The Author(s). Background: The currently accepted ranges for “normal” serum vitamin D have recently been challenged in adults on the basis that healthy bone metabolism requires higher levels of vitamin D than previously thought. Purpose: The purpose of this study was to evaluate whether a new “biologically based” classification based on 25(OH)vitamin D levels that invoke an endocrine biomarker response (<20 ng/mL for deficiency and <32 ng/mL for insufficiency) is more appropriate for children with fractures than historical criteria. Methods: Serum 25(OH)vitamin D levels were collected from 58 children with acute low-energy fractures from an outpatient orthopedic clinic from 2009 to 2012. These vitamin D levels were compared with a cohort of 103 children with chronic kidney disease (CKD) from an adjacent clinic, a condition with acknowledged low levels of vitamin D. Then, the prevalence of vitamin D sufficiency in the fracture cohort was evaluated and compared using both historical guidelines and newer biologically based criteria. Results: 25(OH)vitamin D levels in the fracture cohort did not differ from levels in the CKD cohort (27.5 vs. 24.6 ng/mL) indicating a similar distribution of vitamin D levels. This finding was consistent when controlling for significant covariables using linear regression analyses. In the fracture cohort, there was a discrepancy between historical and biologically based criteria in 64% of children. Conclusions: The results of the current study suggest that fracture patients are more frequently vitamin D deficient than previously thought. This finding is more readily apparent when newer biologically based criteria for vitamin D sufficiency are used.

publication date

  • August 11, 2015

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC4773687

Digital Object Identifier (DOI)

  • 10.1007/s11420-015-9447-7

PubMed ID

  • 26981060

Additional Document Info

start page

  • 249

end page

  • 257

volume

  • 11

number

  • 3