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Published in: Journal of Inherited Metabolic Disease 6/2014

01-11-2014 | Review

A systematic review of bone mineral density and fractures in phenylketonuria

Authors: Karen E. Hansen, Denise Ney

Published in: Journal of Inherited Metabolic Disease | Issue 6/2014

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Abstract

Introduction

Our objective was to systematically review and analyze published data on bone mineral density (BMD) and fracture rates in patients with phenylketonuria (PKU), and relationships between BMD and phenylalanine levels.

Methodology

We searched PubMed, CINAHL, and Cochrane databases from January 1966 to November 2013 for studies of spine BMD or fracture in PKU and control subjects. We excluded studies assessing skeletal health by ultrasound or peripheral quantitative computer tomography. Both authors reviewed abstracts for inclusion, and read full text papers to extract data.

Results

Sixteen studies met eligibility criteria. Meta-analysis of three studies found that spine BMD was 0.100 g/cm2 lower (95% CI, -0.110, -0.090 g/cm2) in 67 subjects with PKU, compared to 161 controls. Among six studies, 20% (53 of 263) of PKU subjects experienced clinical fractures. In the single study with controls, the fracture rate was 2.6 fold higher (95% CI, 1.1-6.1) after age 8 in PKU subjects, compared to healthy sibling controls. When considering a total of 12 studies in 412 subjects, nine or 75% of studies representing 71% of studied subjects reported no association between phenylalanine levels and BMD.

Summary

Spine BMD is lower in PKU than control subjects, but only one study controlled for smaller body size. Existing studies suggest a clinical fracture rate of 20% among PKU subjects, but fracture rates in controls are lacking. Finally, existing data shows no consistent relationship between phenylalanine levels and BMD. Future studies are needed to clarify the etiology and health consequences of low BMD in PKU.
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Metadata
Title
A systematic review of bone mineral density and fractures in phenylketonuria
Authors
Karen E. Hansen
Denise Ney
Publication date
01-11-2014
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 6/2014
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-014-9735-2

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