Normative data on mineralization density distribution in iliac bone biopsies of children, adolescents and young adults

N Fratzl-Zelman, P Roschger, BM Misof, S Pfeffer… - Bone, 2009 - Elsevier
N Fratzl-Zelman, P Roschger, BM Misof, S Pfeffer, FH Glorieux, K Klaushofer, F Rauch
Bone, 2009Elsevier
Bone mineralization density distribution (BMDD) as assessed by quantitative backscattered
electron imaging (qBEI) in iliac crest bone biopsies has become in the last years a powerful
diagnostic tool to evaluate the effect of metabolic bone diseases and/or therapeutic
interventions on the mineralization status of the bone material. However until now, normative
reference data are only available for adults. The aim of the present study is to close this gap
and establish normative data from children and compare them with reference BMDD data of …
Bone mineralization density distribution (BMDD) as assessed by quantitative backscattered electron imaging (qBEI) in iliac crest bone biopsies has become in the last years a powerful diagnostic tool to evaluate the effect of metabolic bone diseases and/or therapeutic interventions on the mineralization status of the bone material. However until now, normative reference data are only available for adults. The aim of the present study is to close this gap and establish normative data from children and compare them with reference BMDD data of adults. qBEI analyses were performed on bone samples from 54 individuals between 1.5 and 23 years without metabolic bone diseases, which were previously used as study population to establish normative histomorphometric standards. In the trabecular compartment, none of the BMDD parameters showed a significant correlation with age. The BMDD was shifted towards lower mineralization density (CaMean −5.6%, p<0.0001; CaPeak −5.6%, p<0.0001; CaLow +39.0% p<0.001; CaHigh −80.7%, p<0.001) and the inter-individual variation was higher compared to the adult population. The cortices appeared to be markedly less mineralized (CaMean −3.1%, p<0.0001) than cancellous bone due to higher amounts of low mineralized secondary bone. However, the cortical BMDD parameters showed a strong correlation (r=0.38 to 0.85, with p<0.001 to<0.0001) with cancellous BMDD parameters. In conclusion, this study provides evidence that BMDD parameters in growing healthy subjects are relatively constant and that these data can be used as normative references in pediatrics osteology. The larger inter-individual variability compared to adults is most likely related to alterations of the bone turnover rate during growth.
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