Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/17840
Title: Cortical Matrix Mineral Density Measured Noninvasively in Pre- and Postmenopausal Women and a Woman With Vitamin D-Dependent Rickets.
Authors: Chiang, Cherie Y;Zebaze, Roger M D;Wang, Xiao-Fang;Ghasem-Zadeh, Ali;Zajac, Jeffrey D;Seeman, Ego
Affiliation: Department of Endocrinology, Austin Health, Heidelberg, Australia
Department of Medicine, University of Melbourne, Parkville, Australia
Institute of Health and Ageing, Australian Catholic University, Melbourne, Australia
Issue Date: 28-Feb-2018
EDate: 2018
Citation: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2018; online first: 28 February
Abstract: Reduced bone mineral density (BMD) may be due to reduced mineralized bone matrix volume, incomplete secondary mineralization, or reduced primary mineralization. Because bone biopsy is invasive, we hypothesized that noninvasive image acquisition at high resolution can accurately quantify matrix mineral density (MMD). Quantification of MMD was confined to voxels attenuation photons above 80% of that produced by fully mineralized bone matrix because attenuation at this level is due to variation in mineralization, not porosity. To assess accuracy, 9 cadaveric distal radii were imaged at a voxel size of 82 microns using high-resolution peripheral quantitative computed tomography (HR-pQCT; XtremeCT, Scanco Medical AG, Bruttisellen, Switzerland) and compared with VivaCT 40 (µCT) at 19-micron voxel size. Associations between MMD and porosity were studied in 94 healthy vitamin D-replete premenopausal women, 77 postmenopausal women, and in a 27-year-old woman with vitamin D-dependent rickets (VDDR). Microstructure and MMD were quantified using StrAx (StraxCorp, Melbourne, Australia). MMD measured by HR-pQCT and µCT correlated (R = 0.87; p < 0.0001). The precision error for MMD was 2.43%. Cortical porosity and MMD were associated with age (r2  = 0.5 and -0.4, respectively) and correlated inversely in pre- and postmenopausal women (both r2  = 0.9, all p < 0.001). Porosity was higher, and MMD was lower, in post- than in premenopausal women (porosity 40.3% ± 7.0 versus 34.7% ± 3.5, respectively; MMD 65.4% ± 1.8 versus 66.6% ± 1.4, respectively, both p < 0.001). In the woman with VDDR, MMD was 5.6 SD lower and porosity was 5.6 SD higher than the respective trait means in premenopausal women. BMD was reduced (Z-scores femoral neck -4.3 SD, lumbar spine -3.8 SD). Low-radiation HR-pQCT may facilitate noninvasive quantification of bone's MMD and microstructure in health, disease, and during treatment. © 2018 American Society for Bone and Mineral Research.
URI: http://ahro.austin.org.au/austinjspui/handle/1/17840
DOI: 10.1002/jbmr.3415
ORCID: 0000-0002-9392-6771
0000-0002-9692-048X
PubMed URL: 29489033
Type: Journal Article
Subjects: BONE QCT/MICRO-CT
MATRIX MINERALIZATION
OSTEOMALACIA AND RICKETS
OSTEOPOROSIS
Appears in Collections:Journal articles

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