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Revista de Osteoporosis y Metabolismo Mineral

On-line version ISSN 2173-2345Print version ISSN 1889-836X

Abstract

LOPEZ PICAZO, M et al. Can 3D measurements obtained by lumbar DXA predict fractures in the dorsal vertebrae?. Rev Osteoporos Metab Miner [online]. 2020, vol.12, n.2, pp.45-52.  Epub Oct 05, 2020. ISSN 2173-2345.  https://dx.doi.org/10.4321/s1889-836x2020000200003.

Objective:

To assess the relation between threedimensional (3D) measurements obtained by lumbar dual energy Xray absorptiometry (DXA) and osteoporotic fractures in dorsal vertebrae.

Material and methods:

We analysed retrospectively 32 postmenopausal women, allocated to two groups: 16 women in the experimental group, who presented incident fractures of the dorsal vertebrae, and 16 women in the control group, who did not show any type of fracture. Measurements of the (aBMD) of vertebrae L1 through L4 were taken at the initial visit (i.e., prior to the fracture event) by lumbar dualenergy xray absorptiometries (DXA). 3D measurements obtained by DXA were evaluated using 3D modelling software (3DSHAPER). Volumetric bone mineral density (vBMD) was calculated in the trabecular, cortical and integral bone. Cortical thickness and cortical surface BMD (sBMD) were also measured. Differences in measurements derived from the DXA between the experimental and control groups were assessed using an unpaired Student ttest. The odds ratio (OR) and the area under the receiver operating characteristic curve (AUC) were also determined.

Results:

In the present ageadjusted casecontrol study, no significant differences were found between the experimental and control groups in terms of weight (ρ=0.44), height (ρ=0.25) and aBMD (ρ=0.11). However, significant differences (ρ<0.05) were found in the integral and trabecular vBMD and in the cortical sBMD. Trabecular vBMD in the vertebral body was the measure that best discriminated between both groups, with an AUC of 0.733, compared to 0.682 of the aBMD.

Conclusion:

This study shows the ability of 3D models resultant from lumbar DXAs to discern between subjects with incident fractures in the dorsal vertebrae and control subjects. It is necessary to analyse larger cohorts to establish if these measurements could improve the prediction of fracture risk in clinical practice.

Keywords : 3D modelling; Fracture risk; Osteoporosis; Trabecular; Cortical; Vertebral fracture; Volumetric bone mineral density; Superficial bone mineral density.

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