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Heterogeneity and Spatial Distribution of Intravertebral Trabecular Bone Mineral Density in the Lumbar Spine is Associated with Prevalent Vertebral Fracture

Kaiser J1Allaire B2Fein PM1Lu D3Adams A1Kiel DP2,4Jarraya M5,6Guermazi A5Demissie S3Samelson EJ7,8Bouxsein ML2,9Morgan EF1.

J Bone Miner Res. 2019 Dec 30. doi: 10.1002/jbmr.3946. [Epub ahead of print]




The spatial heterogeneity in trabecular bone density within the vertebral centrum is associated with vertebral strength and could explain why volumetric bone mineral density (vBMD) exhibits low sensitivity in identifying fracture risk. This study evaluated whether the heterogeneity and spatial distribution of trabecular vBMD are associated with prevalent vertebral fracture. We examined the volumetric QCT scans of the L3 vertebra in 148 participants in the Framingham Heart Study Multidetector CT study. Of these individuals, 37 were identified as cases of prevalent fracture, and 111 were controls, matched on sex and age with three controls per case. vBMD was calculated within 5-mm contiguous cubic regions of the centrum. Two measures of heterogeneity were calculated: 1) interquartile range (IQR); and 2) quartile coefficient of variation (QCV). Spatial distributions of the trabecular vBMD were also calculated: anterior/posterior, central/outer, superior/mid-transverse, and inferior/mid-transverse. Heterogeneity and spatial distributions were compared between cases and controls using Wilcoxon Rank Sum tests and t-tests and tested for association with prevalent fractures with conditional logistic regressions independent of integral vBMD. Prevalent fracture cases had lower mean (SD) integral vBMD (134 (38) vs.165 (42) mg/cm3 , p<0.001), higher QCV (0.22 (0.13) vs. 0.17 (0.09), p=0.003), and lower anterior/posterior rBMD (0.65 (0.13) vs 0.78 (0.16), p<0.001) than controls. QCV was positively associated with increased odds of prevalent fracture (OR=1.61; 95% CI: 1.04-2.49, p=0.034), but this association was not independent of integral vBMD (p=0.598). Increased anterior/posterior trabecular vBMD ratio was associated with decreased odds of prevalent fracture independent of integral vBMD (OR= 0.38; 95% CI: 0.20-0.71, p=0.003). In conclusion, increased trabecular vBMD in the anterior vs. posterior centrum, but not trabecular vBMD heterogeneity, was associated with decreased risk of prevalent fracture independent of integral vBMD. Regional measurements of trabecular vBMD could aid in determining the risk and underlying mechanisms of vertebral fracture.