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In adults, BMD and BMC should change in parallel, as bone area does not change appreciably; thus, discordant BMD and BMC results are biologically implausible and are probably artifacts of DXA.
The finding that only the medullary canal area shows differences among groups, whereas the cortical bone area does not, likely depends on the amount of resorbed bone that is irrelevant when compared to the cortical bone area; this notwithstanding such difference is significant when compared to the medullary canal area.
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Bone area did not clearly show an association with age.
Thus, because bone area did not change with weight loss or partial regain, we verified that the alterations in BMD were likely not the result of artifactual changes in bone area.
In our study, bone resorption in the augmented area did not differ significantly between sinus lifting procedures with or without perforations.
However, areal BMD (bone quantity per unit bone area measured) does not provide information regarding bone distribution (between cortical and cancellous compartments) or bone microarchitecture.
Since bone marrow does not contain different T and B cell areas, tissue segmentation was not applicable and only cell segmentation was performed (Figs. 6a c, 7a c).
The Bone Tree does not follow the filler path.
Regression analyses with BMI as a covariate showed that medial tibial cartilage volume, normalized to bone area, and thickness did not decrease significantly with age (p > 0.05).
A bone scan did not reveal positive areas.
However, in 3 specimens from the indomethacin group, there were small areas within that volume where bone formation did not appear to have occurred.
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