Stereological measures of trabecular bone structure: comparison of 3D micro computed tomography with 2D histological sections in human proximal tibial bone biopsies.

Stereology applied on histological sections is the 'gold standard' for obtaining quantitative information on cancellous bone structure. Recent advances in micro computed tomography (microCT) have made it possible to acquire three-dimensional (3D) data non-destructively. However, before the 3D methods can be used as a substitute for the current 'gold standard' they have to be verified against the existing standard. The aim of this study was to compare bone structural measures obtained from 3D microCT data sets with those obtained by stereology performed on conventional histological sections using human tibial bone biopsies. Furthermore, this study forms the first step in introducing the proximal tibia as a potential bone examination location by peripheral quantitative CT and CT. Twenty-nine trabecular bone biopsies were obtained from autopsy material at the medial side of the proximal tibial metaphysis. The biopsies were embedded in methylmetacrylate before microCT scanning in a Scanco microCT 40 scanner at a resolution of 20 x 20 x 20 microm3, and the 3D data sets were analysed with a computer program. After microCT scanning, 16 sections were cut from the central 2 mm of each biopsy and analysed with a computerized method. Trabecular bone volume (BV/TV) and connectivity density (CD) were estimated in both modalities, whereas trabecular bone pattern factor (TBPf) was estimated on the histological sections only. Trabecular thickness (Tb.Th), number (Tb.N) and separation (Tb.Sp), and structure model index (SMI) were estimated with the microCT method only. Excellent correlations were found between the two techniques for BV/TV (r = 0.95) and CD (r = 0.95). Additionally, an excellent relationship (r = 0.95) was ascertained between TBPf and SMI. The study revealed high correlations between measures of bone structure obtained from conventional 2D sections and 3D microCT data. This indicates that 3D microCT data sets can be used as a substitute for conventional histological sections for bone structural evaluations.

Mutation of the ectodysplasin-A gene results in bone defects in mice.

Anhidrotic ectodermal dysplasia (EDA) is an X-linked, recessive genetic disease characterized by dysfunctional sweat glands, poorly developed teeth, and premature balding in human beings. This disorder results from mutations in the gene for ectodysplasin-A, a type II transmembrane protein with tumour necrosis factor-alpha domains. An animal model of EDA, the Tabby mouse, also has mutations in the ectodysplasin-A gene and defects similar to those of human beings with EDA. In addition to these defects, Tabby mice acquire deformities in the distal portion of their tails at 10-12 weeks of age. Whole-mount staining of the skeleton with Alizarin Red and Alcian Blue revealed that the tail defect resulted from vertebral fractures just distal to the epiphysis. Histological analysis demonstrated that the structure of both the epiphysis and the subepiphyseal zone of the tail vertebrae was dysplastic while the shaft of the diaphysis was relatively normal. The overall structure of the trabecular bone of these animals was examined through 3-dimensional microcomputed tomography of the tibia. This analysis indicated that Tabby mice had a mild increase in the interconnectivity of the intertwined trabecular bone network but that individual trabeculae were relatively normal. Since it has been determined recently that the ectodysplasin-A gene is expressed in the osteoblasts of developing human embryos, it appears likely that this gene plays a role in normal bone development.

High-resolution three-dimensional-pQCT images can be an adequate basis for in-vivo microFE analysis of bone.

Micro-finite element (microFE) models based on high-resolution images have enabled the calculation of elastic properties of trabecular bone in vitro. Recently, techniques have been developed to image trabecular bone structure in vivo, albeit at a lesser resolution. The present work studies the usefulness of such in-vivo images for microFE analyses, by comparing their microFE results to those of models based on high-resolution micro-CT (microCT) images. Fifteen specimens obtained from human femoral heads were imaged first with a 3D-pQCT scanner at 165 microns resolution and a second time with a microCT scanner at 56 microns resolution. A third set of images with a resolution of 165 microns was created by downscaling the microCT measurements. The microFE models were created directly from these images. Orthotropic elastic properties and the average tissue von Mises stress of the specimens were calculated from six FE-analyses per specimen. The results of the 165 microns models were compared to those of the 56 microns model, which was taken as the reference model. The results calculated from the pQCT-based models, correlated excellent with those calculated from the reference model for both moduli (R2 > 0.95) and for the average tissue von Mises stress (R2 > 0.83). Results calculated from the downscaled micro-CT models correlated even better with those of the reference models (R2 > 0.99 for the moduli and R2 > 0.96 for the average von Mises stress). In the case of the 3D-pQCT based models, however, the slopes of the regression lines were less than one and had to be corrected. The prediction of the Poisson's ratios was less accurate (R2 > 0.45 and R2 > 0.67) for the models based on 3D-pQCT and downscaled microCT images respectively). The fact that the results from the downscaled and original microCT images were nearly identical indicates that the need for a correction in the case of the 3D-pQCT measurements was not due to the voxel size of the images but due to a higher noise level and a lower contrast in these images, in combination with the application of a filtering procedure at 165 micron images. In summary: the results of microFE models based on in-vivo images of the 3D-pQCT can closely resemble those obtained from microFE models based on higher resolution microCT system.

The temporal changes of trabecular architecture in ovariectomized rats assessed by MicroCT.

To study the short- and long-term effects of estrogen deficiency on trabecular bone, three-dimensional measurements of proximal tibiae of ovariectomized rats were performed by micro-computed tomography (MicroCT). New three-dimensional (3D) techniques were employed to characterize the trabecular architecture from 0 to 110 days post-ovariectomy (OVX). These new methods no longer assume a plate or rod model of bone, but calculate trabecular thickness, separation, and number and their distribution by placing maximal spheres into the 3D representation of the structure. The model type of bone was quantified with the Structure Model Index (SMI). Utilizing these methods we found a rapid loss of trabecular bone in the first week after OVX. After the first week bone mass declined further, although the rate of loss was lower. In addition there was a complete change in model type from plate-like to rod-like within 7 days post-OVX, and then a very constant SMI after 12 days. After an initial thinning of trabecular structure, further bone loss seems to occur through removal of trabeculae, while the trabecular plate thickness remains constant. The heterogeneity of the network could be quantified by intra-individual standard deviation of local separations, which showed a stair-like progression, with a plateau between 12 and 60 days post-OVX. This study provides new insights into ovariectomy-related changes in cancellous bone structure evaluated by 3D MicroCT. In addition, these data suggest that the rapid change of model from plate-like to rod-like post-OVX may potentially introduce biases in the parameters that are determined using model-based algorithms, and these biases may modify the impact of age-related or therapeutic changes.

Calibration of trabecular bone structure measurements of in vivo three-dimensional peripheral quantitative computed tomography with 28-microm-resolution microcomputed tomography.

It has recently been shown that high-resolution computed tomography and magnetic resonance imaging have the potential to assess information about the microarchitecture of bone in a noninvasive way. However, due to the limited spatial resolution of the in vivo measurements, the individual trabeculae are not depicted with their true thickness. Nevertheless, the spacing of the structural elements allows the assessment of trabecular number. In a previous publication, the ridge number density (RND) was introduced as a measure for this structural index. It can be extracted from high-resolution three-dimensional (3D) images of patients and shows a reproducibility of 1.6%. In this work the Ridge extraction procedure is compared to and calibrated with microcomputed tomography (microCT) measurements. Three-dimensional measurements of 15 bone biopsies are made with a 28-microm-resolution microCT scanner as well as with a 165-microm-resolution peripheral quantitative computed tomography (pQCT) scanner. For the latter, the same settings are used as for patient examinations. The 15 pairs of measurements are analyzed and the resulting structural indices are compared. The results show that structural indices such as trabecular number, mean thickness, and mean separation can be determined from the 3D pQCT data with an r2 of between 0.81 and 0.96 if the microCT data are taken as the gold standard. The calibration equation found for the bone volume fraction has an intercept of 0.04 and a slope of 0.86 (r2 = 0.98), and trabecular number as the main additional structural index shows a nonsignificant intercept and a calibration slope of 0.91 with the microCT. The calibration procedure can be used directly for patient examinations. Applied to time-series measurements it may be of value for monitoring and quantifying microarchitectural changes due to therapy or aging.