Imaging Sci Dent. 2013 Dec;43(4):227-233. English.
Published online Dec 12, 2013.
Copyright © 2013 by Korean Academy of Oral and Maxillofacial Radiology
Original Article

The three-dimensional microstructure of trabecular bone: Analysis of site-specific variation in the human jaw bone

Jo-Eun Kim,1 Jae-Myung Shin,2 Sung-Ook Oh,3 Won-Jin Yi,1 Min-Suk Heo,1 Sam-Sun Lee,1 Soon-Chul Choi,1 and Kyung-Hoe Huh1
    • 1Department of Oral and Maxillofacial Radiology and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, Korea.
    • 2Department of Oral and Maxillofacial Surgery, Ilsan Paik Hospital, Inje University College of Medicine, Goyang, Korea.
    • 3A Plus Dental Clinic, Seoul, Korea.
Received June 30, 2013; Revised July 24, 2013; Accepted August 03, 2013.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose

This study was performed to analyze human maxillary and mandibular trabecular bone using the data acquired from micro-computed tomography (micro-CT), and to characterize the site-specific microstructures of trabeculae.

Materials and Methods

Sixty-nine cylindrical bone specimens were prepared from the mandible and maxilla. They were divided into 5 groups by region: the anterior maxilla, posterior maxilla, anterior mandible, posterior mandible, and mandibular condyle. After the specimens were scanned using a micro-CT system, three-dimensional microstructural parameters such as the percent bone volume, bone specific surface, trabecular thickness, trabecular separation, trabecular number, structure model index, and degrees of anisotropy were analyzed.

Results

Among the regions other than the condylar area, the anterior mandibular region showed the highest trabecular thickness and the lowest value for the bone specific surface. On the other hand, the posterior maxilla region showed the lowest trabecular thickness and the highest value for the bone specific surface. The degree of anisotropy was lowest at the anterior mandible. The condyle showed thinner trabeculae with a more anisotropic arrangement than the other mandibular regions.

Conclusion

There were microstructural differences between the regions of the maxilla and mandible. These results suggested that different mechanisms of external force might exist at each site.

Keywords
Microstructure; Humans; Jaw; Three-Dimensional Image; Micro-CT

Introduction

Prediction of bone quality is very important for evaluating the healing phase after bone fracture, the load-bearing potential after installation of an implant, and the bone change around a pathologic lesion. Therefore, many studies on the parameters predicting bone quality have been performed. The term 'bone quality' has been used ambiguously. The best known bone quality classification in dentistry was proposed by Lekholm and Zarb.1 They classified the bone quality based on both morphology and the proportion of cortical and trabecular bone. This classification has been used widely in clinical practice up to the present; however, the efficacy of the determination of bone types has not yet been scientifically validated.2

Recently, mechanical strength has been accepted as an indicator of bone quality in general. Several studies have reported that, in addition to bone mass, structural architecture also provided a useful predictor of mechanical strength.3-5 Some other approaches used to assess bone quality include evaluation of bone mineral density,6, 7 histologic structure,8 and histomorphometric analysis.9 These methods had limitations in evaluating the mechanical properties of bone in a subjective or quantitative manner.10

Several studies have reported on the variations in the quality and quantity of jaw bone according to the success rate of implant installation at different jaw sites.11 Most of these studies have emphasized the role of cortical bone for achieving primary stabilization due to its stiffness. However, mechanical characteristics of trabecular bone also influence the load-bearing capacity of the implant-bone union while the greater part of the fixture is in contact with trabecular bone. Few studies have investigated the features of maxillary and mandibular trabecular bone, especially their mechanical behavior.12 A number of studies have been published to demonstrate various features in jaw trabeculation;13, 14 however, the three-dimensional (3D) microstructures specific to the maxilla and mandible have not been clearly described.

High resolution scanning by micro-computed tomography (micro-CT) was developed in the late 1990s to image tiny specimens with resolutions as small as a micrometer. This made it possible to assess the trabecular architecture in order to estimate the mechanical properties of bone using specific parameters in three dimensions with micro-CT.15

The purpose of this study was to analyze human maxillary and mandibular trabecular bone with 3D microstructure data acquired with micro-CT, and to characterize site-specific variations in trabecular microstructure.

Materials and Methods

Bone specimens

Four sets of dry human jaw bone were prepared. The protocol for this study was approved by the institutional ethics committee of the associated institution.

Using a micro-cutting and grinding system, the 300 CP precision parallel-control Exakt (Apparatebau GmbH, Norderstedt, Germany), the mandibles and maxillae were cut para-sagittally into consecutive slices 4 mm thick in an approximately perpendicular direction to the occlusal plane under continuous water irrigation. Cylindrical specimens that included trabecular bone only were harvested from each sectioned plate using a trephine bur with a 4.9-mm internal diameter.

The regions were categorized as follows:

  • Anterior maxilla (AX): including the incisors to the distal aspect of the canines (n=10)

  • Posterior maxilla (PX): from the premolar to the maxillary tuberosity (n=18)

  • Anterior mandible (AN): including the incisors to the distal aspect of the canines (n=6)

  • Posterior mandible (PN): from the premolar to the mandibular angle (n=23)

  • Condyle (C): above the sigmoid notch (n=12)

A total of 69 bone samples was obtained and grouped by each region. Figure 1 illustrates the procedures of this study.

Fig. 1
Schematic description of specimen.

Micro-CT

The micro-CT examination of each bone specimen was performed using a SkyScan 1172 (Skyscan, Antwerp, Belgium). The specimen was placed on the holder between the X-ray source and the CCD camera, such that the whole specimen was encompassed in the field of view. The exposure conditions were 192° rotation with 0.4° rotation step, 0.5-mm aluminum filtration, 80 kVp, 100 µA, and 19.57-µm pixel. During image acquisition, the bone specimens were kept moist with wet tissue in water. The projection data were then reconstructed with NRecon (ver. 1.5.1.3, Skyscan, Antwerp, Belgium) to create 3D images. The volume of interest (VOI) was 3.91 mm×3.91 mm×3.91 mm with a 202 pixel ×202 pixel×202 pixel cube in the cylindrical bone specimens. The images were processed using a fixed threshold value of 193 to separate the trabecular bone from the marrow spaces. Threshold was determined as the value of both CT and binary image presenting minimal difference in trabecular portion.

Examples of the 3D reconstructed model from each site are shown in Figure 2. The procedures were performed by Skyscan™ CT analyzer software (CTAn version 1.7, Skyscan, Antwerpen, Belgium).

Fig. 2
Examples of 3D reconstruction of micro-CT data from bone specimens of specific regions.

Three-dimensional image analysis

From each VOI, the following structural parameters were determined: the percent bone volume (BV/TV), bone specific surface (BS/BV), trabecular thickness (Tb.Th), trabecular separation (Tb.Sp), trabecular number (Tb.N), structure model index (SMI), and degrees of anisotropy (DA). The 3D parameters were calculated by SkyScan™ CT analyzer software.

Statistical analysis

The mean value and standard deviation of each parameter was calculated for 4 groups (AX, PX, AN, PN) excluding the condyle group. The values were compared by the analysis of variance (ANOVA). Tukey's multiple comparison test was used to determine whether significant differences existed in the measured parameters in between the regions (at a 95% confidence interval level, α=0.05).

A t test was carried out to compare the parameters of the mandibular body area (N=AN+PN) and the mandibular condyle (C). IBM SPSS Statistics (version 21, SPSS Inc., Chicago, IL, USA) was used for all statistical analyses.

Results

Comparison of 3D microstructural parameters among the regions

Table 1 demonstrates the values of the parameters measured in the various sites other than the mandibular condyle. ANOVA indicated that there were significant differences between the groups (P<0.05) for the BS/BV, Tb.Th, and DA parameters. Notably, the BS/BV was the highest at the PX and the lowest at the AN (Fig. 3). The difference between these two groups was statistically significant (P=0.033).

Fig. 3
Bone specific surface (BS/BV) of the various jaw regions.

Table 1
The values of 3D microstructural parameters from various jaw regions

One of the structural parameters, Tb.Th, ranged from 0.12 mm to 0.41 mm and showed significant differences between groups (P=0.002). The highest value was measured at the AN and the lowest at the PX. The groups showing significant differences are marked in Figure 4.

Fig. 4
Trabecular thickeness (Tb.Th) of the various jaw regions.

BV/TV revealed a wide range of values from 6.75% to 48.92%. Even though there was no statistical significance, the anterior regions showed a higher BV/TV value than the posterior region, and the mandibular region had higher value than the maxillary regions (Fig. 5). This tendency toward a difference was similar to that of Tb.Th, and opposed to that of BS/BV. No significant differences were observed in Tb.Sp, Tb.N, or SMI. Tb.Sp ranged from 0.44 mm to 1.77 mm; however, there was little to no difference between groups (P=0.533). The Tb.N, which ranged from 0.34 to 1.73, was lowest at the AN. DA was lowest at the AN and highest at the PN.

Fig. 5
Percent bone volume (BV/TV) of the various jaw regions.

Tukey's test (α=0.05) revealed that the AN region had a significantly higher Tb.Th value compared with the other regions, but the difference did not attain statistical significance for BV/TV, Tb.Sp, Tb.N, or SMI. The differences in the values from the trabecular bone of each region were not significant, except for Tb.Th and BS/BV, which were highest in the AN (Table 2).

Table 2
Tukey's multiple comparison tests among the different regions

Comparison of 3D microstructural parameters between the mandibular body and mandibular condyle

A t-test revealed differences between the mandibular body and mandibular condyle for the Tb.Th and DA parameters (P=0.032, P=0.002, respectively). The Tb.Th was higher in the mandibular body than the mandibular condyle, and the DA was higher in the mandibular condyle than the mandibular body (Table 3).

Table 3
The values of 3D microstructural parameters from mandible (n=29) and condyle (n=12)

Discussion

Bone quality is considered to be a predictor of implant success; however, the parameters for evaluating bone quality have not been clearly established. There have been many attempts to propose classifications of bone quality. Lekholm and Zarb proposed a classification based on the macrostructure of the morphology and distribution of both cortical and trabecular bone,1 and Jensen proposed a classification correlated with the anatomic site.16 Misch et al proposed a density-related macrostructure bone classification using subjective tactile sensation during bone drilling,12 and Friberg et al used an objective cutting resistance to predict the initial stability of an implant.17

Recently, image-based bone density evaluation by CT using the Hounsfield index was suggested.7 However, quantification of bone mass or bone density itself was not sufficient to describe the mechanical properties of bone. Riggs et al suggested that increasing the bone mass in osteoporotic patients by medication did not guarantee either an increase in bone strength or a decrease in the fracture risk.18 This study showed that bone structure was another important factor influencing the mechanical strength of bone. There have been many attempts at analyzing the trabecular structure in two-dimensional images using the fractal dimension.19, 20 With the development of high-resolution imaging modalities, new methods of analyzing the microstructure in 3D images have made it possible to evaluate and predict bone quality more precisely in a noninvasive manner.

Although many studies have investigated trabecular microstructure, only a few have been conducted on human jaw bone because a high resolution scanner, particularly micro-CT, might be difficult to apply in practice, given the high exposure dose and small field of view. One report demonstrated the site-specific microstructure of the mandible and maxilla.10 However, it provided data from the maxilla and mandible of only one cadaver with one site-specific specimen from each region. Therefore, the results were unlikely to represent human bone microstructure in general.

The present study proposed microstructural parameters from specific jaw sites of the human skull. BV/TV indicated that the amount of bone was the greatest in the anterior mandible, although the difference was not statistically significant. The anterior region showed a greater BV/TV value than the posterior region, and the value was greater in the mandible than the maxilla. This tendency corresponded with Jensen's site-specific variation of bone density measured using CT scan.16 The Tb.Th value showed a similar tendency in this study. On the other hand, BS/BV, a parameter characterizing the complexity of structure, showed an inverse relationship with BV/TV. The values of Tb.N and Tb.Sp showed no significant difference between the regions; however, the tendency toward a difference in Tb. N and Tb.Sp among the jaw regions was opposite that of the study results from Fanuscu and Chang.10 Specifically, the present study demonstrated that the anterior and mandibular regions showed greater Tb.Th and Tb.Sp values, and a smaller Tb.N value, than the posterior and maxillary regions. These parameter values implied that the high bone density of the anterior mandible was due to the thick trabeculae rather than complex structure. On the other hand, Fanuscu and Chang found a greater Tb.N value with a smaller Tb.Sp value in the anterior mandible, suggesting a complex and compact structure in this region.10

The mandibular condyle has been studied as a separate part from the other jaw bone areas because the condyle has a unique trabecular structure and mechanical properties to resist strain.21, 22 For that reason, we compared the 3D structural parameters of the condyle and the other regions of the mandible in this study. The values of Tb.Th and DA showed a significant difference between the mandibular condyle and other mandibular regions. The condylar region had thinner trabeculae and a higher degree of anisotropy than the mandible. A higher DA means that the trabecular bone of the mandibular condyle is structurally anisotropic, and our result was in agreement with other research results. Giesen and van Eijden found that the trabecular bone of the condyle mainly consisted of parallel plates perpendicular to the medio-lateral condylar axis.21 Anisotropy is a measure of 3D asymmetry or the presence or absence of preferential alignment of structures along a particular directional axis, and DA is one of the most important determinants of mechanical strength. It is known that the trabeculae of isotropic structures are related to increased mechanical strength since force might be evenly dispersed among them. Conversely, anisotropic structure has less resistance to external force. However, there is a more complex relationship between mechanical properties and structure. Some studies have revealed the mechanical anisotropy of the mandibular condyle and the microstructural anisotropy of condylar trabecular bone; they concluded the orientation of strain followed the direction of the applied load and the principal mechanical direction correlated significantly with the principal structural direction.23, 24 Therefore, the difference in the DA value between the condyle and mandible might indicate that the directions and types of forces in each region were different. The present study had a number of possible limitations. First, the number of samples of each group was not controlled. This was due to the complicated procedure of bone specimen harvesting. We could not prepare an even number of specimens from each region because we obtained specimens composed of only trabecular bone without cortical bone or tooth structures. Second, the dentate or edentulous condition of the jaw was not considered when harvesting the bone specimens and analyzing the data. Third, there was no consideration of the microstructural difference between alveolar bone and basal bone. It has been revealed that there are physical and mechanical differences between the alveolar and basal trabecular bone.25 The stability of an implant is provided by the alveolar trabecular bone, so further research investigating the microstructural variation of the alveolar bone of specific jaw sites is needed.

To our knowledge, this was the first comprehensive study on specific jaw bone sites using 3D microstructural parameters. Despite some limitations, these results would be useful in implant planning on specific sites and as a reference for comparing the microstructure of abnormal trabecular bone caused by pathologic lesions. However, micro-CT may not be routinely applicable due to its high radiation dosage and small field of view. Further studies to analyze the microstructure of trabecular bone using clinically applicable imaging modalities are needed.

In conclusion, we analyzed and compared the 3D trabecular microarchitecture of various sites on the jaw bone. The anterior mandible had thick trabeculae and lower bone surface density; however, no specific characteristics of the microstructure at each region were identified. The mandibular condyle revealed a higher value of anisotropy. These results suggested that different mechanisms of external force might exist at the condyle than at other sites of the jaw bone.

References

    1. Lekholm U, Zarb GA. Patient selection and preparation. In: Brånemark PI, Zarb GA, Albrektsson T, editors. Tissue-integrated prostheses: osseointegration in clinical dentistry. Chicago: Quintessence; 1985. pp. 199-209.
    1. Ribeiro-Rotta RF, Lindh C, Rohlin M. Efficacy of clinical methods to assess jawbone tissue prior to and during endosseous dental implant placement: a systematic literature review. Int J Oral Maxillofac Implants 2007;22:289–300.
    1. Pothuaud L, Van Rietbergen B, Mosekilde L, Beuf O, Levitz P, Benhamou CL, et al. Combination of topological parameters and bone volume fraction better predicts the mechanical properties of trabecular bone. J Biomech 2002;35:1091–1099.
    1. Thomsen JS, Ebbesen EN, Mosekilde L. Relationships between static histomorphometry and bone strength measurements in human iliac crest bone biopsies. Bone 1998;22:153–163.
    1. Borah B, Dufresne TE, Cockman MD, Gross GJ, Sod EW, Myers WR, et al. Evaluation of changes in trabecular bone architecture and mechanical properties of minipig vertebrae by three-dimensional magnetic resonance microimaging and finite element modeling. J Bone Miner Res 2000;15:1786–1797.
    1. Bassi F, Procchio M, Fava C, Schierano G, Preti G. Bone density in human dentate and edentulous mandibles using computed tomography. Clin Oral Implants Res 1999;10:356–361.
    1. Norton MR, Gamble C. Bone classification: an objective scale of bone density using the computerized tomography scan. Clin Oral Implants Res 2001;12:79–84.
    1. Weinstein RS, Hutson MS. Decreased trabecular width and increased trabecular spacing contribute to bone loss with aging. Bone 1987;8:137–142.
    1. Hahn M, Vogel M, Pompesius-Kempa M, Delling G. Trabecular bone pattern factor - a new parameter for simple quantification of bone microarchitecture. Bone 1992;13:327–330.
    1. Fanuscu MI, Chang TL. Three-dimensional morphometric analysis of human cadaver bone: microstructural data from maxilla and mandible. Clin Oral Implants Res 2004;15:213–218.
    1. Bryant SR. The effects of age, jaw site, and bone condition on oral implant outcomes. Int J Prosthodont 1998;11:470–490.
    1. Misch CE, Qu Z, Bidez MW. Mechanical properties of trabecular bone in the human mandible: implications for dental implant treatment planning and surgical placement. J Oral Maxillofac Surg 1999;57:700–708.
    1. Ulm CW, Kneissel M, Hahn M, Solar P, Matejka M, Donath K. Characteristics of the cancellous bone of edentulous mandibles. Clin Oral Implants Res 1997;8:125–130.
    1. Yi WJ, Heo MS, Lee SS, Choi SC, Huh KH. Comparison of trabecular bone anisotropies based on fractal dimensions and mean intercept length determined by principal axes of inertia. Med Biol Eng Comput 2007;45:357–364.
    1. Ulrich D, van Rietbergen B, Laib A, Rüegsegger P. The ability of three-dimensional structural indices to reflect mechanical aspects of trabecular bone. Bone 1999;25:55–60.
    1. Jensen O. Site classification for the osseointegrated implant. J Prosthet Dent 1989;61:228–234.
    1. Friberg B, Sennerby L, Roos J, Lekholm U. Identification of bone quality in conjunction with insertion of titanium implants. A pilot study in jaw autopsy specimens. Clin Oral Implants Res 1995;6:213–219.
    1. Riggs BL, Hodgson SF, O'Fallon WM, Chao EY, Wahner HW, Muhs JM, et al. Effect of fluoride treatment on the fracture rate in postmenopausal women with osteoporosis. N Engl J Med 1990;322:802–809.
    1. Koh KJ, Park HN, Kim KA. Prediction of age-related osteoporosis using fractal analysis on panoramic radiographs. Imaging Sci Dent 2012;42:231–235.
    1. Amer ME, Heo MS, Brooks SL, Benavides E. Anatomical variations of trabecular bone structure in intraoral radiographs using fractal and particles count analyses. Imaging Sci Dent 2012;42:5–12.
    1. Giesen EB, van Eijden TM. The three-dimensional cancellous bone architecture of the human mandibular condyle. J Dent Res 2000;79:957–963.
    1. Giesen EB, Ding M, Dalstra M, van Eijden TM. Mechanical properties of cancellous bone in the human mandibular condyle are anisotropic. J Biomech 2001;34:799–803.
    1. van Eijden TM, van der Helm PN, van Ruijven LJ, Mulder L. Structural and mechanical properties of mandibular condylar bone. J Dent Res 2006;85:33–37.
    1. van Ruijven LJ, Giesen EB, van Eijden TM. Mechanical significance of the trabecular microstructure of the human mandibular condyle. J Dent Res 2002;81:706–710.
    1. Moon HS, Won YY, Kim KD, Ruprecht A, Kim HJ, Kook HK, et al. The three-dimensional microstructure of the trabecular bone in the mandible. Surg Radiol Anat 2004;26:466–473.

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