Correlations between radiological and histological findings of bone remodelling and root resorption in a rodent cleft model
Head & Face Medicine volume 18, Article number: 33 (2022)
The evaluation of bone remodelling and dental root resorption can be performed by histological techniques or micro-computed tomography (micro-CT). The present study aimed to evaluate the relationship between these two procedures in the context of cleft repair in a rat model.
The reconstructed maxillae and the orthodontically-moved first molar of 12 rats were analysed for correlations between the histological and radiological findings retrospectively. The alveolar cleft repairs were performed using bone autografts or (human) xenografts. Four weeks after the operation, the intervention of the first molar protraction was initiated and lasted for eight weeks. The newly formed bone and the root resorption lacunae were determined via histology. In the micro-CT analysis, the average change of bone mineral density (BMD), bone volume fraction (BV/TV), trabecular thickness and trabecular separation of the jaw, as well as the volume of the root resorptions were determined. The Pearson correlation coefficient was applied to study the associations between groups.
Positive correlations were found only between the newly formed bone (histology) and BMD changes (micro-CT) in the autograft group (r = 0.812, 95% CI: 0.001 to 0.979, p = 0.05). The relationship of newly formed bone and BV/TV was similar but not statistically significant (r = 0.691, 95% CI: −0.274 to 0.963, p = 0.013). Regarding root resorption, no significant correlations were found.
Due to the lack of correlation between histological and radiological findings of bone remodelling and the development of root resorptions, both methods should be combined in this cleft model in rats for a comprehensive analysis.
Osteoplasty is an established treatment for cleft patients. In alveolar ridge repairs, various types of bone grafts have been applied, such as autografts from the iliac crest, cranium, mandibular symphysis, tibia or rib, allografts, xenografts or synthetic bone substitutes (e.g., bioceramics, polymers or biocomposites) [1,2,3]. Particularly, the autologous iliac crest grafts are considered the gold standard for cleft repair due to their osteogenic, osteoinductive and osteoconductive properties . Nevertheless, the bone grafting process implies operational risks and may lead to postoperative donor site morbidities, such as pain, hematoma and delayed ambulation. Furthermore, maxillofacial donor sites entail limited bone supply, indicating the demand for an additional donor site and the associated inherent susceptibility to resorption in the long term [5,6,7,8,9,10]. Therefore, different grafting materials and bone substitutes are constantly being improved to enhance clinical outcomes and limit postoperative morbidities [3, 4, 11].
In this context, we recently introduced a new alveolar cleft model in rats with complete maxillary interruption covered by the epithelial lining, which allows for orthodontic tooth movement after cleft repair [12,13,14,15]. This model permits cleft repairs using autologous bone grafts from a novel donor site, the ischial tuberosity of the hip [12, 13]. This model permits the in vivo radiological analysis of the bone structure of the reconstructed area and the associated tooth roots, as well as the corresponding histopathological examination after the trial. The bone graft quality of different substitutes, including autografts, and the root resorptions after cleft repair in the context of subsequent orthodontic treatment have been analysed and compared via radiology and histology methods [14, 15].
Several studies have shown that micro-computed tomography (micro-CT) measurements of bone morphology are highly consistent and accurate. Morphology assessments with micro-CT have been compared to typical two-dimensional (2D) histomorphometry measurements in both animal [16,17,18,19] and human specimens to determine their compatibility [20,21,22,23,24], revealing that micro-CT assessments of 2D and three-dimensional (3D) morphology correlate with 2D histomorphometry measurements. In this context, Müller et al.  reported high correlations and minor differences between conventional histology and microtomography analyses regarding bone volume density (BV/TV), bone surface density (BS/TV), trabecular thickness (Tb.Th) and trabecular separation (Tb.Sp).
The analysis of orthodontically induced root resorption can also be performed with micro-CT analysis [25, 26]. However, to our knowledge, there are no comparative studies on the differences between micro-CT assessments of 2D and 3D morphology and 2D histomorphometry measurements of root resorptions.
In our recently published articles [14, 15], contradictory results or discrepancies between the radiological and histological analyses were found. As for the bone microarchitecture of substitutes, bone mineral density (BMD) and BV/TV were higher in the micro-CT of the autograft than the human xenograft, while in the histological analysis, the most persistent grafting material was the human xenograft, which also led to the highest percentage of new bone formation . The largest root resorption was detected at the mesial root after orthodontic tooth movement of the autograft with the radiological analysis, followed by the human xenograft . Based on these findings, the previously documented correlation between histological and radiological measurements in different tissues does not seem to exist in this model.
Therefore, this follow-up investigation aimed to evaluate the correlation between histological findings by toluidine blue staining and radiological findings in micro-CT analysis in the case of root resorptions and bone morphology changes after cleft repair. Particularly, we determined whether new bone formation can be deduced from the radiological analysis of bone morphology.
Materials and methods
Detailed information about the study protocol and the procedures was recently published [12, 13]. The a priori sample size calculation was performed applying a one-way ANOVA considering the data in Ru et al. .
The animal trials were authorised by the Governmental Animal Care and Use Committee (Reference No.: 81–02.04.2018.A342; Landesamt für Natur, Umwelt und Verbraucherschutz Recklinghausen, Nordrhein-Westfalen, Germany; date: January 11, 2019) and were conducted in agreement with the German Animal Welfare Law (Tierschutzgesetz, TSchG) and the European Union Directive 2010/63/EU. The study was performed according to the ARRIVE Guidelines  and the Guide for the Care and Use of Laboratory Animals.
In this follow-up investigation, the rats were retrospectively analysed after alveolar cleft repair with either autograft or human xenograft (N = 6 per group). In one group, the cleft repair was performed with autologous bone from the hip, while in the other group, human xenogeneic bone substitute (maxgraft, Botiss Biomaterials, Zossen, Germany) was used.
At the time of the artificial maxillary cleft creation, the rats were 8 weeks old and had a mean average weight of 465 ± 34 g, while after another 4 weeks the cleft repair was performed. Finally, four weeks after the maxillary reconstruction, the orthodontic tooth movement intervention started and lasted for 8 weeks (Fig. 1A–C). At the end of the experimental procedures, the animals were 16 weeks old with an average body weight of 542 ± 32 g. Subsequently, the animals were euthanised by cervical dislocation under general anaesthesia.
Cleft creation, maxillary reconstruction and orthodontic device placement were performed under general anaesthesia with a cocktail of ketamine (80–100 mg/kg, i.p.), medetomidine hydrochloride (0.15–0.25 mg/kg, i.p.) and buprenorphine (0.03–0.05 mg/kg, s.c.). Antibiotic administration (cefuroxime: 15 mg/kg, s.c.) started after the operation at a 24-hour interval for seven consecutive days. Atipamezole hydrochloride (0.75 mg/kg, i.p.) was administered to support the recovery process, and buprenorphine (0.03–0.05 mg/kg, s.c.) was given for maximum 5 days when necessary.
Micro-computed tomography (Mirco-CT) analysis
The required radiological examinations were performed in vivo using a μCT system (U-CT OI, MILabs, Utrecht, the Netherlands) at three time points: immediately after the jaw reconstruction (T0), 4 weeks after cleft repair and before the initiation of the orthodontic tooth movement (T1), and 12 weeks after cleft repair or 8 weeks of orthodontic tooth movement (T2).
The radiology parameters were the following: ultra-focus magnification and rotation of 360° at an increment of 0.75° with 0.3 s/degree. The data were reconstructed at an isotropic voxel size of 40 μm. The Micro-CT data were down-sampled to a voxel size of 80 μm. The images of cross-sectional slices were rendered to 3D iso-surfaces. For the analysis of the reconstructed maxillae and the root resorption of the first molars, both regions were segmented in micro-CT images using all the anatomical planes.
For the bone analysis, a coat with a fixed 10-voxel thickness was calculated around the segment using the morphological operation . Then, the bone tissue was segmented within the coat’s volume via thresholding. The reconstructed maxilla and the surrounding bone were then analysed for BMD, BV/TV, Tb.Th and Tb.Sp (Fig. 2A–D). Radiological changes (Δ = T2-T0) within the reconstructed part of the maxilla were defined by the difference among these measurements.
For the root analysis, all roots were individually delineated, and their volumes were calculated for all three measurements (T0–T2). The root resorption was analysed by subtracting the root volume at T2 from the root volume at T1 (Fig. 2E–H).
After resection of the affected part of the maxilla including the orthodontically moved first molar, the samples were stored in 4% formalin (Otto Fischar GmbH & Co. KG, Saarbrücken, Germany), followed by decalcification in a 20-fold volume of ethylenediaminetetraacetic acid (EDTA, MolDecalcifer, Menarini, Florence, Italy) for 4 weeks at 37 °C. Afterwards, the samples were deposited in 5% sucrose/phosphate-buffered saline for 24 h, followed by shock freezing in liquid nitrogen and finally embedded (TissueTek, Sakura, Alphen, Netherlands).
Subsequently, longitudinal sections through the tooth and the surrounding hard and soft tissue or cross-sections from the area immediately in front of the first molar (all sections were 7 μm thick) were collected and fixed on super frost slides for drying. Then, the samples were submerged in acetone for 10 min and stained with toluidine blue, according to a standard protocol. The specimens were observed under digital microscopy with software support (OLYMPUS digital microscope DSX-1000, Olympus Hamburg, Germany).
The region of the augmented bone, the newly formed bone, and the interior and exterior of the augmented substitutes were observed to evaluate the osseous build-up or the bone substitutes that were still present (Fig. 3). The amount of root resorption was defined as the area between the intact parts of the root surfaces (Fig. 4).
The Shapiro-Wilk test was applied to confirm the normal distribution of the data. Statistical comparisons between the groups were performed with the unpaired nonparametric Mann-Whitney test with compared ranks. The correlations between the radiological (BMD, BV/TV, Tb.Sp and Tb.Th) and the histological measurements to determine the newly formed bone (mm2) and the resorption lacunae (mm2) were analysed with the Pearson correlation coefficient (r). The latter was also used to study the correlation between the radiological and histological determination of root resorptions. All analyses were performed on Prism (version 8, GraphPad Software Inc., La Jolla, CA, USA). The level of significance was set at p ≤ 0.05. All results are expressed as mean ± standard deviation (SD).
The results of the histological analysis (persistent grafting material and new bone formation measured in mm2) and the radiological measurements (changes in BMD, BV/TV, Tb.Th and Tb.Sp) 12 weeks after the cleft repair, including the 8 weeks of tooth movement, are shown in Table 1. The mean values of root resorptions are demonstrated in Table 2. Table 3 presents the results of the correlation analysis. Figure 5 shows the overall relationship between the histological findings of newly formed bones and the radiological measurements of morphometric bone changes. Figure 6 presents the relationship between the histological and radiological measurements of root resorptions.
As for the bone morphometric changes, neither the histological nor the radiological analysis showed statistically significant differences between the autograft and the human xenograft groups, except for Tb.Th (0.031 ± 0.024 vs. -0.003 ± 0.001, p = 0.002). Additionally, no statistically significant differences were found between the autograft and the xenograft groups in the case of the root resorptions, regardless of the analysis method.
The only positive relationship was found between the histological findings of newly formed bone and the radiological measurements of BMD changes in the autograft group (r = 0.812, 95% CI: 0.001 to 0.979, p = 0.05). The comparison between the amount of newly formed bone and BV/TV is of similar magnitude but not statistically significant (r = 0.691, CI [−0.274 to 0.963], p = 0.13). Regarding root resorptions, no significant correlations were found.
A large number of preclinical animal studies on cleft repair have examined materials alternative to autologous bone. The bone substitutes include allografts, xenografts and synthetic substitutes (e.g., bioceramics, polymers, or biocomposites) [1,2,3]. To improve clinical outcomes and decrease postoperative morbidity, bone substitutes have been tested [3, 4, 11]. In this context, various artificial cleft models in rats have been introduced to analyse the bone remodelling processes and the development of root resorptions through evaluation with traditional histological techniques or radiological methods such as Micro-CT [27, 29,30,31,32,33,34,35,36].
Generally, histological methods for morphological analyses require considerable preparation of the samples, i.e., embedding in methylmethacrylate and, subsequently, sectioning. Even though the method offers high longitudinal resolution and image contrast, it is labour-intensive and time-consuming. Additionally, it deteriorates the samples, preventing repeated measurements of the same specimen at different time points.
To overcome these limitations, a variety of 3D visualisation techniques have become popular . Micro-CT is an alternative for 3D imaging and quantification of bone structures. Müller et al.  compared histology (2D) and micro-CT (3D) regarding BV/TV, BS/TV, Tb.Th and Tb.Sp, revealing significant correlations between the two methods for all the morphometric parameters. They concluded that the non-destructive, fast and precise radiological analysis allows the measurement of bone structures without biopsies of small bone samples .
Micro-CT has also been used in experimental research with laboratory animals in the field of cleft treatment [27, 36, 38, 39]. Recently, we published the results of our investigations on different graft materials used in alveolar cleft repair, the subsequent bone healing process and the development of dental root resorptions in the context of orthodontic tooth movement in a rodent model [14, 15]. In the autologous bone graft group, BMD increased from 0.54 ± 0.05 g/cm3 to 0.62 ± 0.11 g/cm3, while in the xenograft group, the values remained unchanged (from 0.43 ± 0.04 g/cm3 to 0.40 ± 0.04 g/cm3) . As for BV/TV, it remained unchanged in the autografts group (from 54.89% ± 5.07 to 54.71% ± 14.74%), while in the human xenografts group, it decreased (from 41.55% ± 5.27 to 36.07% ± 3.99%). In contrast, the histological findings showed an increase in the newly formed bone in both groups (autograft: 0.89 ± 0.29 mm2; xenograft: 0.52 ± 0.84 mm2), which was also reflected in the distribution of the newly formed bone on the persistent bone substitute (autograft: 79.45%; xenograft: 62.18%) . The radiological examination demonstrated an increase in the mesial root resorption in both the autologous (2.38 ± 0.35 mm3) and the xenogeneic groups (2.17 ± 0.26 mm3), while in the histological analysis, resorption in the autologous group was 0.048 ± 0.015 mm2 and in the xenogeneic group 0.078 ± 0.05 mm2 . The bone changes measured with micro-CT were partially in contrast to the histological measurements of new bone formation.
Based on the correlations between histological and radiological findings in other medical fields [21, 23, 40, 41], we investigated this relationship by studying bone repair processes and root resorptions in our rodent cleft model to determine whether both analytical procedures are necessary for the assessment of structural changes or micro-CT is sufficient. Apart from reproducing our previous findings [14, 15], Tb.Th and Tb.Sp changes were now also included in the present follow-up investigation since they represent a feature of histological analysis of the new bone formation.
Concerning the remodelling processes, weak relationships between both analysis methods were found, with the only significant correlation being that of newly formed bones (histology) and BMD changes (radiology) in the autograft group (r = 0.812, CI [0.001 to 0.979], p = 0.05). Therefore, in this experimental model, BMD, BV/TV, Tb.Th and Tb.Sp cannot be used to confirm new bone formation. Likewise, no correlations were found between the 2D root resorptions and the 3D resorption lacunae. Regarding the significantly larger total amount of root resorption in the radiological 3D imaging and the lack of a correlation with histological 2D slices, the use of histology techniques should be considered. The type of bone substitute also has a minor role in X.
Because of the specific study design, comparisons between data from the current literature and data from the present study are impossible. Micro-CT is an established method for bone analysis in different fields of medicine. Recently, Pichone et al.  assessed trabecular and cortical parameters using histomorphometry and micro-CT of the iliac crest bone core in haemodialysis patients, finding a moderate correlation between the techniques in the trabecular bone volume. In different conditions such as osteoporosis, hypoparathyroidism and primary hyperparathyroidism, positive correlations between the two techniques have been documented [21, 23, 40]. However, in patients with ESRD or renal osteodystrophy, no significant correlations were observed [42, 43]. Pereira et al.  investigated paediatric patients with renal osteomalacia, where BV/TV was higher in histomorphometry than in micro-CT, and the osteoid accumulation in histomorphometry negatively correlated with the trabecular density observed in Micro-CT.
Due the missing correlation between the histolgical and radioloigical findings, a detailed and inclusive analysis needs further both kinds of preparations. However, it should be noted that in the present study the sample size was small, possibly influencing the statistical analysis.
Availability of data and materials
The data supporting the findings of this research can be obtained directly from the corresponding author.
Bajaj AK, Wongworawat AA, Punjabi A. Management of alveolar clefts. J Craniofac Surg. 2003;14(6):840–6.
Aalami OO, et al. Applications of a mouse model of calvarial healing: differences in regenerative abilities of juveniles and adults. Plast Reconstr Surg. 2004;114(3):713–20.
Sharif F, et al. Dental materials for cleft palate repair. Mater Sci Eng C Mater Biol Appl. 2016;61:1018–28.
Canady JW, et al. Suitability of the iliac crest as a site for harvest of autogenous bone grafts. Cleft Palate Craniofac J. 1993;30(6):579–81.
Rawashdeh MA, Telfah H. Secondary alveolar bone grafting: the dilemma of donor site selection and morbidity. Br J Oral Maxillofac Surg. 2008;46(8):665–70.
Kamal M, et al. Volumetric comparison of autogenous bone and tissue-engineered bone replacement materials in alveolar cleft repair: a systematic review and meta-analysis. Br J Oral Maxillofac Surg. 2018;56(6):453–62.
Janssen NG, et al. Tissue engineering strategies for alveolar cleft reconstruction: a systematic review of the literature. Clin Oral Investig. 2014;18(1):219–26.
Le BT, Woo I. Alveolar cleft repair in adults using guided bone regeneration with mineralized allograft for dental implant site development: a report of 2 cases. J Oral Maxillofac Surg. 2009;67(8):1716–22.
Schultze-Mosgau S, et al. Analysis of bone resorption after secondary alveolar cleft bone grafts before and after canine eruption in connection with orthodontic gap closure or prosthodontic treatment. J Oral Maxillofac Surg. 2003;61(11):1245–8.
Seifeldin SA. Is alveolar cleft reconstruction still controversial? (Review of literature). Saudi Dent J. 2016;28(1):3–11.
Gimbel M, et al. Repair of alveolar cleft defects: reduced morbidity with bone marrow stem cells in a resorbable matrix. J Craniofac Surg. 2007;18(4):895–901.
Möhlhenrich SC, et al. Ischial tuberosity: new donor site for bone grafts in animal cleft research. Sci Rep. 2020;10(1):20699.
Möhlhenrich SC, et al. Establishing a new alveolar cleft model in rats to investigate the influence of jaw reconstructions on orthodontic tooth movement. Ann Anat. 2021;236:151713.
Möhlhenrich SC, et al. Development of root resorption during orthodontic tooth movement after cleft repair using different grafting materials in rats. Clin Oral Investig. 2022;26(9):5809–21.
Möhlhenrich SC, et al. Evaluation of different grafting materials for alveolar cleft repair in the context of orthodontic tooth movement in rats. Sci Rep. 2021;11(1):13586.
Kapadia RD, et al. Applications of micro-CT and MR microscopy to study pre-clinical models of osteoporosis and osteoarthritis. Technol Health Care. 1998;6(5–6):361–72.
Bonnet N, et al. Assessment of trabecular bone microarchitecture by two different x-ray microcomputed tomographs: a comparative study of the rat distal tibia using Skyscan and Scanco devices. Med Phys. 2009;36(4):1286–97.
Waarsing JH, Day JS, Weinans H. An improved segmentation method for in vivo microCT imaging. J Bone Miner Res. 2004;19(10):1640–50.
Barbier A, et al. The visualization and evaluation of bone architecture in the rat using three-dimensional X-ray microcomputed tomography. J Bone Miner Metab. 1999;17(1):37–44.
Kuhn JL, et al. Evaluation of a microcomputed tomography system to study trabecular bone structure. J Orthop Res. 1990;8(6):833–42.
Müller R, et al. Morphometric analysis of human bone biopsies: a quantitative structural comparison of histological sections and micro-computed tomography. Bone. 1998;23(1):59–66.
Fanuscu MI, Chang TL. Three-dimensional morphometric analysis of human cadaver bone: microstructural data from maxilla and mandible. Clin Oral Implants Res. 2004;15(2):213–8.
Chappard D, et al. Comparison insight bone measurements by histomorphometry and microCT. J Bone Miner Res. 2005;20(7):1177–84.
Akhter MP, et al. Transmenopausal changes in the trabecular bone structure. Bone. 2007;41(1):111–6.
Xu X, et al. Using micro-computed tomography to evaluate the dynamics of orthodontically induced root resorption repair in a rat model. PLoS One. 2016;11(3):e0150135.
Trelenberg-Stoll V, et al. Standardized assessment of bone micromorphometry around teeth following orthodontic tooth movement : a microCT split-mouth study in mice. J Orofac Orthop. 2022;83(6):403–11.
Ru N, et al. BoneCeramic graft regenerates alveolar defects but slows orthodontic tooth movement with less root resorption. Am J Orthod Dentofac Orthop. 2016;149(4):523–32.
Gremse F, et al. Imalytics preclinical: interactive analysis of biomedical volume data. Theranostics. 2016;6(3):328–41.
Mehrara BJ, et al. A rat model of gingivoperiosteoplasty. J Craniofac Surg. 2000;11(1):54–8.
Mostafa NZ, et al. Reliable critical sized defect rodent model for cleft palate research. J Craniomaxillofac Surg. 2014;42(8):1840–6.
Cheng N, et al. Effects of bisphosphonate administration on cleft bone graft in a rat model. Cleft Palate Craniofac J. 2017;54(6):687–98.
Nguyen PD, et al. Establishment of a critical-sized alveolar defect in the rat: a model for human gingivoperiosteoplasty. Plast Reconstr Surg. 2009;123(3):817–25.
Jahanbin A, et al. Success of maxillary alveolar defect repair in rats using osteoblast-differentiated human deciduous dental pulp stem cells. J Oral Maxillofac Surg. 2016;74(4):829 e1-9.
Sun J, Xu Y, Chen Z. Establishment of a rat model for alveolar cleft with bone wax. J Oral Maxillofac Surg. 2015;73(4):733 e1–10.
Sun J, et al. Biological effects of orthodontic tooth movement into the grafted alveolar cleft. J Oral Maxillofac Surg. 2018;76(3):605–15.
Ru N, et al. Microarchitecture and biomechanical evaluation of boneceramic grafted alveolar defects during tooth movement in rat. Cleft Palate Craniofac J. 2018;55(6):798–806.
Mosekilde L. Consequences of the remodelling process for vertebral trabecular bone structure: a scanning electron microscopy study (uncoupling of unloaded structures). Bone Miner. 1990;10(1):13–35.
Ru N, et al. In vivo microcomputed tomography evaluation of rat alveolar bone and root resorption during orthodontic tooth movement. Angle Orthod. 2013;83(3):402–9.
Kamal M, et al. Bone regeneration using composite non-demineralized xenogenic dentin with beta-tricalcium phosphate in experimental alveolar cleft repair in a rabbit model. J Transl Med. 2017;15(1):263.
Cohen A, et al. Assessment of trabecular and cortical architecture and mechanical competence of bone by high-resolution peripheral computed tomography: comparison with transiliac bone biopsy. Osteoporos Int. 2010;21(2):263–73.
Pichone A, et al. Assessment of trabecular and cortical parameters using high-resolution peripheral quantitative computed tomography, histomorphometry and microCT of iliac crest bone core in hemodialysis patients. Bone Rep. 2022;16:101173.
Benillouche E, et al. Cortical bone microarchitecture in dialysis patients. Am J Nephrol. 2020;51(10):833–8.
Tamminen IS, et al. Reproducibility and agreement of micro-CT and histomorphometry in human trabecular bone with different metabolic status. J Bone Miner Metab. 2011;29(4):442–8.
Pereira RC, et al. Micro-CT in the assessment of pediatric renal osteodystrophy by bone histomorphometry. Clin J Am Soc Nephrol. 2016;11(3):481–7.
Our special thanks go to Mrs. Leonie Tix (Institute for Laboratory Animal Science and Central Laboratory for Laboratory Animal Science, University Hospital of Aachen, Aachen, Germany). Without Mrs. Tix, the project could not have been completed successfully. Furthermore, we thank Eva Eberspächer-Schweda (Clinical Department for Anesthesiology and Perioperative Intensive Care Medicine, University Hospital for Small Animals, Vienna, Austria) for supporting us by adjusting the anesthesia protocol.
Open Access funding enabled and organized by Projekt DEAL. This research project is supported by the START-Program of the Faculty of Medicine, RWTH Aachen, Germany (Grant No. 104/18). The ultrasonic surgery device was provided free of charge by Mectron Medical (Carasco, Italy) and the bone substitutes by Botiss biomaterials GmbH (Zossen, Germany).
Ethics approval and consent to participate
The experimental animal study protocol was approved by the Governmental Animal Care and Use Committee (Reference No.: 81–02.04.2018.A342; Landesamt für Natur, Umwelt und Verbraucherschutz Recklinghausen, Nordrhein-Westfalen, Germany; dated: 11.01.2019). The study protocol conforms to the ARRIVE Guidelines and with the Guide for the Care and Use of Laboratory Animals. All applicable international, national, and/or institutional guidelines for the care and use of animals were followed.
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Möhlhenrich, S.C., Kniha, K., Heitzer, M. et al. Correlations between radiological and histological findings of bone remodelling and root resorption in a rodent cleft model. Head Face Med 18, 33 (2022). https://doi.org/10.1186/s13005-022-00338-x
- Micro-computed tomography
- Quantitative bone morphometry
- Root resorption
- Bone substitutes
- Cleft animal model