Abstract
Objectives
To evaluate the outcomes of corrective surgical treatment for craniofacial asymmetry using four different methods with the aim of developing the best technique for craniofacial asymmetry assessment.
Materials and methods
CBCT images of twenty-one class III subjects with surgically corrected craniofacial asymmetry and twenty-one matched controls were analyzed. Twenty-seven hard tissue landmarks were used to quantify asymmetry using the following methodologies: the asymmetry index (AI), asymmetry scores based on the clinically derived midline (CM), Procrustes analysis (PA), and modified Procrustes analysis (MPA).
Results
Modified Procrustes analysis successfully identified pre-operative asymmetry and revealed severe asymmetry at the mandibular regions compared to controls, which was comparable to the asymmetry index and clinically derived midline methods, while Procrustes analysis masked the asymmetric characteristics. Likewise, when comparing the post-surgical outcomes, modified Procrustes analysis not only efficiently determined the changes evidencing decrease in facial asymmetry but also revealed significant residual asymmetry in the mandible, which was congruent with the asymmetry index and clinically derived midline methods but contradictory to the results shown by Procrustes analysis.
Conclusions
In terms of quantifying cranio-facial asymmetry, modified Procrustes analysis has evidenced to produce promising results that were comparable to the asymmetry index and the clinically derived midline, making it a more viable option for craniofacial asymmetry assessment.
Clinical relevance
Modified Procrustes analysis is proficient in evaluating cranio-facial asymmetry with more valid clinical representation and has potential applications in assessing asymmetry in a wide spectrum of patients, including syndromic patients.
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Introduction
Aesthetic faces have been proven to influence individuals’ personality development, which can dictate their social, economic, and health status [1, 2]. In tandem with sexual dimorphism, juvenescence, and uniformity, symmetry is also a prerequisite for an attractive face [2, 3]. However, perfect symmetry in humans continues to be a hypothetical concept [4, 5], thus compelling individuals toward reconstructive surgical procedures to restore facial harmony [2, 6]. Nevertheless, the effect of surgical treatment is directly reliant on the precision of the diagnosis, thereby making accurate evaluation an essential and mandatory step before planning the surgical procedure.
The advent of 3-dimensional (3D) imaging modalities has provided additional diagnostic tools for clinical use [7]. Accurate and comprehensive knowledge of facial discrepancies can be obtained from 3D images, as it is possible to rotate and view 3D images from different angles [8]. There are numerous methods documented in the literature to quantify facial asymmetry. Several studies have calculated asymmetry 3-dimensionally by measuring linear, angular, and surface distances of several landmarks from the plane of symmetry [9,10,11,12]. In addition, others have performed surface area and volumetric measurements [6]. Furthermore, some studies have also used a 3D image-based coordinate assessment approach to compare assorted symmetry factors (region-based asymmetry index) [4, 13, 14], while other studies have calculated asymmetry scores [2, 15].
A midsagittal plane (symmetry plane) is central for the quantification of facial asymmetry and can be constructed by manually selecting the reference landmarks not affected by the asymmetry [6, 16,17,18] or by deriving it mathematically based on a best-fit superimposition method called “Procrustes analysis.” Several studies have analyzed facial asymmetry using clinical midline and Procrustes methods; however, flaws associated with these methods, such as unreliability and falsified presentation of true asymmetric features, have also been reported [2, 19], which might influence the diagnosis and post-operative treatment outcomes. Hence, a method that yields reliable evaluation of asymmetry is required. Therefore, the present study aimed to compare four different methods and develop the best technique for the assessment of facial asymmetry.
Materials and method
Sample size calculation
By considering the mean difference of 0.66 mm (standard deviation of 0.5) as clinically significant [14], together with a power of 95%, an effect size of 1.32, and alpha level set at 0.05, a minimum sample size of 32 (16 in each group) was calculated with G*Power (version 3.1.9.2, Kiel University, Germany) [20].
Subjects
Asymmetry group
Twenty-one subjects (7 male and 14 females) aged 18 to 40 years (23.0 ± 3.4 years) from the orthodontic-orthognathic pool who sought surgical treatment at the Prince Philip Dental Hospital, University of Hong Kong, between April 2012 and July 2019 were chosen if they fulfilled the following inclusion criteria: (1) soft tissue chin deviation > 3 mm, (2) bimaxillary surgery with no genioplasty, (3) pre-operative cone-beam computed tomography (CBCT) scan (T0) and post-surgical CBCT scan (T1) taken at least 6 months after surgery, (4) had no history of craniofacial syndromes or craniofacial surgery, and (5) were not diagnosed with hemifacial microsomia or orbital dystopia.
Control group
Twenty-one age (23.0 ± 3.3 years) and gender (7 males and 14 females) matched subjects from the same hospital who had taken CBCT scans in 2015 for nonsurgical purposes and who satisfied the following inclusion criteria were recruited for the present study. Inclusion criteria: (1) imperceptible maxillo-mandibular asymmetry (soft tissue chin deviation < 3 mm), (2) class I skeletal pattern, (3) decently aligned dental arches, and (4) no previous record of temporomandibular disorder, craniofacial syndromes, or craniofacial surgery. Table 1 represents the baseline characteristics of the subjects in the asymmetry and control groups.
CBCT acquisition
Each patient was scanned using ProMax 3D Mid (Planmeca, Helsinki, Finland) with the following parameters: 90 kVp, 400 μm voxel size, 4.7 s scan time, and 20 cm × 17 cm field of view. Each subject was seated with the head positioned such that the Frankfurt horizontal (FH) plane was parallel to the ground while maintaining a mild contact of the lips to their teeth and labio-mental soft tissue at rest throughout the scanning process. CBCT scans were saved in Digital Imaging and Communications in Medicine (DICOM) format and then imported to 3D Slicer 4.10, an open-source medical image processing software platform (http://www.slicer.org) for analysis [21].
Analysis of asymmetry
Four different methodologies, the asymmetry index (AI) [4, 13, 14, 22] using the landmark-based midsagittal plane, the asymmetry scores using the clinically derived midline (CM) [2], Procrustes analysis (PA) [2, 23], and our new-found technique, modified Procrustes analysis (MPA), were utilized to evaluate the results of corrective surgical treatment of facial asymmetry in class III patients compared with controls.
3D model generation, registration, and 3D analysis
A detailed description of the landmarks and reference planes [6, 23,24,25,26,27] utilized in the current research is presented in Table 2. 3D surface models were generated from the CBCT volumes for each patient through bone segmentation using 3D Slicer’s “Editor tool.” Next, “Markups tool” enabled manual digitization of bilateral orbitale and left porion landmarks, to establish the horizontal plane (HP), while the nasion and sella to define the midsagittal plane (MSP) perpendicular to the HP. Coronal plane (CP) was built passing through the left porion and perpendicular to the HP and MSP. Using slicer extension “Align2FH_SagittalPlane,” the HP plane was aligned along the x–z plane, and MSP was aligned along the y–z plane, while the porion was set to lie on the x-axis. Thereafter, the CBCT volume and its corresponding 3D model underwent automatic reorientation via the “Transform tool” appertaining to the reference planes mentioned above. Later, using a 2-step semiautomated registration technique, pre-operative (T0) and post-operative (T1) CBCTs of each patient were superimposed based on selecting the region of interest (ROI) involving predetermined stable cranial structures unaffected by the surgery. Detailed methodology for orientation and registration of CBCT volumes can be referred from the previously published study [28]. Subsequently, 20 bilateral and 7 midline landmarks (Table 2) were identified on CBCT scans and digitized manually on the 3D reconstructed models of T0, T1 and control patients and the distance of each landmark to the three reference planes was measured as dR, dA, and dS in millimeters (mm) (Fig. 1).
Asymmetry index (AI)-based analysis
To assess facial asymmetry, a region-based AI was created by summing each landmark AI for that region (Table 3). AI must approach zero for a perfectly symmetrical face. The AI for various regions was calculated as follows [14]:
where D = deviated side and N = non-deviated side.
Clinically derived midline based analysis (CM)
For each individual, the comma-separated value files (.CSV file) of the 3D landmark coordinates including the coordinates (Nasion and Sella) for generating the “clinically derived midline” were imported to “MATLAB” (The MathWorks, Inc., USA). Next, the 3D 27-landmark configuration (original configuration) along with a “clinically derived midline” (perpendicular to horizontal plane) was generated. Following this, the centroid (geometric center) for each 3D configuration was determined, and scaled to a common centroid size, which was then used to generate a “reflected” 3D landmark configuration by mirroring the 3D original configuration about the “clinically derived midline.” Thereafter, “Euclidean” distances between each pair of landmarks (original landmark and its reflected configuration) were measured (Fig. 2). Facial asymmetry evaluation was performed by dividing the face into 9 regions (Table 3), and region-wise asymmetry scores were computed for each region by squaring the Euclidean distances between each pair of landmarks and then summing and dividing it by the total number of landmarks assigned to that region. This procedure was repeated for each subject in the asymmetry and control groups. The greater the discrepancy between the landmarks and their reflected configuration, the higher the asymmetry scores, which signifies the severity of facial asymmetry.
Procrustes analysis (PA)
The 3D landmark configuration (original configuration), as mentioned previously, was imported into MATLAB software. The 3D configuration was then aligned with the help of a new code using PA. As described earlier, this technique determined the centroid for each 3D configuration and scaled them to the same centroid size. Next, a reflected configuration was created by mirroring the original 3D configuration, this time about an arbitrary plane instead of the clinically derived plane. Finally, to achieve the best fit between the original 3D configuration and its reflected configuration, the latter configuration was rotated and translated over the static original configuration until the Procrustes distance (sum of the squared distances between all the landmarks) was minimized (Fig. 3 c1, and d1). Finally, a region-based asymmetry score (Table 3) was computed by taking the sum of the squared Euclidean distances between each pair of landmarks and dividing by the total number of landmarks in that region [2, 29].
Modified Procrustes analysis (MPA)
Additional MATLAB code was written to undertake the modified Procrustes analysis (MPA). This involved importing the 3D landmark configuration (original configuration) into MATLAB software, computing the centroid and re-scaling the configuration to a common centroid size. A reflected configuration was then created by mirroring the original version around an arbitrary plane. Next, the original configuration was kept static while rotating the reflected configuration until the sum of the squared distances between four stable landmarks (bilateral porion and orbitale) was minimized to achieve the best fit between them unlike PA, wherein all the landmarks were utilized to obtain the best fit between the original and reflected configurations (Fig. 3c2 and d2). Finally, the asymmetry score for all 9 regions was computed (Table 3). MPA was designed so that the superimposition of the original and reflected 3D configurations was based solely on 4 stable landmarks, in contrast to the Procrustes analysis (PA) method which utilized all the facial landmarks during the alignment process.
Study error
All measurements were carried out by one investigator. Intraexaminer reliability was assessed by repeating the reorientation and landmarking procedures on 13 randomly selected CBCT images from each group (26 in total). A 2-week interval was maintained amid the first and the second alignments and landmarking procedures to minimize memory bias. The Dahlberg formula [30] was used to calculate random error for R, A, and S coordinates separately [31].
Statistical analysis
All statistical analyses were performed using IBM SPSS Statistics for Mac, version 25.0 (IBM Corp., Armonk, N.Y., USA). Facial asymmetry was evaluated by computing the asymmetry scores of 9 regions for all the patients. Patients’ pre-operative and post-operative measured variables were compared using a Students paired t-test. Similarly, an independent t-test was used to assess the pre- and post-operative means against controls. Probabilities of p < 0.05 were considered significant.
Results
The intra-examiner reliability measurements were excellent, with a mean intraclass correlation coefficient (ICC) of 0.95 (range 0.90 to 0.99), and method error ranging from 0.03 to 0.38 mm.
Asymmetry index (AI)-based analysis
The results of the AI comparison between different groups are summarized in Table 4. The regional evaluation of AI showed that before surgery, asymmetry was more severe at all the facial regions (zone AI, part AI, and area AI) compared to controls, specifically at the chin area (9.14 mm, p = 0.023), followed by the lower facial region, including the mandibular midline (7.00 mm, p < 0.001) and mandibular bilateral region (7.36 mm, p = 0.003). After surgery, substantial correction of asymmetry was noticed regarding the total facial skeleton (p = 0.046), total mandible (p = 0.018), and mandibular midline (p < 0.001). However, even after surgery, the asymmetry was more pronounced in the total maxilla, bilateral maxilla, and bilateral mandibular regions. Despite significant improvement in asymmetry post-operatively, the symmetry achieved was not comparable to controls at the total facial skeleton (p = 0.002), total mandible (p = 0.006), and mandibular midline (p < 0.001).
Asymmetry score based on clinically derived midline (CM)
Table 5 shows the results for the comparison of asymmetry scores using the CM method. Before surgery, asymmetry was more severe at the total facial skeleton and total mandible (p < 0.001 and < 0.001, respectively; zone AS), mandible midline and mandible bilateral (p < 0.001 and p < 0.001, respectively; part AS), chin and ramus (p < 0.001 and p < 0.001, respectively; area AS), as assessed by higher mean asymmetry scores compared to C (Fig. 4a). Significant correction of mandibular asymmetry was observed in the total facial skeleton (p = 0.020) and total mandible (p = 0.010) post-surgery when asymmetry scores were compared against T0 (Fig. 4b). Specifically, the mean asymmetry scores significantly decreased from 7.23 to 2.78 for the mandible midline (p < 0.001) and from 6.99 to 3.14 for the chin region (p < 0.001) after surgical correction. When post-surgery asymmetry scores were compared with controls, mean asymmetry scores at all regions of zone AS (total facial skeleton, p < 0.001; total maxilla, p = 0.03; and total mandible, p < 0.001); maxilla bilateral and mandible bilateral (p = 0.03 and p < 0.001, respectively; part AS); and ramus (p < 0.001; area AS) were found to be significantly higher for the post-surgery group (Fig. 4c). In addition, the T1-C results also revealed significant residual asymmetry at the mandible midline (2.78 ± 2.34, p = 0.010) and chin (3.14 ± 2.04, p = 0.020) regions.
Asymmetry score based on Procrustes analysis (PA)
The results for the intergroup comparison of Procrustes-derived asymmetry scores are summarized in Table 6. When asymmetry scores for different regions were compared between the pre-surgery group and controls, Procrustes failed to detect asymmetry at the mandibular midline and chin regions, while significantly higher mean asymmetry scores were noticed at the total facial skeleton and total mandible (p < 0.001 and p < 0.001, respectively; zone AS), mandible bilateral (p < 0.001; part AS), and ramus (p < 0.001; area AS) (Fig. 5a). After correction, there was no significant decrease in the asymmetry characteristics in comparison to T0; instead, the mean asymmetry scores noticed were higher in comparison to T0 for most of the regions except for the total facial skeleton and chin regions, which showed decreased asymmetry scores; however, the change was insignificant (Fig. 5b). In addition, all the regions of zone AS, including the total facial skeleton (p < 0.001), total maxilla (p = 0.02), and total mandible (p < 0.001); bilateral maxilla (p = 0.04) and bilateral mandible (p < 0.001) of part AS; ramus (p < 0.001); and area AS exhibited significantly higher mean asymmetry scores after surgery when compared with controls (Fig. 5c).
Asymmetry score based on modified Procrustes analysis (MPA)
Pre-surgical asymmetry scores were observed to be significantly higher when matched against controls, implying severe asymmetry at all the facial regions including total facial skeleton and total mandible (p < 0.001 and < 0.001, respectively; zone AS), mandible midline and mandible bilateral (p < 0.001 and p < 0.001, respectively; part AS), chin and ramus (p < 0.001 and < 0.001, respectively; area AS) except for the maxillary region (zone AI, part AI and area AI) (Fig. 6a). Substantial improvements were noticed following surgery with respect to the lower jaw at the mandible midline (p < 0.001, part AS) and chin region (p < 0.001; area AS) compared to T0 (Fig. 6b). When post-surgical asymmetry scores were compared with controls, higher asymmetry scores were noticed at all regions except for the maxilla midline (Fig. 6c). In addition, evaluation of the surgical outcomes was indicative of persisting asymmetry at the total mandible (p < 0.01, zone AS), albeit significant correction. The results for the intergroup comparison of MPA-derived asymmetry scores are summarized in Table 7.
Discussion
Matching symmetry or object symmetry defines bilateral symmetry as portrayed in biology. Matching symmetry is characterized as a structure created by 2 distinct replicas (mirror images), each located on either side of the body. Object symmetry refers to a structure that is symmetric within itself, thus devising its own internal plane of symmetry, attributable to the left and right halves as mirror images of each other [23, 32]. Two-pronged symmetry of the facial skeleton is often used during reconstructive procedures in cases with facial deformities where the unaffected side is usually used as a template for the restoration of the other. Effectual management of such cases relies on proper diagnosis and prediction for aesthetic outcomes, which again relies on the correct internal symmetry plane or midsagittal plane to which the measurements are made [8, 15, 23, 33,34,35,36]. Furthermore, the additional knowledge pertaining to the site, severity, and degree of facial deformity contributes to a favorable outcome [28]. However, a good post-surgical outcomes demand a reliable method to quantify asymmetry correctly; therefore, the results of the current study go some way toward achieving this goal.
Assessment of facial asymmetry consists of 2 steps: (1) establishing a symmetry plane that fits the asymmetric craniofacial structures and (2) gauging the degree of deviation from symmetry [37]. In an attempt to achieve an accurate diagnosis of asymmetric craniofacial structures, the present study focused on objectively quantifying the degree of asymmetry obtained using 4 different methodologies with cephalometric and morphometric modus. By comparing the outcomes of 4 different methodologies, it was found that the clinically derived midline (CM) and modified Procrustes analysis (MPA) were capable of detecting asymmetry comprehensively, especially in the mandibular region, which was analogous to AI, whereas Procrustes analysis (PA) showed contrasting results where the mandible midline and chin were symmetric. This could not be clinically valid, as skeletal distortion of the mandible and/or maxilla that sequels to Menton deviation is a chief point of concern to patients with facial asymmetry [27].
In an effort to maintain accuracy, the same coordinate system for pre- and post-surgery craniofacial structures was used for assessing the changes following surgery to avoid the deviation of the clinical midline that could have affected the results. AI, CM, and MPA proved the surgery to be successful in decreasing asymmetric characteristics of the mandibular region, but concomitantly where CM and MPA showed substantial improvement (Fig. 7a and c), AI was unable to signify the change specific to the chin region. In contrast, PA not only failed to demonstrate changes following surgery but also calculated post-surgical asymmetry scores higher than the scores before treatment, suggesting surgery intensifies asymmetry (Fig. 7b). While other methods of quantification also revealed the fact that substantial surgical corrections for some regions could not abet in achieving norms of clinically perceived symmetric faces (controls), for example, MPA identified significant residual asymmetry at the total mandible, whereas AI identified residual asymmetry at the total facial skeleton and mandible midline in addition to the total mandible. Likewise, in addition to the aforementioned regions, CM also identified significant residual asymmetry in the chin region.
Scrutinizing the collected results of asymmetry values with different techniques showed that the results of AI, CM based on cephalometric measurements, and the new “modified Procrustes analysis” stemmed on morphometric analysis quadrate with each other, while PA, a morphometric method, showed quite paradoxical results (Fig. 7a–c). The underlying aim of the PA method is to minimize the sum of squared distances between the corresponding landmark configurations, i.e., to achieve the “best fit” [2]. By definition this means all the landmarks are taken into account and will therefore reduce the asymmetric characteristics [19]. This pronounced “masking effect” led to lower pre-surgery asymmetry scores, thus, lowering its clinical implications (Fig. 7b). The new modified Procrustes analysis (MPA) method only incorporates the landmarks in the upper part of the face (bilateral porions and orbitales) for “best fit,” as these are least affected by asymmetry and could be considered stable [38] (Fig. 7c).
Likewise, it can be observed that the CM shows more asymmetry than the PA and MPA methods, even for the control group, alluding to a drawback of using the CM for calculating the asymmetry score (Fig. 7a). Considering that the CM method is highly reliant on the accuracy of the midsagittal plane, which in turn is dependent on the precision with which the nasion and sella are identified, the slightest landmarking error may induce a yaw deviation in the symmetry plane (midsagittal plane) that might go undetected from the frontal view. A benefit of MPA is that it may be less sensitive to such deviations. The modified Procrustes algorithm is less “rigid” than the calculation of the clinical midline in the sense that it is the solution to a mathematical optimization problem rather than an algebraic problem.
Previous studies [4, 13, 14, 22] have confirmed the clinical legitimacy of calculating AI, and as evident from the present analysis, the quantification of asymmetry through MPA has provided outcomes that are equivalent to the results by AI. Hence, MPA is proficient in evaluating cranio-facial asymmetry with more valid clinical representation when porion and orbitale are unaffected. In the future, additional stable landmarks could be used to improve the validly and generalizability of the MPA method.
Despite meticulous evaluation of cranio-facial deformity, the retrospective nature of this study cannot be overlooked even though this limitation was minimized by selecting consecutive patients. Therefore, further studies are required to analyze craniofacial asymmetry prospectively. Additionally, this study was limited to asymmetry in class III subjects; hence, future studies analyzing asymmetry, e.g., in class II subjects or with syndromic patients, should be conducted to increase the applicability of this method.
Conclusion
True clinical representation of asymmetry in all three dimensions is essential to effective and desirable surgical outcomes. The present study demonstrated that modified Procrustes analysis (MPA) is a promising and reliable method for the assessment of 3D facial asymmetry and is clinically applicable for class III patients seeking orthognathic surgery. Furthermore, this method has potential applications in assessing asymmetry in a wider spectrum of patients, including syndromic patients, given that symmetrical arbitrary landmarks can be located.
Data availability
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
References
Van Der Geld P, Oosterveld P, Van Heck G, Kuijpers-Jagtman AM (2007) Smile attractiveness. Self-perception and influence on personality. Angle Orthod 77:759–765. https://doi.org/10.2319/082606-349
Khambay BS, Lowney CJ, Hsung TC, Morris DO (2019) Fluctuating asymmetry of dynamic smiles in normal individuals. Int J Oral Maxillofac Surg 48:1372–1379. https://doi.org/10.1016/j.ijom.2019.01.032
Bashour M (2006) An objective system for measuring facial attractiveness. Plast Reconstr Surg 118:757–774. https://doi.org/10.1097/01.prs.0000207382.60636.1c. discussion 775–756
Huang CS, Liu XQ, Chen YR (2013) Facial asymmetry index in normal young adults. Orthod Craniofac Res 16:97–104. https://doi.org/10.1111/ocr.12010
Bishara SE, Burkey PS, Kharouf JG (1994) Dental and facial asymmetries: a review. Angle Orthod 64:89–98. https://doi.org/10.1043/0003-3219(1994)064%3c0089:Dafaar%3e2.0.Co;2
Nur RB, Çakan DG, Arun T (2016) Evaluation of facial hard and soft tissue asymmetry using cone-beam computed tomography. Am J Orthod Dentofacial Orthop 149:225–237. https://doi.org/10.1016/j.ajodo.2015.07.038
Ajmera DH, Singh P, Leung YY, Gu M (2021) Three-dimensional evaluation of soft-tissue response to osseous movement after orthognathic surgery in patients with facial asymmetry: a systematic review. J Craniomaxillofac Surg 49:763–774. https://doi.org/10.1016/j.jcms.2021.04.010
Hwang HS, Hwang CH, Lee KH, Kang BC (2006) Maxillofacial 3-dimensional image analysis for the diagnosis of facial asymmetry. Am J Orthod Dentofacial Orthop 130:779–785. https://doi.org/10.1016/j.ajodo.2005.02.021
Lee EH, Yu HS, Lee KJ, Han SS, Jung HD, Hwang CJ (2020) Comparison of three midsagittal planes for three-dimensional cone beam computed tomography head reorientation. Korean J Orthod 50:3–12. https://doi.org/10.4041/kjod.2020.50.1.3
An S, Lee J-Y, Chung CJ, Kim K-H (2017) Comparison of different midsagittal plane configurations for evaluating craniofacial asymmetry by expert preference. Am J Orthod Dentofacial Orthop 152:788–797. https://doi.org/10.1016/j.ajodo.2017.04.024
Zheng X, Wang L, Zhang B, Bai X, Qin K, Tian Y, Zhao R, Liu S, Wang J, Zhao Z (2018) Accuracy of two midsagittal planes in three-dimensional analysis and their measurement in patients with skeletal mandibular deviation: a comparative study. Br J Oral Maxillofac Surg 56:600–606. https://doi.org/10.1016/j.bjoms.2018.06.009
Kim MS, Lee EJ, Song IJ, Lee JS, Kang BC, Yoon SJ (2015) The location of midfacial landmarks according to the method of establishing the midsagittal reference plane in three-dimensional computed tomography analysis of facial asymmetry. Imaging Sci Dent 45:227–232. https://doi.org/10.5624/isd.2015.45.4.227
Katsumata A, Fujishita M, Maeda M, Ariji Y, Ariji E, Langlais RP (2005) 3D-CT evaluation of facial asymmetry. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 99:212–220. https://doi.org/10.1016/j.tripleo.2004.06.072
Chen YF, Liao YF, Chen YA, Chen YR (2019) Treatment outcome of bimaxillary surgery for asymmetric skeletal class II deformity. Clin Oral Investig 23:623–632. https://doi.org/10.1007/s00784-018-2462-6
Willing RT, Roumeliotis G, Jenkyn TR, Yazdani A (2013) Development and evaluation of a semi-automatic technique for determining the bilateral symmetry plane of the facial skeleton. Med Eng Phys 35:1843–1849. https://doi.org/10.1016/j.medengphy.2013.06.006
De Momi E, Chapuis J, Pappas I, Ferrigno G, Hallermann W, Schramm A, Caversaccio M (2006) Automatic extraction of the mid-facial plane for cranio-maxillofacial surgery planning. Int J Oral Maxillofac Surg 35:636–642. https://doi.org/10.1016/j.ijom.2006.01.028
Kim TY, Baik JS, Park JY, Chae HS, Huh KH, Choi SC (2011) Determination of midsagittal plane for evaluation of facial asymmetry using three-dimensional computed tomography. Imaging Sci Dent 41:79–84. https://doi.org/10.5624/isd.2011.41.2.79
Huang L, Wang Z, Shan Z, Yeung AWK, Yang Y, Liang Z, Gu M (2022) Nasal asymmetry changes during growth and development in 6- to 12-year-old children with repaired unilateral cleft lip and palate: a 3D computed tomography analysis. J Anat 240:155–165. https://doi.org/10.1111/joa.13538
Gateno J, Jajoo A, Nicol M, Xia JJ (2016) The primal sagittal plane of the head: a new concept. Int J Oral Maxillofac Surg 45:399–405. https://doi.org/10.1016/j.ijom.2015.11.013
Faul F, Erdfelder E, Lang AG, Buchner A (2007) G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods 39:175–191. https://doi.org/10.3758/BF03193146
Fedorov A, Beichel R, Kalpathy-Cramer J et al (2012) 3D Slicer as an image computing platform for the quantitative imaging network. Magn Reson Imaging 30:1323–1341. https://doi.org/10.1016/j.mri.2012.05.001
Lee MS, Chung DH, Lee JW, Cha KS (2010) Assessing soft-tissue characteristics of facial asymmetry with photographs. Am J Orthod Dentofacial Orthop 138:23–31. https://doi.org/10.1016/j.ajodo.2008.08.029
Damstra J, Fourie Z, De Wit M, Ren Y (2012) A three-dimensional comparison of a morphometric and conventional cephalometric midsagittal planes for craniofacial asymmetry. Clin Oral Investig 16:285–294. https://doi.org/10.1007/s00784-011-0512-4
Jung YJ, Kim MJ, Baek SH (2009) Hard and soft tissue changes after correction of mandibular prognathism and facial asymmetry by mandibular setback surgery: three-dimensional analysis using computerized tomography. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 107:763-771.e768. https://doi.org/10.1016/j.tripleo.2008.12.026
Ercan I, Ozdemir ST, Etoz A, Sigirli D, Tubbs RS, Loukas M, Guney I (2008) Facial asymmetry in young healthy subjects evaluated by statistical shape analysis. J Anat 213:663–669. https://doi.org/10.1111/j.1469-7580.2008.01002.x
Leung MY, Leung YY (2018) Three-dimensional evaluation of mandibular asymmetry: a new classification and three-dimensional cephalometric analysis. Int J Oral Maxillofac Surg 47:1043–1051. https://doi.org/10.1016/j.ijom.2018.03.021
Suzuki-Okamura E, Higashihori N, Kawamoto T, Moriyama K (2015) Three-dimensional analysis of hard and soft tissue changes in patients with facial asymmetry undergoing 2-jaw surgery. Oral Surg Oral Med Oral Pathol Oral Radiol 120:299–306. https://doi.org/10.1016/j.oooo.2015.05.020
Ajmera DH, Hsung RTC, Singh P, Wong NSM, Yeung AWK, Lam WYH, Khambay BS, Leung YY, Gu M (2022) Three-dimensional assessment of facial asymmetry in class III subjects. Part 1: a retrospective study evaluating postsurgical outcomes. Clin Oral Investig. https://doi.org/10.1007/s00784-022-04463-4
Darby LJ, Millett DT, Kelly N, McIntyre GT, Cronin MS (2015) The effect of smiling on facial asymmetry in adults: a 3D evaluation. Aust Orthod J 31:132–137. https://doi.org/10.21307/aoj-2020-147
Kim H-Y (2013) Statistical notes for clinical researchers: evaluation of measurement error 2: Dahlberg’s error, Bland-Altman method, and Kappa coefficient. Restor Dent Endod 38:182–185
Djordjevic J, Pirttiniemi P, Harila V, Heikkinen T, Toma AM, Zhurov AI, Richmond S (2011) Three-dimensional longitudinal assessment of facial symmetry in adolescents. Eur J Orthod 35:143–151. https://doi.org/10.1093/ejo/cjr006
Klingenberg CP, Barluenga M, Meyer A (2002) Shape analysis of symmetric structures: quantifying variation among individuals and asymmetry. Evolution 56:1909–1920. https://doi.org/10.1111/j.0014-3820.2002.tb00117.x
Yáñez-Vico RM, Iglesias-Linares A, Torres-Lagares D, Gutiérrez-Pérez JL, Solano-Reina E (2011) Three-dimensional evaluation of craniofacial asymmetry: an analysis using computed tomography. Clin Oral Investig 15:729–736. https://doi.org/10.1007/s00784-010-0441-7
Tuncer BB, Ataç MS, Yüksel S (2009) A case report comparing 3-D evaluation in the diagnosis and treatment planning of hemimandibular hyperplasia with conventional radiography. J Craniomaxillofac Surg 37:312–319. https://doi.org/10.1016/j.jcms.2009.01.004
Baek SH, Cho IS, Chang YI, Kim MJ (2007) Skeletodental factors affecting chin point deviation in female patients with class III malocclusion and facial asymmetry: a three-dimensional analysis using computed tomography. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 104:628–639. https://doi.org/10.1016/j.tripleo.2007.03.002
Kwon TG, Park HS, Ryoo HM, Lee SH (2006) A comparison of craniofacial morphology in patients with and without facial asymmetry–a three-dimensional analysis with computed tomography. Int J Oral Maxillofac Surg 35:43–48. https://doi.org/10.1016/j.ijom.2005.04.006
Berssenbrügge P, Berlin NF, Kebeck G, Runte C, Jung S, Kleinheinz J, Dirksen D (2014) 2D and 3D analysis methods of facial asymmetry in comparison. J Craniomaxillofac Surg 42:e327-334. https://doi.org/10.1016/j.jcms.2014.01.028
Severt TR, Proffit WR (1997) The prevalence of facial asymmetry in the dentofacial deformities population at the University of North Carolina. Int J Adult Orthodon Orthognath Surg 12:171–176
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This work was partially supported by the Hong Kong General Research Fund (RGC Ref No. 17107321 and No. 17210419).
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D.H.A. and M.G. conceptualized the methodology, D.H.A. and J.H.H.N. performed data curation, investigation, and formal analysis. D.H.A. wrote, reviewed, and edited the original draft. M.G., C.Z., R.T.H., and W.W. supervised the methodology. M.G. and W.Y.H.L. provided the resources, C.Z., Y.Y.L., and B.S.K. reviewed and edited the original draft. M.G. also administered the project and validation. All authors reviewed the manuscript.
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Ajmera, D.H., Zhang, C., Ng, J.H.H. et al. Three-dimensional assessment of facial asymmetry in class III subjects, part 2: evaluating asymmetry index and asymmetry scores. Clin Oral Invest 27, 5813–5826 (2023). https://doi.org/10.1007/s00784-023-05193-x
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DOI: https://doi.org/10.1007/s00784-023-05193-x