Subjects. The sample size was estimated based on a similar study by Hu et al., in which a standard deviation of 0.58 mm of buccal alveolar bone thickness of maxillary posterior teeth at 3 mm apical to the enamelo-cemental junction (CEJ) was reported.16 If 0.45 mm was set as clinically significant difference, the sample size was supposed to be 36 patients with a significance level (α) of 0.05 and a statistical power (1 - β) of 90%. The calculation was conducted with the PASS software (Version 21.0.3; NCSS, LLC).
The records of 36 patients with unilateral second molar SB (14 males, 22 females; average age, 24.11 ± 3.72 years old) and 36 adults with normal occlusion (8 males, 28 females; average age, 24.00 ± 3.29 years old) were selected. They were divided into SB group and Control group, respectively. The inclusion criteria of SB group were as follows: (1) Age over 18 years old; (2) No missing teeth except the third molar; (3) SB involving at least one pair of second molars. The inclusion criteria of Control group were as follows: (1) Age over 18 years old; (2) No missing teeth except the third molar; (3) Angle class I with normal alignment in the posterior segment; (4) Normal posterior overjet and overbite in the intercuspal position. The exclusion criteria of two groups included: (1) History of orthodontic treatment; (2) CBCT data with artifacts or distortion; (3) Tooth defect, crown restoration or moderate or severe periodontitis with the measuring tooth.
ICE design and treatment progress. In this study, SB was corrected before placement of brackets to reduce overall discomfort and retain muscle activity. Before ICE treatment, mandibular thermoplastic retainer without SB area was made. Based on the retainer, self-curing denture acrylic was constructed on bilateral posterior segments to serve as a removable bite turbo, thus increasing the interocclusal space to allow SB correction. Two buttons were bonded on the buccal side of maxillary second molar and lingual side of mandibular second molar, respectively. The mechanic of SB correction was 3 cross-elastics (3/16-inch 3.5 oz; Ormco Corporation, USA) applied on the malpositioned molars. Patients were advised to change the elastics daily with a monthly follow-up visit. Once SB molars had nearly normal occlusal contact, the patients were instructed to stop wearing removable bite turbos, wear one elastic at night to retain the correction, and do masticatory exercises by clenching their molars as hard as possible for 15 seconds for 3 times as suggested.17 After one-month masticatory training, routine orthodontic treatment was initiated.
CBCT protocol and measurements. CBCT scans were conducted for each patient before and after the comprehensive orthodontic treatment, which encompassed both SB correction and other routine orthodontic procedures. All CBCT data was achieved with NNT Viewer software (version 9.0) from October 2016 to August 2023. The settings are as follows: 16 cm×16 cm field of view, 110kV, 25mA, axial slice thickness of 0.25 mm, exposure time of 20–25 seconds for all subjects. All images were reconstructed with Dolphin Imaging software (version 11.95; Dolphin Imaging and Management Solutions, Chatsworth, Calif). To standardize the process of measuring, the orientation of head position for each subject was performed based on Frankfort plane.16
All cephalometric measurements are shown in Fig. 1, including FMA, SN-GoGn, facial height (N-Me), upper anterior facial height (N-ANS), lower anterior facial height (ANS-Me), posterior facial height (S-Go) and facial height ratio (ANS-Me / N-Me).
To further explore the vertical control after ICE, molar height was measured based on CBCT according to previous studies.18,19 Two reference planes were used: (1) for the upper molars, the palatal plane (projecting a line through Anterior Nasal Spine and Posterior Nasal Spine) was applied; (2) for the lower molars, the mandibular plane (projecting a line between Gonion and menton points) was applied.19 The vertical distance between cusps and reference planes were recorded before and after ICE treatment (Fig. 2A,B).
Long axis of tooth and alveolar body were defined according to previous studies.20,21 The angle from long axis of tooth and alveolar body to a vertical line that was perpendicular to the Frankfort plane were defined as inclination of tooth (In-T) and bone (In-B), respectively (Fig. 2C-F). If the tooth or alveolar body was buccally inclined, the angle would be positive (+), otherwise, the angle would be negative (-). The buccal and lingual ABT at 4 mm, 6 mm, 8 mm apical to CEJ were measured according to Hu’s study.16 Vertical distance between buccal and lingual alveolar bone crest to CEJ were defined as B-ABH and L-ABH. The measurement of ABH and ABT are described in Fig. 3. If the measurement plane is above the lowest point of maxillary sinus, ABT at this level would be recorded as not available.
Statistical analysis. The reproducibility of measuring procedure was verified by reperforming all measurement of 20 patients at two-week intervals, randomly chosen from two groups, and utilizing intraclass correlation coefficients (ICC) test with confidence level set at 95%. Shapiro-Wilk test was applied for normality of the data and all measures demonstrates normally distributed. Therefore, the measuring values were presented as mean and standard deviation. Independent t test was used to analyze the differences between SB group and Control group, while differences between SB-T0 and SB-T1 were analyzed with paired t test. Missing values were filled with mean value when comparing SB-T1 and Control group. All statistically significant tests were two-sided, computed by using SPSS software (version 23; IBM, Armonk, NY). The significance level was set at 0.05.
Ethics approval and consent to participate. All patients’ data in this study were collected from Nanjing Stomatological Hospital, Affiliated Hospital of Medical School, Research Institute of Stomatology, Nanjing University. The study was approved by Institutional Ethics Committee and the approval number is NJSH-2023NL-082-1. All subjects signed informed consent forms.
Approval for human experiments. The study protocol was evaluated and approved by the local ethics committee (Nanjing Stomatological Hospital, Affiliated Hospital of Medical School, Research Institute of Stomatology, Nanjing University, NJSH-2023NL-082-1). Written consent was obtained from participants. All subjects signed informed consent forms. Additionally, this study follows the recommendations proposed by the CONSORT Statement.
1. We identify the institutional and/or licensing committee that approved the experiments, including any relevant details.
2. We confirm that all experiments were performed in accordance with relevant named guidelines and regula- tions.
3. We confirm that informed consent was obtained from all participants and/or their legal guardians.