ABSTRACT
Objectives
The biomechanical mechanism of brace intervention on bone, muscle, and disc should be comprehensively considered for AIS patients. We aimed to developmentally construct a musculoskeletal finite element model of adolescent idiopathic scoliosis to simulate the coupling of corrective forces and analyze the mechanical properties of bone, muscle, and disc. Investigateing, more effective clinical interventions to break the vicious cycle of patients during growth.
Methods
A finite element model, including muscle, bone, and disc, was established using computed tomography data of a patient with RigoA3 adolescent idiopathic scoliosis. The three‐point force coupling, antigravity, and bending effects of the Chêneau brace were simulated, and the correction force of the secondary lumbar bend was gradually reduced while observing the mechanical characteristics of bone, muscle, and disc. The correction force in line with symmetrical spine growth was comprehensively evaluated.
Results
The correction rate of the main thoracic (MT) curve, the intervertebral space height on the concave side of the vertebrae at the apex, and the stress ratio of the intervertebral discs were optimal when the maximum corrective pressure threshold was reached. However, the proximal thoracic (PT) curve was aggravated and the axial forces on the concave side were unbalanced. At this time, the biomechanical performance of the model is also not optimal. The correction rate of the Cobb Angle of the MT curve decreased with the decrease of the correction pressure in the lumbar region. When reduced to 25% of the maximum threshold, the convex side of disc stress, intervertebral space, and muscle axial force is more in line with the biomechanical mechanism of correction and can avoid sacrificing the PT curve.
Conclusions
Downward adjustment of the corrective force to the secondary lumbar curve, using the Chêneau brace, results in better primary thoracic curvature mechanics in the musculoskeletal finite element model, suggesting that breaking the vicious cycle of scoliosis progression to guide benign spinal growth is beneficial.
Keywords: downward correction pressure, finite element simulation, improved performance, lumbar spine curve, tensegrity
A Rigo A‐classified finite element model of adolescent idiopathic scoliosis was constructed, which included muscles, bones, and intervertebral discs conforming to the tensegrity of the spine. Reducing the corrective force of the compensatory lumbar curve of Rigo‐Chêneau brace results in preferable radiological parameters, muscle axial force, and intervertebral disc height and stress balance, which would be beneficial to break the vicious cycle of deformity during growth.

1. Introduction
Adolescent idiopathic scoliosis (AIS) is a three‐dimensional, structural deformity of the spine, defined as a radiological lateral Cobb angle ≥ 10°. AIS affects 1%–3% of children (aged 10–16 years) at or around puberty, and a proportion of children with AIS require corrective intervention to control the progression of the scoliosis [1]. Patients with AIS usually present with uneven shoulders, waistline asymmetry, or rib prominence [2]. Although most AIS curves do not require surgical intervention, a Cobb angle of ≥ 30 poses the most health risks, especially in skeletally immature patients [3]. Health risks include back pain, mental health issues related to appearance [4], and cardiac risks [5]. Although the etiopathological mechanisms of curve occurrence and progression of AIS remain unclear, biomechanical mechanisms are involved in the development of asymmetric spinal malformations.
Stokes' vicious cycle states that spinal deformity produces asymmetrical spinal loads that induce asymmetrical growth in patients with AIS. The spine deformity results from a combination of disc and vertebral wedging. However, the relative contributions of these two structures are not well defined [5]. A longitudinal study of patients with progressive AIS demonstrated that spinal deformities begin with intervertebral disc (IVD) changes, and wedging of the IVDs precedes wedging of the vertebra during the growth spurt [6]. Disc torsional deformation causes greater anterior overgrowth and coronal wedging in the discs than in the vertebral bodies [7]. Furthermore, mechanobiological studies demonstrated significantly greater disc height asymmetry in patients with AIS, suggesting that excessive disc pressure on the concave side leads to annular fibrosis and longitudinal ligamentous tension, which may lead to the inability to remodel and grow. Differences in IVD pressures on the concave and convex sides may drive the development and progression of AIS [8].
Bracing is the most effective treatment for the patients with mild to moderate AIS [9]. AIS patients with immature skeletons are at the greatest risk of curve progression, particularly those with a Cobb angle ≥ 30°. The goal of bracing is to prevent the progression of the curve to a severity that requires surgery [3]. The Rigo‐Chêneau brace, which is frequently recommended to control curve progression, exhibits excellent clinical results [10, 11]. In clinical studies, the brace resulted in a 72% success rate, indicating that many patients with AIS are still at risk of progression, even with the brace [12].
Recently, the biomechanical mechanism of bracing has been investigated to improve the predictability of brace correction results. Finite element models (FEMs) have been applied to the biomechanical studies of scoliosis treatment [13].
Furthermore, computer‐aided design (CAD) using FEMs has been proposed as a time‐ and cost‐efficient approach for managing scoliosis. These models have resulted in promising brace corrections and improved clinical satisfaction outcomes [14, 15]. However, little research has focused on musculoskeletal and finite element studies of patients with AIS. Previous studies revealed that the center of reaction the deviates from the IVD, resulting in uneven stress distribution on the IVD disc and increased reaction torque in FEMs [16]. Stress changes in the disc affect the growth of the scoliosis curve, which affects the final correction result.
FEMs have been used to simulate the correction effects of braces and optimize the design and management of braces [17, 18]. However, brace corrections involve the coupling of multiple three‐dimensional three‐point forces rather than a simple single plane. Moreover, few finite element simulation studies have focused on how brace corrections change the stress characteristics of the concave and convex sides of the IVD. The Chêneau brace controls the curve of scoliosis, but some patients are still at risk of correction failure, especially in the thoracic curve [19]. Our previous studies showed that when there are two curves, lowering the corrective stress of the secondary curve results in a superior correction rate for the primary curve [20]. This mechanism may also influence the height and stress of the discs involved in differential growth. Therefore, the purposes of this study included: (i) To developmentally construct a musculoskeletal FEM of spinal tensegrity for AIS. (ii) The biomechanical responses of bone, muscle, and IVD to different bracing force combinations were comprehensively measured. (iii) Investigating a combination of brace correction forces aimed at improving clinical predictability that optimizes biomechanical performance of muscles and IVDs to help break the vicious cycle of malformations.
2. Materials and Methods
This study was approved by the Human Subject Committee of Guangzhou Sport University (2021LC LL‐16), and informed consent was obtained from the patients or parents of minors.
Musculoskeletal models of trunk muscles are based on the coordinates of the muscle fascicle attachment points [16]. Muscle reaction moments, which are calculated using musculoskeletal models, and gravity loads and muscle forces after Chêneau brace correction force simulation were prescribed using patient‐specific FEMs to estimate the stress distribution within the T1 to L3 IVDs. The Cobb angles and Cobb angle correction ratios were also analyzed.
2.1. Data Acquisition
A 13‐year‐old female patient with Rigo A3 scoliosis, a height of 152 cm, and a weight of 42 kg was included in the study. A Siemens dual‐source computed tomography (CT) scanner (Siemens Somatom Definition 2012B; Siemens Healthineers, Erlangen, Germany) was used for transverse scanning of the entire spine and pelvis, covering T1 through S1, with a layer thickness of 0.7 mm. All CT images were saved in DICOM format.
2.2. Building the Three‐Dimensional Musculoskeletal Model
The DICOM format CT images were imported into Mimics 21.0 software (Materialize, Leuven, Belgium) [18]. The model coordinates were defined as follows: coronal axis, X; sagittal axis, Y; and horizontal axis, Z. The cervical, thoracic, lumbar, sacral, and pelvic vertebral regions were identified based on the gray values of different tissues. The identified bones were imported into Geomagic Studio 2017 (Geomagic Inc. Research Triangle Park, NC, USA) in STL format to process the uneven surface of the medical image accumulation (Figure 1A). Each surface component was imported into SolidWorks 2020 (SolidWorks Corporation, MA, USA) to create a solid individual model fitting for the spine‐pelvis assembly [18]. The models included the articular cartilage, cortical bone, cancellous bone, fibrous annulus, nucleus pulposus and endplate, and muscle. The attachment positions of muscle bundles and bones in the FEM were added based on the classic skeletal muscle model. The muscle was idealized based on previous reports, and the physiologic cross‐sectional area of the skeletal muscle was determined to establish the trunk muscle model [21, 22, 23, 24, 25, 26, 27, 28, 29]. The curve of the whole extensor muscle [30] and the curve of the internal and external oblique muscles of the abdomen were simulated using the elliptical torso model [27]. Finally, the models were combined and saved in the SLDPRT part format.
FIGURE 1.

The musculoskeletal finite element model was constructed for Rigo A classification. (A) Radiographic data of the spine and pelvis were obtained by CT. (B) The skeleton of the model was optimized and the whole spine‐pelvis musculoskeletal assembly model was established.
Ansys Workbench 19.0 was used to perform the finite element analysis (ANSYS Inc. Cannon Sburg, USA). To ensure the accuracy and validity of the model and optimize the demand for computing resources, the solid model of each vertebra was divided into a high‐quality mesh using the adaptive dynamic mesh of the modeler. Bone, cartilage, and other tissues, including the anterior longitudinal, posterior longitudinal, Ligamenta flavum, supraspinous, and interspinous ligaments, were specified as the tetrahedral solid units of a network using Ansys Workbench 19.0. Spring elements were used to simulate ligaments between the vertebrae (Figure 1B). All components were defined as elastomers, and the bone structure and discs were modeled as isotropic elastic materials. The material properties of bone, IVD, and ligament were determined based on experimental literature [16, 17, 21, 31, 32, 33, 34, 35, 36]. The material parameters of bone and soft tissue are summarized in Table 1 [15]. Different materials can be distinguished according to their differences in elastic modulus and Poisson's ratio.
TABLE 1.
Material properties of each part in the finite element model (FEM).
| Competent name | Elastic modulus (MPa) | Poisson's ratio (v) |
|---|---|---|
| Cortical bone | 12,000 | 0.30 |
| Cancellous bone | 100 | 0.20 |
| Posterior structure of vertebral body | 3500 | 0.25 |
| Nucleus pulposus of intervertebral disc | 1 | 0.49 |
| Annulus fibrosus of intervertebral disc | 4.2 | 0.45 |
| Rib | 5000 | 0.10 |
| Sternum | 9592 | 0.20 |
| Pelvis | 5000 | 0.20 |
| Sacrum | 5000 | 0.20 |
| Costal cartilage | 300 | 0.20 |
| Ligament | 31.5 | 0.45 |
| Skin | 31.5 | 0.42 |
To observe the important effects of muscles and ligaments on the stability and mobility of the spine, a muscle ligament model was constructed. Muscle forces and reaction moments were estimated in the upright‐standing posture under load gravity simulation, which was constrained to equilibrium and stability conditions, and the scoliotic curvature and stress distribution were calculated (Figure 1B). According to Hueter–Volkmann's law, increased pressure on the concave side of the epiphysis and increased tension on the convex side change the growth rate of the vertebral body, manifested by concave inhibition and convex acceleration [37]. Loading on the spine includes gravitational forces acting on the vertebrae and muscle forces that maintain spinal stability [38]. Based on previous studies [39, 40], we assumed that the load on the vertebral body is closely related to the body's self‐gravity. The musculoskeletal FEM of the AIS‐simulated forces in the upright‐standing position of the patient is shown in Figure 2. The actual weight of the patient with AIS was 42 kg. The simulated forces act along the Z‐axis at the center of the vertebral body, constraining all degrees of freedom of the sacrum. The simulated forces allow T1 forward flexion, lateral flexion, and vertical translation to maintain balance. The equation used to calculate the loads on the patient at each vertebral level [20] is shown below.
where g = 9.81 m/s; Massi, mass corresponding to the ith vertebral body level; Ptoti, cumulative mass of the part above the level of vertebral i.
FIGURE 2.

Red arrows represent the direction of gravity and muscle force application, (A) represents the mixing force, C–K (B) represents magnitude of the applied force.schematic diagram of loads at different vertebral levels under FEM simulated gravity and muscle factors (spine–plevis FEM) vertical and downward gravity load is applied to the surface of the vertebrae.
2.3. Mesh Sensitivity Analysis
Sensitivity analysis was performed after each parametric FEM was generated. The reason for the analysis is to determine the correct size of the part, as well as the type of part used and its numerical formula to ensure excellent results at the lowest computational cost [41, 42]. According to the previous study on the FEM of scoliosis, Ansys Workbench 19.0 was used to divide tetrahedral elements. We selected T7 as the research object to divide the number of four groups of mesh and conduct axial load simulation analysis [43]. It can be seen from Table 1 that the number of meshs has a corresponding impact on the results.
When the number of meshs is < 20,215, the difference of results is obvious. With the increase of the number of meshs, the stress–strain of the vertebrae divided by the number of adjacent meshs also decreases. The difference between the number of grids D and the number of grids C is the smallest, The difference between stress and displacement is 4.37% and 0.05%, respectively. Therefore, it can be considered that Group C satisfies the verification.
Therefore, it can be considered that in Group C, the meshes number of the vertebral body is 29,308, which meets the verification. The meshs quality check criteria are as follows: aspect ratio ≤ 5°, maximum Angle ≥ 30°, minimum angle ≤ 120°, Jacob ratio > 0.7, warpage ratio ≤ 0.6.At this time, the meshs of vertebrae and the whole torso is shown in Figure 3A. The overall torso meshes model is shown in Figure 3C.
FIGURE 3.

Schematic diagram of the meshs, where (A) is the vertebra, (B) is the disc, and (C) is the torso and pelvis.
2.4. Loading and Boundary Conditions
The intermodel contacts were defined based on the structure and motion characteristics of the spinal–pelvic region. The types of contact between models were defined in the connections. The contact type of the joint surfaces was defined as no separation, which does not allow the surfaces of the contact area to separate but allows small frictionless sliding along the contact surface. High pressure on the body causes discomfort and pressure ulcers. A reasonable stress range and area were selected to ensure acceptable local pressure generation by the body brace. Modifications due to human gravity and muscle forces were comprehensively considered, and correction forces within the range of the human pain threshold were guaranteed. Therefore, the corresponding ceiling thresholds for the area and correction force were set according to the model previously reported in this study (Table 2) [44, 45].
TABLE 2.
Area and force direction of the brace pressure region simulated by the FEM model.
| Pressure area location | Pressure area location (cm2) | The direction of force |
|---|---|---|
| Left arm | 38.5 | From ventrolateral to dorsomeally |
| Left waist | 116.0 | From the dorsolateral to the ventromedial direction |
| The right chest | 143.9 | From the dorsolateral to the ventromedial direction |
| Left underarm | 47.1 | Vertical up |
| On the right arm | 23.5 | Vertical up |
2.5. FEM Validation
Number of grids influences the results of the numerical calculation. Improving the grid quality gradually reduces the performance prediction error [46]. When grid increases have little influence on the calculated results, the numerical results are meaningful [17]. The model was meshed to ensure the accuracy of the calculations. The grid type was a tetrahedral mesh, and the grid size of the joint surfaces was set to 0.8 mm; the other grids were set at 1.5 mm. Therefore, the model was divided into 1,353,236 elements and 2,381,761 nodes.
The biomechanical properties of the FEM were validated to ensure the reliability of the mechanical response analysis during the brace correction simulation [47]. The geometry, range of motion (ROM) of the vertebral segments, and muscle axial force of the model were validated. To verify the geometric similarity of the model, the spinal imaging parameters of the model were measured after gravity loading (Figure 4). The model was adjusted to the coronal plane, and the Cobb angles of the main and near chest bends were measured using the x‐ray sheet Cobb measurement method. The model was adjusted to the sagittal plane to measure the thoracic kyphosis (TK) and lumbar lordosis (LL) angles. The model was adjusted to the axial position, the vertebra T2 and T7 were located, the respective axial vertebral rotations were measured, and the measured values were compared with the parameters from the patient's EOS imaging. The numerical difference between this model and the clinical imaging parameters was < 5°. Therefore, this model exhibited geometric similarity with the clinical data (Table 3).
FIGURE 4.

Comparison of the geometric shape of the patient's full spine anterior‐lateral radiographs with the finite element model.
TABLE 3.
Radiological parameter measurements were compared between the finite element model and the x‐ray examination.
| Parameters | MT | PT | L | TK (°) | LL (°) |
|---|---|---|---|---|---|
| Radiological measurements | 38.5 | 19.8 | 34 | 10 | 40.5 |
| FEM Model | 39.6 | 22.5 | 33 | 11 | 42.4 |
Abbreviations: L, lumbar curve; MT, main thoracic curve; PT, proximal thoracic curve.
The ROMs of the T1–T8 joints in this model were previously verified. All degrees of freedom were constrained on the lower surface of the T4 vertebra, and 4 Nm torques were applied to the upper surface of the T1 vertebra. Forward flexion and backward extension, left and right lateral flexion, and axial rotation were simulated to verify the T1–T4 segment ROM. Similarly, the ROM of T5–T8 in the model was verified [48, 49, 50]. The T1–T4 segment ROM simulation results were verified (Figure 5A); the stimulated ROM values in this model were consistent with anterior flexion, dorsal extension, left/right flexion, and left/right rotation ROM values from previous research models [48, 49, 50]. However, structural changes near the chest bend differed in this model; the left/right ROM values were slightly lower than the ROM values in the three preceding models but were within an acceptable range. Verification of the T5–T8 segment ROM (Figure 5B) revealed that the anterior flexion values and left/right rotation ROM simulated in the selected segments of this model were higher than those values obtained by Busscher et al. [48] and Xin et al. [50]. The location of the top of the main thoracic (MT) curvature, the different degrees and types of lateral curvatures, and the older age in the previous models may make the ROM values of this model slightly larger than those of previous models.
FIGURE 5.

Comparison of vertebral segment ROM with previous studies. (A) Comparison of ROM from T1 to T4. (B) Comparison of ROM from T1 to T4.
Herein, the musculoskeletal model incorporated an optimization algorithm based on balance and stability conditions to measure the axial force of muscles in the upright‐standing position and compared the overall concave/convex ratio of the axial force of muscles, including the concave–convex multifidus and longissimus muscles, with the musculoskeletal model of Kamal and Rouhi [51]. In our model, the ratios of the multifidus were 0.95 for the concave–convex muscle, 0.82 for the longissimus psoas, 0.89 for the longissimus pectoris, 0.75 for the quadratus psoas, and 0.86 for the psoas major. The overall ratio was 0.86, which was close to the concave/convex ratio of the paravertebral muscle group in the previous FEM (0.88). In summary, the new model is reliable and complies with the biomechanical simulations.
2.6. Boundary and Loading Conditions for Brace Correction FEM Simulation
The Chêneau brace provides space for tissue displacement, growth, and respiratory movement by applying corrective force on the convex side of the spine and releasing pressure on the concave side. According to the correction mechanism of the Chêneau brace, the model's pelvis and sacral canals were restricted to X, Y, and Z axis of freedom, and T1 was allowed to do lateral bending, forward bending, and upward extension. Previous studies [52, 53] have shown that the corrective thrust was applied to the right chest to correct the right thoracic curve, the corrective reaction force was applied to the left axilla and the left lumbar side, and an upward extension force was applied to the axillae (400 N on the left and 200 N on the right) to simulate the “bending effect” and the “antigravity effect” of the brace (Figure 6).
FIGURE 6.

Correct force finite element model of Chêneau brace Simulate the correction mechanism according to the concept of the Chêneau brace. (A) Arrows indicate the direction of the applied correction force and the red areas represent the area of the corrected force applied. (B) The direction of applied stress force is as follows: α represents a thrust applied on left axillary lateral (α₁ represents upward axillary extension inferior), β represents a thrust applied on Right thorax lateral (β₁ represents‐upward axillary extension inferior), γ represents a thrust applied on Left lumbar posterior, and δ represents gravity and muscle force applied on trunk. The model's pelvis and sacral canals were restricted to X, Y, and Z axis of freedom, and T1 was allowed to do lateral bending, forward bending and upward extension.
The FEM was used to simulate the corrective force coupling of the brace in three regions of the torso, including the left axilla, left lumbar, and right lateral thoracic region (Table 4). The correction pressure of the left lumbar region (CPLL) was scaled down gradually, and the effects of the downward adjustment of the CPLL were simulated based on the three‐point correction force principle of the brace. According to our previous clinical study [20], lowering the correction pressure for the compensatory lumbar curvature induces a better correction rate for the MT curve. Therefore, in the simulation, the CPLL was reduced by 25%, 50%, 75%, and 100%, and the biological characteristics of the correction according to the maximum threshold setting were observed in other areas. The internal pressure threshold for the trunk tolerance was 0.035 MPa [45] and the axillary brace tolerance was 0.085 MPa [54]. Using these pressure threshold values, four different correct pressures were set (Table 3), including correct finite model element (CFME)1, CFME2, CFME3, and CFME4. The effective pressure area was determined based on previous studies, patient conditions, and clinical experience [38, 55]. The area of the correction force varied in different body parts (Table 4).
TABLE 4.
The area and direction of the correcting force of the Chêneau brace are simulated.
| Combination groups | Left axillary | Left lumbar | Right thorax | Left axillary inferior | Right axillary inferior |
|---|---|---|---|---|---|
| CFEM1 | 0.035 | 0.009 | 0.035 | 0.085 | 0.085 |
| CFEM2 | 0.035 | 0.018 | 0.035 | 0.085 | 0.085 |
| CFEM3 | 0.035 | 0.026 | 0.035 | 0.085 | 0.085 |
| CFEM4 | 0.035 | 0.035 | 0.035 | 0.085 | 0.085 |
2.7. Biomechanical Analysis of the Brace Correction Simulation
The relevant parameters for the mechanical response of the corrected model were measured. First, the Cobb angle, TK, LL, and apical vertebral translation (AVT) were measured radiologically. The AVT in the proximal thoracic (PT) and MT regions were recorded as AVTPT and AVTMT, respectively. The correction rate for the Cobb angle was calculated using the following formula:
Second, the height ratios of the concave and convex sides of the upper and lower intervertebral spaces at the apex of vertebrae T7 and T2 (for T1–T2, T2–T3, T6–T7, and T7–T8) were measured and calculated. Third, the von Mises stress ratios for the concavities and convexities of the T1–T2, T2–T3, T6–T7, and T7–T8 discs were determined. The average value for the IVD stress was obtained by taking 10 points in the convex and concave, respectively (Figure 7) [56]. A larger concave/convex ratio of the height of the intervertebral space means that the concave side of the intervertebral space increased to create favorable conditions for disc remodeling. A smaller stress ratio for the concave side of the disc indicates that the originally overstressed concave side of the disc is released, breaking the vicious cycle of scoliosis progression by creating favorable remodeling through the disc. The ratio of axial forces in the concave and convex side muscles was measured. Based on the premise that the spinal skeleton returns to the midline, balanced axial force on the concave and convex sides of the muscle is beneficial to the construction of reasonable tensegrity.
FIGURE 7.

Schematic representation of the convex and concave lateral pressure points of the intervertebral disc. (A) Convex side and the concave side points of T1–T2 disc. (B) Anterior and posterior points of T1–T2 disc.
3. Results
3.1. Radiological Parameter
The radiological parameters when different combinations of corrective forces were applied in the model are given in Table 5. In the coronal plane, the Cobb angle correction rates were highest in the MT curve and lumbar curve when the CPLL was 0.035 MPa (100% threshold), followed by 75%, 50%, and 25% thresholds. In contrast, the correction rates of the PT curve were 25%, 50%, 75%, and 100% in the order of high to low. The distance reduction sequences for AVTT7 were 100%, 75%, 50%, and 25%. The distance reduction sequences for AVTT2 were 25%, 50%, 75%, and 100%. The TK angle for the sagittal plane was 7.4° when the CPLL was 0.09 MPa, which was the maximum value at 25%. A TK angle of < 10° is diagnosed as a flatback deformity. The remaining correction force pressure combination of TK was in the range of 10°–40°. In the simulation, LL decreased when the correction threshold of the left lumbar region reached 50% and 75%, which was still in the normal physiological range.
TABLE 5.
Simplified term.
| Abbreviations | Full term |
|---|---|
| AIS | Adolescent idiopathic scoliosis |
| AVT | Apical vertebral translation |
| CAD | Computer‐aided design |
| CPLL | Correction pressure of the left lumbar region |
| CSVL | Center sacral vertical line |
| EO | Externus oblique |
| EOS imaging | |
| FEM | Finite element model |
| ICPL | Iliocostalis lumborum pars lumborum |
| ICPT | Iliocostalis lumborum pars thoracic |
| IO | Internus oblique |
| IP | Iliopsoas |
| IVD | Intervertebral disc |
| LGPL | Longissimus thoracis pars lumborum |
| LGPT | Longissimus thoracis pars thoracic |
| LL | Lumbar lordosis |
| MF | Multifidus |
| MT | Main thoracic |
| PT | Proximal thoracic |
| PM | Psoas muscle |
| QL | Quadratus lumborum |
| RA | Rectus abdominis |
| ROM | Range of motion |
| TK | Thoracic kyphosis |
3.2. Intervals Height Concave to Convex Ratios
Variations in the concave/convex height ratios in the upper and lower IVDs at the apical vertebra when simulating four combinations of corrective pressures are shown in Figure 8. For the concave–convex ratio of the intervertebral space height of the vertebrae at the apex of the PT curvature, the most satisfactory performance was achieved at 25% CPLL, followed by 50%, 70%, and 100%. In the MT region, the best performance was achieved when CPLL was 100%, followed by 75%, 50%, and 25%. Lumbar curve measurements were most satisfactory when the CPLL was 75%, followed by 100%, 50%, and 25%.
FIGURE 8.

Concave/convex height ratios of intervertebral gaps under four simulated conditions.
3.3. The von Mises Stress Ratios From Concave to Convex in IVDs
The concave/convex stress ratios of the disc at the apex are shown in Figure 9. The most satisfactory performance in the concave/convex ratio of the upper and lower discs at the apex of the PT region was at 25% CPLL, followed by 75%, 50%, and 100% CPLL. At the apex of the MT, the most satisfactory performance was at 100% CPLL, followed by 75%, 50%, and 25% CPLL. The most satisfactory performance of the concave/convex ratio of the upper and lower discs at the apex of the lumbar curve was at 75% CPLL, followed by 50%, 100%, and 25%.
FIGURE 9.

Concave/convex stress ratios of intervertebral discs under four simulated conditions.
3.4. Muscles Axial Force in Concave to Convex Ratios
Changes in the axial stress ratio of muscles on the concave and convex sides after different corrective pressures loading are shown in Figure 10. After the correction group was applied, the ICPL/IO/EO/LGPL tended to be balanced; when the CPLL boundaries were 25%, 50%, 75%, and 100%, the balance changed from best to worst. The other muscles were more unbalanced than before the correction in each correction combination, especially when the LGPT reached 100%. Conversely, imbalances occurred in the axial force ratio of muscles, including an increase in MF and a decrease in RA, QL, and PM.
FIGURE 10.

The concave/convex ratio of muscle axial stress under four simulation conditions. EO, external oblique; ICPL, iliocostalis lumborum pars lumborum; ICPT, iliocostalis lumborum pars thoracic; IO, internal oblique; LGPL, longissimus thoracis pars lumborum; LGPT, longissimus thoracis pars thoracic; MF, multifidus; PM, psoas muscle; QL, quadratus lumborum; RA, rectus abdominus.
4. Discussion
4.1. Main Findings
In this study, the FEM of “tensegrity” of AIS was constructed and effectively verified as the first innovative result of this study. Another unprecedented result from the simulation of brace intervention was that different combinations of corrective forces showed different characteristics in terms of radiological measurements, disc stress distribution and height, and muscle axial tension. Specifically, the combination with the highest correction pressure resulted in a high Cobb correction rate for the MT curve, whereas the correction rate for PT and the disc stress at the apex of PT and MT exhibited unsatisfactory characteristics. Interestingly, the biomechanical performance of Rigo A classification can be achieved by properly downregulating the correction force of the lumbar lateral curve. It was a combination of radiometric measurements, disc, and muscle axial force parameters that gave us evidence to support our initial clinical observations and hypotheses that were consistent. These results suggest that when brace intervention is used to break the vicious cycle, it should not only consider the correction rate of Cobb Angle, but also focus on the asymmetry of IVD and muscle axial force.
4.2. Verification for Tensegrity of FEM
The geometry of the EFM in this study is consistent with the radiological measurements, and the ROM verification of the main curve is close to the previous model, supporting the validity of the model. The ROM of the T1–T4 spinal segments was within a reasonable range and close to the ROM reported by previous authors [48, 49, 50]. The simulated T5–T8 spinal segment ROM in the left and right lateral flexion directions exhibited a 6° difference compared with the autopsy results of Busscher et al. [48] and the differences in the rest of the directions were in the range of 1°–2°. The experimental results were also similar but slightly lower than the results of Xin et al. [50] and Sheng et al. [49]. The differences may be related to the individual morphologic differences in age, gender, and spinal and other skeletal morphologic characteristics that affect joint mobility in AIS patients.
4.3. Simulation of Chêneau Brace Intervention
4.3.1. Changes in Radiological Parameters During Simulation
Model simulations with brace corrections were performed to observe changes in radiological parameters. Like studies [49, 57], the main curve correction rate increased with increased correction pressure. However, this study adopted the Chêneau brace correction concept and set a specific correction area. The left armpit was elevated to produce antigravity and lateral flexion effects, which may also cause compensatory PT increases when the maximum correction pressure is reached.
According to the Rigo classification, Rigo A consists of three subtypes. Compared with A1 and A2, A3 has more functional waist bending. The waist bending arc is small but has a greater impact on the overall curve, so the design of the waist correction force for Rigo A3 bracing is particularly important [58]. The simulated corrected pressure reached the tolerance threshold of patients in the thoracic vertebra region, and only the corrected pressure in the left lumbar region changed in different correction combinations. The correction rate for the MT curve Cobb angle was low in this experimental simulation, except for a 54% correction rate when CPLL reached the maximum threshold. Simultaneously, a compensatory increase in PT curvature was observed. In general, the present model simulations exhibit unsatisfactory Cobb correction rates, similar to previous studies. For the lumbar curve, the correction was the greatest when the corrective force at the lumbar region reached 75% (CFEM3), which was rarely reported in previous studies. The maximum corrective stress of the secondary curve is not the primary consideration of this study and should be analyzed in conjunction with the corrective performance of the primary curve in future studies [18].
Overall, the correction of the Cobb angle was low in this simulation. However, the Cobb angle may be progressively increased by creep when the brace is worn. According to Périé et al. [36], the correction force in the finite element simulation only corrects the Cobb angle of the coronal plane by 9°, while the actual correction is 16°. Therefore, in addition to the passive correction force, the orthopedic mechanism of the brace may involve other factors that jointly promote mechanical balance in the brace. The simulation results of Andriacchi et al. [59] demonstrate that the brace cannot achieve a large immediate correction effect due to the relatively small corrective force applied in actual clinical practice. Andriacchi et al. also suggested that the corrective effect of the brace can be extended by spinal growth, gradual soft tissue relaxation, and sustained muscle activity after a few months of applied corrective force. Creep, which is an important concept in the treatment of scoliosis, refers to the deformation of a material under constant load that increases with time. When a constant corrective force is applied during the correction of spinal deformities, subsequent correction will occur due to creep [60]. Our model simplifies the biomechanical changes in vivo while wearing the brace but does not simulate the creep of the musculoskeletal system or the changes in tension or support force caused by creep of the brace and brace materials. These differences may affect the correction rates of the brace.
In our model, the displacement (AVT) of T2 and T7 on the X‐axis is consistent with the correction force direction of the main chest curve, resulting in T2 being further away from the CSVL line and T7 being closer to the CSVL line than the original model. Thus, wearing braces can improve the Cobb angle of the main chest curvature in AIS patients, but may affect the standing balance or lead to effects similar to the Crankshaft phenomenon in AIS patients after surgery. With the downward adjustment of CPLL pressure, the correction rate of the MT curve is decreased, but the correction rate of PT curve does not decrease. The biological characteristics of the IVDs with the double thoracic curve are more reasonable, which is more conducive to reversing the vicious cycle law of Stoke and Hutter. Reversing this cycle may increase spinal growth in the central axis in teenagers. These results suggest that a better coronal balance can be obtained by adjusting the corrective force of the left lumbar lateral curvature area appropriately.
The correction simulation did not cause significant changes in TK. The most significant change was an increase of only 3.3°–14.3° when the CPLL pressure was at 50% of the maximum threshold. These results suggest that the sagittal curve was not reshaped in the simulation. When the CPLL pressure was 100%, the Cobb correction rate was the highest, but TK was not affected. Like previous studies, achieving optimal correction may cause a flat back deformity. The risk of a flat back may be reduced by adjusting the corrective force coupling [17]. Nonetheless, high‐quality evidence supporting improvements in flat back remodeling of the sagittal curve using the Chêneau brace is lacking, and flat back remodeling remains a challenge [58].
Matsumoto et al. [61] showed that AVT is closely related to the postoperative distal attachment phenomenon. Liu et al. [62] investigated the correlation between three‐dimensional spinal–pelvic parameters and standing balance and gait characteristics in AIS and showed that the standing balance of Lenke V AIS patients is influenced by their AVT, PT, and pelvic axial rotation.
4.3.2. Changes in IVD Parameters During Simulation
The height of IVD, which is related to the height of intervertebral space, is the main reason for changes in the vertebral body height. Therefore, understanding the height of concavity and convexity in the intervertebral space and the distribution of IVD stress is crucial for the long‐term effectiveness of scoliosis correction. The clinical observations of de Reuver et al. [63] showed that the height of the concave side of the spine was smaller than the height of the convex side at the curve apex.
Differential growth of the spine may occur within the IVD first. The growth is manifested as early wedge‐shaped changes in the IVD, ending with sudden growth and severe vertebral deformation [6]. Therefore, the height and stress parameters of the disc should be considered when wearing the corrective stent. To our knowledge, few finite element analyses of these problems have been reported. Our study shows that progressively decreasing the corrective force in the lumbar region can ameliorate the concave–convex height asymmetry in the parietal space near the thoracic curve. When the correction force of the lumbar curve was gradually increased to the maximum, the concave/convex space ratio of the thoracic apex curve gradually increased. The same pattern was observed in the stress values of the convex side of the IVD. Thus, when the maximum correction force of the lumbar curve reaches the upper limit of the threshold, the correction rate of the chest curve is optimal and may break the vicious cycle. However, the compensatory increase in the PT curve should be considered. Gradually reducing the correction force of the lumbar curve may prevent the compensatory aggravation of the near thoracic curve, but the correction rate of the MT curve will decrease. Improving the concavity‐to‐convexity ratio in intervertebral space height means that the asymmetric stress on both sides of the concavity and convexity during IVD growth in AIS tends to be balanced. According to Hutte Volkman's Law, this may break the vicious cycle of asymmetric growth of the spine and improve the deformity.
4.3.3. The Change of Muscle Axial Force During Simulation
We simulated the forces of the muscles that stabilize the spine. Our model was similar to the model of Kamal and Rouhi [64] in that the axial force on the convex side of the muscle was greater than the force on the concave side. This may be due to a compensatory change in the muscle to maintain the mechanical stability of the spine. The more the curve deviates from the center line, the more unbalanced the trunk muscle force [65, 66].
In general, ICPL/IO/EO/LGPL tend to be balanced in simulation corrections. When the CPLL pressure gradually decreases, this trend is clearer. Synchronous, LGPT, MF, RA, QL, and PM are still out of balance, which may further explain the complexity of scoliosis deformity. The cumulative force of the multifidus muscle is increased by approximately 27%. Our model simulated a more pronounced abdominal muscle imbalance during brace correction. This can be explained by Stoke's theory. To maintain the mechanical stability of the spine, antagonistic muscles in the abdomen are activated to strengthen the spine during continuous load tasks with different heights, constant posture, and external torque [67].
The balance constraint allocates more force to the active muscles in the back to maintain a balanced state. When corrective force is applied to open the concave and convex sides of the spine, the muscles on the concave side of the back are activated to maintain balance and the axial force of the muscles increases. Other electromyography and optimized models indicate that the spine is more stable in more demanding activities. However, the finite element simulation conducted by Hajihosseinali et al. [18] demonstrated that coactivation occurred in the abdominal muscles, unlike other in vivo studies. This is consistent with our experimental results. The correction force of the lumbar curve is reduced to obtain a more balanced representation of the overall radiology, disc, and muscle axial force. We believe this simulation can be used to design more effective conservative clinical treatments for patients with AIS. Specifically, the pros and cons of disc and radiographic parameters should be weighed when facing a double thoracic curve. If asymmetry of muscle axial force occurs under a relatively reasonable central axis after wearing the brace, physical therapy intervention may be needed.
4.4. Limitations and Strengths
To our knowledge, this study is the first to developmentally construct a musculoskeletal FEM that embodies the tensegrity of the spine as a brace intervention simulation for AIS. It is possible to obtain excellent biomechanical performance by reducing the correcting force of the compensation curve. Musculoskeletal models fitted with biomechanical characteristics may enrich the multidimensional thinking of clinical intervention with braces. There are several limitations to this study. First, the effects of immediate correction of the brace were modeled, and the effects of long‐term correction of the brace were not analyzed. Immediate correction may correlate with long‐term treatment. However, to obtain a more detailed long‐term treatment effect, future studies should include dynamic simulations of individual growth. Second, no complete soft tissue model such as muscle was available to compare and validate the model. This experiment did not construct tissues such as internal organs and did not fully model the effects of human internal organs on the axial forces of spinal bones, IVDs, and muscles. Finally, the effects of individual patient differences cannot be excluded. In the future, a larger number of patients with more classifications will be included to enhance the generality of the findings.
4.5. Prospect of Clinical Application
Our simulation study has implications for brace correction in patients with challenging multiple curves. Theoretically, the design of the brace would be different depending on the type of scoliosis. As more scoliosis models are developed, the biomechanical effects of different types of scoliosis braces should be analyzed to improve the predictability of clinical outcomes.
5. Conclusion
The FEM of AIS patients including musculoskeletal is effectively established, which provides a numerical platform for the correction of the Chêneau brace. Downregulating CPLL pressure may improve the radiological parameters and biomechanical manifestations of the thoracic curve. Muscle imbalances that occur during bracing may be a concern for physical therapy.
Author Contributions
Xiaohui Zhang: writing review and editing, writing original draft, validation, software, methodology, formal analysis, data curation, and conceptualization. Di Wang: writing review and editing. Danyu Lv: writing review and editing, resources. Jinmiao Lv: writing review and editing, writing original draft, validation, formal analysis, conceptualization. Bagen Liao: writing review and editing, writing original draft, validation, supervision, formal analysis, conceptualization. Huiyi Tang: writing review and editing. Jinlin Qian: writing original draft.
Ethics Statement
The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Scientific Board of Guangzhou Sport University (2021LC LL‐16).
Consent
Written informed consent to participate in this study was provided by the participantsandapos.legal guardian written informed consent was obtained from the individual.
Conflicts of Interest
The authors declare no conflicts of interest.
Acknowledgments
We thank the Engineering Technology Research Center for Adolescent Scoliosis in Guangdong Province (2019GCZX009) and the Guangzhou Sport University‐Klarity United Laboratory for technical support.
Funding: This work was supported by the Guangzhou Sports Science and Technology Collaborative Innovation Center (2023B04J0466), Open Fund of the Guangdong Provincial Key Laboratory of Physical Activity and Health Promotion (2021B1212040014), Higher Education Teaching Reform Project of Guangdong Provincial Department of Education (Strategy and Practice Exploration of Innovative Training Mode for Sports Rehabilitation Professionals Under the Guidance Of Supply‐Side Reform), The Basic and Applied Basic Research Project of Guangzhou City (2023A04J0554), and The Key Scientific Research Project of Guangdong Province Education Department (2024ZDZX2064).
Xiaohui Zhanga, Di Wanga, Danyu Lva, Jinmiao Lva, and Huiyi Tanga are co‐first authors.
Data Availability Statement
Data for this study are available upon request as the data contained patient privacy and other sensitive information. Data requests can be sent to corresponding author (bagenliao@sina.com) and obtained after obtaining informed consent from the patient.
References
- 1. Weinstein S. L., Dolan L. A., Cheng J. C., Danielsson A., and Morcuende J. A., “Adolescent Idiopathic Scoliosis,” Lancet 371 (2008): 1527–1537, 10.1016/s0140-6736(08)60658-3. [DOI] [PubMed] [Google Scholar]
- 2. Altaf F., Gibson A., Dannawi Z., and Noordeen H., “Adolescent Idiopathic Scoliosis,” BMJ 346 (2013): f2508, 10.1136/bmj.f2508. [DOI] [PubMed] [Google Scholar]
- 3. Cheng J. C., Castelein R. M., Chu W. C., et al., “Adolescent Idiopathic Scoliosis,” Nature Reviews. Disease Primers 1 (2015): 15030, 10.1038/nrdp.2015.30. [DOI] [PubMed] [Google Scholar]
- 4. Zhang H., Wang B., Wu A., et al., “Assessment of Neck Imbalance in Adolescent Idiopathic Scoliosis Patients: A Cross‐Section Study Based on Body Image of 115 Patients With Main or Double Thoracic Curve,” Orthopaedic Surgery 15 (2023): 572–578, 10.1111/os.13583. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Yang S., Andras L. M., Redding G. J., and Skaggs D. L., “Early‐Onset Scoliosis: A Review of History, Current Treatment, and Future Directions,” Pediatrics 137 (2016): E20150709. 10.1542/peds.2015-0709. [DOI] [PubMed] [Google Scholar]
- 6. Will R. E., Stokes I. A., Qiu X., Walker M. R., and Sanders J. O., “Cobb Angle Progression in Adolescent Scoliosis Begins at the Intervertebral Disc,” Spine (Phila Pa 1976) 34 (2009): 2782–2786, 10.1097/BRS.0b013e3181c11853. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Schlösser T. P., van Stralen M., Brink R. C., et al., “Three‐Dimensional Characterization of Torsion and Asymmetry of the Intervertebral Discs Versus Vertebral Bodies in Adolescent Idiopathic Scoliosis,” Spine (Phila Pa 1976) 39 (2014): E1159–E1166, 10.1097/brs.0000000000000467. [DOI] [PubMed] [Google Scholar]
- 8. Smit T. H., “Adolescent Idiopathic Scoliosis: The Mechanobiology of Differential Growth,” JOR Spine 3 (2020): e1115, 10.1002/jsp2.1115. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Clin J., Aubin C. E., Parent S., and Labelle H., “A Biomechanical Study of the Charleston Brace for the Treatment of Scoliosis,” Spine (Phila Pa 1976) 35 (2010): E940–E947, 10.1097/BRS.0b013e3181c5b5fa. [DOI] [PubMed] [Google Scholar]
- 10. Rigo M., Quera‐Salvá G., Puigdevall N., and Martínez M., “Retrospective Results in Immature Idiopathic Scoliotic Patients Treated With a Chêneau Brace,” Studies in Health Technology and Informatics 88 (2002): 241–245. [PubMed] [Google Scholar]
- 11. Ovadia D., Eylon S., Mashiah A., Wientroub S., and Lebel E. D., “Factors Associated With the Success of the Rigo System Chêneau Brace in Treating Mild to Moderate Adolescent Idiopathic Scoliosis,” Journal of Children's Orthopaedics 6 (2012): 327–331, 10.1007/s11832-012-0429-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Weinstein S. L., Dolan L. A., Wright J. G., and Dobbs M. B., “Effects of Bracing in Adolescents With Idiopathic Scoliosis,” New England Journal of Medicine 369 (2013): 1512–1521, 10.1056/NEJMoa1307337. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Li J., An Z., Wu J., et al., “Construction of the Adjusted Scoliosis 3D Finite Element Model and Biomechanical Analysis Under Gravity,” Orthopaedic Surgery 15 (2023): 606–616, 10.1111/os.13572. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Guy A., Labelle H., Barchi S., et al., “Braces Designed Using CAD/CAM Combined or Not With Finite Element Modeling Lead to Effective Treatment and Quality of Life After 2 Years: A Randomized Controlled Trial,” Spine (Phila Pa 1976) 46 (2021): 9–16, 10.1097/brs.0000000000003705. [DOI] [PubMed] [Google Scholar]
- 15. Bidari S., Kamyab M., Ghandhari H., and Komeili A., “Efficacy of Computer‐Aided Design and Manufacturing Versus Computer‐Aided Design and Finite Element Modeling Technologies in Brace Management of Idiopathic Scoliosis: A Narrative Review,” Asian Spine Journal 15 (2021): 271–282, 10.31616/asj.2019.0263. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16. Kamal Z., Rouhi G., Arjmand N., and Adeeb S., “A Stability‐Based Model of a Growing Spine With Adolescent Idiopathic Scoliosis: A Combination of Musculoskeletal and Finite Element Approaches,” Medical Engineering & Physics 64 (2019): 46–55, 10.1016/j.medengphy.2018.12.015. [DOI] [PubMed] [Google Scholar]
- 17. Guan T., Zhang Y., Anwar A., Zhang Y., and Wang L., “Determination of Three‐Dimensional Corrective Force in Adolescent Idiopathic Scoliosis and Biomechanical Finite Element Analysis,” Frontiers in Bioengineering and Biotechnology 8 (2020): 963, 10.3389/fbioe.2020.00963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Hajihosseinali M., Arjmand N., Shirazi‐Adl A., Farahmand F., and Ghiasi M. S., “A Novel Stability and Kinematics‐Driven Trunk Biomechanical Model to Estimate Muscle and Spinal Forces,” Medical Engineering & Physics 36 (2014): 1296–1304, 10.1016/j.medengphy.2014.07.009. [DOI] [PubMed] [Google Scholar]
- 19. Hawary R. E., Zaaroor‐Regev D., Floman Y., Lonner B. S., Alkhalife Y. I., and Betz R. R., “Brace Treatment in Adolescent Idiopathic Scoliosis: Risk Factors for Failure‐a Literature Review,” Spine Journal 19 (2019): 1917–1925, 10.1016/j.spinee.2019.07.008. [DOI] [PubMed] [Google Scholar]
- 20. Yuan C., A Retrospective Study and Finite Element Analysis of Compensatory Proximal Thoracic Curves in Rigo Type A AIS Following Brace Treatment (Master's thesis of Guangzhou Sport University, 2023), 10.27042/d.cnki.ggztc.2023.000239. [DOI] [Google Scholar]
- 21. Sharma M., Langrana N. A., and Rodriguez J., “Role of Ligaments and Facets in Lumbar Spinal Stability,” Spine 20 (1995): 887–900, 10.1097/00007632-199504150-00003. [DOI] [PubMed] [Google Scholar]
- 22. Bogduk N., Macintosh J. E., and Pearcy M. J., “A Universal Model of the Lumbar Back Muscles in the Upright Position,” Spine (Phila Pa 1976) 17 (1992): 897–913, 10.1097/00007632-199208000-00007. [DOI] [PubMed] [Google Scholar]
- 23. Stokes I. A. and Gardner‐Morse M., “Quantitative Anatomy of the Lumbar Musculature,” Journal of Biomechanics 32 (1999): 311–316, 10.1016/s0021-9290(98)00164-x. [DOI] [PubMed] [Google Scholar]
- 24. Bogduk N., Pearcy M., and Hadfield G., “Anatomy and Biomechanics of Psoas Major,” Clinical Biomechanics (Bristol, Avon) 7, no. 2 (1992): 109–119, 10.1016/0268-0033(92)90024-x. [DOI] [PubMed] [Google Scholar]
- 25. Macintosh J. E., Valencia F., Bogduk N., and Munro R. R., “The Morphology of the Human Lumbar Multifidus,” Clinical Biomechanics (Bristol, Avon) 1, no. 4 (1986): 196–204, 10.1016/0268-0033(86)90146-4. [DOI] [PubMed] [Google Scholar]
- 26. Macintosh J. E. and Bogduk N., “Volvo Award in Basic Science. The Morphology of the Lumbar Erector Spinae,” Spine (Phila Pa 1976) 12, no. 7 (1987): 658–668, 10.1097/00007632-198709000-00004. [DOI] [PubMed] [Google Scholar]
- 27. Gatton M., Pearcy M., and Pettet G., “Modelling the Line of Action for the Oblique Abdominal Muscles Using an Elliptical Torso Model,” Journal of Biomechanics 34 (2001): 1203–1207, 10.1016/s0021-9290(01)00079-3. [DOI] [PubMed] [Google Scholar]
- 28. Arjmand N., Gagnon D., Plamondon A., Shirazi‐Adl A., and Larivière C., “A Comparative Study of Two Trunk Biomechanical Models Under Symmetric and Asymmetric Loadings,” Journal of Biomechanics 43 (2010): 485–491, 10.1016/j.jbiomech.2009.09.032. [DOI] [PubMed] [Google Scholar]
- 29. Dumas G. A., Poulin M. J., Roy B., Gagnon M., and Jovanovic M., “A Three‐Dimensional Digitization Method to Measure Trunk Muscle Lines of Action,” Spine (Phila Pa 1976) 13 (1988): 532–541, 10.1097/00007632-198805000-00017. [DOI] [PubMed] [Google Scholar]
- 30. Arjmand N., Shirazi‐Adl A., and Bazrgari B., “Wrapping of Trunk Thoracic Extensor Muscles Influences Muscle Forces and Spinal Loads in Lifting Tasks,” Clinical Biomechanics (Bristol, Avon) 21, no. 7 (2006): 668–675, 10.1016/j.clinbiomech.2006.03.006. [DOI] [PubMed] [Google Scholar]
- 31. Roberts S. B. and Chen P. H., “Elastostatic Analysis of the Human Thoracic Skeleton,” Journal of Biomechanics 3 (1970): 527–545, 10.1016/0021-9290(70)90037-0. [DOI] [PubMed] [Google Scholar]
- 32. Brown N., Saputa C., and Black J., “Young's Modulus of Living Human Bone Transactions of the Orthopaedic Research Society,” (1981).
- 33. Wang H., “Development of a Side Impact Finite Element Human Thoracic Model,” (PhD thesis, Wayne State University, 1995).
- 34. Clin J., Aubin C., Parent S., and Labelle H., “Biomechanical Modeling of Brace Treatment of Scoliosis: Effects of Gravitational Loads,” Medical & Biological Engineering & Computing 49 (2011): 743–753, 10.1007/s11517-011-0737-z. [DOI] [PubMed] [Google Scholar]
- 35. Clin J., Aubin C. E., and Labelle H., “Virtual Prototyping of a Brace Design for the Correction of Scoliotic Deformities,” Medical & Biological Engineering & Computing 45 (2007): 467–473, 10.1007/s11517-007-0171-4. [DOI] [PubMed] [Google Scholar]
- 36. Périé D., Aubin C. E., Petit Y., Labelle H., and Dansereau J., “Personalized Biomechanical Simulations of Orthotic Treatment in Idiopathic Scoliosis Clinical,” Biomechanics (Bristol, Avon) 19 (2004): 190–195, 10.1016/j.clinbiomech.2003.11.003. [DOI] [PubMed] [Google Scholar]
- 37. Mehlman C. T., Araghi A., and Roy D. R., “Hyphenated History: The Hueter–Volkmann Law,” American Journal of Orthopedics (Belle Mead, NJ) 26 (1997): 798–800. [PubMed] [Google Scholar]
- 38. Villemure I., Aubin C. E., Dansereau J., and Labelle H., “Biomechanical Simulations of the Spine Deformation Process in Adolescent Idiopathic Scoliosis From Different Pathogenesis Hypotheses,” European Spine Journal 13 (2004): 83–90, 10.1007/s00586-003-0565-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39. Nachemson A., “The Load on Lumbar Disks in Different Positions of the Body,” Clinical Orthopaedics and Related Research 45 (1966): 107–122. [PubMed] [Google Scholar]
- 40. Schultz A., Andersson G., Ortengren R., Haderspeck K., and Nachemson A., “Loads on the Lumbar Spine. Validation of a Biomechanical Analysis by Measurements of Intradiscal Pressures and Myoelectric Signals,” Journal of Bone and Joint Surgery (American Volume) 64 (1982): 713–720. [PubMed] [Google Scholar]
- 41. Íñiguez‐Macedo S., Lostado‐Lorza R., Escribano‐García R., and Martínez‐Calvo M., “Finite Element Model Updating Combined With Multi‐Response Optimization for Hyper‐Elastic Materials Characterization,” Materials (Basel) 12 (2019): 109, 10.3390/ma12071019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42. Lostado‐Lorza R., Corral‐Bobadilla M., and Somovilla‐Gomez I. M., “Characterization, LCA and FEA for an Efficient Ecodesign of Novel Stainless Steel Woven Wire Mesh Reinforced Recycled Aluminum Alloy Matrix Composite,” Journal of Cleaner Production 411 (2023): 13780. [Google Scholar]
- 43. Dong R., To Study the Modular Design of ScoliosisOrthosis Considering Multiple Factors (Master's Thesis of Dalian Jiaotong University, 2023), 10.26990/d.cnki.gsltc.2023.000910. [DOI] [Google Scholar]
- 44. Desbiens‐Blais F., Clin J., Parent S., Labelle H., and Aubin C. E., “New Brace Design Combining CAD/CAM and Biomechanical Simulation for the Treatment of Adolescent Idiopathic Scoliosis,” Clinical Biomechanics (Bristol, Avon) 27, no. 10 (2012): 999–1005, 10.1016/j.clinbiomech.2012.08.006. [DOI] [PubMed] [Google Scholar]
- 45. Cobetto N., Aubin C. E., Parent S., et al., “Effectiveness of Braces Designed Using Computer‐Aided Design and Manufacturing (CAD/CAM) and Finite Element Simulation Compared to CAD/CAM Only for the Conservative Treatment of Adolescent Idiopathic Scoliosis: A Prospective Randomized Controlled Trial,” European Spine Journal 25 (2016): 3056–3064, 10.1007/s00586-016-4434-3. [DOI] [PubMed] [Google Scholar]
- 46. Ferziger J. H. and Peric M., “Computational Methods in Computational Fluid Dynamics,” Artificial Intelligence and Sustainable Computing Conference paper (Springer, Online: 24 September 2023). [Google Scholar]
- 47. Gould S. L., Cristofolini L., Davico G., and Viceconti M., “Computational Modelling of the Scoliotic Spine: A Literature Review,” International Journal for Numerical Methods in Biomedical Engineering 37 (2021): e3503, 10.1002/cnm.3503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48. Busscher I., van Dieën J. H., Kingma I., van der Veen A. J., Verkerke G. J., and Veldhuizen A. G., “Biomechanical Characteristics of Different Regions of the Human Spine: An In Vitro Study on Multilevel Spinal Segments,” Spine (Phila Pa 1976) 34 (2009): 2858–2864, 10.1097/BRS.0b013e3181b4c75d. [DOI] [PubMed] [Google Scholar]
- 49. Sheng W., Finite Element Modeling and Analysis of Personalized Scoliosis (Taiyuan, China:Taiyuan University of Technology, 2022), Master's Thesis. 10.27352/d.cnki.gylgu.2021.000790. [DOI] [Google Scholar]
- 50. Xin D., Huo H., Hu J., et al., “Construction of Lenke3 Type Adult Idiopathic Scoliosis Finite Element Model and Thoracic Screw Guide Target 3D Model,” Chinese Journal of Tissue Engineering Research 19 (2015): 8597–8602, 10.3969/j.issn.2095-4344.2015.53.012. [DOI] [Google Scholar]
- 51. Kamal Z. and Rouhi G., “Stress Distribution Changes in Growth Plates of a Trunk With Adolescent Idiopathic Scoliosis Following Unilateral Muscle Paralysis: A Hybrid Musculoskeletal and Finite Element Model,” Journal of Biomechanics 111 (2020): 109997, 10.1016/j.jbiomech.2020.109997. [DOI] [PubMed] [Google Scholar]
- 52. Sylvestre P. L., Villemure I., and Aubin C. E., “Finite Element Modeling of the Growth Plate in a Detailed Spine Model,” Medical & Biological Engineering & Computing 45 (2007): 977–988, 10.1007/s11517-007-0220-z. [DOI] [PubMed] [Google Scholar]
- 53. Mac‐Thiong J. M., Petit Y., Aubin C. E., Delorme S., Dansereau J., and Labelle H., “Biomechanical Evaluation of the Boston Brace System for the Treatment of Adolescent Idiopathic Scoliosis: Relationship Between Strap Tension and Brace Interface Forces,” Spine (Phila Pa 1976) 29 (2004): 26–32, 10.1097/01.Brs.0000103943.25412.E9. [DOI] [PubMed] [Google Scholar]
- 54. Cobetto N., Aubin C. E., Clin J., et al., “Braces Optimized With Computer‐Assisted Design and Simulations Are Lighter, More Comfortable, and More Efficient Than Plaster‐Cast Braces for the Treatment of Adolescent Idiopathic Scoliosis,” Spine Deformity 2 (2014): 276–284, 10.1016/j.jspd.2014.03.005. [DOI] [PubMed] [Google Scholar]
- 55. Visser D., Xue D., Ronsky J. L., Harder J., and Zernicke R. F., “Computer‐Aided Optimal Design of Custom Scoliosis Braces Considering Clinical and Patient Evaluations,” Computer Methods and Programs in Biomedicine 107 (2012): 478–489, 10.1016/j.cmpb.2010.12.017. [DOI] [PubMed] [Google Scholar]
- 56. Wang Yidan X., Yangyang W. H., Xiaohe L., et al., “Finite Element Analysis of Facet Joint Between Normal and Lumbar Disc Herniation in Adolescents,” Acta Anatomica Sinica 53 (2022): 776–784, 10.16098/j.issn.0529-1356.2022.06.012. [DOI] [Google Scholar]
- 57. Mingxing T., Finite Element Model Construction and Its Biomechanics Study of Lenke Type 1A‐Adolescent Idiopathic Scoliosis (Changsha: Central South University, 2009), 10.7666/d.y1538667. [DOI] [Google Scholar]
- 58. Rigo M. and Jelačić M., “Brace Technology Thematic Series: The 3D Rigo Chêneau‐Type Brace,” Scoliosis and Spinal Disorders 12 (2017): 10, 10.1186/s13013-017-0114-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59. Andriacchi T. P., Schultz A. B., Belytschko T. B., and Dewald R., “Milwaukee Brace Correction of Idiopathic Scoliosis. A Biomechanical Analysis and a Restrospective Study,” Journal of Bone and Joint Surgery (American Volume) 58 (1976): 806–815, 10.2106/00004623-197658060-00011. [DOI] [PubMed] [Google Scholar]
- 60. A. A. White, 3rd and Panjabi M. M., “The Clinical Biomechanics of Scoliosis,” Clinical Orthopaedics and Related Research 118 (1976): 100–112. [PubMed] [Google Scholar]
- 61. Matsumoto M., Watanabe K., Hosogane N., et al., “Postoperative Distal Adding‐On and Related Factors in Lenke Type 1A Curve,” Spine (Phila Pa 1976) 38 (2013): 737–744, 10.1097/BRS.0b013e318279b666. [DOI] [PubMed] [Google Scholar]
- 62. Liu Y., Li X., Dou X., et al., “Correlational Analysis of Three‐Dimensional Spinopelvic Parameters With Standing Balance and Gait Characteristics in Adolescent Idiopathic Scoliosis: A Preliminary Research on Lenke V,” Frontiers in Bioengineering and Biotechnology 10 (2022): 1022376, 10.3389/fbioe.2022.1022376. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63. de Reuver S., Brink R. C., Homans J. F., et al., “Anterior Lengthening in Scoliosis Occurs Only in the Disc and Is Similar in Different Types of Scoliosis,” Spine Journal 20 (2020): 1653–1658, 10.1016/j.spinee.2020.03.005. [DOI] [PubMed] [Google Scholar]
- 64. Kamal Z. and Rouhi G., “Significance of Spine Stability Criteria on Trunk Muscle Forces Following Unilateral Muscle Weakening: A Comparison Between Kinematics‐Driven and Stability‐Based Kinematics‐Driven Musculoskeletal Models,” Medical Engineering & Physics 73 (2019): 51–63, 10.1016/j.medengphy.2019.07.008. [DOI] [PubMed] [Google Scholar]
- 65. Duncombe P., Izatt M. T., Pivonka P., Claus A., Little J. P., and Tucker K., “Quantifying Muscle Size Asymmetry in Adolescent Idiopathic Scoliosis Using Three‐Dimensional Magnetic Resonance Imaging,” Spine (Phila Pa 1976) 48 (2023): 1717–1725, 10.1097/brs.0000000000004715. [DOI] [PubMed] [Google Scholar]
- 66. Barba N., Ignasiak D., Villa T. M. T., Galbusera F., and Bassani T., “Assessment of Trunk Muscle Activation and Intervertebral Load in Adolescent Idiopathic Scoliosis by Musculoskeletal Modelling Approach,” Journal of Biomechanics 114 (2021): 110154, 10.1016/j.jbiomech.2020.110154. [DOI] [PubMed] [Google Scholar]
- 67. Stokes I. A., Gardner‐Morse M. G., and Henry S. M., “Abdominal Muscle Activation Increases Lumbar Spinal Stability: Analysis of Contributions of Different Muscle Groups,” Clinical Biomechanics (Bristol, Avon) 26 (2011): 797–803, 10.1016/j.clinbiomech.2011.04.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Data for this study are available upon request as the data contained patient privacy and other sensitive information. Data requests can be sent to corresponding author (bagenliao@sina.com) and obtained after obtaining informed consent from the patient.
