Warning: mkdir(): Permission denied in /home/virtual/lib/view_data.php on line 87 Warning: chmod() expects exactly 2 parameters, 3 given in /home/virtual/lib/view_data.php on line 88 Warning: fopen(/home/virtual/e-kjs/journal/upload/ip_log/ip_log_2025-04.txt): failed to open stream: No such file or directory in /home/virtual/lib/view_data.php on line 95 Warning: fwrite() expects parameter 1 to be resource, boolean given in /home/virtual/lib/view_data.php on line 96 Correlation Between the Spinopelvic Parameters and Morphological Characteristics of Pedicle-Facet Joints in Different Lumbar Spondylolisthesis

Correlation Between the Spinopelvic Parameters and Morphological Characteristics of Pedicle-Facet Joints in Different Lumbar Spondylolisthesis

Article information

Neurospine. 2025;22(1):231-242
Publication date (electronic) : 2025 March 31
doi : https://doi.org/10.14245/ns.2448900.450
1Department of Orthopedics, The Affiliated Hospital, Southwest Medical University, Luzhou, China
2Department of Spine Surgery, Suining Central Hospital, Suining, China
3Meishan Tianfu New Area People’s Hospital, Meishan, China
4Department of Gastroenterology, The Affiliated Hospital, Southwest Medical University, Luzhou, China
Corresponding Author Dejun Zhong Department of Orthopedics, Affiliated Hospital of Southwest Medical University, No. 25 Taiping Street, Luzhou 646000, China Email: zdj_1974@163.com
Co-corresponding Author Chao Tang Department of Orthopedics, Affiliated Hospital of Southwest Medical University, No. 25 Taiping Street, Luzhou 646000, China Email: tc_spine211@swmu.edu.cn
*Baoqiang He and Yebo Leng contributed equally to this study as co-first authors.
Received 2024 September 9; Revised 2024 October 25; Accepted 2024 November 4.

Abstract

Objective

Based on spinopelvic parameters and biomechanical principles, the pedicle-facet joint (PFJ) morphological characteristics of isthmic and degenerative spondylolisthesis were analyzed, and the mechanism of their onset and progression was discussed.

Methods

This retrospective cross-sectional study included 194 patients with L5 spondylolysis or L5–S1 low-grade isthmic spondylolisthesis (IS group), 172 patients with L4–5 degenerative spondylolisthesis (DS group), and 366 patients with nonlumbar spondylolysis (NL group). The spinopelvic parameters and PFJ morphological parameters of the patients were measured, the differences in these parameters among and within the 3 groups were compared, and the correlations were analyzed.

Results

Sacral slope (SS) and lumbar lordosis (LL) were the highest in the IS group, the second highest in the DS group, and the lowest in the NL group. Among the 3 groups, the L4 facet joint angle (FJA) was the largest in the IS group, the second largest in the NL group, and the smallest in the DS group. The L4 pedicle-facet joint angle (PFA) was the largest in the DS group, the second largest in the IS group, and the smallest in the NL group. Pearson correlation analysis showed that within each group, SS and LL were negatively correlated with FJA and positively correlated with PFA.

Conclusion

This study found a correlation between the PFJ morphological characteristics of patients with lumbar spondylolisthesis and spinopelvic parameters, suggesting that the morphological characteristics of PFJs may be caused by varying stresses under different spinopelvic morphologies.

INTRODUCTION

Lumbar spondylolisthesis refers to the abnormal connection between adjacent vertebrae due to congenital dysplasia, trauma, degeneration, and other factors of the lumbar spine, which leads to partial or total slippage of the upper vertebrae relative to the lower vertebrae. It is one of the common diseases leading to lumbar and leg pain in clinical practice. Wiltse et al. [1] classified lumbar spondylolisthesis into dysplastic, isthmic, degenerative, traumatic, and pathologic spondylolisthesis based on the cause of occurrence, of which isthmic and degenerative lumbar spondylolisthesis are the most common. Degenerative lumbar spondylolisthesis was first identified and described by Junghannsyu in 1930, who named it pseudospondylolisthesis, mainly due to the occurrence of slippage of the upper vertebrae relative to the lower vertebrae because of degeneration without pars interarticularis defect. As discovered and reported by Killam, isthmic spondylolisthesis (IS) generally refers to vertebral slippage of the diseased vertebrae due to loss of traction from the posterior facet joints (FJs) due to pars defects. However, the pathogenesis of isthmic and degenerative lumbar spondylolisthesis remains unclear [2,3].

Previous studies have reported that the spinopelvic parameters of the 2 types of spondylolisthesis are significantly different compared with those of normal populations; that is, patients with lumbar spondylolisthesis have greater pelvic incidence (PI) and sacral slope (SS) [4-7]. Recently, relevant biomechanical studies have shown that under different spinopelvic types, there are significant differences in the distribution of stress in the lower lumbar spine [8], and the differences in stress will lead to differences in the morphology of the local bone structure of the lumbar spine [9-11]. To date, few studies have analyzed isthmic and degenerative lumbar spondylolisthesis from the perspective of bony morphology combined with biomechanics under different spinopelvic types. Therefore, we hypothesize that isthmic and degenerative lumbar spondylolisthesis, due to their unique spinopelvic morphology, result in an abnormal distribution of local stress in the lower lumbar spine, and we want to determine whether this stress abnormality is related to their pedicle-facet joint (PFJ) morphological characteristics.

The objectives of this study were to: (1) measure the spinopelvic parameters and morphological parameters of PFJs using radiographs and 3-dimensional (3D) reconstructed computed tomography (CT) images of patients with IS, those with degenerative spondylolisthesis (DS), and those without lumbar spondylolysis; (2) analyze the differences in the spinopelvic parameters and morphological parameters of PFJs between patients with spondylolysis and those without spondylolysis; (3) analyze the correlation between the spinopelvic parameters and morphological characteristics of the PFJs in combination with biomechanical principles; and (4) investigate the mechanism of the onset and development of lumbar spondylolysis and evaluate the clinical significance.

MATERIALS AND METHODS

1. Study Design and Participants

We conducted a retrospective cross-sectional analysis of the medical records and imaging data of all patients (Asian, from Southwest China) who visited our hospital from August 1, 2018, to May 1, 2023. This study was approved by the Institutional Review Board (IRB) of the Affiliated Hospital of Southwest Medical University (IRB No. KY2202058). Informed consent was not required, as the study was retrospective in nature. Based on the inclusion and exclusion criteria (Fig. 1), 194 patients with L5 spondylolysis or L5–S1 low-grade IS and 172 patients with L4–5 DS were included in the IS group and the DS group, respectively. A random numerical table method was used to select 366 patients from 682 patients with normal L4–5 but lumbar disc herniation in other segments as the control group (i.e., nonlumbar spondylolysis [NL] group). All of the aforementioned patients were diagnosed by spine surgeons (CT, YL) on the basis of lumbosacral frontal and lateral radiographs and 3D reconstructed lumbar CT images, and when there was disagreement between the diagnoses of these 2 surgeons, the final decision was made by a third, more senior spine surgeon (DZ).

Fig. 1.

Flowchart demonstrating the inclusion process for research subjects. All participants were randomly selected by a computer-generated random number table. 3D, 3-dimensional; CT, computed tomography; PACS, picture archiving and communication system; IS, isthmic spondylolisthesis and spondylolysis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis.

2. Data Source

Lumbosacral radiographs of all patients were obtained in the standing neutral position, and the patients were scanned in the supine position using a Siemens 128-slice spiral CT scanner with scan parameters of a 1.0-mm thickness and 1.0 mm-spacing. The original image data of all patients were stored in the postprocessing workstation for reconstruction, and the relevant parameters were measured using the measurement tool in the Siemens Syngo software workstation, with accuracy values of 0.1 mm and 0.1° for distance and angle measurements, respectively.

3. Measurements

Vertebral body slip percentage (SP) and spinopelvic parameters, i.e., PI, pelvic tilt (PT), SS, and lumbar lordosis (LL), were measured on radiographs according to the method proposed by Legaye et al. [12] and Bourassa-Moreau et al. [13] (Fig. 2). Lumbar spondylolisthesis was then graded in accordance with the Meyerding classification (grades I–IV).

Fig. 2.

Measurements of the spinopelvic parameters and pedicle-facet joint morphological parameters. (A) Pelvic incidence (PI) is the angle between the line perpendicular to the sacral plate (line a) and the line connecting the midpoint of the sacral plate to the bicoxofemoral axis (line b). Pelvic tilt (PT) is the angle between line b and the vertical line. Sacral slope (SS) is the angle between the horizontal line and the superior plate of S1 (line c). Lumbar lordosis (LL) is the angle between line c and the superior endplate of L1 (line d), and vertebral body slip percentage (SP) is the ratio of the anterior slip distance of the slipped vertebral body (distance d) to the length of the superior endplate of the lower vertebral body (distance D) expressed as a percentage. (B) The following reference lines were drawn on the axial image at the plane parallel to the inferior border of the superior endplate: line e) was drawn to divide the vertebral body equally along the central axis, and line f was drawn to connect the anteromedial and posterolateral points of the articular facet. The facet joint angle (FJA) is the angle between the 2 lines (lines e and f). The facet joint tropism is the difference between the right and left FJAs (angles α and β). Inset: Sagittal view showing where the cross-section is located. (C) The pedicle-facet joint angle (PFA) was measured on the sagittal computed tomography image at the plane parallel to the medial wall of the spinal canal as the angle between line g via the central axis of the pedicle and parallel to the pedicle and line h via the facet joint space. Inset: axial view showing where the sagittal section is located.

The morphological parameters of the L4–5 and L5–S1 FJs, including the facet joint angle (FJA), pedicle-facet joint angle (PFA), facet joint osteoarthritis (FJOA), and facet joint tropism (FT), were measured on 3D reconstructed lumbar CT images according to the method proposed by Grobler et al. [14] and Boden et al. [15] (Fig. 2). In addition, FJOA was evaluated using the FJOA grading method suggested by Kalichman et al. [16], which classifies FJOA into 4 grades based on subchondral cysts, subarticular erosions, joint space, the vacuum phenomenon, sclerosis, and articular process hypertrophy (grade I, normal; grade II, mild; grade III, moderate; and grade IV, severe).

Two spine surgeons (CT, YL) performed each measurement independently, and the final results were averaged for statistical analysis. In addition, 2 spine surgeons separately evaluated the results for FJOA grading, and in cases of disagreement, the results were evaluated by a third spine surgeon (DZ) who made a decision based on the combined evaluations. General information about all patients, including age, sex, weight, height, and body mass index (BMI), was obtained from their medical records.

4. Statistical Analysis

Statistical analysis was performed using IBM SPSS Statistics ver. 25.0 (IBM Co., Armonk, NY, USA). Independent-samples t-test was used to analyze differences in the spinopelvic parameters and PFJ morphological parameters by sex (men vs. women) and to analyze the differences in SP between the IS and DS groups. Paired-samples t-test was used to analyze differences in the PFJ morphological parameters between different segments. Analysis of variance was used to analyze the differences in general information (age, height, weight, and BMI) among the 3 groups. With age as a covariate, analysis of covariance was used to analyze the differences in the spinopelvic and PFJ morphological parameters among the 3 groups, and all between-group comparisons were performed using Bonferroni post hoc tests. Differences in Meyerding grade between the IS and DS groups and differences in FJOA severity between groups and between segments were analyzed using nonparametric tests, and between-group comparisons were performed. Categorical variables were compared using the chi-square test. Correlation analysis was performed using the Pearson correlation coefficient. At p< 0.05, differences were considered statistically significant.

RESULTS

General information and clinical features of the patients in the IS, DS, and NL groups are compared in Table 1. The differences in age and sex between the 3 groups were statistically significant (p< 0.001). The SP values in the IS group (27.3%± 10.8%) were significantly higher than those in the DS group (19.8%± 5.0%) (p < 0.001). Based on the Meyerding classification of lumbar spondylolisthesis, there were 57 cases (47.1%) of grade I and 64 cases (52.9%) of grade II in the IS group, while there were 136 cases (79.1%) of grade I and 36 cases (20.9%) of grade II in the DS group, and the difference was statistically significant (p<0.001). There were no significant differences in height, weight, and BMI among the IS, DS, and NL groups (p> 0.05).

General information and clinical features of patients in the IS, DS, and NL groups

1. Comparison of the Spinopelvic Parameters and PFJ Morphological Parameters of L4–5 and L5–S1 Among the IS, DS, and NL Groups

The results of the comparisons between the 3 groups of patients were consistent irrespective of whether the confounding factor of age was considered or not (Table 2). The differences in the spinopelvic parameters among the 3 groups were statistically significant. PI (56.7± 11.2, 58.3± 9.9), SS (38.6± 9.0, 33.2± 10.5), and LL (54.4± 12.0, 47.8± 14.6) in the IS and DS groups were significantly higher than those in the NL group (48.8± 9.2, 30.2± 8.3, 30.2± 8.3) (p< 0.001). While SS and LL were significantly higher in the IS group than in the DS group (p< 0.001), there was no significant difference in PI between the IS and DS groups (p> 0.999). PT values in both the IS and NL groups (18.3± 8.5, 18.6± 7.6) were significantly lower than those in the DS group (25.1± 9.2) (p< 0.001), but there was no significant difference in PT between the IS and NL groups (p= 0.573).

Comparison of the spinopelvic parameters and facet joint morphological parameters among the IS, DS, and NL groups

As for the morphological parameters of the L4–5 FJs, FJA in the IS group (47.4± 4.6) was significantly larger than that in the DS group (30.8± 5.9) and the NL group (46.2± 4.1) (p< 0.001), while FJA in the DS group was significantly smaller than that in the NL group (p< 0.001); PFA in the IS and DS groups (106.1± 3.4, 114.6± 4.6) was significantly larger than that in the NL group (104.2± 3.3) (p< 0.001), while PFA in the IS group was significantly smaller than that in the DS group (p< 0.001). The degree of FJOA in the DS group was significantly more severe than the degree of FJOA in the IS and NL groups (p< 0.001), while there was no significant difference in the degree of FJOA between the IS and NL groups (p> 0.999).

As for the morphological parameters of the L5–S1 FJs, FJA in the IS and NL groups (51.3 ± 7.5, 51.2 ± 3.2) was significantly larger than that in the DS group (49.5± 4.2) (p= 0.006), while there was no significant difference in FJA between the IS and NL groups (p> 0.999); PFA in the DS group (106.0± 4.5) was significantly larger than that in the NL group (102.7± 3.5) (p<0.001). The degree of FJOA in the IS and DS groups was significantly more severe than that in the NL group (p< 0.001), while there was no significant difference in the degree of FJOA between the IS and DS groups (p> 0.999).

In addition, to exclude the interference of gender, we stratified the 3 groups of patients according to gender before comparing the imaging parameters (Table 3), and the comparative results were largely consistent with the aforementioned results.

Comparison of the spinopelvic parameters and facet joint morphological parameters among members of the same sex in the IS, DS, and NL groups

2. Correlation Between the Spinopelvic Parameters and PFJ Morphological Parameters Within the IS, DS, and NL Groups

Pearson correlation analysis showed correlations between the spinopelvic parameters and lumbar PFJ morphological parameters within the IS, DS, and NL groups (Table 4). SS negatively correlated with L4 FJA in the IS group (r = -0.446, p < 0.001), DS group (r= -0.642, p< 0.001), and NL group (r= -0.563, p< 0.001), but it positively correlated with L4 PFA in the IS group (r = 0.571, p < 0.001), DS group (r = 0.677, p < 0.001), and NL group (r = 0.654, p < 0.001). LL negatively correlated with L4 FJA in the IS group (r= -0.343, p< 0.001), DS group (r= -0.574, p< 0.001), and NL group (r= -0.443, p< 0.001), and positively correlated with L4 PFA in the IS group (r= 0.437, p< 0.001), DS group (r= 0.625, p< 0.001), and NL group (r= 0.590, p< 0.001).

Correlation between the spinopelvic parameters and facet joint morphological parameters within the IS, DS, and NL groups

3. Comparison of the PFJ Morphological Parameters Between the L4–5 and L5–S1 Segments Within the IS, DS, and NL Groups

Within the IS, DS, and NL groups, L4 FJA was smaller than L5 FJA (p< 0.001), while L4 PFA was larger than L5 PFA (p<0.001). L5 FJOA was more severe than L4 FJOA in the IS group (p< 0.001); L4 FJOA was more severe than L5 FJOA in the DS group (p<0.001); and there was no significant difference between L4 FJOA and L5 FJOA in the NL group (p= 0.968) (Table 5).

Comparison of the facet joint morphological parameters between different segments within the IS, DS, and NL groups

DISCUSSION

The lumbar PFJs refer to a bony region consisting of the pedicle, the superior and inferior articular processes, and the isthmus between them. They play an important role in maintaining spinal stability and transmitting stresses [17,18]. First, under the influence of LL, the lower lumbar spine is subjected to a forward shear force that can be transmitted through the intact pedicles and the pars interarticularis to the FJs [18]. Second, through biomechanical studies, Yang and King [17] found that the distribution of spinal axial loads shared by the vertebral body and FJs was significantly different due to the differences in lumbar spine morphology and that these axial loads could be transmitted between the superior and inferior articular processes through the lumbar pars interarticularis (LPI) [18]. In a histological study, Sagi et al. [19] found the pars interarticularis of the lower lumbar spine to be a stress-weak area. Thus, both the structural features and biomechanical properties of the lower lumbar PFJs contribute to their susceptibility to morphological changes. Recently, multiple biomechanical studies have demonstrated that different spinopelvic types result in significantly different stress distribution patterns in the lumbar spine [8-11]. A large number of prior studies have found differences in spinopelvic parameters in patients with isthmic and degenerative lumbar spondylolisthesis compared with the normal population, but it has never been possible to determine whether this is related to the onset and progression of lumbar spondylolisthesis [20,21]. Considering that few studies have analyzed the PFJ morphological characteristics of patients with lumbar spondylolisthesis from a biomechanical view under different spinopelvic types, our study aimed to explore this issue based on spinopelvic parameters.

In this study, we first compared the spinopelvic parameters among the IS, DS, and NL groups. The results indicated that there were significant differences in the spinopelvic parameters among the 3 groups, and SS and LL were significantly higher in the IS group than in the DS and NL groups, and they were also significantly higher in the DS group than in the NL group. Initially, the lower lumbar spine was mechanically analyzed based on the lumbar static force equation [9,10,22]. The contact force (CF) acting on the lumbar spine is the sum of gravity and posterior spinal muscle forces. The anterior shear force (F1) is equal to CF × sinα, and the vertical compression force (F2) is equal to CF× cosα, where α is the angle between F2 and CF, and α positively correlated with SS. In this study, the patients in the IS group with higher SS were subjected to a greater forward shear force in the lower lumbar spine, particularly at L5, compared with the DS and NL groups, which could lead to the onset or even progression of lumbar spondylolisthesis (Fig. 3). At the same time, when the forward shear force is transmitted to the posterior FJs, the superior articular process of the inferior vertebra prevents the slippage by exerting a reverse resistance to the inferior articular process of the slipping vertebra, and the entire morphology of the PFJ undergoes stress-related remodeling changes or even stress fracture of the LPI under long-term stress. In addition, the stress distribution of the lumbar spine is also affected by lumbar curvature; as lumbar curvature increases, the lumbar force line gradually moves backward, and the load exerted on the posterior FJs and LPI gradually increases [9,18,23]. According to the biomechanical studies reported by Schendel et al. [23] and Dunlop et al. [24], the FJs are subjected to greater axial compressive loads in the hyperextension position of the lumbar spine, and this compressive load can be transmitted primarily through the articular surfaces, tip contacts, and LPI. Moreover, Terai et al. [25] found that when the lumbar spine was in the hyperextension position, the stress exerted on the LPI was the greatest and more likely to cause the “nutcracker” mechanism, leading to microtrauma or even fracture of the LPI. Therefore, with the increase of lumbar curvature, the LPI and FJs are subjected to greater forward shear and axial compression forces (Fig. 3), making the LPI more susceptible to fracture at greater stress and the morphological changes of the PFJs more pronounced in response to long-term stress. In this study, compared with the NL group, the PFJ morphology of the patients in the IS group with the highest SS and LL manifested pars defects, while the patients in the DS group with the second highest SS and LL showed significant morphological changes of the PFJs, i.e., a smaller FJA, a larger PFA, and more severe FJOA, due to the traction of the stress through the intact pedicle and LPI (Fig. 4). Meanwhile, SP was significantly higher in the IS group than in the DS and NL groups and was higher in the DS group than in the NL group. Moreover, within the IS, DS, and NL groups, the patients with higher SS and LL had more pronounced morphological changes of the PFJs and more severe vertebral body slippage, i.e., a smaller FJA, a larger FPA, more severe FJOA, and higher SP (Fig. 5). These findings are in agreement with our previously mentioned hypotheses, i.e., that the differences in the spinopelvic parameters among the IS, DS, and NL groups result in the entire region of the PFJs showing different structural characteristics under different stresses (Fig. 4).

Fig. 3.

Panels A–C show typical standing lateral lumbosacral radiographs and their biomechanical characteristics in the IS, DS, and NL groups, respectively. Contact force (CF) is the vector force being exerted on the vertebrae and discs; F1 is a forward shear force parallel to the endplate; F2 is a compression force perpendicular to the plate; and α is the angle between F2 and CF. CF1 is the compression force being exerted on the posterior facet joints and pars. Among the 3 groups of patients, SS and LL were the highest in the IS group, the second highest in the DS group, and the lowest in the NL group. Similarly, the force analysis showed that F1 and CF1 were the greatest in the IS group, the second greatest in the DS group, and the smallest in the NL group. IS, isthmic spondylolisthesis and spondylolysis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis.

Fig. 4.

Diagrams showing the characteristics of the forces and morphologies of the pedicle-facet joint in patients with IS, DS, and NL. F1 is a forward shear force parallel to the endplate, and F2 is the reverse resistance force of the facet joints due to the traction of F1. f1 is the axial compression force transmitted to the pars interarticularis through the facet joints, and f2 is the reverse resistance force acting on the pars interarticularis generated by the superior articular process of the inferior vertebra due to the impact of f1. The shear stresses comprise F1 and F2, whereas the pincer forces involve f1 and f2. (A) IS patients with the highest SS and LL, which means that they were subjected to the greatest shear stresses and pincer forces and manifested pars defects in the pedicle-facet joints (insets). (B) DS patients with the second greatest shear stresses and pincer forces exhibited significant morphological changes in the pedicle-facet joints (insets), i.e., smaller FJA, larger PFA, and more severe FJOA. (C) NL patients with the smallest shear stresses and pincer forces exhibited the least morphological changes in the pedicle-facet joints (insets). Insets show illustrative computed tomography scans. IS, isthmic spondylolisthesis and spondylolysis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis; FJA, facet joint angle; PFA, pediclefacet joint angle; FJOA, facet joint osteoarthritis.

Fig. 5.

Radiographs of NL patients who exhibited differences in the pedicle-facet joint morphology and biomechanics under different spinopelvic types. Contact force (CF) is the vector force being exerted on the vertebrae and discs; F1 is a forward shear force parallel to the endplate; F2 is a compression force perpendicular to the plate; and α is the angle between F2 and CF. CF1 is the compression force being exerted on the posterior facet joints and pars. The higher the SS and LL, the greater the F1 and CF1 to which the posterior facet joints and pars interarticularis are subjected, resulting in more pronounced morphological changes in the facet joints, i.e., a smaller FJA and larger PFA. The illustrative imaging of NL patients in all panels clearly shows significant differences in PFA and FJA between different spinopelvic types. SS, sacral slope; LL, lumbar lordosis; FJA, facet joint angle; PFA, pedicle-facet joint angle.

In addition, previous studies have also reported that isthmic lumbar spondylolisthesis occurs predominantly in the L5 vertebra, while degenerative lumbar spondylolisthesis tends to occur more commonly in the L4 vertebra. We believe that this difference is due to the differences in local structure and stress. First, compared with L1–4 vertebrae, the L5 vertebra has the greatest difference between the upper and lower parts of the LPI as well as cephalad and caudal lateral inclinations, and there is the narrowest lateral buttress in the L5 vertebra, so the LPI of the L5 vertebra is anatomically the most fragile [26,27]. Second, the L5 vertebra is located at the lumbosacral junction, and according to the static force equation, the forward shear force (F1) is equal to CF× sin α, where CF is the largest and α= SS, so the L5 vertebra is subjected to the greatest forward shear force. Furthermore, compared with the L4–5 FJs, the articular surfaces of the L5–S1 FJs are wider, coronally oriented in FJA, and vertically oriented in PFA (Fig. 6). In addition, there is a strong iliolumbar ligament at the posterior aspect of L5, as a result of which when the L5 vertebra is subjected to forward shear force, the posterior FJs and ligaments can generate greater reverse resistance, making the L5 vertebra less susceptible to slippage. Therefore, when faced with a strong forward shear force, the strong reverse resistance generated by the L5 vertebra due to these special anatomical structures results in a greater shear stress acting on the LPI, which may lead to its fracture or even spondylolisthesis when the stress that exceeds the bone strength (Fig. 4A). In contrast, the L4 vertebra, with its FJs oriented more sagittally in FJA and horizontally in PFA, and with smaller articular surfaces (Fig. 5), can generate a weaker resistance to a forward shear force than the L5 vertebra in both the posterior FJs and the ligaments, and is therefore more prone to pseudospondylolisthesis with an intact LPI, often resulting in significant morphological changes in the FJs with repetitive traction of shear force (Fig. 4B). In this study, L5 FJA was larger and L5 PFA was smaller compared with those of L4 in the 3 groups. Degeneration of the L4–5 FJs was significantly more severe in the DS group than in the IS and NL groups. In addition, the correlations of SS with FJA and PFA were stronger in the L4 than in the L5 vertebra in all 3 groups. These results were consistent with our analysis described above.

Fig. 6.

Comparison of the pedicle-facet joint morphology between the L4–5 and L5–S1 segments in a typical patient of the NL group. (A) At the L4–5 segment, this patient’s PFA and FJA were 105.8° and 39.3°, respectively. (B) At the L5–S1 segment, this patient’s PFA and FJA were 102.8° and 48.8°, respectively. Compared with the L4–5 facet joints, the articular surfaces of the L5–S1 facet joints were wider, coronally oriented in FJA, and vertically oriented in PFA. NL, nonlumbar spondylolysis; PFA, pediclefacet joint angle; FJA, facet joint angle.

Finally, in this study, we often observed significant disc degeneration below the slipped segment in both the IS and DS groups compared with the patients in the NL group. The mechanisms may be as follows. First, patients in the IS and DS groups have a greater forward shear force of the vertebral body compared with those in the NL group, which may lead to lumbar slippage under the traction of the shear stress; at the same time, the intervertebral discs show significant degeneration under the effect of shear stress during lumbar slippage. Second, because of the LPI defect in patients in the IS group, the role of the posterior FJs in resisting the forward shear force disappears and sharing the axial load of the spine is significantly weakened; therefore, the forward shear force and greater axial compression loads exerted on the disc increase. All of these abnormal stresses can accelerate disc degeneration (Fig. 4A and B). On imaging, we also observed that patients in the IS group tended to have more severe disc degeneration than patients of the same age in the DS group. As the disc degenerates further, its ability to maintain the stability of the lumbar spine is greatly reduced, potentially leading to the onset and progression of spondylolisthesis. Therefore, for patients with lumbar spondylolysis or low-grade isthmic lumbar spondylolisthesis presenting with high SS and LL and surgical indication, the surgical protocol recommends internal fixation treatment to correct the biomechanical imbalance and thereby restore the stability of the lumbar spine caused by the defect of the LPI. This is because direct repair of the LPI, decompression alone, or fusion without internal fixation cannot correct the biomechanical imbalance triggered by the pars defect, which can easily lead to the subsequent progression of slippage due to accelerated degeneration of the remaining stabilizing structures, such as the intervertebral disc, or can even cause severe sagittal imbalance of the lumbar spine or nerve damage.

This study has some limitations. This is a single-center, retrospective, cross-sectional study, and the conclusions need to be further validated by multicenter, large-sample, prospective cohort studies.

CONCLUSION

In this study, we found a correlation between the PFJ morphological characteristics of patients with lumbar spondylolisthesis with the spinopelvic parameters. This was evident from the fact that, compared with NL patients, patients with IS had a larger SS and LL, followed by patients with degenerative lumbar spondylolisthesis, and as SS and LL increased, the changes in the morphology of PFJs became more pronounced, and the lumbar slippage became more severe. This result suggests that different spinopelvic morphologies may result in different morphological characteristics in the PFJ region due to stress differences and the progression of lumbar spondylolisthesis. The present study provides new clues and ideas for further study into the mechanism of the onset and development of lumbar spondylolisthesis.

Notes

Conflict of Interest

The authors have nothing to disclose.

Funding/Support

This research was supported by the Sichuan Science and Technology Program (2024NSFSC0682), the Sichuan Medical Association Fund (No. S17075, Q22008, Q21005), the Science and Technology Strategic Cooperation Project Fund between the People's Government of Luzhou City and Southwest Medical University (No. 2020LZXNYDJ22), and the Doctoral Research Initiation Fund of Affiliated Hospital of Southwest Medical University (No. 22155).

Author Contribution

Conceptualization: BH, YL, CT, DZ; Data curation: BH, YL, SX, YL, JZ, MK, YL, MT, QT, FM, QW, CT, DZ; Formal analysis: BH, YL, CT, DZ; Funding acquisition: DZ; Investigation: BH, YL, XSC, CT, DZ; Methodology: BH, YL, CT, DZ; Project administration: CT, DZ; Software: HBQ, LYB; Validation: BH, YL, CT, DZ; Writing – original draft: BH, YL; Writing – review & editing: BH, YL, SX, YL, JZ, MK, YL, MT, QT, FM, QW, CT, DZ.

References

1. Wiltse LL, Newman PH, Macnab I. Classification of spondylolisis and spondylolisthesis. Clin Orthop Relat Res 1976;(117):23–9.
2. Yoshihara H. Pathomechanisms and predisposing factors for degenerative lumbar spondylolisthesis: a narrative review. JBJS Rev 2020;8e2000068.
3. Leone A, Cianfoni A, Cerase A, et al. Lumbar spondylolysis: a review. Skeletal Radiol 2011;40:683–700.
4. Lemoine T, Fournier J, Odent T, et al. The prevalence of lumbar spondylolysis in young children: a retrospective analysis using CT. Eur Spine J 2018;27:1067–72.
5. Sakai T, Goda Y, Tezuka F, et al. Characteristics of lumbar spondylolysis in elementary school age children. Eur Spine J 2016;25:602–6.
6. Sakai T, Sairyo K, Takao S, et al. Incidence of lumbar spondylolysis in the general population in Japan based on multidetector computed tomography scans from two thousand subjects. Spine (Phila Pa 1976) 2009;34:2346–50.
7. Sonne-Holm S, Jacobsen S, Rovsing HC, et al. Lumbar spondylolysis: a life long dynamic condition? A cross sectional survey of 4.151 adults. Eur Spine J 2007;16:821–8.
8. Sterba M, Arnoux PJ, Labelle H, et al. Biomechanical analysis of spino-pelvic postural configurations in spondylolysis subjected to various sport-related dynamic loading conditions. Eur Spine J 2018;27:2044–52.
9. Roussouly P, Pinheiro-Franco JL. Biomechanical analysis of the spino-pelvic organization and adaptation in pathology. Eur Spine J 2011;20 Suppl 5(Suppl 5):609–18.
10. Leng Y, Tang C, He B, et al. Correlation between the spinopelvic type and morphological characteristics of lumbar facet joints in degenerative lumbar spondylolisthesis. J Neurosurg Spine 2022;38:425–35.
11. Leng Y, Tang C, Liao Y, et al. Correlation between sacral slope and pedicle morphology of the fourth lumbar vertebra in degenerative lumbar spondylolisthesis. Global Spine J 2024;14:583–92.
12. Legaye J, Duval-Beaupère G, Hecquet J, et al. Pelvic incidence: a fundamental pelvic parameter for three-dimensional regulation of spinal sagittal curves. Eur Spine J 1998;7:99–103.
13. Bourassa-Moreau E, Mac-Thiong JM, Labelle H. Redefining the technique for the radiologic measurement of slip in spondylolisthesis. Spine (Phila Pa 1976) 2010;35:1401–5.
14. Grobler LJ, Robertson PA, Novotny JE, et al. Etiology of spondylolisthesis. Assessment of the role played by lumbar facet joint morphology. Spine (Phila Pa 1976) 1993;18:80–91.
15. Boden SD, Riew KD, Yamaguchi K, et al. Orientation of the lumbar facet joints: association with degenerative disc disease. J Bone Joint Surg Am 1996;78:403–11.
16. Kalichman L, Suri P, Guermazi A, et al. Facet orientation and tropism: associations with facet joint osteoarthritis and degeneratives. Spine (Phila Pa 1976) 2009;34:E579–85.
17. Yang KH, King AI. Mechanism of facet load transmission as a hypothesis for low-back pain. Spine (Phila Pa 1976) 1984;9:557–65.
18. Inoue N, Orías AAE, Segami K. Biomechanics of the lumbar facet joint. Spine Surg Relat Res 2020;4:1–7.
19. Sagi HC, Jarvis JG, Uhthoff HK. Histomorphic analysis of the development of the pars interarticularis and its association with isthmic spondylolysis. Spine (Phila Pa 1976) 1998;23:1635–9. discussion 1640.
20. Roussouly P, Gollogly S, Berthonnaud E, et al. Sagittal alignment of the spine and pelvis in the presence of L5-s1 isthmic lysis and low-grade spondylolisthesis. Spine (Phila Pa 1976) 2006;31:2484–90.
21. Vialle R, Ilharreborde B, Dauzac C, et al. Is there a sagittal imbalance of the spine in isthmic spondylolisthesis? A correlation study. Eur Spine J 2007;16:1641–9.
22. Lai Q, Gao T, Lv X, et al. Correlation between the sagittal spinopelvic alignment and degenerative lumbar spondylolisthesis: a retrospective study. BMC Musculoskelet Disord 2018;19:151.
23. Schendel MJ, Wood KB, Buttermann GR, et al. Experimental measurement of ligament force, facet force, and segment motion in the human lumbar spine. J Biomech 1993;26:427–38.
24. Dunlop RB, Adams MA, Hutton WC. Disc space narrowing and the lumbar facet joints. J Bone Joint Surg Br 1984;66:706–10.
25. Terai T, Sairyo K, Goel VK, et al. Spondylolysis originates in the ventral aspect of the pars interarticularis: a clinical and biomechanical study. J Bone Joint Surg Br 2010;92:1123–7.
26. Sairyo K, Goel VK, Grobler LJ, et al. The pathomechanism of isthmic lumbar spondylolisthesis. A biomechanical study in immature calf spines. Spine (Phila Pa 1976) 1998;23:1442–6.
27. Weiner BK, Walker M, Wiley W, et al. The lateral buttress: an anatomic feature of the lumbar pars interarticularis. Spine (Phila Pa 1976) 2002;27:E385–7.

Article information Continued

Fig. 1.

Flowchart demonstrating the inclusion process for research subjects. All participants were randomly selected by a computer-generated random number table. 3D, 3-dimensional; CT, computed tomography; PACS, picture archiving and communication system; IS, isthmic spondylolisthesis and spondylolysis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis.

Fig. 2.

Measurements of the spinopelvic parameters and pedicle-facet joint morphological parameters. (A) Pelvic incidence (PI) is the angle between the line perpendicular to the sacral plate (line a) and the line connecting the midpoint of the sacral plate to the bicoxofemoral axis (line b). Pelvic tilt (PT) is the angle between line b and the vertical line. Sacral slope (SS) is the angle between the horizontal line and the superior plate of S1 (line c). Lumbar lordosis (LL) is the angle between line c and the superior endplate of L1 (line d), and vertebral body slip percentage (SP) is the ratio of the anterior slip distance of the slipped vertebral body (distance d) to the length of the superior endplate of the lower vertebral body (distance D) expressed as a percentage. (B) The following reference lines were drawn on the axial image at the plane parallel to the inferior border of the superior endplate: line e) was drawn to divide the vertebral body equally along the central axis, and line f was drawn to connect the anteromedial and posterolateral points of the articular facet. The facet joint angle (FJA) is the angle between the 2 lines (lines e and f). The facet joint tropism is the difference between the right and left FJAs (angles α and β). Inset: Sagittal view showing where the cross-section is located. (C) The pedicle-facet joint angle (PFA) was measured on the sagittal computed tomography image at the plane parallel to the medial wall of the spinal canal as the angle between line g via the central axis of the pedicle and parallel to the pedicle and line h via the facet joint space. Inset: axial view showing where the sagittal section is located.

Fig. 3.

Panels A–C show typical standing lateral lumbosacral radiographs and their biomechanical characteristics in the IS, DS, and NL groups, respectively. Contact force (CF) is the vector force being exerted on the vertebrae and discs; F1 is a forward shear force parallel to the endplate; F2 is a compression force perpendicular to the plate; and α is the angle between F2 and CF. CF1 is the compression force being exerted on the posterior facet joints and pars. Among the 3 groups of patients, SS and LL were the highest in the IS group, the second highest in the DS group, and the lowest in the NL group. Similarly, the force analysis showed that F1 and CF1 were the greatest in the IS group, the second greatest in the DS group, and the smallest in the NL group. IS, isthmic spondylolisthesis and spondylolysis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis.

Fig. 4.

Diagrams showing the characteristics of the forces and morphologies of the pedicle-facet joint in patients with IS, DS, and NL. F1 is a forward shear force parallel to the endplate, and F2 is the reverse resistance force of the facet joints due to the traction of F1. f1 is the axial compression force transmitted to the pars interarticularis through the facet joints, and f2 is the reverse resistance force acting on the pars interarticularis generated by the superior articular process of the inferior vertebra due to the impact of f1. The shear stresses comprise F1 and F2, whereas the pincer forces involve f1 and f2. (A) IS patients with the highest SS and LL, which means that they were subjected to the greatest shear stresses and pincer forces and manifested pars defects in the pedicle-facet joints (insets). (B) DS patients with the second greatest shear stresses and pincer forces exhibited significant morphological changes in the pedicle-facet joints (insets), i.e., smaller FJA, larger PFA, and more severe FJOA. (C) NL patients with the smallest shear stresses and pincer forces exhibited the least morphological changes in the pedicle-facet joints (insets). Insets show illustrative computed tomography scans. IS, isthmic spondylolisthesis and spondylolysis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis; FJA, facet joint angle; PFA, pediclefacet joint angle; FJOA, facet joint osteoarthritis.

Fig. 5.

Radiographs of NL patients who exhibited differences in the pedicle-facet joint morphology and biomechanics under different spinopelvic types. Contact force (CF) is the vector force being exerted on the vertebrae and discs; F1 is a forward shear force parallel to the endplate; F2 is a compression force perpendicular to the plate; and α is the angle between F2 and CF. CF1 is the compression force being exerted on the posterior facet joints and pars. The higher the SS and LL, the greater the F1 and CF1 to which the posterior facet joints and pars interarticularis are subjected, resulting in more pronounced morphological changes in the facet joints, i.e., a smaller FJA and larger PFA. The illustrative imaging of NL patients in all panels clearly shows significant differences in PFA and FJA between different spinopelvic types. SS, sacral slope; LL, lumbar lordosis; FJA, facet joint angle; PFA, pedicle-facet joint angle.

Fig. 6.

Comparison of the pedicle-facet joint morphology between the L4–5 and L5–S1 segments in a typical patient of the NL group. (A) At the L4–5 segment, this patient’s PFA and FJA were 105.8° and 39.3°, respectively. (B) At the L5–S1 segment, this patient’s PFA and FJA were 102.8° and 48.8°, respectively. Compared with the L4–5 facet joints, the articular surfaces of the L5–S1 facet joints were wider, coronally oriented in FJA, and vertically oriented in PFA. NL, nonlumbar spondylolysis; PFA, pediclefacet joint angle; FJA, facet joint angle.

Table 1.

General information and clinical features of patients in the IS, DS, and NL groups

Variable IS group DS group NL group p-value
Age (yr) 51.8 ± 12.9 62.4 ± 10.0 46.4 ± 12.3 < 0.001
Sex < 0.001
 Male 88 (45.4) 35 (20.3) 203 (55.5)
 Female 106 (54.6) 137 (79.7) 163 (44.5)
Height (cm) 159.7.0 ± 7.9 158.7 ± 6.4 159.6 ± 7.4 0.385
Weight (kg) 60.7 ± 10.0 59.9 ± 8.0 61.3 ± 10.0 0.290
BMI (kg/m2) 23.8 ± 3.3 24.2 ± 4.9 24.1 ± 3.2 0.424
SP (%) 27.3 ± 10.8 19.8 ± 5.0 - < 0.001
Meyerding grade < 0.001
 Grade I 57 (47.1) 136 (79.1) NA
 Grade II 64 (52.9) 36 (20.9) NA
 Grade III 0 (0) 0 (0) NA
 Grade IV 0 (0) 0 (0) NA

Values are presented as mean±standard deviation or number (%).

IS, isthmic spondylolisthesis and spondylolysis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis; BMI, body mass index; SP, slip percentage; NA, not applicable.

Table 2.

Comparison of the spinopelvic parameters and facet joint morphological parameters among the IS, DS, and NL groups

Variable IS group DS group NL group p-value p-value
PI (°) 56.7 ± 11.2§ 58.3 ± 9.9§ 48.8 ± 9.2 < 0.001 < 0.001
PT (°) 18.3 ± 8.5§ 25.1 ± 9.2 18.6 ± 7.6 < 0.001 < 0.001
SS (°) 38.6 ± 9.0 33.2 ± 10.5 30.2 ± 8.3 < 0.001* < 0.001*
LL (°) 54.4 ± 12.0 47.8 ± 14.6 42.3 ± 13.5§ < 0.001* < 0.001*
L4 FJA (°) 47.4 ± 4.6 30.8 ± 5.9 46.2 ± 4.1 < 0.001* < 0.001*
L4 PFA (°) 106.1 ± 3.4 114.6 ± 4.6 104.2 ± 3.3 < 0.001* < 0.001*
L4 FT (°) 5.7 ± 4.8 6.2 ± 3.2 2.8 ± 2.3 < 0.001 < 0.001
L5 FJA (°) 51.3 ± 7.5 49.5 ± 4.2 51.2 ± 3.2 < 0.001 0.006
L5 PFA (°) NA 106.0 ± 4.5§ 102.7 ± 3.5 < 0.001 < 0.001
L5 FT (°) 6.2 ± 5.1 6.9 ± 7.3 7.4 ± 6.3 0.138 0.172
L4 FJOA < 0.001
 Grade I 264 (68.0) 0 (0) 504 (68.9)
 Grade II 99 (25.5) 18 (5.2) 200 (27.3)
 Grade III 21 (5.4) 122 (35.5) 26 (3.6)
 Grade IV 4 (1.0) 204 (59.3) 2 (0.3)
L5 FJOA < 0.001
 Grade I 149 (38.4) 141 (41.0) 504 (68.9)
 Grade II 181 (46.6) 144 (41.9) 198 (27.0)
 Grade III 47 (12.1) 28 (8.1) 30 (4.1)
 Grade IV 11 (2.8) 31 (9.0) 0 (0)

Values are presented as mean±standard deviation or number (%).

IS, spondylolysis and low-grade isthmic spondylolisthesis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis; PI, pelvic incidence; PT, pelvic tilt; SS, sacral slope; LL, lumbar lordosis; FJA, facet joint angle; PFA, pedicle-facet joint angle; FT, facet joint tropism; FJOA, facet joint osteoarthritis; ANCOVA, analysis of covariance; NA, not applicable.

L5 PFA values were not measured in the IS group due to pars defect interference.

There was a significant difference in age among the 3 groups of patients; therefore, differences in PI, PT, LL, FJA, and PFA parameters were compared using ANCOVA (age as a covariate) to exclude the interference of the age factor.

*

Post hoc analysis revealed that there were significant differences among the IS, DS, and NL groups.

Post hoc analysis revealed that there were significant differences between the IS and DS groups and between the DS and NL groups.

Post hoc analysis revealed that there were significant differences between the IS and NL groups and between the DS and NL groups.

§

The value was larger in women than in men, and the difference was statistically significant (p<0.05). There was no statistical difference in the remaining parameters between men and women (p>0.05).

Table 3.

Comparison of the spinopelvic parameters and facet joint morphological parameters among members of the same sex in the IS, DS, and NL groups

Variable Female
Male
IS (n = 106) DS (n = 137) NL (n = 163) p-value IS (n = 88) DS (n = 35) NL (n = 203) p-value
PI (°) 59.3 ± 11.5 59.2 ± 9.7 49.7 ± 9.0 < 0.001 53.6 ± 10.0 54.8 ± 10.2 48.0 ± 9.2 < 0.001
PT (°) 20.3 ± 8.8 25.6 ± 8.8 19.3 ± 7.6 < 0.001 15.7 ± 7.4 23.2 ± 10.6 18.0 ± 7.6 < 0.001*
SS (°) 39.3 ± 9.4 33.8 ± 10.3 30.3 ± 8.0 < 0.001* 37.9 ± 8.6 31.1 ± 11.4 30.0 ± 8.7 < 0.001§
LL (°) 55.3 ± 11.7 48.6 ± 13.8 44.1 ± 13.3 < 0.001§ 53.3 ± 12.3 44.5 ± 17.4 40.8 ± 13.5 < 0.001§
L4 PFA (°) 105.9 ± 3.4 114.8 ± 4.6 104.4 ± 3.3 < 0.001 106.4 ± 3.3 113.7 ± 4.5 104.1 ± 3.3 < 0.001*
L5 PFA (°) NA 106.5 ± 4.4 102.5 ± 3.5 < 0.001 NA 103.8 ± 4.1 102.8 ± 3.5 0.435
L4 FJA (°) 47.0 ± 4.4 30.7 ± 5.9 46.6 ± 4.0 < 0.001 47.9 ± 4.9 31.0 ± 6.0 46.0 ± 4.2 < 0.001*
L4 FT (°) 5.1 ± 4.1 6.3 ± 3.3 2.8 ± 2.0 < 0.001* 6.5 ± 5.4 5.6 ± 2.7 2.8 ± 2.5 < 0.001
L5 FJA (°) 51.3 ± 7.1 49.4 ± 3.9 51.2 ± 3.2 0.007 51.3 ± 7.9 50.1 ± 5.3 51.2 ± 3.2 0.689
L5 FT (°) 5.9 ± 5.0 6.9 ± 7.3 7.8 ± 7.1 0.097 6.7 ± 5.2 6.8 ± 7.4 7.0 ± 5.7 0.922

Values are presented as mean±standard deviation.

IS, spondylolysis and low-grade isthmic spondylolisthesis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis; PI, pelvic incidence; PT, pelvic tilt; SS, sacral slope; LL, lumbar lordosis; PFA, pedicle-facet joint angle; FJA, facet joint tropism; FT, facet joint tropism; ANCOVA, analysis of covariance; NA, not applicable.

L5 PFA values were not measured in the IS group due to pars defect interference.

There was a significant difference in age among the 3 groups of patients; therefore, differences in PI, PT, LL, FJA, and PFA parameters were compared using ANCOVA (age as a covariate) to exclude the interference of the age factor.

*

Post hoc analysis revealed that there were significant differences between the IS, DS, and NL groups.

Post hoc analysis revealed that there were significant differences between the IS and DS groups and between the DS and NL groups.

Post hoc analysis revealed that there were significant differences between the IS and NL groups and between the DS and NL groups.

§

Post hoc analysis revealed that there were significant differences between the IS and DS groups and between the IS and NL groups.

Table 4.

Correlation between the spinopelvic parameters and facet joint morphological parameters within the IS, DS, and NL groups

Variable IS group
DS group
NL group
PI SS LL PI SS LL PI SS LL
L4 FJA -0.251* -0.446* -0.343* -0.397* -0.642* -0.574* -0.378* -0.563* -0.443*
L4 PFA 0.316* 0.571* 0.437* 0.540* 0.677* 0.625* 0.540* 0.654* 0.590*
L4 FT -0.019 0.024 0.024 -0.012 0.002 0.021 0.066 0.054 0.037
L5 FJA -0.086 -0.167* -0.126 -0.256* -0.448* -0.428 -0.259* -0.405* -0.349*
L5 PFA NA NA NA 0.362* 0.542* 0.566* 0.327* 0.510* 0.446*
L5 FT -0.006 -0.01 -0.087 0.022 -0.019 -0.036 0.055 0.115* 0.061
SP 0.359* 0.345* 0.254* 0.328* 0.293* 0.232* NA NA NA

IS, spondylolysis and low-grade isthmic spondylolisthesis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis; FJA, facet joint angle; PFA, pedicle-facet joint angle; FT, facet joint tropism; SP, slip percentage; NA, not applicable.

*

p<0.05, statistically significant differences.

Table 5.

Comparison of the facet joint morphological parameters between different segments within the IS, DS, and NL groups

Variable IS group
DS group
NL group
L4 L5 p-value L4 L5 p-value L4 L5 p-value
FJA (°) 47.4 ± 4.6 51.3 ± 7.5 < 0.001 30.8 ± 5.9 49.5 ± 4.2 < 0.001 46.2 ± 4.1 51.2 ± 3.2 < 0.001
PFA (°) 106.1 ± 3.4 NA 114.6 ± 4.6 106.0 ± 4.5 < 0.001 104.2 ± 3.3 102.7 ± 3.5 < 0.001
FT (°) 5.7 ± 4.8 6.2 ± 5.1 0.300 6.2 ± 3.2 6.9 ± 7.3 0.240 2.8 ± 2.3 7.4 ± 6.3 < 0.001
FJOA < 0.001 < 0.001 0.968
 Grade I 264 (68.0) 149 (38.4) 0 (0) 141 (41.0) 504 (68.9) 504 (68.9)
 Grade II 99 (25.5) 181 (46.6) 18 (5.2) 144 (41.9) 200 (27.3) 198 (27.0)
 Grade III 21 (5.4) 47 (12.1) 122 (35.5) 28 (8.1) 26 (3.6) 30 (4.1)
 Grade IV 4 (1.0) 11 (2.8) 204 (59.3) 31 (9.0) 2 (0.3) 0 (0)

Values are presented as mean±standard deviation or number (%).

IS, isthmic spondylolisthesis and spondylolysis; DS, degenerative spondylolisthesis; NL, nonlumbar spondylolysis; FJA, facet joint tropism; PFA, pedicle-facet joint angle; FT, facet joint tropism; FJOA, facet joint osteoarthritis; NA, not applicable.