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. 2024 Feb 15;14:3813. doi: 10.1038/s41598-024-54472-4

Hip-sacroiliac joint-spine syndrome in total hip arthroplasty patients

Ayumi Kaneuji 1,✉, Makoto Fukui 1, Eiji Takahashi 1, Yusuke Sanji 1, Hiroaki Hirata 1, Norio Kawahara 1
PMCID: PMC10869769  PMID: 38361017

Abstract

This study is designed to compare the extent of sacroiliac joint (SIJ) degeneration at total hip arthroplasty (THA) for two pathologies: osteoarthritis of the hip (OA) and osteonecrosis of the femoral head (ON). We also assessed the prevalence of SIJ degeneration in patients with lumbar spondylolisthesis or degenerative scoliosis. A total of 138 hips from 138 patients (69 OA and 69 ON) were assessed in this study, including 66 hips affected by OA secondary to developmental dysplasia of the hip. The degenerative changes in the SIJ and lumbar spine were evaluated prior to THA using radiographs and computed tomography (CT) scans, showing 9 instances of spondylolisthesis and 38 of degenerative scoliosis. The OA group exhibited longer duration from onset to surgery than the ON group. The OA group also included more cases with significant pelvic obliquity (3 degrees or more) and with significant increases in SIJ sclerosis and irregularities. Patients with lumbar spondylolisthesis or degenerative scoliosis were significantly more likely to have SIJ irregularities. The prevalence of SIJ degeneration was higher in cases of THA for OA than for ON. This study also suggests the possibility of Hip-SIJ-Spine syndrome in THA patients with OA.

Subject terms: Diseases, Medical research

Introduction

Hip-spine syndrome was first described by Offierski and Macnab in 19831. It is classified into four types: simple, complex, mixed, and misdiagnosed. The simple type involves degenerative changes in either the hip joint or the spine, with that degeneration being the primary cause of the condition. The complex type involves degenerative changes in both the hip joint and the spine, with both contributing to the pathology. The mixed type refers to the interaction between hip and spinal pathologies, so that the conditions of the hip joint and the spine mutually affect each other. The misdiagnosed type occurs when incorrect treatment is provided due to a lack of awareness of the involvement of both hip and spine pathologies. An anatomical study also has detailed the mutual influence of degenerative changes in the spine and the hip joint2.

In recent years, researchers have suggested that lumbosacral fusion and long fusion of the lumbar spine can lead to progressive hip osteoarthritis (hip OA)3,4. Additionally, sacroiliac joint (SIJ) fixation has been linked to a two-fold increase in the risk of dislocation after total hip arthroplasty5, suggesting a mechanical influence on the SIJ between the lumbar spine and the hip joint. Credible reports indicate that 14–30% of low back pain originates from the SIJ7–9, and extensive study of the nerve supply to the SIJ suggests that not only the SIJ capsule but also the surrounding tissues such as ligaments can manifest pain10–18. However, the origin of SIJ pain remains unclear6,16,17. While excessive motion is restricted by ligaments, the SIJ joint has some limited mobility6, and increased instability or stress on the posterior ligaments of the SIJ may cause pain and dysfunction. In fact, symptomatic relief has been reported from immobilization by external fixation of the pelvis or injections into the posterior ligaments19,20.

There have been reports of increased stress on the SIJ due to lumbosacral fusion21,22, as well as reports of increased degeneration of the SIJ23, strongly indicating an interrelationship between the lumbar spine and the SIJ, and a link between hip OA and SIJ dysfunction has been suggested24,25. Asada et al.25 analyzed preoperative CT scans of patients with hip OA who underwent total hip arthroplasty (THA) and noted a significantly higher incidence of narrowed joint space, osteophyte formation, and vacuum phenomena in the SIJ compared with a control group. Elucidating the relationship between the hip, spine, and SIJ disorders is thus of considerable clinical importance.

In this study, we formulated two hypotheses: first, that long-term degeneration of the hip joint has a major impact on the SIJ, making it more susceptible to Hip-SIJ syndrome, and second, that patients with the condition termed “Hip-Spine syndrome” show a higher prevalence of SIJ degeneration, suggesting the existence of what we have designated as “Hip-SIJ-Spine syndrome”. We then conducted a comparative study of patients undergoing THA for hip OA and for idiopathic osteonecrosis of the femoral head (ON).

THA for OA is often performed after a long duration of illness, while ON frequently requires THA within a short timeframe. This is the reason for selecting these two conditions for comparison. Furthermore, in our facility, a significant proportion of OA cases are associated with developmental dysplasia of the hip (DDH), and ON often occurs in the unaffected hip joint, making it easier to compare and study in the context of this research.

Methods

The subjects of this study were patients who underwent THA for the treatment of OA or ON. A total of 93 patients (100 hips) who received THA for OA between June 2016 and December 2016 were enrolled. Since there was a possibility of changes in findings after unilateral surgery, seven cases of bilateral procedures were included only for analysis of the first operated side. An additional 24 patients (24 hips) were excluded because of inadequate CT confirmation of SIJ, so that 69 patients (69 hips) were included in analysis for the OA group. Because the annual number of cases of ON is relatively small, the treatment period for ON was extended from January 2010 to October 2022, and 83 patients (109 hips) were enrolled. Of those, 26 bilateral cases were counted on one side only. Seven patients (7 hips) were excluded because the patient had already undergone THA on one side, and an additional seven patients (7 hips) were excluded because of inadequate confirmation of the SIJ by CT or because of significant collapse of the necrotic area from advanced OA. This resulted in 69 cases (69 hips) that were included in analysis for the ON group.

Patient demographics are shown in Table 1. There were no significant differences in age, height, weight and BMI between the groups. However, due to a higher prevalence of OA resulting from developmental dysplasia of the hip (DDH), female patients made up a significantly higher portion of the OA group (87%) than of the ON group (55%). In the OA group, only 3 hips were classified as primary OA, while 66 hips (96%) were classified as secondary OA from DDH. Crowe classification Group I accounted for 61 hips (92%), indicating a relatively low degree of hip dislocation in this group. In the ON group, 38 hips (55%) were classified as Group 4, indicating narrowing of the joint space but not reaching terminal OA.

Table 1.

Demographic data for all patients.

OA ON p value
Cases 69 69 NS
Hips 69 69 NS
Female : Male 60 : 9 38 : 31  < 0.01
Right : Left 38 : 31 39 : 30 NS
Age (years)* 62.0 (44–87) 59.4 (33–81) NS
Height (cm)* 156.3 (142.6–181.0) 160.2 (140.0–178.6) NS
Weight (kg)* 58.5 (36.8–98.8) 61.5 (40.8–99.0) NS
BMI (kg/m2)* 23.9 (15.6–40.7) 23.9 (14.6–36.8) NS
Tönnis grade (0:1:2:3) 0:0:7:62 NA
Crowe classification34 (group I:II:III:IV) 61:5:0:0 NA
Stage classification35 for ON (1:2:3:4) NA 0:6:25:38

OA osteoarthritis of the hip joint, ON osteonecrosis of the femoral head, BMI body mass index.

*Values are mean and range, NA not applicable, NS not significant.

Preoperative leg length discrepancy was measured by assessing the difference in Spina Malleolar Distance between the left and right sides before surgery, and was classified as an absolute value of ≤ 5 mm or ≥ 6 mm. A difference of ≥ 6 mm was defined as leg length discrepancy.

Radiographic and CT analysis

The following items were investigated using imaging:

I. Preoperative anteroposterior pelvic radiographs

  1. Pelvic tilt angle: Confirmation of the presence of lateral tilt of the iliac wings, with a tilt of 3 degrees or more in either direction classified as tilt present.

  2. Discrepancy in the obturator foramen: Confirmation of any obvious left–right asymmetry in the shape of the obturator foramen.

II. Preoperative frontal and lateral lumbar spine images

  1. Lumbar scoliosis: Confirmation of the presence of lumbar scoliosis and measurement of the Cobb angle. A Cobb angle of 5 degrees or more was classified as scoliosis present.

  2. Lumbar degenerative spondylolisthesis: Presence of more than 25% slip of a lumbar vertebra was classified as spondylolisthesis present.

III. Preoperative CT images

SIJ degenerative changes26,27: CT cross-sectional images with a slice interval of 1 mm were examined for the following:

  1. Sclerosis: Presence of sclerosis adjacent to either the sacral or iliac side of the SIJ was classified as sclerosis present.

  2. Vacuum phenomenon: Presence of CT attenuation similar to air in the joint space of the SIJ was classified as vacuum phenomenon present.

  3. Discrepancy in joint space width: Confirmation of asymmetry in the width of the SIJ space was classified as discrepancy in joint space width.

  4. Irregularities: Slight narrowing of the SIJ space, non-parallel joint surfaces of the sacral or iliac side, or erosive changes in a portion of the joint surface were classified as irregularities present.

  5. Discrepancy in iliac wing opening angle: Measurement of the angle formed by drawing a perpendicular line from the midline sacral ridge to the vertebral body at the second sacrum level and drawing a line from the midpoint of the width of the most anterior part of the iliac wing visible on the CT slice to the sacral ridge. A difference in absolute values of 3 degrees or more between the left and right sides was classified as iliac wing opening angle discrepancy present.

Statistical analysis

Statistical analysis was performed using the chi-square test or Fisher's exact test by Microsoft Excel. A p-value of 0.05 or less was considered statistically significant.

All methods in this study were performed in accordance with the relevant guidelines and regulations, and approval was granted by the Ethics Committee of Kanazawa Medical University.

Ethical approval

Approval was granted by the Ethics Committee of Kanazawa Medical University.

Consent to participate

Written informed consent was obtained from the all patients.

Results

The OA group differed significantly from the ON group in several parameters. Significantly more prevalent in the OA group were duration of illness, angle of pelvic outward tilt, instances of pelvic outward tilt of 3 degrees or more, and sclerotic and irregular images in the SIJ (Table 2). No significant intergroup differences were noted in the frequency of lumbar spondylolisthesis and scoliosis. However, the presence of lumbar spondylolisthesis and of 5 degrees or more of scoliosis were significantly associated with a higher prevalence of irregular SIJ images (P = 0.027) and (P = 0.00373), respectively (Table 3). Further analysis revealed that the presence of SIJ irregularities was significantly associated with asymmetry in the SIJ joint space in the entire group (P < 0.0001). No significant differences were observed in other parameters.

Table 2.

Comparison of OA and ON groups.

OA ON p value
Duration from onset to surgery (years)# 5.0 (0.25–20) 0.75 (0.1–24) < 0.01
Leg length discrepancy (LLD) at surgery (mm)* 10.0 (0–40) 5.7 (0–20) 0.409
LLD >  = 6 mm (yes:no) 44:25 26:43 0.07
Lateral inclination angle of pelvis (°)* 1.6 (0–9) 0.7 (0–11) < 0.01
Lateral inclination angle of pelvis >  = 3°(yes:no) 25:44 6:63 < 0.01
Asymmetry of obturator foramen (yes : no) 52:17 7:62 0.198
Spondylolisthesis (cases) 8:61 1:68 0.374
Cobb angle at lumbar spine (°)* 3.5 (0–17) 2.9 (0–26) 0.121
Cobb angle >  = 5°(yes:no) 20:49 18:51 0.751
Sclerotic change of SIJ (yes:no) 30:39 14:55 < 0.01
Vacuum phenomenon of SIJ (yes:no) 32:37 17:52 0.828
Asymmetry of SIJ space (yes:no) 20:49 7:62 0.464
Irregularity of SIJ (yes:no) 38:31 9:60  < 0.01
Angle of right iliac wing (°)* 44.7 (34–58) 45.8 (36–58) 0.464
Angle of left iliac wing (°)* 44.9 (33–59) 45.5 (34–58) 0.134
Difference in bilateral iliac wing angle (°)* 4.5 (0–25) 3.5 (0–15) 0.598

SIJ sacro-iliac joint, OA osteoarthritis of the hip joint, ON osteonecrosis of the femoral head.

#Values are median and range. *Values are mean and range.

Statistical analysis for continuous values was performed using a t-test. A chi-square test was conducted for the other variables.

Table 3.

Relationship between lumbar spine degeneration and SIJ degeneration.

Spondylolisthesis Cobb angle >  = 5°
Yes (cases) No (cases) p value Yes (cases) No (cases) p value
Irregularity of SIJ Yes 7 40 0.027 15 32 0.0037
No 2 89 23 68
Sclerotic change in SIJ Yes 5 47 0.35 13 39 0.5733
No 4 82 25 61
Asymmetry of SIJ space Yes 5 22 0.518 7 20 0.0861
No 4 107 31 80
Asymmetry of obturator foramen Yes 3 21 0.482 7 17 0.2877
No 6 108 31 83
Vacuum phenomenon in SIJ Yes 5 45 0.485 12 38 0.6745
No 4 84 26 62
Lateral inclination of pelvis >  = 3° Yes 5 78 0.122 22 61 0.2769
No 4 51 16 39

SIJ sacro-iliac joint, Fisher's exact test was conducted for all analyses.

Case study 1 (Fig. 1a–c): A 58-year-old female presented with bilateral hip OA. She had been experiencing bilateral hip pain for the past 10 years. The pain gradually worsened, leading to limited range of motion, and she underwent left THA. Subsequently, a right THA was also performed.

Figure 1.

Figure 1

Hip OA secondary to DDH. (a) Pre-operative x-ray. The patient had bilateral terminal-stage OA of the hip joint. The SIJ space differed visibly between right and left sides. (b) Prior to left-side surgery, the patient was diagnosed with a 25% slip of the fourth lumbar vertebra indicative of spondylolisthesis. Scoliosis with a Cobb angle of 7 degrees was also observed. (c) CT imaging showed SIJ irregularities and the presence of vacuum phenomena (yellow arrows). OA: osteoarthritis, DDH: developmental dysplasia of the hip, SIJ: sacroiliac joint, CT: computed tomography.

Case study 2 (Fig. 2a–c): A 51-year-old male presented with left hip pain continuing for the past 3 months and was diagnosed with stage 3 ON on the left side. Due to severe pain, he underwent left THA.

Figure 2.

Figure 2

Alcohol-induced ON. (a) The sclerotic boundary was visible (white triangles), with bone collapse on the left femoral head (yellow arrows). (b) X-ray images showed no lumbar spondylolisthesis except for slight scoliosis. (c) CT images showed no abnormalities, including SIJ irregularities. ON: osteonecrosis of the femoral head, SIJ: sacroiliac joint, CT: computed tomography.

Discussion

The results of this study suggested that THA was associated with significantly more degenerative change in the SIJ of the OA group than the ON group. In addition, the presence of irregularities in the SIJ was significantly associated with greater asymmetry in the SIJ space, indicating that excessive load on the SIJ due to hip OA may have led to degenerative changes24,25. This study showed little correlation with leg length discrepancy, suggesting that SIJ degeneration may progress even in the absence of conditions such as DDH-related leg shortening. However, it is also possible that DDH itself increases stress on the SIJ. Toyohara et al. analyzed SIJ stress using finite element models based on CT images before and after periacetabular osteotomy in four DDH patients28. They reported that stress on the SIJ and the posterior sacroiliac ligament, which is commonly observed in preoperative dysplastic hips, often decreased after surgery, indicating that excessive load on the SIJ was reduced after formation of a near-normal acetabulum. This suggests that the morphology of DDH itself may increase the load on the SIJ.

A significant association was noted between SIJ joint irregularities and the presence of more than 25% of lumbar spondylolisthesis or scoliosis of 5° or more, indicating a higher prevalence of SIJ degeneration in the patient group that underwent THA and had degenerative spinal diseases. Kwon et al. reported a higher prevalence of SIJ degeneration in patients with spinopelvic imbalance compared to those with lumbar spinal canal stenosis (LSCS)29, and Chen has stated that SIJ degeneration was more common in patients with spondylolisthesis30. Although a systematic review has shown no consensus regarding SIJ degeneration after lumbar spinal fixation31, there has been some suggestion that the SIJ degeneration described in the previous reports24,25,30 might have been caused by spinal disease or hip OA. However, our study showed SIJ degeneration in some cases of Hip-Spine syndrome, in which spinal degeneration is associated with hip OA. Although further investigation is needed in a larger number of clinical cases, of course, with careful consideration of clinical symptoms, the new concept of “Hip-SIJ-Spine syndrome” should be focused on patients with Hip-Spine syndrome.

This study indicated that long-term degeneration of the hip joint has a major impact on the SIJ, making it more susceptible to Hip-SIJ syndrome. And patients with the condition termed “Hip-Spine syndrome” may show a higher prevalence of SIJ degeneration, suggesting the existence of what we have designated as “Hip-SIJ-Spine syndrome”.

This study did not make use of the SIJ degeneration score developed by Backlund et al. or Eno's classification32,33. This was because previous reports on the relationship between hip OA and SIJ degeneration25 showed no significant difference in scores between the OA and control groups, and data on osteophyte levels were contradictory. In the present study, SIJ joint irregularities, which were not included in the SIJ degeneration score, were found to be associated with hip OA. SIJ joint irregularities are often observed on CT scans as early changes and may be interpreted as the first imaging of SIJ degeneration27. Considering that SIJ instability can induce symptoms19, these changes may also represent the first imaging of instability. Further investigation is needed in the future.

This study had several limitations. First, observations were limited to cases that underwent THA, and it is unclear whether similar occurrences of Hip-SIJ-Spine syndrome are more likely in cases of DDH or femoroacetabular impingement. Second, no data is currently available on whether SIJ degeneration is similarly likely to occur in simple Hip-Spine syndrome where pathology extends from the lumbar spine to the hip. Third, clinical symptoms were not confirmed, so it is unclear whether the concept of Hip-SIJ-Spine syndrome is clinically relevant or clearly expressed. Fourth, cases of DDH-related hip OA predominated in this study, and we do not know whether the same pathology would occur in cases of primary hip OA. Fifth, the sample size was small.

Diagnosing SIJ dysfunction was not easy in the past, but it has been facilitated by the SIJ scoring system developed by Kurosawa et al.18 and based on physical examination and pain region. The SIJ score has a total of 9 possible points, including 2 points for groin pain. In this context, for physicians working with OA patients who require THA, our findings may be useful clinically as a warning that groin pain should be differentiated from SIJ if the spine also has degenerative disease. Further research is warranted.

Acknowledgements

Medical editor Lee Seaman (Seaman Medical Inc., Bellingham WA) provided professional English-language editing of this article.

Author contributions

Conceptualization: A.K.; Data curation: M.F., Y.S., H.H.; Formal analysis: A.K., E.T.; Investigation: A.K., M.F., Y.S., H.H.; Methodology: A.K.; Resources: A.K., E.T.; Supervision: N.K.; Validation: A.K., E.T., N.K.; Writing—original draft: A.K.; Writing—review and editing: A.K., N.K.

Data availability

The datasets analyzed during this given study are available from the corresponding author on reasonable request.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Offierski CM, MacNab I. Hip-spine syndrome. Spine. 1983;8:316–321. doi: 10.1097/00007632-198304000-00014. [DOI] [PubMed] [Google Scholar]
  • 2.Weinberg DS, Gebhart JJ, Liu RW. Hip-spine syndrome: A cadaveric analysis between osteoarthritis of the lumbar spine and hip joints. Orthop. Traumatol. Surg. Res. 2017;103:651–656. doi: 10.1016/j.otsr.2017.05.010. [DOI] [PubMed] [Google Scholar]
  • 3.Kozaki T, et al. Adjacent segment disease on hip joint as a complication of spinal fusion surgery including sacroiliac joint fixation. Eur. Spine J. 2021;30:1314–1319. doi: 10.1007/s00586-020-06700-4. [DOI] [PubMed] [Google Scholar]
  • 4.Kawai T, et al. Number of levels of spinal fusion associated with the rate of joint-space narrowing in the hip. J. Bone Jt. Surg. Am. 2021;103:953–960. doi: 10.2106/JBJS.20.01578. [DOI] [PubMed] [Google Scholar]
  • 5.Ramamurti P, et al. Increased dislocation rates after total hip arthroplasty in patients with prior isolated sacroiliac joint arthrodesis. J. Arthroplasty. 2023;38(7S):S105. doi: 10.1016/j.arth.2023.03.051. [DOI] [PubMed] [Google Scholar]
  • 6.Kiapour A, Joukar A, Elgafy H, Erbulut DU, Agarwal AK, Goel VK. Biomechanics of the sacroiliac joint: anatomy, function, biomechanics, sexual dimorphism, and causes of pain. Int. J. Spine Surg. 2020;14(Suppl 1):3–13. doi: 10.14444/6077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Schwarzer AC, Aprill CN, Bogduk N. The sacroiliac joint in chronic low back pain. Spine. 1995;20:31–37. doi: 10.1097/00007632-199501000-00007. [DOI] [PubMed] [Google Scholar]
  • 8.Maigne JY, Aivaliklis A, Pfefer F. Results of sacroiliac joint double block and value of sacroiliac pain provocation tests in 54 patients with low back pain. Spine. 1996;21:1889–1892. doi: 10.1097/00007632-199608150-00012. [DOI] [PubMed] [Google Scholar]
  • 9.Sembrano JN, Polly DW., Jr How often is low back pain not coming from the back? Spine. 2009;34:E27–E32. doi: 10.1097/BRS.0b013e31818b8882. [DOI] [PubMed] [Google Scholar]
  • 10.Solonen KA. The sacroiliac joint in the light of anatomical, roentgenological and clinical studies. Acta Orthop. Scand. Suppl. 1957;27:1–127. [PubMed] [Google Scholar]
  • 11.Nakagawa T. Study on the distribution of nerve filaments over the iliosacral joint and its adjacent region in the Japanese. Nihon Seikeigeka Gakkai zasshi. 1966;40:419–430. [PubMed] [Google Scholar]
  • 12.Fortin JD, Kissling RO, O’Connor BL, Vilenski JA. Sacroiliac joint innervation and pain. Am. J. Orthop. 1999;28:687–690. [PubMed] [Google Scholar]
  • 13.Forst SL, Wheeler MT, Fortin JD, Vilenski JA. The sacroiliac joint: Anatomy, physiology and clinical significance. Pain Physician. 2006;9:61–67. [PubMed] [Google Scholar]
  • 14.Sakamoto N, Yamashita T, Takebayashi T, Sekine M, Ishii S. An electrophysiologic study of mechanoreceptors in the sacroiliac joint and adjacent tissues. Spine. 2001;26:E468–471. doi: 10.1097/00007632-200110150-00008. [DOI] [PubMed] [Google Scholar]
  • 15.Yang AJ, Schneider BJ, Miller S. Sacroiliac joint interventions. Phys. Med. Rehabil. Clin. N. Am. 2022;33:251–265. doi: 10.1016/j.pmr.2022.01.002. [DOI] [PubMed] [Google Scholar]
  • 16.Cohen SP. Sacroiliac joint pain: A comprehensive review of anatomy, diagnosis, and treatment. Anesth. Analg. 2005;101:1440–1453. doi: 10.1213/01.ANE.0000180831.60169.EA. [DOI] [PubMed] [Google Scholar]
  • 17.Le Huec JC, Tsoupras A, Leglise A, Heraudet P, Celarier G, Sturresson B. The sacro-iliac joint: A potentially painful enigma. Update on the diagnosis and treatment of pain from micro-trauma. Orthop. Traumatol. Surg. Res. 2019;105(1S):S31–S42. doi: 10.1016/j.otsr.2018.05.019. [DOI] [PubMed] [Google Scholar]
  • 18.Kurosawa D, et al. A diagnostic scoring system for sacroiliac joint pain originating from the posterior ligament. Pain Med. 2017;18:228–238. doi: 10.1093/pm/pnw117. [DOI] [PubMed] [Google Scholar]
  • 19.Sturesson B, Udén A, Onsten I. Can an external frame fixation reduce the movements in the sacroiliac joint? A radiostereometric analysis of 10 patients. Acta Orthop. Scand. 1999;70:42–46. doi: 10.3109/17453679909000956. [DOI] [PubMed] [Google Scholar]
  • 20.Murakami E, Kurosawa D, Aizawa T. Treatment strategy for sacroiliac joint-related pain at or around the posterior superior iliac spine. Clin. Neurol. Neurosurg. 2018;165:43–46. doi: 10.1016/j.clineuro.2017.12.017. [DOI] [PubMed] [Google Scholar]
  • 21.Ivanov AA, Kiapour A, Ebraheim NA, Goel V. Lumbar fusion leads to increases in angular motion and stress across sacroiliac joint: a finite element study. Spine. 2009;34:E162–E169. doi: 10.1097/BRS.0b013e3181978ea3. [DOI] [PubMed] [Google Scholar]
  • 22.Kozaki T, et al. Lumbar fusion including sacroiliac joint fixation increases the stress and angular motion at the hip joint: A finite element study. Spine Surg. Relat. Res. 2022;6:681–688. doi: 10.22603/ssrr.2021-0231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Ha KY, Lee JS, Kim KW. Degeneration of sacroiliac joint after instrumented lumbar or lumbosacral fusion: A prospective cohort study over five-year follow-up. Spine. 2008;33:1192–1198. doi: 10.1097/BRS.0b013e318170fd35. [DOI] [PubMed] [Google Scholar]
  • 24.Okuzu Y, Goto K, Shimizu Y, Kawai T, Kuroda Y, Matsuda S. Sacroiliac joint degeneration is common in patients with end-stage hip osteoarthritis secondary to unilateral developmental dysplasia of the hip: Factors associated with its severity and laterality. J. Orthop. Sci. 2021;26:135–140. doi: 10.1016/j.jos.2020.02.005. [DOI] [PubMed] [Google Scholar]
  • 25.Asada M, et al. Degeneration of the sacroiliac joint in hip osteoarthritis patients: A three-dimensional image analysis. J. Belg. Soc. Radiol. 2019;103(36):1–7. doi: 10.5334/jbsr.1648. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Fewins HE, Whitehouse GH, Bucknall RC. Role of computed tomography in the evaluation of suspected sacroiliac joint disease. J. R. Soc. Med. 1990;83:430–432. doi: 10.1177/014107689008300706. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Wolharn L, et al. Detailed bone assessment of the sacroiliac joint in a prospective imaging study: Comparison between computed tomography, zero echo time, and black bone magnetic resonance imaging. Skelet. Radiol. 2022;51:2307–2315. doi: 10.1007/s00256-022-04097-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Toyohara R, et al. A patient-cohort study of numerical analysis on sacroiliac joint stress distribution in pre- and post-operative hip dysplasia. Sci. Rep. 2022;12:14500. doi: 10.1038/s41598-022-18752-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Kwon BT, Kim HJ, Yang HJ, Park SM, Chang BS, Yeom JS. Comparison of sacroiliac joint degeneration between patients with sagittal imbalance and lumbar spinal stenosis. Eur. Spine J. 2020;29:3038–3043. doi: 10.1007/s00586-020-06558-6. [DOI] [PubMed] [Google Scholar]
  • 30.Chen X, et al. Sacroiliac joint degeneration in degenerative lumbar spondylolisthesis and related risk factors: A retrospective study. Eur. Spine J. 2023;32:1375–1382. doi: 10.1007/s00586-023-07558-y. [DOI] [PubMed] [Google Scholar]
  • 31.Longo UG, Loppini M, Berton A, Laverde L, Maffulli N, Denaro V. Degenerative changes of the sacroiliac joint after spinal fusion: An evidence-based systematic review. Br. Med. Bull. 2014;112:47–56. doi: 10.1093/bmb/ldu030. [DOI] [PubMed] [Google Scholar]
  • 32.Backlund J, Clewett Dahl E, Skorpil M. Is CT indicated in diagnosing sacroiliac joint degeneration? Clin. Radiol. 2017;72:693e9–693e13. doi: 10.1016/j.crad.2017.03.006. [DOI] [PubMed] [Google Scholar]
  • 33.Eno JJ, Boone CR, Bellino MJ, Bishop JA. The prevalence of sacroiliac joint degeneration in asymptomatic adults. J. Bone Jt. Surg. Am. 2015;97:932–936. doi: 10.2106/JBJS.N.01101. [DOI] [PubMed] [Google Scholar]
  • 34.Crowe JF, Mani VJ, Ranawat CS. Total hip replacement in congenital dislocation and dysplasia of the hip. J. Bone Jt. Surg. Am. 1979;61:15–23. doi: 10.2106/00004623-197961010-00004. [DOI] [PubMed] [Google Scholar]
  • 35.Sugano N, Atsumi T, Ohzono K, Kubo T, Hotokebuchi T, Takaoka K. The 2001 revised criteria for diagnosis, classification, and staging of idiopathic osteonecrosis of the femoral head. J. Orthop. Sci. 2002;7:601–605. doi: 10.1007/s007760200108. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets analyzed during this given study are available from the corresponding author on reasonable request.


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