BACKGROUND: Sacro-pelvic morphology and orientation are usually described in terms of pelvic incidence (PI), pelvic tilt (PT), and sacral slope (SS). Orientation and morphology of pelvis can affect degenerative changes in the lumbar spine. Thus, here we investigated the relationships between various sagittal spinopelvic parameters and the degree of disc degeneration in young adults. MATERIAL AND METHODS: A hospital-based cross-sectional study with a total of 60 cases was done. Patients presenting with back or leg pain having prolapsed disc on magnetic resonance imaging (MRI) were included in the study. A standing X-ray of LS spine from dorso-lumbar junction to mid-thigh was taken. Various spinopelvic parameters were assessed from the scannogram using the software. RESULTS: The mean age was 39.27 years. L5S1 was the most common level. Mean SS, PT, PI, and LL were 37.78°, 13.52°, 51.33°, and 41.01°. Disc pathologies at L1L2, L2L3, and L4L5 level showed a positive correlation with PT, PI, and LL. Disc pathology at the L5S1 level shows a positive correlation with PT and LL. A statistically significant correlation between SS and degenerative spondylolisthesis at L4L5 was found from data with P = 0.023. DISCUSSION: An increase in SS statistically significantly increases the chance of development of degenerative spondylolisthesis at L4L5. An increase in PT, PI, and LL will cause an increase in disc pathology at L1L2. An increase in SS, PT, PI, and LL will cause an increase in disc pathology at L2L3. An increase in SS, PT, PI, and LL will cause an increase in disc pathology at L4L5. An increase in PT and LL will cause an increase in disc pathology at L5S1. CONCLUSION: Standing lateral view radiograph from dorso-lumbar junction to the mid-thigh is as good as standing whole spine radiograph for measurement of spinopelvic parameters. Degenerative spondylolisthesis at L4L5 has a statistically significant correlation with an increase in SS. Copyright:
BACKGROUND: Sacro-pelvic morphology and orientation are usually described in terms of pelvic incidence (PI), pelvic tilt (PT), and sacral slope (SS). Orientation and morphology of pelvis can affect degenerative changes in the lumbar spine. Thus, here we investigated the relationships between various sagittal spinopelvic parameters and the degree of disc degeneration in young adults. MATERIAL AND METHODS: A hospital-based cross-sectional study with a total of 60 cases was done. Patients presenting with back or leg pain having prolapsed disc on magnetic resonance imaging (MRI) were included in the study. A standing X-ray of LS spine from dorso-lumbar junction to mid-thigh was taken. Various spinopelvic parameters were assessed from the scannogram using the software. RESULTS: The mean age was 39.27 years. L5S1 was the most common level. Mean SS, PT, PI, and LL were 37.78°, 13.52°, 51.33°, and 41.01°. Disc pathologies at L1L2, L2L3, and L4L5 level showed a positive correlation with PT, PI, and LL. Disc pathology at the L5S1 level shows a positive correlation with PT and LL. A statistically significant correlation between SS and degenerative spondylolisthesis at L4L5 was found from data with P = 0.023. DISCUSSION: An increase in SS statistically significantly increases the chance of development of degenerative spondylolisthesis at L4L5. An increase in PT, PI, and LL will cause an increase in disc pathology at L1L2. An increase in SS, PT, PI, and LL will cause an increase in disc pathology at L2L3. An increase in SS, PT, PI, and LL will cause an increase in disc pathology at L4L5. An increase in PT and LL will cause an increase in disc pathology at L5S1. CONCLUSION: Standing lateral view radiograph from dorso-lumbar junction to the mid-thigh is as good as standing whole spine radiograph for measurement of spinopelvic parameters. Degenerative spondylolisthesis at L4L5 has a statistically significant correlation with an increase in SS. Copyright:
The human lumbar spine consists of five lumbar vertebrae articulating with each other at intervertebral discs anteriorly and facets joints posteriorly. Intervertebral disc functions physiologically as a shock absorber of the spine and helps to maintain the lordotic curve of lumbar spine. The functional and clinical importance of lumbar lordosis is being recognized increasingly.[12] Loss of normal lordotic alignment may induce pathologic changes in the spine from load-bearing and accelerate degeneration of the functional motion units.[3] The lumbar spine rests on the first sacral vertebra which is an integral part of the pelvis. The lumbar spine and pelvis are biomechanically connected, pathology of one affecting other, and vice-versa. Orientation and morphology of pelvis can, therefore, affect degenerative changes in the lumbar spine due to altered biomechanical forces.Sacropelvic morphology refers to the anatomy (shape) specific to each individual. On the contrary, sacropelvic orientation depends on the position of the individual in space and is best measured from standing lateral radiographs with the hips and knees extended [Figure 1]. Sacro-pelvic morphology and orientation are usually described in terms of pelvic incidence (PI), pelvic tilt (PT), and sacral slope (SS). The PI is a morphological parameter describing the sacro-pelvis, which is specific and constant for each individual. This parameter introduced by Duval-Beaupère et al.[4] is defined as the angle between the line perpendicular to the upper sacral endplate and the line joining the middle of the upper sacral endplate and the hip axis [Figure 2]. The mean value of PI in the Indian population as given by Singh et al.[5] is 48.52 ± 8.99. In contrast to the PI, the PT and SS measure the orientation of the Sacro-pelvis in the sagittal plane. SS is defined as the angle between the sacral endplate and the horizontal reference line (HRL) [Figure 2], whereas PT is defined as the angle between the vertical reference line (VRL) and the line joining the middle of the sacral endplate and the hip axis [Figure 2]. The mean values of SS and PT in the Indian population are 39.14 ± 7.05 and 9.30 ± 7.16, respectively.[5] PI represents the arithmetic sum of the PT and SS (PI = PT + SS).
Figure 1
Lateral view lumbo-sacral spine with hip joints overlapped and extended. (patient in standing position)
Figure 2
Measurement of PI, SS, PT, and LL
Lateral view lumbo-sacral spine with hip joints overlapped and extended. (patient in standing position)Measurement of PI, SS, PT, and LLIn a static standing position, the way SS and PT balance themselves refers to the concept of acro-pelvic balance. Patients with high PI and SS would increase the shear stresses at the lumbosacral junction, causing more tension on L5S1 articulations, i.e., intervertebral disc anteriorly and facets joints posteriorly. This increased stress, in theory, will increase disc degeneration and prolapse at this level [Figure 3].
Figure 3
Increase in PI and henceforth SS will cause increased shear stress on lumbo-sacral junction and will accelerate degenerative changes
Increase in PI and henceforth SS will cause increased shear stress on lumbo-sacral junction and will accelerate degenerative changesIn normal individuals, studies have shown that the sacropelvic morphology determines the sacro-pelvic orientation, which in turn greatly influences the shape and orientation of the spine, especially the lumbar lordosis.[67] This results in an open linear chain linking the head to the pelvis where the shape and orientation of each successive anatomical segment are closely related and influence the adjacent segment[678] to maintain the center of gravity over the femoral heads. Hence, any change in SS will affect LL. The normal physiological orientation of the lumbar spine is that of lordosis which ranges between 40° and 60°. Change in lumbar lordosis outside of normal range affects load transmission along the lumbar spine and hence leads to accelerated disc degeneration. Recently, Keorochana et al.[3] reported that sagittal spinopelvic alignment may alter spinal load and mobility, thereby possibly influencing segmental degeneration; moreover, alterations in sagittal spinopelvic alignment may lead to kinematic changes that influence load bearing and the distribution of disc degeneration at each level. Consequently, the analysis of sagittal balance recently seems to be essential in the management of lumbar degenerative pathologies.[9] Nevertheless, the relationship between sagittal balance and the degree of disc degeneration has not been extensively explored. Thus, here we investigated the relationships between various sagittal spinopelvic parameters and the degree of disc degeneration in young adults. LL is measured as an angle between lines along the superior endplate of the L1 vertebra and the inferior endplate of the L5 vertebra [Figure 2]. The mean value of LL in the Indian population is 58.78 ± 9.51.[5]
Our study population comprised young adults in the age group between 20 years to 50 years. The mean age was 39.27 years with a standard deviation of ± 8.93. The maximum number of patients was in the age group between 41 and 50 years. Females comprised of major sex group among the study population. There were 37 female patients making 61.7% of the total group as compared to 23 male patients making 38.3% of the total population. Patients with two levels of disc pathologies were major group comprising of 58.3% of cases. L5S1 was the most common level followed by L4 L5 in cases with a single level of disc pathologies. L4L5 + L5S1 were the most commonly involved levels in cases with two-level involvement however L4L5 was the most common level involved in combination with other levels in cases with two-level involvement. Diffuse disc bulge was the commonest type of disc pathology comprising 31 (51.7%) cases. Disc protrusion was the second commonest type with 20 (33.3%) cases.
SS, PT, PI, and LL
Mean SS in the study population was 37.78° with a standard deviation of ± 9.34 [Table 1]. The median value of SS was 37.08° with a range of 13.11 to 58.39. Mean PT in the study population was 13.52° with a standard deviation of ± 5.84. The median value of PT was 12.64° with a range of 1.52 to 25.24. Mean PI in the study population was 51.33° with a standard deviation of ± 9.19. The median value of PI was 50.94° with a range of 30.44 to 71.62. Mean LL in the study population was 41.01° with a standard deviation of ± 14.52. The median value of SS was 42.46° with a range of 1.51–70.28. The sum of the mean of SS and PT (37.78 + 13.52 = 51.3) is equal to PI mean (51.33). So, the correlation between SS, PT, and PI that is PI = PT + SS stands true in the result of our study.
Table 1
Values of SS, PT, PI, and LL in study population
Mean±SD
Median
Min-Max
SS
37.78±9.34
37.08
13.11-58.39
PT
13.52±5.84
12.64
1.52-25.24
PI
51.33±9.19
50.94
30.44-71.62
LL
41.01±14.52
42.46
1.51-70.28
Values of SS, PT, PI, and LL in study population
Correlation between SS, PT, and PI
Pearson correlation shows that SS, PT, and PI are linearly correlated. A change in the value of one will correspondingly change the other two linearly [Table 2 and Figures 5–7]. This linear correlation is statistically significant in all the cases with P < 0.05. SS had positive linear correlation with PI (Pearson correlation coefficient = 0.798) and negative linear correlation with PT (Pearson correlation coefficient = - 0.303). Similarly, PT had a positive linear correlation with PI (Pearson correlation coefficient = 0.330) and a negative linear correlation with SS (Pearson correlation coefficient = - 0.303). PI had positive linear correlation with both SS (Pearson correlation coefficient = 0.798) and PT (Pearson correlation coefficient = 0.330).
Table 2
Pearson correlation (linear correlation) between SS, PT, and PI
Correlations
SS
PT
PI
SS
Pearson correlation
1
-0.303*
0.798**
P
0.019
<0.001
n
60
60
60
PT
Pearson correlation
-0.303*
1
0.330**
P
0.019
0.010
n
60
60
60
PI
Pearson correlation
0.798**
0.330**
1
P
<0.001
0.010
N
60
60
60
N
60
60
60
Figure 5
Pearson correlation (linear correlation) between SS and PT
Figure 7
Pearson correlation (linear correlation) between PT and PI
Pearson correlation (linear correlation) between SS, PT, and PIPearson correlation (linear correlation) between SS and PTPearson correlation (linear correlation) between SS and PIPearson correlation (linear correlation) between PT and PI
Correlation between LL and SS, PT, and PI
LL was found to be linearly correlated to SS and in turn to PI and this correlation was statistically significant with P < 0.05. No such statistically significant correlation was found between LL and PT [Table 3 and Figures 8–10].
Table 3
Pearson correlation (linear correlation) between LL and SS, PT, PI
Correlations
SS
PT
PI
LL
Pearson correlation
0.759**
0.049
0.781**
P
<0.001
0.712
<0.001
n
60
60
60
Figure 8
Pearson correlation (linear correlation) between LL and SS
Figure 10
Pearson correlation (linear correlation) between LL and PI
Pearson correlation (linear correlation) between LL and SS, PT, PIPearson correlation (linear correlation) between LL and SSPearson correlation (linear correlation) between LL and PTPearson correlation (linear correlation) between LL and PI
Correlation between Disc pathology at L1L2 and pelvic parameters (SS, PT, PI, and LL)
In cases with L1L2 disc pathology, mean SS, PT, PI, and LL were 36.59 ± 8.23, 16.22 ± 5.06, 53.18 ± 7.10 and 41.07 ± 13.90, respectively [Figure 11]. Disc pathologies at L1L2 level showed positive monotonic correlation with PT, PI, and LL (Spearman's rho correlation coefficient of 0.173, 0.083, and 0.016, respectively). These correlations however were not statistically significant [Table 4].
Figure 11
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L1L2 and no disc pathology at L1L2
Table 4
Spearman's rank correlation coefficient (Spearman's rho) between disc pathologies at various levels and SS, PT, PI, and LL.
Correlations
Disc level
SS
PT
PI
LL
Spearman's rho
L1-L2
Correlation coefficient
-0.042
0.173
0.083
0.016
P
0.752
0.186
0.526
0.903
N
60
60
60
60
L2-L3
Correlation coefficient
0.031
0.042
0.074
0.136
P
0.813
0.747
0.576
0.301
N
60
60
60
60
L3-L4
Correlation coefficient
-0.035
-0.013
-0.004
0.027
P
0.79
0.922
0.979
0.839
N
60
60
60
60
L4-L5
Correlation coefficient
0.106
0.014
0.086
0.106
P
0.422
0.913
0.516
0.422
N
60
60
60
60
L5-SI
Correlation coefficient
0
0.038
-0.04
0.003
P
0.994
0.775
0.764
0.982
n
60
60
60
60
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L1L2 and no disc pathology at L1L2Spearman's rank correlation coefficient (Spearman's rho) between disc pathologies at various levels and SS, PT, PI, and LL.
Correlation between Disc pathology at L2L3 and pelvic parameters (SS, PT, PI, and LL)
In cases with L2L3 disc pathology, mean SS, PT, PI, and LL were 39.42 ± 9.26, 13.86 ± 8.09, 53.36 ± 8.39 and 46.92 ± 13.89, respectively [Figure 12]. Disc pathologies at the L2L3 level showed positive monotonic correlation with SS, PT, PI, and LL (Spearman's rho correlation coefficient of 0.031, 0.042, 0.074, and 0.136, respectively). These correlations however were not statistically significant [Table 4].
Figure 12
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L2L3 and no disc pathology at L2L3
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L2L3 and no disc pathology at L2L3
Correlation between disc pathology at L3L4 and pelvic parameters (SS, PT, PI, and LL)
In cases with L3L4 disc pathology, mean SS, PT, PI, and LL were 37.41 ± 6.21, 13.86 ± 7.56, 51.34 ± 5.39 and 42.09 ± 7.49, respectively [Figure 13]. Disc pathology at L3L4 level show positive monotonic correlation with LL (Spearman's rho correlation coefficient of 0.027) only and shows a negative correlation with SS, PT, and PI (Spearman's rho correlation coefficient of –0.035, -0.013, and –0.004, respectively). These correlations however were not statistically significant [Table 4].
Figure 13
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L3L4 and no disc pathology at L3L4
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L3L4 and no disc pathology at L3L4
Correlation between Disc pathology at L4L5 and pelvic parameters (SS, PT, PI, and LL)
In cases with L4L5 disc pathology, mean SS, PT, PI, and LL were 38.36 ± 9.43, 13.58 ± 5.77, 51.93 ± 9.69, and 41.92 ± 15.06, respectively [Figure 14]. Disc pathology at L4L5 level shows a positive monotonic correlation with SS, PT, PI, and LL (Spearman's rho correlation coefficient of 0.106, 0.014, 0.086, and 0.106, respectively). These correlations however were not statistically significant [Table 4].
Figure 14
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L4L5 and no disc pathology at L4L5
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L4L5 and no disc pathology at L4L5
Correlation between Disc pathology at L5S1 and pelvic parameters (SS, PT, PI, and LL)
In cases with L5S1 disc pathology, mean SS, PT, PI, and LL were 37.44 ± 10.35, 13.63 ± 5.10, 51.06 ± 10.23, and 40.49 ± 15.18, respectively [Figure 15]. Disc pathology at L5S1 level shows a positive monotonic correlation with PT and LL (Spearman's rho correlation coefficient of 0.038 and 0.003, respectively). Disc pathology at L5S1 however showed a negative monotonic correlation with PI (Spearman's rho correlation coefficient of –0.004). These correlations however were not statistically significant [Table 4].
Figure 15
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L5S1 and no disc pathology at L5S1
Comparison of mean and median values of SS, PT, PI, and LL among cases with disc pathology at L5S1 and no disc pathology at L5S1
Correlation between degenerative spondylolisthesis at L4L5 and SS, PT, PI, LL
A total of four (6.7%) cases had degenerative listhesis and all of them had it at the level of L4L5. A statistically significant correlation between SS and degenerative spondylolisthesis at L4L5 was found from data with P = 0.023 [Table 5]. This correlation was found to be a monotonic direct correlation with Spearman's rho correlation coefficient of 0.293 [Table 6]. A similar trend is shown by PI (Spearman's rho correlation coefficient of 0.177) and LL (Spearman's rho correlation coefficient of 0.201) i.e., increase in PI and LL lordosis increase chance of development of degenerative spondylolisthesis at L4L5 but this increase was not found to be statistically significant for PI and LL.
Table 5
Correlation between degenerative spondylolisthesis at L4L5 and SS, PT, PI, LL.
Degenerative spondylolisthesis L4L5
Spondylolisthesis=No
P
Mean±SD
Median (IQR)
Mean±SD
Median (IQR)
SS
47.97±7.13
45.51 (42.96-55.43)
37.05±9.10
36.81 (30.54-43.21)
0.023
PT
11.48±8.53
11.12 (3.52-19.79)
13.67±5.69
12.82 (9.73-17.73)
0.475
PI
59.20±11.20
59.47 (48.57-69.56)
50.77±8.88
50.58 (45.56-57.40)
0.076
LL
52.47±12.26
50.57 (42.02-64.81)
40.20±14.41
41.29 (33.10-49.05)
0.103
Table 6
Spearman's rank correlation coefficient (Spearman's rho) between degenerative spondylolisthesis at L4L5 and SS, PT, PI, LL
Correlations
SS
PT
PI
LL
Spearman's rho
Spondylolisthesis
Correlation coefficient
0.293*
-0.073
0.177
0.201
P
0.023
0.578
0.175
0.124
n
60
60
60
60
Correlation between degenerative spondylolisthesis at L4L5 and SS, PT, PI, LL.Spearman's rank correlation coefficient (Spearman's rho) between degenerative spondylolisthesis at L4L5 and SS, PT, PI, LL
Discussion
The adoption of vertical posture represents the main transformation in the evolution of humans. Spine and spinopelvic complex played a major role in vertical posture development and bipedalism. To achieve this marvellous feat, the human spine comprises of successive, opposing curves that allow the trunk to assume an erect position. The lumbar lordosis is unique and is not found in any other species. Pelvis also underwent tremendous modifications to alter posture to a vertical one. The pelvis attempts to couple lumbar lordosis with hip extension in the erect position with minimal expense of energy. However, some pelvis can accomplish this task better than others. Progressive knowledge has demonstrated that the shape of the pelvis and its relation to the SS influence dramatically the type of lumbar lordosis in a single individual.[10] Due to the work of Duval-Beaupère et al.[41112] it became possible to define the pelvic geometry and the relation of this geometry with the position of the pelvis. Recently, some authors have highlighted the correlation between lumbar spine disc pathologies and degeneration with the spinopelvic organization.[13]The key for it is the pelvic incidence (PI) angle. It is now crystal clear that the PI and the SS are important in determining the type of lumbar lordosis in a specific individual. The specific spinopelvic geometry will result in mechanical stress at the lumbar spine.Any pattern of the degenerative spine is not a static entity. This is a result of dynamic forces acting on it because of its spatial orientation in space and resulting in biomechanical forces. There is a strong correlation in shape and positioning, and form and function, between the pelvis and the spine. The morphology of the pelvis is identified by PI, with consequences on the morphology of the spine. With time, depending on the individual morphology of a person, specific degenerative evolutions may occur. Sagittal parameters may be considered as predictive regarding the respective shape of the spine and pelvis. A better understanding of this relation may lead to improved diagnosis of degenerative spine diseases and a better strategy of treatment.The mean age in our study falls in the young adult category. Age group was similar in the study by Endo et al.[14] with a mean age of 32.7 years. Although other studies by P. Rajnics et al.[15] and Barrey et al.[9] constituted a higher age group with a mean age of 47.70 ± 14.15 years and 49 ± 12 years, respectively. Sex distribution in our study was female dominant as was in the study by Barrey et al.[9] while in a study by Endo et al.[14] males formed a majority group.A statistically significant monotonic direct correlation of SS with degenerative spondylolisthesis at L4L5 was found in our study. A monotonic direct relationship is where an increase in the independent variable causes an increase in the dependent variable; never to remain constant or decrease, i.e., our study signifies that an increase in SS statistically significantly increases the chance of development of degenerative spondylolisthesis at L4L5. A similar trend is shown by PI and LL although it was not statistically significant. Similar findings were reported by Wang et al.[16] They reported that cases with single-level degenerative spondylolisthesis have higher PI and SS than those without degenerative spondylolisthesis. Ferrero et al.[17] reported that patients with degenerative spondylolisthesis had higher PI as compared to asymptomatic volunteers. Similarly, Lai et al.[18] found that PI was associated with degenerative spondylolisthesis and that among patients with degenerative spondylolisthesis, SS has higher values compared to a control group.A statistically significant linear correlation was found between SS, PI, and PT [Table 2]. In our study, increase in SS linearly increased PI as PI is the mathematical sum of SS and PT. On the contrary, an increase in SS decreased PT because the pelvis has to compensate for increase SS to maintain a straight posture of the body, and pelvis does this by reducing its tilt, i.e., PT. Increase in PT linearly increased PI as PI is mathematical sum of PT and SS. On the contrary, an increase in PT decreased SS because the spine has to compensate for increase PT to maintain a straight posture of body and spine does this by reducing SS i.e., SS.LL showed a statistically significant linear correlation with SS and PI. Any increase in SS will increase LL. This is on expected lines to compensate for increased SS, the lumbar spine will have to increase its curve to maintain an erect standing posture.Disc pathologies at the L1L2 level showed a positive monotonic correlation with PT, PI, and LL [Figure 16]. It implies that an increase in PT, PI, and LL will cause an increase in disc pathology at L1L2 in a monotonic fashion, i.e., disc pathology at L1L2 always increasing; never remaining constant or decreasing with increase in PT, PI, and LL.
Figure 16
Correlation between disc pathology at L1L2 and spino-pelvic parameters
Correlation between disc pathology at L1L2 and spino-pelvic parametersDisc pathologies at L2L3 and L4L5 level showed positive monotonic correlation with SS, PT, PI, and LL [Figures 17 and 18]. It implies that an increase in SS, PT, PI, and LL will cause an increase in disc pathology at L2L3 and L4L5 in a monotonic fashion.
Figure 17
Correlation between disc pathology at L2L3 and spino-pelvic parameters
Figure 18
Correlation between disc pathology at L4L5 and spino-pelvic parameters
Correlation between disc pathology at L2L3 and spino-pelvic parametersCorrelation between disc pathology at L4L5 and spino-pelvic parametersDisc pathology at L3L4 level shows a positive monotonic correlation with LL only and shows a negative correlation with SS, PT, and PI [Figure 19].
Figure 19
Correlation between disc pathology at L3L4 and spino-pelvic parameters
Correlation between disc pathology at L3L4 and spino-pelvic parametersDisc pathology at L5S1 level shows positive monotonic correlation with PT and LL [Figure 20]. Disc pathology at L5S1 however showed negative monotonic correlation with PI. This implies that with an increase in PI, disc pathology at L5S1 will always decrease; never remaining constant or increase.
Figure 20
Correlation between disc pathology at L5S1 and spino-pelvic parameters
Disc herniation has multifactorial pathophysiology. Correlation of sacropelvic parameters with disc herniation in the young population is a new paradigm for research and should be explored further with prospective randomized controlled studies to validate results. Standing lateral view radiograph from dorso-lumbar junction to the mid-thigh is as good as standing whole spine radiograph for measurement of spinopelvic parameters.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Authors: C Boulay; C Tardieu; J Hecquet; C Benaim; B Mouilleseaux; C Marty; D Prat-Pradal; J Legaye; G Duval-Beaupère; J Pélissier Journal: Eur Spine J Date: 2005-09-23 Impact factor: 3.134
Authors: P Stagnara; J C De Mauroy; G Dran; G P Gonon; G Costanzo; J Dimnet; A Pasquet Journal: Spine (Phila Pa 1976) Date: 1982 Jul-Aug Impact factor: 3.468