The correlation analysis between sagittal alignment and cross-sectional area of paraspinal muscle in patients with lumbar spinal stenosis and degenerative spondylolisthesis

Muscle mass decreases with age. Observational studies have shown an annual decline of approximately 1% after the age of 40 [1]. In recent years, the relationship between low back pain (LBP) and the mass of trunk muscles, including skeletal muscles, has attracted attention. The density of the paraspinal muscles and their cross sectional area (CSA) size are known to be associated with variables such as age, gender, and weight [2‐4]. It is generally agreed that muscle CSA and density reflect muscle performance and physical function of individuals [5].

Various imaging techniques (computed tomography, magnetic resonance imaging (MRI), and ultrasound) have been reported as reliable and useful tools for measuring CSA, density, and fat infiltration of paraspinal muscles [3, 6‐8]. Bioimpedance analysis (BIA) has been used in various contexts for the measurement of the nutritional components of body composition, such as fat mass or fat-free mass, using the electrical properties of body tissues. It is easy, non-invasive, relatively inexpensive, and can be performed in almost any subject because of its portability [9]. It has also recently shown promise as a tool for the measurement of water volume status of body [10, 11].

The alteration in sagittal alignment is thought to be one of the potential risk factors influencing disorders of the lower back. Especially in older people, spinal sagittal malalignment causes poor health-related quality of life (QOL) [12].Various factors affecting spinal alignment have been studied, including patient demographics (gender and age) and radiographic factors [13, 14]. Generally, sagittal imbalance results in increased muscular effort and energy expenditure, causing pain, fatigue, and disability. Yagi et al. reported that trunk muscles play an important role in spinal structure and, based on the evaluation of the CSA in spinal deformity, that paraspinal muscle degeneration is related to spinal deformity [15]. However, the relationship between body composition measured by BIA and paraspinal muscle CSA measured by MRI in patients with spinal disease has not been studied, and their correlation with spinal alignment is not clear. Therefore, this study was conducted to elucidate the role of the multifidus (MF) and psoas major (PS) muscles in maintaining global spinal alignment in patients with lumbar spinal stenosis (LSS) and degenerative spondylolisthesis (DS), and to analyze whether muscle CSA correlates with SMM measured by BIA.

Of the included 288 patients, complete analysis was possible in 140 patients. Patients were excluded when MRI images were insufficient to measure CSAs of the MF and PS muscles or when spinal parameters could not be accurately measured on radiographs. The field of view in axial images were unfortunately often too narrow to measure PS CSA especially at the L5-S1 level, leading to exclusion of many cases.

The demographics and radiological parameters of the 140 patients are listed in Table 1. The mean age at the time of operation was 70.6 ± 9.0 years and 52.1% of the patients were female. Height and body weight were significantly higher in males compared to females, while the spinal parameters PI and PT were significantly higher in females compared to males.

BIA measurements are shown in Table 2. The SMM, soft lean mass, protein and mineral measured by BIA were significantly higher in males compared to females. ICW and ECW also had similar results.

CSA measured by MRI revealed no difference found between the right and left sides, but demonstrated that CSA of both PS and MF muscles were significantly higher in males compared to females. PS AveCSA was highest at the L4-L5 level, whereas MF AveCSA was the highest at the L5-S1 level (PS AveCSA; L3-L4, 770.8 ± 304.6 mm²; L4-L5, 1005.8 ± 333.9 mm²; and L5-S1, 887.1 ± 319.5 mm². MF AveCSA; L3-L4, 358.9 ± 106.6 mm²; L4-L5, 464.9 ± 140.5 mm²; and L5-S1, 484.1 ± 144.6 mm²) (Table 3). Measurement of the CSA of both PS and MF muscles using MRI showed to excellent intraobserver reliability (PS AveCSA; L3-L4, 0.905; L4-L5, 0.945; and L5-S1, 0.981. MF AveCSA; L3-L4, 0.914; L4-L5, 0.905; and L5-S1, 0.919)).

The mean interobserver reliability was also good to excellent in measurement of the CSA of both PS and MF muscles in MRI. There were no significant differences between the three observers.

Analysis of the correlation between SMM and the AveCSA of each muscle was also performed for all lower lumbar levels. Correlations between SMM and PS AveCSA was found, in decreasing order of correlation coefficient, at L4-L5 (r = 0.739, P < 0.001), L3-L4 (r = 0.723, P < 0.001), and L5-S1 (r = 0.654, P < 0.001). Similarly, correlations between SMM and MF AveCSA were also found in L4-L5 (r = 0.582, P < 0.001), L5-S1 (r = 0.563, P < 0.001), and L3-L4 (r = 0.546, P < 0.001) (Table 4). These results demonstrated that PS AveCSA at the L4-L5 level was most positively correlated with SMM in patients with LSS and DS (Fig. 3). Correlation coefficient analysis showed weak correlation between SMM and PT (r = − 0.184, P < 0.05). Moreover, PS AveCSA (L4-L5) correlated with the PT (r = − 0.183, P < 0.05) and age (r = − 0.156, P < 0.05) (Table 5), while PT correlated with PS AveCSA (L4-L5) (r = − 0.183, P < 0.05) and whole body SMM (r = − 0.184, P < 0.05) but not with age. Analysis of the correlation between NRS of LBP and SMM did not show any correlation (SMM and NRS of LBP; r = − 0.014, P = 0.880). The mean score of NRS for 140 patients was 5.5 ± 2.8, and it did not show a statistically significant correlation with the PS AveCSA or MF AveCSA (Table 6).

There are several reports on the effects of aging on the morphology of the lumbar paraspinal muscles evaluated by MRI and the association of paraspinal muscle degeneration with LBP [7, 22]. We have also previously investigated whether SMM measured by BIA affects spinal alignment in patients with spinal degenerative disease and showed that SMM decreases with age [18]. To the best of our knowledge, this analysis is the largest investigation of the relationship between SMM and paraspinal muscle CSA in symptomatic LSS and/or DS patients. Our results show a high correlation between PS AveCSA (L4-L5) and whole body SMM and suggest a correlation with the spinal parameter PT.

Only a few studies have examined age-related changes in lumbar paraspinal muscle size, and these studies have reported inconsistent findings [1, 23, 24]. Takayama et al. examined the CSA of paraspinal muscles using T2-weighted MRI in 160 patients aged 10 to 88 years-old with an average lumbar lordosis of 20 degrees [23]. They demonstrated that the CSA of paraspinal muscles tended to decrease with age, which was also reported by Sasaki et al. [25]. On the other hand, Crawford et al. examined the volume of the erector spinae and multifidus muscles with 2-point Dixon 3 T MRI in 80 healthy volunteers aged 20 to 62, but the muscle volume did not depend on age [24]. Discrepancies between studies may be due to methodology, because differences in measurement techniques (CSA vs. volume), definition of paravertebral area, and research target population may influence the results.

In addition, males are known to have a larger CSA than females [23, 24]. In our analysis, as well as previous reports, there was a difference by gender, with larger PS and MF CSA in males than females. This result was similar for SMM measured by BIA. Chan et al. previously reported that male stenosis patients showed larger PS CSA than females, while elderly patients showed smaller PS CSA and more fat infiltration than younger stenosis patients [6]. Furthermore, in previous studies, the PS was known to exhibit the least fat infiltration, with Sasaki et al. reporting that the PS is highly unlikely to be affected by age-dependent degeneration [25]. However, our analysis suggests that SMM and PS AveCSA at the L4-L5 level are correlated, and that PS AveCSA at the L4-L5 has also a weak correlation with age.

To date, several studies reported the association between the size and fat content of the paraspinal muscles and LBP [3, 26, 27], but conflicting data has been obtained with regard to changes in PS CSA in cases of LBP. Arbanas et al. reported that LBP patients have significantly bigger PS CSA compared to control subjects [28], while Parkkola et al. described smaller PS CSA in patients with chronic LBP compared to healthy volunteers [27]. Unfortunately in this study, we were unable to determine whether PS CSA in patients with degenerative spine disease was smaller compared to healthy control subjects, as we focused only on patients with LSS and/or DS. However, we found that PS or MF CSA was highly correlated with whole body SMM, and that whole body SMM correlated with age. Regarding the relationship between LBP and paraspinal muscle, it is also known that there is a correlation between LBP and fatty infiltration of the paraspinal muscles [29]. In this study, we did not investigate fat infiltration, but focused on whole-body SMM and CSA of paraspinal muscles which showed no correlation between the CSA of paraspinal muscles and the intensity of LBP. These findings suggest that degeneration of paraspinal muscles and decrease in whole body SMM do not directly cause LBP. Or putting it into different terms, age-related degeneration of paraspinal muscles may not strongly correlate with LBP.

In large cohorts looking into spinal parameters in adult patients with degenerative lumbar disease, LL, PT, and PI were significantly smaller in males than in females, SVA, TK, and PT increased with age, and LL was reported to decrease with age [30]. In this study, we examined the relationship between spinal parameters, the paraspinal muscles, and SMM, because although it is well known that the spinal column and ligaments are important for maintaining spinal alignment, the relationship between sagittal alignment and paraspinal muscle CSA has not been sufficiently examined. MF and PS plays a role in the segmental stability of the lumbar spine [31, 32]. The MF and PS are also important for the motor control of the pelvis because they are directly attached to the pelvis. In this study, we found that the correlation between SMM and PS Ave CSA was higher than that between SMM and MF Ave CSA. The results suggests that PS may be related to anterior and posterior pelvic tilting than MF in patients with lumbar degenerative diseases. We also found that reduction of whole body SMM and decrease in PS CSA was correlated with PT. In other words, we believe that the inclination of the pelvis due to the reduction of SMM and especially the paraspinal muscles might be one factor that precipitates the onset of LBP. There are several limitations in our study. Study design prevents a strong conclusion about the role of MF and PS in spinal alignment or LBP. Longitudinal analysis is needed to determine whether a loss of muscle mass results in a spinal deformity or a spinal deformity results in a loss of muscle mass. Furthermore, the small number of participants and the lack of a control group limits the analytic power of the results. In this study, only patients with degenerative spinal disease were compared and not healthy volunteers. In order to confirm the results of our research, further studies recruiting more participants and a control group will be necessary. Furthermore, in this analysis, we did not analyze for adult patients with spinal deformities (kyphosis and scoliosis) such as Parkinson’s disease. The loss of muscle mass can cause disruption of the balance between extensors and flexors muscles of the spine. This imbalance along with all alterations take place in different parts of the spine, might have a consequence of spinal deformity. Finally, in this study, we focused on CSA of the paraspinal muscles and did not evaluate paraspinal muscles density because previous reports concerning fat infiltration in LBP patients were inconsistent. However, additional studies will be necessary to improve our understanding of the association and causal relationships between changes in the paraspinal muscle CSA or density and spinal alignment as well as LBP.

Whole body SMM and paraspinal muscle CSA in 140 LSS and/or DS patients were evaluated. The whole body SMM showed strong correlation with PS AvCSA (L4-L5). In addition, whole body SMM as well as PS AvCSA (L4-L5) correlated with the spinal parameter PT. A significant correlation between PS AvCSA and PT suggests a causal relationship between muscle function and global spinal alignment. Inferring from randomized controlled trials conducted so far, intensive exercise programs can improve muscular strength, density and increase CSA of paraspinal muscles in LBP patients [33, 34], but this cannot be confirmed in this retrospective study. In the future, it will be necessary to analyze the influence of these paraspinal muscle strength and LBP with a prospective multicenter study.