TY - JOUR
T1 - Scoliosis and skeletal muscle mass are strongly associated with low back pain-related disability in humans
T2 - An evolutionary anthropology point of view
AU - Tarabeih, Nader
AU - Masharawi, Youssef
AU - Shalata, Adel
AU - Higla, Orabi
AU - Kalinkovich, Alexander
AU - Livshits, Gregory
N1 - Publisher Copyright:
© 2022 Wiley Periodicals LLC.
PY - 2022/8
Y1 - 2022/8
N2 - Objectives: To clarify the potential risk factors and etiology of low back pain (LBP)-related disability, including structural changes of the spine (spinal scoliosis) and body composition components in a population with a high prevalence of LBP. Methods: In this cross-sectional study, two self-reported validated questionnaires were used to collect back pain and disability data in an ethnically homogeneous family-based population sample (N = 1078). The scoliosis angle of trunk rotation was measured by a scoliometer on three spinal levels while the patient was bent forward. Body composition parameters, including relative to weight (WT), fat, relative skeletal muscle mass (SMM/WT), and total body water were determined by bioelectrical impedance analysis. Statistical analysis was conducted, accounting for the familial composition of the sample. Results: The mixed multiple regression analyses with several LBP-related phenotypes as dependent variables consistently showed significant independent associations with scoliosis and SMM/WT, irrespective of other covariates. The odds ratios (OR)/95% CI for scoliosis ranged between 1.40 (1.19–1.64) and 1.51 (1.27–1.80), and from 0.61(0.51–0.72), to 0.71(0.58–0.87) for SMM/WT, depending on the LBP phenotype. The genetic components of the respective correlations between the LBP-phenotypes and scoliosis or SMM/WT were negligible. Conclusions: The associations between LBP-related conditions and postured scoliosis and SMM/WT were consistent and significant and therefore may serve as markers in predicting the development of LBP-related disability. We interpret the origin of these correlations as the evolutionary event due to the imperfect spine anatomy adaptation to a vertical posture resulting from a quick transition to bipedalism from a quadrupedal ancestor.
AB - Objectives: To clarify the potential risk factors and etiology of low back pain (LBP)-related disability, including structural changes of the spine (spinal scoliosis) and body composition components in a population with a high prevalence of LBP. Methods: In this cross-sectional study, two self-reported validated questionnaires were used to collect back pain and disability data in an ethnically homogeneous family-based population sample (N = 1078). The scoliosis angle of trunk rotation was measured by a scoliometer on three spinal levels while the patient was bent forward. Body composition parameters, including relative to weight (WT), fat, relative skeletal muscle mass (SMM/WT), and total body water were determined by bioelectrical impedance analysis. Statistical analysis was conducted, accounting for the familial composition of the sample. Results: The mixed multiple regression analyses with several LBP-related phenotypes as dependent variables consistently showed significant independent associations with scoliosis and SMM/WT, irrespective of other covariates. The odds ratios (OR)/95% CI for scoliosis ranged between 1.40 (1.19–1.64) and 1.51 (1.27–1.80), and from 0.61(0.51–0.72), to 0.71(0.58–0.87) for SMM/WT, depending on the LBP phenotype. The genetic components of the respective correlations between the LBP-phenotypes and scoliosis or SMM/WT were negligible. Conclusions: The associations between LBP-related conditions and postured scoliosis and SMM/WT were consistent and significant and therefore may serve as markers in predicting the development of LBP-related disability. We interpret the origin of these correlations as the evolutionary event due to the imperfect spine anatomy adaptation to a vertical posture resulting from a quick transition to bipedalism from a quadrupedal ancestor.
UR - http://www.scopus.com/inward/record.url?scp=85129688086&partnerID=8YFLogxK
U2 - 10.1002/ajhb.23757
DO - 10.1002/ajhb.23757
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C2 - 35533002
AN - SCOPUS:85129688086
SN - 1042-0533
VL - 34
JO - American Journal of Human Biology
JF - American Journal of Human Biology
IS - 8
M1 - e23757
ER -