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Adolescent idiopathic scoliosis

A Correction to this article was published on 15 October 2015

Abstract

Adolescent idiopathic scoliosis (AIS) is the most common form of structural spinal deformities that have a radiological lateral Cobb angle — a measure of spinal curvature — of ≥10°. AIS affects between 1% and 4% of adolescents in the early stages of puberty and is more common in young women than in young men. The condition occurs in otherwise healthy individuals and currently has no recognizable cause. In the past few decades, considerable progress has been made towards understanding the clinical patterns and the three-dimensional pathoanatomy of AIS. Advances in biomechanics and technology and their clinical application, supported by limited evidence-based research, have led to improvements in the safety and outcomes of surgical and non-surgical treatments. However, the definite aetiology and aetiopathogenetic mechanisms that underlie AIS are still unclear. Thus, at present, both the prevention of AIS and the treatment of its direct underlying cause are not possible.

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Figure 1: Measuring the Cobb angle.
Figure 2: Classification of scoliosis on the basis of the location of the spinal curve.
Figure 3: Global prevalence of AIS.
Figure 4: The cascade concept of AIS pathogenesis.
Figure 5: A proposed model of the aetiopathogenesis of AIS.
Figure 6: Summary of the morphological changes in the central nervous system involved in AIS.
Figure 7: Influence of shear loads on the spine.
Figure 8: Scoliosis screening tests.
Figure 9: The Hong Kong scoliosis screening protocol.
Figure 10: A patient with AIS treated with rigid bracing.
Figure 11: Spinal surgery for the treatment of AIS.
Figure 12: Potential role of early development in AIS.

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References

  1. Grivas, T. B. in SOSORT 2014 — 4th Educational Courses (ed. SOSORT Educational Committee) 38–43 (SOSORT, 2014).

    Google Scholar 

  2. Grivas, T. B., Vasiliadis, E., Mouzakis, V., Mihas, C. & Koufopoulos, G. Association between adolescent idiopathic scoliosis prevalence and age at menarche in different geographic latitudes. Scoliosis 1, 9 (2006). This study reviews the prevalence of idiopathic scoliosis across 13 countries and suggests the possible roles of geographic latitude and sunlight in the pathogenesis of AIS.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Fong, D. Y. et al. A meta-analysis of the clinical effectiveness of school scoliosis screening. Spine 35, 1061–1071 (2010). This meta-analysis on 36 studies found that the use of the forward bending test alone in school scoliosis screening is insufficient, suggesting that a combination of screening tools is required.

    Article  PubMed  Google Scholar 

  4. Luk, K. D. et al. Clinical effectiveness of school screening for adolescent idiopathic scoliosis: a large population-based retrospective cohort study. Spine 35, 1607–1614 (2010). This is the largest retrospective cohort of any AIS study and includes 157,444 students who were undergoing scoliosis screening. The results of this study suggest that a well-designed, tiered screening protocol can avoid over-referrals and achieve good predictability and sensitivity for the diagnosis and treatment of AIS.

    Article  PubMed  Google Scholar 

  5. Ueno, M. et al. A 5-year epidemiological study on the prevalence rate of idiopathic scoliosis in Tokyo: school screening of more than 250,000 children. J. Orthop. Sci. 16, 1–6 (2011).

    Article  PubMed  Google Scholar 

  6. de Souza, F. I. et al. Epidemiology of adolescent idiopathic scoliosis in students of the public schools in Goiânia-GO. Acta Ortop. Bras. 21, 223–225 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  7. Asher, M. A. & Burton, D. C. Adolescent idiopathic scoliosis: natural history and long term treatment effects. Scoliosis 1, 2 (2006).

    Article  PubMed  PubMed Central  Google Scholar 

  8. Lee, C. F. et al. A new risk classification rule for curve progression in adolescent idiopathic scoliosis. Spine J. 12, 989–995 (2012).

    Article  CAS  PubMed  Google Scholar 

  9. Wang, W. J. et al. Top theories for the etiopathogenesis of adolescent idiopathic scoliosis. J. Pediatr. Orthoped. 31, S14–S27 (2011).

    Article  Google Scholar 

  10. Burwell, R. G., Dangerfield, P. H., Moulton, A., Grivas, T. B. & Cheng, J. C. Whither the etiopathogenesis (and scoliogeny) of adolescent idiopathic scoliosis? Incorporating presentations on scoliogeny at the 2012 IRSSD and SRS meetings. Scoliosis 8, 4 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  11. Lowe, T. G. et al. Etiology of idiopathic scoliosis: current trends in research. J. Bone Joint Surg. 82, 1157–1168 (2000).

    Article  PubMed  Google Scholar 

  12. Wong, C. Mechanism of right thoracic adolescent idiopathic scoliosis at risk for progression; a unifying pathway of development by normal growth and imbalance. Scoliosis 10, 2 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  13. Veldhuizen, A. G., Wever, D. J. & Webb, P. J. The aetiology of idiopathic scoliosis: biomechanical and neuromuscular factors. Eur. Spine J. 9, 178–184 (2000). This paper reviews and evaluates evidence that supports a role for biomechanics and neuromuscular factors in the initiation and progression of idiopathic scoliosis. This paper also discusses the difficulty in distinguishing between primary and secondary (consequential) effects of biomechanics in idiopathic scoliosis.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Roth, M. Idiopathic scoliosis from the point of view of the neuroradiologist. Neuroradiology 21, 133–138 (1981).

    CAS  PubMed  Google Scholar 

  15. Porter, R. W. The pathogenesis of idiopathic scoliosis: uncoupled neuro-osseous growth? Eur. Spine J. 10, 473–481 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Chu, W. et al. Relative shortening and functional tethering of spinal cord in adolescent scoliosis — result of asynchronous neuro-osseous growth, summary of an electronic focus group debate of the IBSE. Scoliosis 3, 8 (2008).

    Article  PubMed  PubMed Central  Google Scholar 

  17. Stokes, I. A. F., Burwell, R. G. & Dangerfield, P. H. Biomechanical spinal growth modulation and progressive adolescent scoliosis — a test of the ‘vicious cycle’ pathogenetic hypothesis: summary of an electronic focus group debate of the IBSE. Scoliosis 1, 16 (2006).

    Article  PubMed  PubMed Central  Google Scholar 

  18. Sevastik, J., Burwell, R. G. & Dangerfield, P. H. A new concept for the etiopathogenesis of the thoracospinal deformity of idiopathic scoliosis: summary of an electronic focus group debate of the IBSE. Eur. Spine J. 12, 440–450 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Azeddine, B., Letellier, K., Wang da, S., Moldovan, F. & Moreau, A. Molecular determinants of melatonin signaling dysfunction in adolescent idiopathic scoliosis. Clin. Orthop. Relat. Res. 462, 45–52 (2007).

    Article  PubMed  Google Scholar 

  20. Moreau, A. et al. Melatonin signaling dysfunction in adolescent idiopathic scoliosis. Spine 29, 1772–1781 (2004). This paper describes a new molecular classification system for patients with AIS according to their differential Gi-coupled receptor signalling response.

    Article  PubMed  Google Scholar 

  21. Lowe, T. G., Burwell, R. G. & Dangerfield, P. H. Platelet calmodulin levels in adolescent idiopathic scoliosis (AIS): can they predict curve progression and severity? Eur. Spine J. 13, 257–265 (2004).

    Article  PubMed  PubMed Central  Google Scholar 

  22. Castelein, R. M., van Dieën, J. H. & Smit, T. H. The role of dorsal shear forces in the pathogenesis of adolescent idiopathic scoliosis — a hypothesis. Med. Hypotheses 65, 501–508 (2005). This landmark paper postulates that dorsal shear forces, acting exclusively on specific regions of the human spine, might contribute to rotational instability of the spine.

    Article  PubMed  Google Scholar 

  23. Courvoisier, A., Drevelle, X., Dubousset, J. & Skalli, W. Transverse plane 3D analysis of mild scoliosis. Eur. Spine J. 22, 2427–2432 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  24. Illés, T. & Somoskeöy, S. Comparison of scoliosis measurements based on three-dimensional vertebra vectors and conventional two-dimensional measurements: advantages in evaluation of prognosis and surgical results. Eur. Spine J. 22, 1255–1263 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  25. Schlösser, T. P. et al. Three-dimensional characterization of torsion and asymmetry of the intervertebral discs versus vertebral bodies in adolescent idiopathic scoliosis. Spine 39, E1159–E1166 (2014).

    Article  PubMed  Google Scholar 

  26. Drevelle, X. et al. Analysis of idiopathic scoliosis progression by using numerical simulation. Spine 35, E407–E412 (2010).

    Article  CAS  PubMed  Google Scholar 

  27. Wang, D. et al. Altered topological organization of cortical network in adolescent girls with idiopathic scoliosis. PLoS ONE 8, e83767 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Domenech, J. et al. Abnormal activation of the motor cortical network in idiopathic scoliosis demonstrated by functional MRI. Eur. Spine J. 20, 1069–1078 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  29. Burwell, R. G., Clark, E., Dangerfield, P. H. & Moulton, A. Adolescent idiopathic scoliosis (AIS): cascade concept of pathogenesis. Clin. Anat. (in the press).

  30. Steppan, C. M. & Swick, A. G. A role for leptin in brain development. Biochem. Biophys. Res. Commun. 256, 600–602 (1999).

    Article  CAS  PubMed  Google Scholar 

  31. Clark, E. M. et al. Association between components of body composition and scoliosis: a prospective cohort study reporting differences identifiable before the onset of scoliosis. J. Bone Miner. Res. 29, 1729–1736 (2014). This is the first population-based large prospective study to show that a decrease in both lean and fat mass at 10 years of age is associated with an increased incidence of scoliosis at 15 years of age, providing important evidence of the link between endocrine metabolic abnormalities and the development of scoliosis.

    Article  PubMed  Google Scholar 

  32. Burwell, R. G. et al. Pathogenesis of adolescent idiopathic scoliosis in girls — a double neuro-osseous theory involving disharmony between two nervous systems, somatic and autonomic expressed in the spine and trunk: possible dependency on sympathetic nervous system and hormones with implications for medical therapy. Scoliosis 4, 24 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  33. Craig, J. Complex diseases: research and applications. Nat. Educ. 1, 184 (2008).

    Google Scholar 

  34. Wynne-Davies, R. Familial (idiopathic) scoliosis. A family survey. J. Bone Joint Surg. Br. 50, 24–30 (1968).

    Article  CAS  PubMed  Google Scholar 

  35. Kesling, K. L. & Reinker, K. A. Scoliosis in twins. A meta-analysis of the literature and report of six cases. Spine 22, 2009–2014 (1997).

    Article  CAS  PubMed  Google Scholar 

  36. Grauers, A., Rahman, I. & Gerdhem, P. Heritability of scoliosis. Eur. Spine J. 21, 1069–1074 (2012).

    Article  PubMed  Google Scholar 

  37. Miller, N. H. et al. Identification of candidate regions for familial idiopathic scoliosis. Spine 30, 1181–1187 (2005).

    Article  PubMed  Google Scholar 

  38. Gao, X. et al. CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. Am. J. Hum. Genet. 80, 957–965 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Patten, S. A. et al. Functional variants of POC5 identified in patients with idiopathic scoliosis. J. Clin. Invest. 125, 1124–1128 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  40. Cheng, J. C., Tang, N. L., Yeung, H. Y. & Miller, N. Genetic association of complex traits: using idiopathic scoliosis as an example. Clin. Orthop. Relat. Res. 462, 38–44 (2007).

    Article  PubMed  Google Scholar 

  41. Tang, N. L. et al. Genetic epidemiology and heritability of AIS: a study of 415 Chinese female patients. J. Orthop. Res. 30, 1464–1469 (2012).

    Article  PubMed  Google Scholar 

  42. Wise, C. A., Gao, X., Shoemaker, S., Gordon, D. & Herring, J. A. Understanding genetic factors in idiopathic scoliosis, a complex disease of childhood. Curr. Genom. 9, 51–59 (2008).

    Article  CAS  Google Scholar 

  43. Ward, K. et al. Polygenic inheritance of adolescent idiopathic scoliosis: a study of extended families in Utah. Am. J. Med. Genet. 152A, 1178–1188 (2010).

    Article  PubMed  Google Scholar 

  44. Kruse, L. M., Buchan, J. G., Gurnett, C. A. & Dobbs, M. B. Polygenic threshold model with sex dimorphism in adolescent idiopathic scoliosis: the Carter effect. J. Bone Joint Surg. Am. 94, 1485–1491 (2012).

    Article  PubMed  Google Scholar 

  45. Gorman, K. F., Julien, C. & Moreau, A. The genetic epidemiology of idiopathic scoliosis. Eur. Spine J. 21, 1905–1919 (2012).

    Article  PubMed  PubMed Central  Google Scholar 

  46. Inoue, M. et al. Prediction of curve progression in idiopathic scoliosis from gene polymorphic analysis. Stud. Health Technol. Inform. 91, 90–96 (2002).

    PubMed  Google Scholar 

  47. Yeung, H. Y. et al. Genetic association study of insulin-like growth factor-I (IGFI) gene with curve severity and osteopenia in adolescent idiopathic scoliosis. Stud. Health Technol. Inform. 123, 18–24 (2006).

    CAS  PubMed  Google Scholar 

  48. Sharma, S. et al. Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. Hum. Mol. Genet. 20, 1456–1466 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Takahashi, Y. et al. A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis. Nat. Genet. 43,1237–1240 (2011). This is one of the largest GWAS of AIS in which genome-wide significant variants near LBX1 were identified in a study of 1,050 Japanese female patients with AIS and 1,474 unaffected individuals.

    Article  CAS  PubMed  Google Scholar 

  50. Londono, D. et al. A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups. J. Med. Genet. 51, 401–406 (2014).

    Article  CAS  PubMed  Google Scholar 

  51. Kou, I. et al. Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis. Nat. Genet. 45, 676–679 (2013).

    Article  CAS  PubMed  Google Scholar 

  52. Sharma, S. et al. A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females. Nat. Commun. 6, 6452 (2015).

    Article  CAS  PubMed  Google Scholar 

  53. Wallin, J. et al. The role of PAX1 in axial skeleton development. Development 120, 1109–1121 (1994).

    CAS  PubMed  Google Scholar 

  54. Hillmer, A. M. et al. Susceptibility variants for male-pattern baldness on chromosome 20p11. Nat. Genet. 40, 1279–1281 (2008).

    Article  CAS  PubMed  Google Scholar 

  55. Buchan, J. G. et al. Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis. Hum. Mol. Genet. 23, 5271–5282 (2014). This is one of the first rare variant association studies of AIS, providing evidence that some rare fibrillin gene variants contribute to a phenotype of scoliosis.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Baschal, E. E. et al. Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis. G3 (Bethesda) 5, 167–174 (2015).

    Article  CAS  Google Scholar 

  57. Chen, Z., Qiu, Y., Ma, W., Qian, B. & Zhu, Z. Comparison of somatosensory evoked potentials between adolescent idiopathic scoliosis and congenital scoliosis without neural axis abnormalities. Spine J. 14, 1095–1098 (2014).

    Article  PubMed  Google Scholar 

  58. Lao, M. L. M., Chow, D. H. K., Guo, X., Cheng, J. C. Y. & Holmes, A. D. Impaired dynamic balance control in adolescents with idiopathic scoliosis and abnormal somatosensory evoked potentials. J. Pediatr. Orthopaed. 28, 846–849 (2008).

    Article  Google Scholar 

  59. Simoneau, M. et al. Evidence for cognitive vestibular integration impairment in idiopathic scoliosis patients. BMC Neurosci. 10, 102 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  60. Chu, W. C. W. et al. Relative shortening and functional tethering of spinal cord in adolescent idiopathic scoliosis?: Study with multiplanar reformat magnetic resonance imaging and somatosensory evoked potential. Spine 31, E19–E25 (2006).

    Article  PubMed  Google Scholar 

  61. Chu, W. C. et al. Morphological and functional electrophysiological evidence of relative spinal cord tethering in adolescent idiopathic scoliosis. Spine 33, 673–680 (2008). This is the first study to show the morphological features of relative spinal cord tethering in AIS using imaging and lends support to the hypothesis that uncoupled neuro-osseous growth between the spinal cord and the vertebral column could contribute to the aetiopathogenesis of AIS.

    Article  PubMed  Google Scholar 

  62. Abul-Kasim, K., Overgaard, A., Karlsson, M. K. & Ohlin, A. Tonsillar ectopia in idiopathic scoliosis: does it play a role in the pathogenesis and prognosis or is it only an incidental finding? Scoliosis 4, 25 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  63. Kong, Y. et al. Variation in anisotropy and diffusivity along the medulla oblongata and the whole spinal cord in adolescent idiopathic scoliosis: a pilot study using diffusion tensor imaging. AJNR Am. J. Neuroradiol. 35, 1621–1627 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Liu, T. et al. MR analysis of regional brain volume in adolescent idiopathic scoliosis: neurological manifestation of a systemic disease. J. Magn. Reson. Imaging 27, 732–736 (2008).

    Article  PubMed  PubMed Central  Google Scholar 

  65. Wang, D. et al. A comparison of morphometric techniques for studying the shape of the corpus callosum in adolescent idiopathic scoliosis. Neuroimage 45, 738–748 (2009).

    Article  CAS  PubMed  Google Scholar 

  66. Joly, O., Rousié, D., Jissendi, P., Rousié, M. & Frankó, E. A new approach to corpus callosum anomalies in idiopathic scoliosis using diffusion tensor magnetic resonance imaging. Eur. Spine J. 23, 2643–2649 (2014).

    Article  PubMed  Google Scholar 

  67. Wang, D. et al. Abnormal cerebral cortical thinning pattern in adolescent girls with idiopathic scoliosis. Neuroimage 59, 935–942 (2012). This is the first study to show a different thinning pattern of the cerebral cortex in girls with AIS compared with unaffected children. Focal cortical thickness was also found to be different in areas related to motor and vestibular functions in these patients.

    Article  PubMed  Google Scholar 

  68. Shi, L. et al. Volumetric changes in cerebellar regions in adolescent idiopathic scoliosis compared with healthy controls. Spine J. 13, 1904–1911 (2013).

    Article  PubMed  Google Scholar 

  69. Shi, L. et al. Automatic MRI segmentation and morphoanatomy analysis of the vestibular system in adolescent idiopathic scoliosis. Neuroimage 54, S180–S188 (2011).

    Article  PubMed  Google Scholar 

  70. Rousie, D. L., Deroubaix, J. P., Joly, O., Baudrillard, J. C. & Berthoz, A. Abnormal connection between lateral and posterior semicircular canal revealed by a new modeling process: origin and physiological consequences. Ann. NY Acad. Sci. 1164, 455–457 (2009).

    Article  PubMed  Google Scholar 

  71. Sanders, J. O. et al. Predicting scoliosis progression from skeletal maturity: a simplified classification during adolescence. J. Bone Joint Surg. Am. 90, 540–553 (2008).

    Article  PubMed  Google Scholar 

  72. Cole, A. A. in Spine: State of Art Reviews (eds Burwell, R. G. et al.) 411–421 (Hanley & Belfus, 2000).

    Google Scholar 

  73. Normelli, H., Sevastik, J. & Akrivos, J. The length and ash weight of the ribs of normal and scoliotic persons. Spine 10, 590–592 (1985).

    Article  CAS  PubMed  Google Scholar 

  74. Burwell, R. G. et al. Patterns of extra-spinal left-right skeletal asymmetries in adolescent girls with lower spine scoliosis: relative lengthening of the ilium on the curve concavity and of right lower limb segments. Stud. Health Technol. Inform. 123, 57–65 (2006).

    CAS  PubMed  Google Scholar 

  75. Shohat, M. et al. Growth and ethnicity in scoliosis. Acta Orthop. Scand. 59, 310–313 (1988).

    Article  CAS  PubMed  Google Scholar 

  76. Ramírez, M. et al. Body composition in adolescent idiopathic scoliosis. Eur. Spine J. 22, 324–329 (2013).

    Article  PubMed  Google Scholar 

  77. Liu, Z. et al. Abnormal leptin bioavailability in adolescent idiopathic scoliosis: an important new finding. Spine 37, 599–604 (2012).

    Article  PubMed  Google Scholar 

  78. Tam, E. M. et al. Are volumetric bone mineral density and bone micro-architecture associated with leptin and soluble leptin receptor levels in adolescent idiopathic scoliosis? — A case–control study. PLoS ONE 9, e87939 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. Cheng, J. C. et al. Generalized low areal and volumetric bone mineral density in adolescent idiopathic scoliosis. J. Bone Miner. Res. 15, 1587–1595 (2000).

    Article  CAS  PubMed  Google Scholar 

  80. Cheung, C. S. et al. Generalized osteopenia in adolescent idiopathic scoliosis — association with abnormal pubertal growth, bone turnover, and calcium intake? Spine 31, 330–338 (2006).

    Article  PubMed  Google Scholar 

  81. Cheng, J. C. et al. Persistent osteopenia in adolescent idiopathic scoliosis — longitudinal monitoring of bone mineral density until skeletal maturity. Stud. Health Technol. Inform. 123, 47–51 (2006).

    CAS  PubMed  Google Scholar 

  82. Hung, V. W. et al. Osteopenia: a new prognostic factor of curve progression in adolescent idiopathic scoliosis. J. Bone Joint Surg. Am. 87, 2709–2716 (2005). This large prospective study of 324 girls with AIS followed them longitudinally until they reached skeletal maturity. The study shows that osteopenia in the femoral neck is a risk factor for curve progression, with an odds ratio of 2.3.

    CAS  PubMed  Google Scholar 

  83. Yu, W. S. et al. Bone structural and mechanical indices in adolescent idiopathic scoliosis evaluated by high-resolution peripheral quantitative computed tomography (HR-pQCT). Bone 61, 109–115 (2014).

    Article  PubMed  Google Scholar 

  84. Cheng, J. C., Tang, S. P., Guo, X., Chan, C. W. & Qin, L. Osteopenia in adolescent idiopathic scoliosis: a histomorphometric study. Spine 26, E19–E23 (2001).

    Article  CAS  PubMed  Google Scholar 

  85. Kouwenhoven, J. W. & Castelein, R. M. The pathogenesis of adolescent idiopathic scoliosis: review of the literature. Spine 33, 2898–2908 (2008).

    Article  PubMed  Google Scholar 

  86. Janssen, M. M., de Wilde, R. F., Kouwenhoven, J. W. & Castelein, R. M. Experimental animal models in scoliosis research: a review of the literature. Spine J. 11, 347–358 (2011).

    Article  PubMed  Google Scholar 

  87. Schlösser, T. P. et al. Evolution of the ischio-iliac lordosis during natural growth and its relation with the pelvic incidence. Eur. Spine J. 23, 1433–1441 (2014).

    Article  PubMed  Google Scholar 

  88. Kouwenhoven, J. W. et al. Effects of dorsal versus ventral shear loads on the rotational stability of the thoracic spine: a biomechanical porcine and human cadaveric study. Spine 32, 2545–2550 (2007).

    Article  PubMed  Google Scholar 

  89. Janssen, M. M. et al. Analysis of preexistent vertebral rotation in the normal infantile, juvenile, and adolescent spine. Spine 36, E486–E491 (2011).

    Article  PubMed  Google Scholar 

  90. Schlösser, T. P., Vincken, K. L., Rogers, K., Castelein, R. M. & Shah, S. A. Natural sagittal spino-pelvic alignment in boys and girls before, at and after the adolescent growth spurt. Eur. Spine J. 24,1158–1167 (2014).

    Article  PubMed  Google Scholar 

  91. Wang, W. et al. Are there gender differences in sagittal spinal pelvic inclination before and after the adolescent pubertal growth spurt? Eur. Spine J. 24, 1168–1174 (2014).

    Article  PubMed  Google Scholar 

  92. Schlösser, T. P. et al. Differences in early sagittal plane alignment between thoracic and lumbar adolescent idiopathic scoliosis. Spine J. 14, 282–290 (2014).

    Article  PubMed  Google Scholar 

  93. Janssen, M. M. et al. Pre-existent vertebral rotation in the human spine is influenced by body position. Eur. Spine J. 19, 1728–1734 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  94. Kouwenhoven, J. W., Vincken, K. L., Bartels, L. W. & Castelein, R. M. Analysis of preexistent vertebral rotation in the normal spine. Spine 31, 1467–1472 (2006).

    Article  PubMed  Google Scholar 

  95. Stokes, I. A. Mechanical modulation of spinal growth and progression of adolescent scoliosis. Stud. Health Technol. Inform. 135, 75–83 (2008).

    PubMed  Google Scholar 

  96. Millner, P. A. & Dickson, R. A. Idiopathic scoliosis: biomechanics and biology. Eur. Spine J. 5, 362–373 (1996).

    Article  CAS  PubMed  Google Scholar 

  97. Jarvis, J. G., Ashman, R. B., Johnston, C. E. & Herring, J. A. The posterior tether in scoliosis. Clin. Orthop. Relat. Res. 227, 126–134 (1988).

    CAS  PubMed  Google Scholar 

  98. Villemure, I. & Stokes, I. A. Growth plate mechanics and mechanobiology. A survey of present understanding. J. Biomech. 42, 1793–1803 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  99. Bobyn, J. D., Little, D. G., Gray, R. & Schindeler, A. Animal models of scoliosis. J. Orthop. Res. 33, 458–467 (2014).

    Article  Google Scholar 

  100. Weinstein, S. L., Dolan, L. A., Wright, J. G. & Dobbs, M. B. Effects of bracing in adolescents with idiopathic scoliosis. N. Engl. J. Med. 369, 1512–1521 (2013). This landmark NIH multicentre clinical trial definitively shows the efficacy of bracing in preventing high-risk patients with AIS from reaching the surgical threshold of curve with a Cobb angle of ≥50°. A significant positive association between hours of brace wear and rate of treatment success was also found.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  101. Roaf, R. Vertebral growth and its mechanical control. J. Bone Joint Surg. Br. 42-B, 40–59 (1960).

    Article  CAS  PubMed  Google Scholar 

  102. Stokes, I. A., Spence, H., Aronsson, D. D. & Kilmer, N. M. D. Mechanical modulation of vertebral body growth: implications for scoliosis progression. Spine 21, 1162–1167 (1996).

    Article  CAS  PubMed  Google Scholar 

  103. Mehlman, C. T., Araghi, A. & Roy, D. R. Hyphenated history: the Hueter–Volkmann law. Am. J. Orthop. (Belle Mead NJ) 26, 798–800 (1997).

    CAS  Google Scholar 

  104. Eastwood, D. M. & Sanghrajka, A. P. Guided growth: recent advances in a deep-rooted concept. J. Bone Joint Surg. Br. 93, 12–18 (2011).

    Article  CAS  PubMed  Google Scholar 

  105. Hasler, C. C., Mehrkens, A. & Hefti, F. Efficacy and safety of VEPTR instrumentation for progressive spine deformities in young children without rib fusions. Eur. Spine J. 19, 400–408 (2010).

    Article  PubMed  Google Scholar 

  106. Stokes, I. A. Analysis and simulation of progressive adolescent scoliosis by biomechanical growth modulation. Eur. Spine J. 16, 1621–1628 (2007). In this analytical computerized simulated spine model, modulation of vertebral growth by estimated compressive loading shows that a substantial component of scoliosis progression during growth is biomechanically mediated through the vertebral growth plates.

    Article  PubMed  PubMed Central  Google Scholar 

  107. Stokes, I. A., Aronsson, D. D., Dimock, A. N., Cortright, V. & Beck, S. Endochondral growth in growth plates of three species at two anatomical locations modulated by mechanical compression and tension. J. Orthop. Res. 24, 1327–1334 (2006).

    Article  PubMed  PubMed Central  Google Scholar 

  108. Will, R. E., Stokes, I. A., Qiu, X., Walker, M. R. & Sanders, J. O. Cobb angle progression in adolescent scoliosis begins at the intervertebral disc. Spine 34, 2782–2786 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  109. Valteau, B., Grimard, G., Londono, I., Moldovan, F. & Villemure, I. In vivo dynamic bone growth modulation is less detrimental but as effective as static growth modulation. Bone 49, 996–1004 (2011).

    Article  PubMed  Google Scholar 

  110. Lombardi, G., Akoume, M. Y., Colombini, A., Moreau, A. & Banfi, G. Biochemistry of adolescent idiopathic scoliosis. Adv. Clin. Chem. 54, 165–182 (2011).

    Article  CAS  PubMed  Google Scholar 

  111. Suh, K. T., Lee, S. S., Hwang, S. H., Kim, S. J. & Lee, J. S. Elevated soluble receptor activator of nuclear factor-κB ligand and reduced bone mineral density in patients with adolescent idiopathic scoliosis. Eur. Spine J. 16, 1563–1569 (2007).

    Article  PubMed  PubMed Central  Google Scholar 

  112. Sabirin, J., Bakri, R., Buang, S. N., Abdullah, A. T. & Shapie, A. School scoliosis screening programme a systematic review. Med. J. Malaysia 65, 261–267 (2010).

    CAS  PubMed  Google Scholar 

  113. Qiu, Y. et al. Decreased circulating leptin level and its association with body and bone mass in girls with adolescent idiopathic scoliosis. Spine 32, 2703–2710 (2007).

    Article  PubMed  Google Scholar 

  114. Wang, B., Chen, Z. J., Qiu, Y. & Liu, W. J. Decreased circulating matrilin-1 levels in adolescent idiopathic scoliosis. Zhonghua Wai Ke Za Zhi 47, 1638–1641 (in Chinese) (2009).

    PubMed  Google Scholar 

  115. Akoume, M. Y. et al. Cell-based screening test for idiopathic scoliosis using cellular dielectric spectroscopy. Spine 35, E601–E608 (2010). This paper presents new evidence that supports the idea that the melatonin signalling dysfunction occurring in AIS also affects other Gi-coupled receptors. The study also shows that osteopontin treatment for AIS further exacerbates the signalling dysfunction in patients classified as FG2 and FG3 endophenotypes.

    Article  PubMed  Google Scholar 

  116. Alonso-Vale, M. I. et al. Melatonin enhances leptin expression by rat adipocytes in the presence of insulin. Am. J. Physiol. Endocrinol. Metab. 288, E805–E812 (2005).

    Article  CAS  PubMed  Google Scholar 

  117. Gottesman, I. I. & Gould, T. D. The endophenotype concept in psychiatry: etymology and strategic intentions. Am. J. Psychiatry 160, 636–645 (2003).

    Article  PubMed  Google Scholar 

  118. Julien, C., Gorman, K. F., Akoume, M.-Y. & Moreau, A. Towards a comprehensive diagnostic assay for scoliosis. Personalized Med. 10, 97–103 (2013).

    Article  CAS  Google Scholar 

  119. Akoume, M. Y., Franco, A. & Moreau, A. Cell-based assay protocol for the prognostic prediction of idiopathic scoliosis using cellular dielectric spectroscopy. J. Vis. Exp. 80, e50768 (2013).

    Google Scholar 

  120. Yadav, M. C. et al. Ablation of osteopontin improves the skeletal phenotype of Phospho1−/− mice. J. Bone Miner. Res. 29, 2369–2381 (2014).

    Article  CAS  PubMed  Google Scholar 

  121. Xie, N. et al. Does elevated osteopontin level play an important role in the development of scoliosis in bipedal mice? Spine J. 15, 1660–1664 (2015).

    Article  PubMed  Google Scholar 

  122. Perdriolle, R. & Vidal, J. Morphology of scoliosis:three-dimensional evolution. Orthopedics 10, 909–915 (1987).

    CAS  PubMed  Google Scholar 

  123. Dubousset, J. et al. A new 2D and 3D imaging approach to musculoskeletal physiology and pathology with low-dose radiation and the standing position: the EOS system. Bull. Acad. Natl Med. 189, 287–297 (in French) (2005).

    PubMed  Google Scholar 

  124. Legaye, J. in Recent Advances in Scoliosis (ed. Grivas, T. ) 119–144 (InTech, 2012).

    Google Scholar 

  125. Nault, M.-L. et al. Three-dimensional spinal morphology can differentiate between progressive and nonprogressive patients with adolescent idiopathic scoliosis at the initial presentation: a prospective study. Spine 39, E601–E606 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  126. Studer, D. Clinical investigation and imaging. J. Child Orthop. 7, 29–35 (2013).

    Article  PubMed  Google Scholar 

  127. Lee, C. F. et al. Costs of school scoliosis screening: a large, population-based study. Spine 35,2266–2272 (2010).

    Article  CAS  PubMed  Google Scholar 

  128. Lee, C. F. et al. Referral criteria for school scoliosis screening: assessment and recommendations based on a large longitudinally followed cohort. Spine 35, E1492–E1498 (2010).

    Article  CAS  PubMed  Google Scholar 

  129. Labelle, H. et al. Screening for adolescent idiopathic scoliosis: an information statement by the scoliosis research society international task force. Scoliosis 8, 17 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  130. Grivas, T. B. et al. The pendulum swings back to scoliosis screening: screening policies for early detection and treatment of idiopathic scoliosis — current concepts and recommendations. Scoliosis 8, 16 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  131. Ascani, E. et al. Natural history of untreated idiopathic scoliosis after skeletal maturity. Spine 11, 784–789 (1986).

    Article  CAS  PubMed  Google Scholar 

  132. Pehrsson, K., Bake, B., Larsson, S. & Nachemson, A. Lung function in adult idiopathic scoliosis: a 20 year follow up. Thorax 46, 474–478 (1991).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  133. Weinstein, S. L., Zavala, D. C. & Ponseti, I. V. Idiopathic scoliosis: long-term follow-up and prognosis in untreated patients. J. Bone Joint Surg. Am. 63, 702–712 (1981).

    Article  CAS  PubMed  Google Scholar 

  134. Weinstein, S. L. & Ponseti, I. V. Curve progression in idiopathic scoliosis. J. Bone Joint Surg. Am. 65, 447–455 (1983).

    Article  CAS  PubMed  Google Scholar 

  135. Collis, D. K. & Ponseti, I. V. Long-term follow-up of patients with idiopathic scoliosis not treated surgically. J. Bone Joint Surg. Am. 51, 425–445 (1969).

    Article  CAS  PubMed  Google Scholar 

  136. Ponseti, I. V. & Friedman, B. Prognosis in idiopathic scoliosis. J. Bone Joint Surg. Am. 32A, 381–395 (1950).

    Article  CAS  PubMed  Google Scholar 

  137. Weinstein, S. L. et al. Health and function of patients with untreated idiopathic scoliosis: a 50-year natural history study. JAMA 289, 559–567 (2003). This study describes a natural history study of a cohort of patients with AIS who had follow-up evaluation for an average of 51 years. The study shows there is an increased risk of shortness of breath associated with a thoracic Cobb angle of >80° and an increased incidence of chronic back pain in this group, although patients remained productive and functional at a high level.

    Article  PubMed  Google Scholar 

  138. Fowles, J. V., Drummond, D. S., L'Ecuyer, S., Roy, L. & Kassab, M. T. Untreated scoliosis in the adult. Clin. Orthop. Relat. Res. 134, 212–217 (1978).

    Google Scholar 

  139. Kolind-Sorensen, V. A follow-up study of patients with idiopathic scoliosis. Acta Orthop. Scand. 44, 5 (1973).

    Google Scholar 

  140. Nachemson, A. A long term follow-up study of non-treated scoliosis. Acta Orthop. Scand. 39, 466–476 (1968).

    Article  CAS  PubMed  Google Scholar 

  141. Nilsonne, U. & Lundgren, K. D. Long-term prognosis in idiopathic scoliosis. Acta Orthop. Scand. 39, 456–465 (1968).

    Article  CAS  PubMed  Google Scholar 

  142. Bunnell, W. P. The natural history of idiopathic scoliosis before skeletal maturity. Spine 11, 773–776 (1986).

    Article  CAS  PubMed  Google Scholar 

  143. Lonstein, J. E. & Carlson, J. M. The prediction of curve progression in untreated idiopathic scoliosis during growth. J. Bone Joint Surg. Am. 66, 1061–1071 (1984).

    Article  CAS  PubMed  Google Scholar 

  144. Nachemson, A. L., Lonstein, J. E. & Weinstein, S. L. Scoliosis Research Society (Denver, 1982).

    Google Scholar 

  145. Peterson, L. E. & Nachemson, A. L. Prediction of progression of the curve in girls who have adolescent idiopathic scoliosis of moderate severity. Logistic regression analysis based on data from The Brace Study Scoliosis Research Society. J. Bone Joint Surg. Am. 77, 823–827 (1995).

    Article  CAS  PubMed  Google Scholar 

  146. Picault, C., deMauroy, J. C., Mouilleseaux, B. & Diana, G. Natural history of idiopathic scoliosis in girls and boys. Spine 11, 777–778 (1986).

    Article  CAS  PubMed  Google Scholar 

  147. Kafer, E. R. Respiratory and cardiovascular functions in scoliosis. Bull. Eur. Physiopathol. Respir. 13, 299–321 (1977).

    CAS  PubMed  Google Scholar 

  148. Kearon, C., Viviani, G. R., Kirkley, A. & Killian, K. J. Factors determining pulmonary function in adolescent idiopathic thoracic scoliosis. Am. Rev. Respir. Dis. 148, 288–294 (1993).

    Article  CAS  PubMed  Google Scholar 

  149. Lin, M. C. et al. Pulmonary function and spinal characteristics: their relationships in persons with idiopathic and postpoliomyelitic scoliosis. Arch. Phys. Med. Rehabil. 82, 335–341 (2001).

    Article  CAS  PubMed  Google Scholar 

  150. Branthwaite, M. A. Cardiorespiratory consequences of unfused idiopathic scoliosis. Br. J. Dis. Chest 80, 360–369 (1986).

    Article  CAS  PubMed  Google Scholar 

  151. Edgar, M. A. & Mehta, M. H. Long-term follow-up of fused and unfused idiopathic scoliosis. J. Bone Joint Surg. Br. 70, 712–716 (1988).

    Article  CAS  PubMed  Google Scholar 

  152. Weinstein, S. L. The Pediatric Spine: Principles and Practice (Raven Press, 1994).

    Book  Google Scholar 

  153. Pehrsson, K., Danielsson, A. & Nachemson, A. Pulmonary function in adolescent idiopathic scoliosis: a 25 year follow up after surgery or start of brace treatment. Thorax 56, 388–393 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  154. Deyo, R. A., Mirza, S. K. & Martin, B. I. Back pain prevalence and visit rates: estimates from U. S. national surveys, 2002. Spine 31, 2724–2727 (2006).

    Article  PubMed  Google Scholar 

  155. Danielsson, A. J., Wiklund, I., Pehrsson, K. & Nachemson, A. L. Health-related quality of life in patients with adolescent idiopathic scoliosis: a matched follow-up at least 20 years after treatment with brace or surgery. Eur. Spine J. 10, 278–288 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  156. Mayo, N. E., Goldberg, M. S., Poitras, B., Scott, S. & Hanley, J. The Ste-Justine adolescent idiopathic scoliosis cohort study. Part III: back pain. Spine 19, 1573–1581 (1994).

    Article  CAS  PubMed  Google Scholar 

  157. Parent, S., Newton, P. O. & Wenger, D. R. Adolescent idiopathic scoliosis: etiology, anatomy, natural history, and bracing. Instr. Course Lect. 54, 529–536 (2005).

    Google Scholar 

  158. Negrini, S. et al. Italian guidelines on rehabilitation treatment of adolescents with scoliosis or other spinal deformities. Europa Medicophys. 41, 183–201 (2005).

    CAS  Google Scholar 

  159. Negrini, A., Verzini, N., Parzini, S. & Negrini, S. Role of physical exercise in the treatment of mild idiopathic adolescent scoliosis. Europa Medicophys. 37, 181–190 (2001).

    Google Scholar 

  160. Weiss, H. R. et al. Indications for conservative management of scoliosis (guidelines). Scoliosis 1, 5 (2006).

    Article  PubMed  PubMed Central  Google Scholar 

  161. Richards, B. S., Bernstein, R. M., D'Amato, C. R. & Thompson, G. H. Standardization of criteria for adolescent idiopathic scoliosis brace studies: SRS Committee on Bracing and Nonoperative Management. Spine 30, 2068–2075 (2005).

    Article  PubMed  Google Scholar 

  162. Verma, K. et al. Simplified skeletal maturity scoring system: learning curve and methods to improve reliability. Spine 39, E1592–E1598 (2014).

    Article  PubMed  Google Scholar 

  163. Weinstein, S. L., Dolan, L. A., Wright, J. G. & Dobbs, M. B. Design of the Bracing in Adolescent Idiopathic Scoliosis Trial (BrAIST). Spine 38, 1832–1841 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  164. Lebel, D. E., Al-Aubaidi, Z., Shin, E. J., Howard, A. & Zeller, R. Three dimensional analysis of brace biomechanical efficacy for patients with AIS. Eur. Spine J. 22, 2445–2448 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  165. Courvoisier, A., Drevelle, X., Vialle, R., Dubousset, J. & Skalli, W. 3D analysis of brace treatment in idiopathic scoliosis. Eur. Spine J. 22, 2449–2455 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  166. Weinstein, S. L., Dolan, L. A., Cheng, J. C., Danielsson, A. & Morcuende, J. A. Adolescent idiopathic scoliosis. Lancet 371, 1527–1537 (2008).

    Article  PubMed  Google Scholar 

  167. Coe, J. D. et al. Complications in spinal fusion for adolescent idiopathic scoliosis in the new millennium. A report of the Scoliosis Research Society Morbidity and Mortality Committee. Spine 31, 345–349 (2006). This paper discusses morbidity and mortality data collected by members of the Scoliosis Research Society and provides valuable information regarding the incidence and type of complications associated with spinal fusion procedures in AIS.

    Article  PubMed  Google Scholar 

  168. de Kleuver, M. et al. Optimal surgical care for adolescent idiopathic scoliosis: an international consensus. Eur. Spine J. 23, 2603–2618 (2014).

    Article  PubMed  Google Scholar 

  169. Clements, D. H. et al. Did the Lenke classification change scoliosis treatment? Spine 36, 1142–1145 (2011).

    Article  PubMed  Google Scholar 

  170. Lenke, L. G. et al. Adolescent idiopathic scoliosis: a new classification to determine extent of spinal arthrodesis. J Bone Joint Surg. Am. 83-A, 1169–1181 (2001). The new scoliosis classification system presented in this paper has become widely used to determine surgical treatment strategies for scoliosis using an algorithmic approach to identify ‘structural minor’ curves that need inclusion in the spinal fusion.

    Article  CAS  Google Scholar 

  171. Newton, P. O. et al. Factors involved in the decision to perform a selective versus nonselective fusion of Lenke 1B and 1C (King-Moe II) curves in adolescent idiopathic scoliosis. Spine 28, S217–S223 (2003).

    Article  PubMed  Google Scholar 

  172. Imrie, M., Yaszay, B., Bastrom, T. P., Wenger, D. R. & Newton, P. O. Adolescent idiopathic scoliosis: should 100% correction be the goal? J. Pediatr. Orthop. 31, S9–S13 (2011).

    Article  PubMed  Google Scholar 

  173. Dohin, B. & Dubousset, J. F. Prevention of the crankshaft phenomenon with anterior spinal epiphysiodesis in surgical treatment of severe scoliosis of the younger patient. Eur. Spine J. 3, 165–168 (1994).

    Article  CAS  PubMed  Google Scholar 

  174. Papin, P. et al. Long-term three-dimensional changes of the spine after posterior spinal instrumentation and fusion in adolescent idiopathic scoliosis. Eur. Spine J. 8, 16–21 (1999).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  175. Helenius, I. et al. Harrington and Cotrel-Dubousset instrumentation in adolescent idiopathic scoliosis. Long-term functional and radiographic outcomes. J. Bone Joint Surg. Am. 85-A, 2303–2309 (2003).

    Article  Google Scholar 

  176. Kim, Y. J. et al. Comparative analysis of pedicle screw versus hook instrumentation in posterior spinal fusion of adolescent idiopathic scoliosis. Spine 29, 2040–2048 (2004).

    Article  PubMed  Google Scholar 

  177. Newton, P. O. et al. Surgical treatment of Lenke 1 main thoracic idiopathic scoliosis: results of a prospective, multicenter study. Spine 38, 328–338 (2013). This prospective non-randomized study compares the favourable outcomes of posterior instrumented fusion and open and endoscopic anterior approaches for thoracic curves in AIS.

    Article  PubMed  Google Scholar 

  178. Sudo, H., Ito, M., Kaneda, K., Shono, Y. & Abumi, K. Long-term outcomes of anterior dual-rod instrumentation for thoracolumbar and lumbar curves in adolescent idiopathic scoliosis: a twelve to twenty-three-year follow-up study. J. Bone Joint Surg. Am. 95, e49 (2013).

    Article  PubMed  Google Scholar 

  179. Lykissas, M. G. et al. Mid- to long-term outcomes in adolescent idiopathic scoliosis after instrumented posterior spinal fusion: a meta-analysis. Spine 38, E113–E119 (2013).

    Article  PubMed  Google Scholar 

  180. Marks, M. et al. Postoperative segmental motion of the unfused spine distal to the fusion in 100 patients with adolescent idiopathic scoliosis. Spine 37, 826–832 (2012).

    Article  PubMed  Google Scholar 

  181. Pehrsson, K., Larsson, S., Oden, A. & Nachemson, A. Long-term follow-up of patients with untreated scoliosis. A study of mortality, causes of death, and symptoms. Spine 17, 1091–1096 (1992). This study shows that patients with AIS with adolescent onset do not have increased mortality compared with the general population. The risk of respiratory failure occurs 20 years after AIS onset if the vital capacity is reduced below 45% of that predicted and the curve has a Cobb angle >110° at skeletal maturity.

    Article  CAS  PubMed  Google Scholar 

  182. Asher, M., Min Lai, S., Burton, D. & Manna, B. Scoliosis research society-22 patient questionnaire: responsiveness to change associated with surgical treatment. Spine 28, 70–73 (2003).

    Article  PubMed  Google Scholar 

  183. Padua, R. et al. Patient outcomes after Harrington instrumentation for idiopathic scoliosis: a 15- to 28-year evaluation. Spine 26, 1268–1273 (2001).

    Article  CAS  PubMed  Google Scholar 

  184. Andersen, M. O., Christensen, S. B. & Thomsen, K. Outcome at 10 years after treatment for adolescent idiopathic scoliosis. Spine 31, 350–354 (2006).

    Article  PubMed  Google Scholar 

  185. Danielsson, A. J. & Nachemson, A. L. Back pain and function 22 years after brace treatment for adolescent idiopathic scoliosis: a case–control study-part I. Spine 28, 2078–2085 (2003). This paper describes a follow-up investigation of patients 22 years after they completed brace treatment. The study found that these patients experienced minimal back pain and dysfunction, which was comparable to what has been found in unaffected individuals.

    Article  PubMed  Google Scholar 

  186. Akazawa, T. et al. Long-term clinical outcomes of surgery for adolescent idiopathic scoliosis 21 to 41 years later. Spine 37, 402–405 (2012).

    Article  PubMed  Google Scholar 

  187. Danielsson, A. J. & Nachemson, A. L. Back pain and function 23 years after fusion for adolescent idiopathic scoliosis: a case–control study-part II. Spine 28, E373–E383 (2003). This paper presents a follow-up investigation 23 years after patients with AIS were treated with surgery. This study found that 25% of patients reported daily pain, but analgesics were sparsely used. No major differences in back function and general HRQOL were noted between patients and unaffected individuals. The length of the fusion carried out in the lower spine did not affect the occurrence of pain.

    Article  PubMed  Google Scholar 

  188. Lange, J. E., Steen, H. & Brox, J. I. Long-term results after Boston brace treatment in adolescent idiopathic scoliosis. Scoliosis 4, 17 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  189. Brox, J. I., Lange, J. E. & Steen, H. Comorbidity influenced health-related quality of life of 390 patients with idiopathic scoliosis at long-term follow-up. Eur. J. Phys. Rehabil. Med. 50, 73–81 (2014).

    CAS  PubMed  Google Scholar 

  190. Cochran, T., Irstam, L. & Nachemson, A. Long-term anatomic and functional changes in patients with adolescent idiopathic scoliosis treated by Harrington rod fusion. Spine 8, 576–584 (1983).

    Article  CAS  PubMed  Google Scholar 

  191. Blount, W. P. & Mellencamp, D. The effect of pregnancy on idiopathic scoliosis. J. Bone Joint Surg. Am. 62, 1083–1087 (1980).

    Article  CAS  PubMed  Google Scholar 

  192. Danielsson, A. J. & Nachemson, A. L. Childbearing, curve progression, and sexual function in women 22 years after treatment for adolescent idiopathic scoliosis: a case–control study. Spine 26, 1449–1456 (2001).

    Article  CAS  PubMed  Google Scholar 

  193. Orvomaa, E., Hiilesmaa, V., Poussa, M., Snellman, O. & Tallroth, K. Pregnancy and delivery in patients operated by the Harrington method for idiopathic scoliosis. Eur. Spine J. 6, 304–307 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  194. Olafsson, Y., Saraste, H. & Ahlgren, R. M. Does bracing affect self-image? A prospective study on 54 patients with adolescent idiopathic scoliosis. Eur. Spine J. 8, 402–405 (1999).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  195. Tones, M. J. & Moss, N. D. The impact of patient self assessment of deformity on HRQL in adults with scoliosis. Scoliosis 2, 14 (2007).

    Article  PubMed  PubMed Central  Google Scholar 

  196. Benli, I. T. et al. Minimum 10 years follow-up surgical results of adolescent idiopathic scoliosis patients treated with TSRH instrumentation. Eur. Spine J. 16, 381–391 (2007).

    Article  PubMed  Google Scholar 

  197. Burwell, R. G., Dangerfield, P. H., Moulton, A. & Grivas, T. B. Adolescent idiopathic scoliosis (AIS), environment, exposome and epigenetics: a molecular perspective of postnatal normal spinal growth and the etiopathogenesis of AIS with consideration of a network approach and possible implications for medical therapy. Scoliosis 6, 26 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  198. Grivas, T. B., Burwell, R. G., Dangerfield, P. H. & Moulton, A. Genetics, epigenetics and the scoliogeny of adolescent idiopathic scoliosis: how much is genetics and how much is it epigenetics as a new paradigm? Bone& Joint[online], (2014).

  199. Moresi, V., Marroncelli, N., Coletti, D. & Adamo, S. Regulation of skeletal muscle development and homeostasis by gene imprinting, histone acetylation and microRNA. Biochim. Biophys. Acta 1849, 309–316 (2015).

    Article  CAS  PubMed  Google Scholar 

  200. Grivas, T. B. et al. Maternal age at birth: does it dictate the epigenotypic expression of the trunkal asymmetry of a child? Stud. Health Technol. Inform. 176, 36–42 (2012). The findings from this study indicate that maternal age at conception, considered as an environmental factor, might influence the occurrence of trunkal asymmetry and idiopathic scoliosis during growth through epigenetic mechanisms.

    PubMed  Google Scholar 

  201. Doi, T. et al. Right thoracic curvature in the normal spine. J. Orthop. Surg. Res. 6, 4 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  202. Negrini, S., Negrini, A., Atanasio, S. & Santambrogio, G. C. Three-dimensional easy morphological (3-DEMO) classification of scoliosis, part I. Scoliosis 1, 20 (2006).

    Article  PubMed  PubMed Central  Google Scholar 

  203. Poncet, P., Dansereau, J. & Labelle, H. Geometric torsion in idiopathic scoliosis: three-dimensional analysis and proposal for a new classification. Spine 26, 2235–2243 (2001).

    Article  CAS  PubMed  Google Scholar 

  204. Weiss, H.-R. The method of Katharina Schroth — history, principles and current development. Scoliosis 6, 17 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  205. Rigo, M., Villagrasa, M. & Gallo, D. A specific scoliosis classification correlating with brace treatment: description and reliability. Scoliosis 5, 1 (2010). This article develops specific principles of correction required for effective brace design and fabrication on the basis of radiological and clinical criteria.

    Article  PubMed  PubMed Central  Google Scholar 

  206. Qiu, G. et al. A new operative classification of idiopathic scoliosis: a peking union medical college method. Spine 30, 1419–1426 (2005).

    Article  PubMed  Google Scholar 

  207. Gilbert, S. F. Developmental Biology (Sinauer, 2014).

    Google Scholar 

  208. Chiru, M. Adolescent idiopathic scoliosis and osteopenia. Maedica (Buchar.) 6, 17–22 (2011).

    Google Scholar 

  209. Chen, Z. et al. Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population. Eur. J. Hum. Genet. 17, 525–532 (2009).

    Article  CAS  PubMed  Google Scholar 

  210. Gerdhem, P. et al. Serum level of cartilage oligomeric matrix protein is lower in children with idiopathic scoliosis than in non-scoliotic controls. Eur. Spine J. 24, 256–261 (2015).

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

The authors thank the following people for their help during the preparation of the manuscript: D.Y.T. Fong (School of Nursing, University of Hong Kong, Hong Kong); J.P.Y. Cheung (Department of Orthopaedics and Traumatology, University of Hong Kong, Hong Kong); P.H. Dangerfield (University of Liverpool and Staffordshire University, UK); A. Moulton (Sherwood Forest Hospitals NHS Foundation Trust, King's Mil Hospital, Mansfield, Nottinghamshire, UK); L. Shi (Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong); S.C.N. Hui (Department of Imaging and Interventional Radiology, The Chinese University of Hong Kong, Hong Kong); E.L.S. Tam (Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong, Hong Kong); T.P. Lam (Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong, Hong Kong); W.W. Chau (Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong, Hong Kong); and D. Colo (Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands).

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Contributions

Introduction (T.B.G.); Epidemiology (K.D.L.); Mechanisms/pathophysiology (R.G.B., J.C.C., M.B.D., C.A.G., W.C.C., R.M.C., A.M. and I.A.S.); Diagnosis, screening and prevention (K.D.L.); Management (S.L.W. and P.O.N.); Quality of life (A.J.D.); Outlook (R.G.B. and J.C.C.); Overview of Primer (J.C.C.).

Corresponding author

Correspondence to Jack C. Cheng.

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Competing interests

A.M. declares research grants from Paradigm Spine LLC (New York City, New York, USA), two patent applications on behalf of Sainte-Justine University Hospital and nine issued patents owned by Centre hospitalier universitaire Sainte-Justine, which has signed a licensing agreement with Paradigm Spine LLC. I.A.S. declares a consulting agreement with K Spine Inc. (Minnetonga, Minnesota, USA). P.O.N. declares consulting and royalty agreements with DePuy Synthes Spine regarding posterior spinal implant systems. He holds patents on anterior and posterior spinal instruments and implants for spinal fusion, as well as implants for spinal growth modulation from DePuy Synthes through the Setting Scoliosis Straight Foundation/Harms Study Group. All other authors declare no conflict of financial interest.

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Cheng, J., Castelein, R., Chu, W. et al. Adolescent idiopathic scoliosis. Nat Rev Dis Primers 1, 15030 (2015). https://doi.org/10.1038/nrdp.2015.30

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