The genetic architecture of adolescent idiopathic scoliosis

Anas M. Khanshour, Carol A. Wise

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Adolescent idiopathic scoliosis (AIS) is the most common pediatric spinal deformity, affecting 2-3% of school-age children worldwide. This disease is typically classified by age at onset, with the great majority occurring around the time of the adolescent growth spurt, the so-called AIS. AIS can progress rapidly, threatening pain, deformity, and pulmonary dysfunction. Heritability of AIS is high, and population studies have consistently found that AIS is best explained by a polygenic inheritance model, in which many genetic risk factors combine to cause the disease. Population studies have associated AIS with genetic markers near interesting candidate genes, including the homeobox transcription factor LBX1, the G protein-coupled receptor GPR126, the paired box transcription factors PAX1 and PAX3, as well as the SRY-box SOX9. Moreover, gene targeting in zebrafish and mouse model systems have identified candidate genes, which offer an exciting new area of investigation into molecular mechanisms of AIS. AIS candidate genes thus far identified function in muscle, nerve, and cartilage specification in early development, suggesting neuromuscular and/or cartilage disease origins, but their role in later human development and growth of the axial spine is an unexplored area of developmental biology. Continued gene discovery efforts, aided by next-generation genomic platforms, are a priority for the field and will provide the tools for biological investigations of AIS pathogenesis.

Original languageEnglish (US)
Title of host publicationPathogenesis of Idiopathic Scoliosis
PublisherSpringer Japan
Pages51-74
Number of pages24
ISBN (Electronic)9784431565413
ISBN (Print)9784431565390
DOIs
StatePublished - Jan 1 2018

Fingerprint

Scoliosis
Paired Box Transcription Factors
Cartilage Diseases
Multifactorial Inheritance
Developmental Biology
Neuromuscular Diseases
Gene Targeting
Homeobox Genes
Genetic Association Studies
Human Development
Zebrafish
Growth
G-Protein-Coupled Receptors
Genetic Markers
Age of Onset
Population
Genes
Cartilage
Spine
Transcription Factors

Keywords

  • Animal modeling
  • Genetics
  • Idiopathic scoliosis
  • Musculoskeletal disorder
  • Neuromuscular system
  • Next-generation genomics

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Khanshour, A. M., & Wise, C. A. (2018). The genetic architecture of adolescent idiopathic scoliosis. In Pathogenesis of Idiopathic Scoliosis (pp. 51-74). Springer Japan. https://doi.org/10.1007/978-4-431-56541-3_3

The genetic architecture of adolescent idiopathic scoliosis. / Khanshour, Anas M.; Wise, Carol A.

Pathogenesis of Idiopathic Scoliosis. Springer Japan, 2018. p. 51-74.

Research output: Chapter in Book/Report/Conference proceedingChapter

Khanshour, AM & Wise, CA 2018, The genetic architecture of adolescent idiopathic scoliosis. in Pathogenesis of Idiopathic Scoliosis. Springer Japan, pp. 51-74. https://doi.org/10.1007/978-4-431-56541-3_3
Khanshour AM, Wise CA. The genetic architecture of adolescent idiopathic scoliosis. In Pathogenesis of Idiopathic Scoliosis. Springer Japan. 2018. p. 51-74 https://doi.org/10.1007/978-4-431-56541-3_3
Khanshour, Anas M. ; Wise, Carol A. / The genetic architecture of adolescent idiopathic scoliosis. Pathogenesis of Idiopathic Scoliosis. Springer Japan, 2018. pp. 51-74
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