AI Article Synopsis

  • Adolescent idiopathic scoliosis (AIS) is a common spinal deformity in children, with limited understanding of its genetic causes, prompting a study involving 79,211 Japanese individuals to identify new susceptibility loci.
  • The study discovered 20 loci associated with AIS, 14 of which were newly identified, accounting for 4.6% of the condition's phenotypic variance, and highlighted 21 related genes.
  • The research also revealed genetic links between AIS and factors like body mass index and uric acid, emphasizing the complex genetic backgrounds contributing to AIS.

Article Abstract

Adolescent idiopathic scoliosis (AIS) is the most common pediatric spinal deformity. Several AIS susceptibility loci have been identified; however, they could explain only a small proportion of AIS heritability. To identify additional AIS susceptibility loci, we conduct a meta-analysis of the three genome-wide association studies consisting of 79,211 Japanese individuals. We identify 20 loci significantly associated with AIS, including 14 previously not reported loci. These loci explain 4.6% of the phenotypic variance of AIS. We find 21 cis-expression quantitative trait loci-associated genes in seven of the fourteen loci. By a female meta-analysis, we identify additional three significant loci. We also find significant genetic correlations of AIS with body mass index and uric acid. The cell-type specificity analyses show the significant heritability enrichment for AIS in multiple cell-type groups, suggesting the heterogeneity of etiology and pathogenesis of AIS. Our findings provide insights into etiology and pathogenesis of AIS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695451PMC
http://dx.doi.org/10.1038/s41467-019-11596-wDOI Listing

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