# Genome-wide association study identifies GAK and KLF12 associated with curve severity of adolescent idiopathic scoliosis

**Authors:** Zhicheng Dai, Zhichong Wu, Leilei Xu, Zhenhua Feng, Yong Qiu, Zezhang Zhu

PMC · DOI: 10.7717/peerj.20638 · PeerJ · 2026-01-19

## TL;DR

This study finds two genes, GAK and KLF12, linked to the severity of spinal curvature in adolescent idiopathic scoliosis.

## Contribution

The study identifies GAK and KLF12 as novel susceptibility genes associated with curve severity in adolescent idiopathic scoliosis.

## Key findings

- rs2061846 in GAK and rs7330031 in KLF12 were successfully replicated as associated with severe scoliosis curves.
- KLF12 mRNA expression in paraspinal muscle was negatively correlated with Cobb angle and related to muscle fiber-specific gene expression.

## Abstract

Genetic factors have been increasingly recognized as important contributors to the development and progression of adolescent idiopathic scoliosis (AIS). However, the genetic basis underlying AIS curve severity remains largely unclear. The objective of this study is to identify novel genetic variants associated with curve severity in AIS through a genome-wide association study (GWAS).

In the discovery stage, 620 female AIS patients were enrolled, including 323 with severe curves (> 40°) and 297 with mild curves (< 30°). Top single nucleotide polymorphisms (SNPs) from each locus were selected for replication in an independent cohort of 634 severe and 546 mild cases. Associations between gene expression and Cobb angle were evaluated using Spearman correlation, while correlations with myofiber–related genes were analyzed using Pearson correlation.

Fifteen novel SNPs showed potential association with AIS curve severity in the discovery stage (P < 1 × 10−4). Six lead SNPs were selected for replication, including rs2061846 (GAK), rs12200301 (DST), rs10820637 (SMC2/NIPSNAP3A), rs7330031 (KLF12), rs2469472 (ST8SIA5-DT), and rs738650 (SEZ6L). Among these, rs2061846 and rs7330031 were successfully replicated. For rs2061846 in GAK, the frequency of the G allele was significantly higher in the severe group (P = 0.001; OR = 1.32). For rs7330031 in KLF12, the C allele was significantly more frequent in the severe group than in the mild group (P = 0.001; OR = 1.46). Moreover, KLF12 mRNA expression in the paraspinal muscle of AIS patients was negatively correlated with Cobb angle and associated with muscle fiber–specific gene expression.

This study identified GAK and KLF12 as novel susceptibility genes associated with AIS curve severity, providing new insights into the genetic basis of curve progression. These findings may contribute to improved risk stratification and personalized management in AIS.

## Linked entities

- **Genes:** GAK (cyclin G associated kinase) [NCBI Gene 2580], KLF12 (KLF transcription factor 12) [NCBI Gene 11278], DST (dystonin) [NCBI Gene 667], SMC2 (structural maintenance of chromosomes 2) [NCBI Gene 10592], NIPSNAP3A (nipsnap homolog 3A) [NCBI Gene 25934], ST8SIA5-DT (ST8SIA5 divergent transcript) [NCBI Gene 105372097], SEZ6L (seizure related 6 homolog like) [NCBI Gene 23544]
- **Diseases:** adolescent idiopathic scoliosis (MONDO:0005488)

## Full-text entities

- **Genes:** SEZ6L (seizure related 6 homolog like) [NCBI Gene 23544] {aka SEZ6L1}, NIPSNAP3A (nipsnap homolog 3A) [NCBI Gene 25934] {aka HSPC299, NIPSNAP4, TASSC}, SMC2 (structural maintenance of chromosomes 2) [NCBI Gene 10592] {aka CAP-E, CAPE, SMC-2, SMC2L1}, KLF12 (KLF transcription factor 12) [NCBI Gene 11278] {aka AP-2rep, AP2REP, HSPC122}, DST (dystonin) [NCBI Gene 667] {aka BP240, BPA, BPAG1, CATX-15, CATX15, CMYO29}, GAK (cyclin G associated kinase) [NCBI Gene 2580] {aka DNAJ26, DNAJC26}, ST8SIA5 (ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5) [NCBI Gene 29906] {aka SIAT8-E, SIAT8E, ST8SiaV}
- **Diseases:** AIS (OMIM:181800)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs2469472, rs7330031, rs12200301, rs738650, rs2061846, rs10820637

## Full text

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## Figures

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## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12826036/full.md

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Source: https://tomesphere.com/paper/PMC12826036