Department of Orthodontics, Institute of Craniofacial Deformity, Yonsei University College of Dentistry, Seoul, Korea.
Department of Biomedical and Pharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul, Korea.
Prog Orthod. 2024 Jun 10;25(1):23. doi: 10.1186/s40510-024-00521-7.
External apical root resorption (EARR) is a common undesirable outcome of orthodontic treatment, this study aimed to identify genetic polymorphisms associated with the susceptibility to extreme orthodontic-induced EARR in a Korean population using extreme phenotype analysis sampling.
Genomic DNA was isolated from the saliva of 77 patients who underwent orthodontic treatment involving two maxillary premolar extractions. The patients were divided into two groups based on EARR values measured on periapical radiographs: The significant resorption group (SG, EARR ≥ 4 mm) and the normal group (NG, EARR < 2 mm). In the NG group, patients with EARR < 1 mm were named the non-resorption group (NonG). Targeted next-generation sequencing was performed using the screened single nucleotide polymorphisms (SNPs), and firth logistic regression analysis was used to determine genetic associations with EARR. Haplotype-based association analysis was performed for specific SNPs.
SNPs related to genes TNFSF11, TNFRSF11B, WNT3A, SFRP2, LRP6, P2RX7, and LRP1 were found to be significantly associated with severe EARR (p < 0.05, pre-Bonferroni correction p-values). Additionally, the haplotype CCA of rs17525809, rs208294, and rs1718119 P2RX7 had a higher frequency in the SG group.
Extreme phenotype analysis has identified eleven SNPs related to genes TNFSF11, TNFRSF11B, WNT3A, SFRP2, LRP6, P2RX7, and LRP1 that are associated with severe root resorption in the Korean population. These findings will contribute to the development of predictive diagnostic tools for identifying severe root resorption that may occur during orthodontic treatment.
正畸治疗后发生的根尖外部吸收(EARR)是一种常见的不良后果。本研究旨在通过极端表型分析抽样,在韩国人群中鉴定与正畸治疗引起的极端 EARR 易感性相关的遗传多态性。
从 77 名接受正畸治疗的患者的唾液中提取基因组 DNA,这些患者接受了上颌两颗前磨牙拔牙治疗。根据根尖片上测量的 EARR 值将患者分为两组:显著吸收组(SG,EARR≥4mm)和正常组(NG,EARR<2mm)。在 NG 组中,EARR<1mm 的患者被命名为无吸收组(NonG)。使用筛选出的单核苷酸多态性(SNP)进行靶向下一代测序,并进行 Firh 逻辑回归分析以确定与 EARR 相关的遗传关联。对特定 SNP 进行基于单倍型的关联分析。
与 TNFSF11、TNFRSF11B、WNT3A、SFRP2、LRP6、P2RX7 和 LRP1 基因相关的 SNP 被发现与严重 EARR 显著相关(p<0.05,预 Bonferroni 校正 p 值)。此外,rs17525809、rs208294 和 rs1718119 P2RX7 的单倍型 CCA 在 SG 组中的频率更高。
极端表型分析确定了与 TNFSF11、TNFRSF11B、WNT3A、SFRP2、LRP6、P2RX7 和 LRP1 基因相关的 11 个 SNP 与韩国人群中严重的根吸收相关。这些发现将有助于开发预测性诊断工具,以识别正畸治疗过程中可能发生的严重根吸收。