Suppr超能文献

一项在中国汉族人群中进行的病例对照研究表明,白细胞介素-17RC 基因中的单核苷酸多态性 rs708567 与青少年特发性脊柱侧凸的易感性和曲线严重程度相关。

A single-nucleotide polymorphism rs708567 in the IL-17RC gene is associated with a susceptibility to and the curve severity of adolescent idiopathic scoliosis in a Chinese Han population: a case-control study.

机构信息

Spine Surgery Department, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.

出版信息

BMC Musculoskelet Disord. 2012 Sep 21;13:181. doi: 10.1186/1471-2474-13-181.

Abstract

BACKGROUND

Although the pathogenesis of adolescent idiopathic scoliosis (AIS) remains controversial, genetic factors are thought to play key roles in the development of AIS. In a recent genome-wide association study, a polymorphism in the interleukin-17 receptor C (IL-17RC) gene was reported to be associated with the susceptibility to AIS, implicating IL-17RC as a novel predisposing gene for AIS. However, as this association has not been replicated in other populations, its global applicability remains unclear.

METHODS

A total of 529 Chinese girls with AIS and 512 healthy age-matched controls were recruited in this case-control study from June 2007 to December 2009. Polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) analysis was performed to detect the genotype of the single-nucleotide polymorphism (SNP) rs708567 in the IL-17RC gene. Case-control and case-only studies were performed to determine the association between the IL-17RC gene polymorphism and the susceptibility to and curve severity of AIS.

RESULTS

The GG genotype and G allele frequencies were significantly higher in the AIS patients than in the controls (χ2 test: P = 0.023 and 0.028, respectively). The risk for the GG genotype is 1.550-fold (95% CI: 1.062 - 2.261) higher than the AG genotype, and the risk for the G allele is 1.507-fold (95% CI: 1.046 - 2.172) higher than the A allele. Additionally, a subgroup of skeletally mature AIS patients (n = 241) who carried the GG genotype showed a significantly higher mean maximum Cobb angle than those carrying the AG genotype (36.01 ± 13.12° vs. 28.92 ± 7.43°, P = 0.007).

CONCLUSIONS

This study confirms the significant association between the IL-17RC gene polymorphism and the susceptibility to and curve severity of AIS in a Chinese Han population, suggesting that the IL-17RC gene is an AIS-predisposing gene in Chinese Han population.

摘要

背景

尽管青少年特发性脊柱侧凸(AIS)的发病机制仍存在争议,但遗传因素被认为在 AIS 的发展中起关键作用。在最近的全基因组关联研究中,白细胞介素-17 受体 C(IL-17RC)基因中的一个多态性被报道与 AIS 的易感性相关,表明 IL-17RC 是 AIS 的一个新的易感基因。然而,由于该关联尚未在其他人群中得到复制,其全球适用性尚不清楚。

方法

本病例对照研究共纳入 2007 年 6 月至 2009 年 12 月期间的 529 例中国女孩 AIS 患者和 512 名年龄匹配的健康对照。采用聚合酶链反应限制片段长度多态性(PCR-RFLP)分析检测 IL-17RC 基因中单核苷酸多态性(SNP)rs708567 的基因型。进行病例对照和病例仅研究以确定 IL-17RC 基因多态性与 AIS 的易感性和曲线严重程度之间的关联。

结果

AIS 患者的 GG 基因型和 G 等位基因频率明显高于对照组(卡方检验:P = 0.023 和 0.028)。GG 基因型的风险是 AG 基因型的 1.550 倍(95%CI:1.062-2.261),G 等位基因的风险是 A 等位基因的 1.507 倍(95%CI:1.046-2.172)。此外,携带 GG 基因型的骨骼成熟 AIS 患者亚组(n = 241)的平均最大 Cobb 角明显高于携带 AG 基因型的患者(36.01 ± 13.12°比 28.92 ± 7.43°,P = 0.007)。

结论

本研究在中国汉族人群中证实了 IL-17RC 基因多态性与 AIS 的易感性和曲线严重程度之间的显著关联,表明 IL-17RC 基因是中国汉族人群中 AIS 的易感基因。

相似文献

引用本文的文献

2
Genetics and pathogenesis of scoliosis.脊柱侧弯的遗传学与发病机制。
N Am Spine Soc J. 2024 Sep 6;20:100556. doi: 10.1016/j.xnsj.2024.100556. eCollection 2024 Dec.

本文引用的文献

7
IL-17RC: a partner in IL-17 signaling and beyond.IL-17RC:IL-17 信号通路的伙伴及其它作用。
Semin Immunopathol. 2010 Mar;32(1):33-42. doi: 10.1007/s00281-009-0185-0. Epub 2009 Dec 13.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验