Department of Pediatrics, Islamic Azad University of Yazd, Yazd, Iran.
Department of Medical Genetics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
J Orthop Surg Res. 2024 Jun 10;19(1):345. doi: 10.1186/s13018-024-04834-5.
Congenital talipes equinovarus (CTEV) is a prevalent pediatric deformity with a multifactorial etiology. The objective of this meta-analysis was to explore the association between genetic variations in COL9A1 and the susceptibility to CTEV.
A comprehensive analysis of pertinent literature released before November 15, 2023, in electronic bibliographic databases was carried out. The importance of the connection was clarified through odds ratios (ORs) with 95% confidence intervals (CIs), utilizing random or fixed-effects models depending on study heterogeneity. Statistical analysis was executed using Comprehensive Meta-Analysis software (Version 4.0).
A total of eight case-control studies involving 833 CTEV patients and 1280 healthy individuals were included in the analysis. Among these, four studies investigated the rs1135056 variant, encompassing 432 CTEV cases and 603 controls; two studies examined the rs35470562 variant, with 189 CTEV cases and 378 controls; and two studies explored the rs592121 variant, including 212 CTEV cases and 299 controls. The results revealed a significant association between the rs1135056 and rs35470562 polymorphisms in the COL9A1 gene, suggesting an increased risk of CTEV in the overall population. Conversely, no such association was found for the rs592121 variant.
Our findings reveal a substantial association between the genetic variants COL9A1 rs1135056 and rs35470562 and susceptibility to CTEV. Conversely, the variant rs592121 did not exhibit any corresponding link. However, the limitations imposed by the small study population have compromised the statistical reliability and generalizability of the results.
先天性马蹄内翻足(CTEV)是一种常见的儿科畸形,具有多因素病因。本荟萃分析的目的是探讨 COL9A1 基因遗传变异与 CTEV 易感性之间的关系。
对 2023 年 11 月 15 日前电子文献数据库中发布的相关文献进行全面分析。通过优势比(OR)及其 95%置信区间(CI),利用随机或固定效应模型,根据研究异质性来阐明相关性的重要性。统计分析使用 Comprehensive Meta-Analysis 软件(版本 4.0)进行。
共纳入 8 项病例对照研究,包括 833 例 CTEV 患者和 1280 名健康对照者。其中,4 项研究探讨了 rs1135056 变异,包括 432 例 CTEV 病例和 603 例对照者;2 项研究检测了 rs35470562 变异,包括 189 例 CTEV 病例和 378 例对照者;2 项研究研究了 rs592121 变异,包括 212 例 CTEV 病例和 299 例对照者。结果表明,COL9A1 基因的 rs1135056 和 rs35470562 多态性与 CTEV 之间存在显著相关性,提示总体人群 CTEV 风险增加。相反,rs592121 变异与 CTEV 之间无相关性。
本研究结果表明,COL9A1 基因的 rs1135056 和 rs35470562 遗传变异与 CTEV 易感性之间存在显著相关性。相反,rs592121 变异与 CTEV 之间无相关性。然而,研究人群较小限制了结果的统计可靠性和普遍性。