Kermanshah University of Medical Sciences, School of Dentistry, Department of Orthodontics, Kermanshah, Iran.
Kermanshah University of Medical Sciences, School of Dentistry, Department of Oral and Maxillofacial Surgery, Kermanshah, Iran.
Int Orthod. 2020 Jun;18(2):191-202. doi: 10.1016/j.ortho.2020.01.012. Epub 2020 Mar 4.
The present meta-analysis is intended to assess the association between NSCL/P risk and methylenetetrahydrofolate reductase (MTHFR) A1298C polymorphism in case-control studies.
The Web of Science, PubMed/Medline, Scopus, and Cochrane Library databases were searched for related articles published by April 2019. Review Manager 5.3 was applied to measure the odds ratios (ORs) with 95% confidence interval (CI) in the analyses assessing the strength of the association between A1298C polymorphism and NSCL/P risk. Results Sixteen studies were involved and analysed in this meta-analysis. Altogether, the reviewed articles included 2677 NSCL/P patients and 3669 controls. The pooled ORs of the allele, homozygote, heterozygote, dominant, and recessive models were 1.11 (95% CI: 0.94, 1.30; P=0.21), 1.14 (95% CI: 0.94, 1.37; P=0.18), 0.98 (95% CI: 0.80, 1.20; P=0.87), 1.03 (95% CI: 0.86, 1.22; P=0.79), and 1.18 (95% CI: 0.99, 1.41; P=0.07), respectively. The analysis did not identify any significant association between the polymorphism and the risk of NSCL/P in any ethnicity or source of controls.
This meta-analysis revealed that A1298C polymorphism is not associated with NSCL/P susceptibility, and the subgroup analyses based on ethnicity and the source of cases further confirmed this result.
本荟萃分析旨在评估病例对照研究中 NSCL/P 风险与亚甲基四氢叶酸还原酶(MTHFR)A1298C 多态性之间的关联。
检索了 Web of Science、PubMed/Medline、Scopus 和 Cochrane Library 数据库,以获取截至 2019 年 4 月发表的相关文章。使用 Review Manager 5.3 评估评估 A1298C 多态性与 NSCL/P 风险之间关联强度的分析中的优势比(OR)和 95%置信区间(CI)。结果:共有 16 项研究纳入本荟萃分析。总共,回顾性文章包括 2677 例 NSCL/P 患者和 3669 例对照。等位基因、纯合子、杂合子、显性和隐性模型的汇总 OR 分别为 1.11(95%CI:0.94,1.30;P=0.21)、1.14(95%CI:0.94,1.37;P=0.18)、0.98(95%CI:0.80,1.20;P=0.87)、1.03(95%CI:0.86,1.22;P=0.79)和 1.18(95%CI:0.99,1.41;P=0.07)。分析未发现该多态性与任何种族或对照来源的 NSCL/P 风险之间存在任何显著关联。
本荟萃分析表明,A1298C 多态性与 NSCL/P 易感性无关,基于种族和病例来源的亚组分析进一步证实了这一结果。