Department of Oral and Maxillofacial Surgery, Fellowship in Maxillofacial Trauma, Health Services, Kurdistan University of Medical Sciences, Sanandaj 6617713446, Iran.
Department of Oral and Maxillofacial Surgery, Fellowship in Maxillofacial Trauma, School of Dentistry, Tehran University of Medical Sciences, Tehran 1439955991, Iran.
Medicina (Kaunas). 2021 Oct 13;57(10):1095. doi: 10.3390/medicina57101095.
( and ) genes have polymorphisms in accordance with slow and rapid acetylator phenotypes with a role in the development of head and neck cancers (HNCs). Herein, we aimed to evaluate the association of and polymorphisms with susceptibility to HNCs in an updated meta-analysis. A search was comprehensively performed in four databases (Web of Science, Scopus, PubMed/Medline, and Cochrane Library until 8 July 2021). The effect sizes, odds ratio (OR) along with 95% confidence interval (CI) were computed. Trial sequential analysis (TSA), publication bias and sensitivity analysis were conducted. : Twenty-eight articles including eight studies reporting polymorphism and twenty-five studies reporting polymorphism were involved in the meta-analysis. The results showed that individuals with slow acetylators of polymorphism are at higher risk for HNC OR: 1.22 (95% CI: 1.02, 1.46; = 0.03). On subgroup analysis, ethnicity, control source, and genotyping methods were found to be significant factors in the association of polymorphism with the HNC risk. TSA identified that the amount of information was not large enough and that more studies are needed to establish associations. Slow acetylators in polymorphism were related to a high risk of HNC. However, there was no relationship between polymorphism and the risk of HNC.
( NAT1 和 NAT2 )基因存在与慢乙酰化和快乙酰化表型相符的多态性,与头颈部癌症(HNCs)的发展有关。在此,我们旨在通过更新的荟萃分析来评估 NAT1 和 NAT2 多态性与 HNC 易感性的相关性。在四个数据库(Web of Science、Scopus、PubMed/Medline 和 Cochrane Library)中全面进行了搜索,截至 2021 年 7 月 8 日。计算了效应大小、比值比(OR)及其 95%置信区间(CI)。进行了试验序贯分析(TSA)、发表偏倚和敏感性分析。结果:纳入了 28 篇文章,其中 8 篇报道了 NAT1 多态性,25 篇报道了 NAT2 多态性。结果表明, NAT1 多态性的慢乙酰化个体患 HNC 的风险更高 OR:1.22(95%CI:1.02,1.46; P = 0.03)。亚组分析显示,种族、对照来源和基因分型方法是 NAT1 多态性与 HNC 风险相关性的重要因素。TSA 确定信息数量不够大,需要更多的研究来建立相关性。 NAT1 多态性中的慢乙酰化与 HNC 的高风险相关。然而, NAT2 多态性与 HNC 的风险之间没有关系。