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Association Signals Unveiled by a Comprehensive Gene Set Enrichment Analysis of Dental Caries Genome-Wide Association Studies

机译:龋病基因组全范围关联研究的全面基因集富集分析揭示关联信号

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摘要

Gene set-based analysis of genome-wide association study (GWAS) data has recently emerged as a useful approach to examine the joint effects of multiple risk loci in complex human diseases or phenotypes. Dental caries is a common, chronic, and complex disease leading to a decrease in quality of life worldwide. In this study, we applied the approaches of gene set enrichment analysis to a major dental caries GWAS dataset, which consists of 537 cases and 605 controls. Using four complementary gene set analysis methods, we analyzed 1331 Gene Ontology (GO) terms collected from the Molecular Signatures Database (MSigDB). Setting false discovery rate (FDR) threshold as 0.05, we identified 13 significantly associated GO terms. Additionally, 17 terms were further included as marginally associated because they were top ranked by each method, although their FDR is higher than 0.05. In total, we identified 30 promising GO terms, including ‘Sphingoid metabolic process,’ ‘Ubiquitin protein ligase activity,’ ‘Regulation of cytokine secretion,’ and ‘Ceramide metabolic process.’ These GO terms encompass broad functions that potentially interact and contribute to the oral immune response related to caries development, which have not been reported in the standard single marker based analysis. Collectively, our gene set enrichment analysis provided complementary insights into the molecular mechanisms and polygenic interactions in dental caries, revealing promising association signals that could not be detected through single marker analysis of GWAS data.
机译:最近,基于基因组的全基因组关联研究(GWAS)数据分析成为一种有用的方法,可用于检查多种风险基因座在复杂人类疾病或表型中的联合作用。龋齿是一种常见,慢性和复杂的疾病,导致世界范围内生活质量的下降。在这项研究中,我们将基因组富集分析的方法应用于主要的龋齿GWAS数据集,该数据集由537例病例和605例对照组成。使用四种互补的基因组分析方法,我们分析了从分子签名数据库(MSigDB)收集的1331个基因本体论(GO)术语。将错误发现率(FDR)阈值设置为0.05,我们确定了13个显着相关的GO项。此外,尽管FDR高于0.05,但每种方法都将17个术语列为边缘关联,因为它们在每种方法中均排名最高。总共,我们确定了30个有前途的GO术语,包括“鞘氨醇代谢过程”,“泛素蛋白连接酶活性”,“细胞因子分泌的调节”和“神经酰胺代谢过程”。这些GO术语包含可能相互作用并有助于与龋齿发展相关的口腔免疫反应,在基于标准单标记的分析中尚未报道。总的来说,我们的基因集富集分析提供了龋齿的分子机制和多基因相互作用的互补见解,揭示了有希望的关联信号,这些信号无法通过GWAS数据的单标记分析来检测。

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