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Genome-wide association Scan of dental caries in the permanent dentition

机译:全基因组关联恒牙中龋齿的扫描

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Background Over 90% of adults aged 20 years or older with permanent teeth have suffered from dental caries leading to pain, infection, or even tooth loss. Although caries prevalence has decreased over the past decade, there are still about 23% of dentate adults who have untreated carious lesions in the US. Dental caries is a complex disorder affected by both individual susceptibility and environmental factors. Approximately 35-55% of caries phenotypic variation in the permanent dentition is attributable to genes, though few specific caries genes have been identified. Therefore, we conducted the first genome-wide association study (GWAS) to identify genes affecting susceptibility to caries in adults. Methods Five independent cohorts were included in this study, totaling more than 7000 participants. For each participant, dental caries was assessed and genetic markers (single nucleotide polymorphisms, SNPs) were genotyped or imputed across the entire genome. Due to the heterogeneity among the five cohorts regarding age, genotyping platform, quality of dental caries assessment, and study design, we first conducted genome-wide association (GWA) analyses on each of the five independent cohorts separately. We then performed three meta-analyses to combine results for: (i) the comparatively younger, Appalachian cohorts (N?=?1483) with well-assessed caries phenotype, (ii) the comparatively older, non-Appalachian cohorts (N?=?5960) with inferior caries phenotypes, and (iii) all five cohorts (N?=?7443). Top ranking genetic loci within and across meta-analyses were scrutinized for biologically plausible roles on caries. Results Different sets of genes were nominated across the three meta-analyses, especially between the younger and older age cohorts. In general, we identified several suggestive loci (P-value?≤?10E-05) within or near genes with plausible biological roles for dental caries, including RPS6KA2 and PTK2B, involved in p38-depenedent MAPK signaling, and RHOU and FZD1, involved in the Wnt signaling cascade. Both of these pathways have been implicated in dental caries. ADMTS3 and ISL1 are involved in tooth development, and TLR2 is involved in immune response to oral pathogens. Conclusions As the first GWAS for dental caries in adults, this study nominated several novel caries genes for future study, which may lead to better understanding of cariogenesis, and ultimately, to improved disease predictions, prevention, and/or treatment.
机译:背景技术超过90%的20岁或以上拥有恒牙的成年人患有龋齿,导致疼痛,感染甚至牙齿脱落。尽管在过去十年中龋齿患病率下降了,但在美国仍有约23%的齿状成年人患有未经治疗的龋齿病变。龋齿是一种复杂的疾病,受个体易感性和环境因素的影响。永久性牙列中大约35-55%的龋齿表型变异可归因于基因,尽管目前尚未鉴定出特定的龋齿基因。因此,我们进行了首次全基因组关联研究(GWAS),以鉴定影响成年人对龋齿敏感性的基因。方法本研究包括5个独立的队列,共有7000多名参与者。对于每个参与者,评估龋齿并在整个基因组中对基因标记(单核苷酸多态性,SNP)进行基因分型或估算。由于年龄,基因分型平台,龋齿评估质量和研究设计这五个队列之间的异质性,我们首先分别对五个独立队列中的每一个进行了全基因组关联(GWA)分析。然后,我们进行了三项荟萃分析,以结合以下方面的结果:(i)相对年轻的阿巴拉契亚队列(N?=?1483)和良好评估的龋齿表型;(ii)相对较老的非阿巴拉契亚队列(N?= (5960)具有较差的龋表型,和(iii)所有五个队列(N == 7443)。对荟萃分析内和跨荟萃分析中排名靠前的遗传基因座进行仔细检查,以确定其在龋齿上的生物学上可能的作用。结果在三项荟萃分析中,特别是在年轻人和老年人之间,提名了不同的基因组。总的来说,我们确定了在龋齿可能具有生物学作用的基因内或附近的几个暗示性位点(P值≤10E-05),包括参与p38依赖的MAPK信号传导的RPS6KA2和PTK2B,以及涉及的RHOU和FZD1在Wnt信号级联中。这两种途径都与龋齿有关。 ADMTS3和ISL1参与牙齿发育,而TLR2参与对口腔病原体的免疫反应。结论作为第一个成人龋齿的GWAS,该研究提名了几个新的龋齿基因用于未来的研究,这可能导致人们更好地了解龋齿,并最终改善疾病的预测,预防和/或治疗。

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