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量化与龋齿相关的变异可以揭示不同人群中效应等位基因频率的差异。

Quantifying variations associated with dental caries reveals disparity in effect allele frequencies across diverse populations.

机构信息

Ancient DNA Lab, Birbal Sahni Institute of Palaeosciences, 226607, Lucknow, Uttar Pradesh, India.

Department of Prosthodontics, Faculty of Dental Sciences, King George's Medical University, 226003, Lucknow, India.

出版信息

BMC Genom Data. 2024 Jun 3;25(1):50. doi: 10.1186/s12863-024-01215-z.

Abstract

BACKGROUND

Dental caries (DC) is a multifaceted oral condition influenced by genetic and environmental factors. Recent advancements in genotyping and sequencing technologies, such as Genome-Wide Association Studies (GWAS) have helped researchers to identify numerous genetic variants associated with DC, but their prevalence and significance across diverse global populations remain poorly understood as most of the studies were conducted in European populations, and very few were conducted in Asians specifically in Indians.

AIM

This study aimed to evaluate the genetic affinity of effect alleles associated with DC to understand the genetic relationship between global populations with respect to the Indian context.

METHODOLOGY

This present study used an empirical approach in which variants associated with DC susceptibility were selected. These variants were identified and annotated using the GWAS summary. The genetic affinity was evaluated using Fst.

RESULTS

The effect of allele frequencies among different populations was examined, revealing variations in allele distribution. African populations exhibited higher frequencies of specific risk alleles, whereas East Asian and European populations displayed distinct profiles. South Asian populations showed a unique genetic cluster.

CONCLUSION

Our study emphasises the complex genetic landscape of DC and highlights the need for population-specific research as well as validation of GWAS-identified markers in Indians before defining them as established candidate genes.

摘要

背景

龋齿(DC)是一种受遗传和环境因素影响的多方面口腔状况。基因分型和测序技术的最新进展,如全基因组关联研究(GWAS),帮助研究人员识别了许多与 DC 相关的遗传变异,但由于大多数研究是在欧洲人群中进行的,而在亚洲人群,特别是在印度人中进行的研究很少,因此这些遗传变异在不同全球人群中的普遍性和意义仍知之甚少。

目的

本研究旨在评估与 DC 相关的效应等位基因的遗传亲和力,以了解全球人群与印度人群之间的遗传关系。

方法

本研究采用实证方法,选择与 DC 易感性相关的变异。这些变异是使用 GWAS 摘要进行识别和注释的。使用 Fst 评估遗传亲和力。

结果

研究检查了不同人群中等位基因频率的影响,揭示了等位基因分布的变化。非洲人群显示出特定风险等位基因的更高频率,而东亚和欧洲人群则显示出不同的特征。南亚人群表现出独特的遗传聚类。

结论

我们的研究强调了 DC 的复杂遗传景观,并强调需要进行特定于人群的研究,以及在将 GWAS 确定的标记定义为既定候选基因之前,在印度人中验证这些标记。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b075/11149341/81011e8ed869/12863_2024_1215_Fig1_HTML.jpg

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