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

IF 1.9 Q3 GENETICS & HEREDITY BMC genomic data Pub Date : 2024-06-03 DOI:10.1186/s12863-024-01215-z
Sangram Sandhu, Varun Sharma, Sachin Kumar, Niraj Rai, Pooran Chand
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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.

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通过量化与龋齿相关的变异,可以发现不同人群中影响等位基因频率的差异。
背景:龋齿(DC)是一种受遗传和环境因素影响的多方面口腔疾病。基因分型和测序技术的最新进展,如全基因组关联研究(GWAS),帮助研究人员确定了许多与龋齿相关的遗传变异,但由于大多数研究是在欧洲人群中进行的,而在亚洲人,特别是印度人中进行的研究很少,因此人们对这些变异在全球不同人群中的流行率和意义仍然知之甚少:本研究采用经验方法,筛选出与 DC 易感性相关的变体。使用 GWAS 摘要对这些变异进行了识别和注释。使用 Fst 对遗传亲和性进行了评估:对不同人群中等位基因频率的影响进行了研究,揭示了等位基因分布的差异。非洲人群的特定风险等位基因频率较高,而东亚和欧洲人群则表现出不同的特征。南亚人群显示出独特的遗传集群:我们的研究强调了 DC 遗传图谱的复杂性,并强调在将 GWAS 确定的标记物定义为确定的候选基因之前,需要在印度人中进行特定人群研究和验证。
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