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对亚马逊地区土著人群中与汞代谢相关基因的基因组研究。

Genomic investigation on genes related to mercury metabolism in Amazonian indigenous populations.

机构信息

Núecleo de Pesquisas em Oncologia, Unidade de Alta Complexidade em Oncologia, Hospital Universitário João de Barros Barreto, 66073-005 Belém, Pará, Brazil.

Núecleo de Pesquisas em Oncologia, Unidade de Alta Complexidade em Oncologia, Hospital Universitário João de Barros Barreto, 66073-005 Belém, Pará, Brazil.

出版信息

Sci Total Environ. 2024 May 1;923:171232. doi: 10.1016/j.scitotenv.2024.171232. Epub 2024 Feb 23.

Abstract

Studies have identified elevated levels of mercury in Amazonian Indigenous individuals, highlighting them as one of the most exposed to risks. In the unique context of the Brazilian Indigenous population, it is crucial to identify genetic variants with clinical significance to better understand vulnerability to mercury and its adverse effects. Currently, there is a lack of research on the broader genomic profile of Indigenous people, particularly those from the Amazon region, concerning mercury contamination. Therefore, the aim of this study was to assess the genomic profile related to the processes of mercury absorption, distribution, metabolism, and excretion in 64 Indigenous individuals from the Brazilian Amazon. We aimed to determine whether these individuals exhibit a higher susceptibility to mercury exposure. Our study identified three high-impact variants (GSTA1 rs1051775, GSTM1 rs1183423000, and rs1241704212), with the latter two showing a higher frequency in the study population compared to global populations. Additionally, we discovered seven new variants with modifier impact and a genomic profile different from the worldwide populations. These genetic variants may predispose the study population to more harmful mercury exposure compared to global populations. As the first study to analyze broader genomics of mercury metabolism pathways in Brazilian Amazonian Amerindians, we emphasize that our research aims to contribute to public policies by utilizing genomic investigation as a method to identify populations with a heightened susceptibility to mercury exposure.

摘要

研究已经确定亚马逊地区的土著人群体体内的汞含量升高,突显了他们是面临最大风险的群体之一。在巴西土著人群体这一独特的背景下,确定具有临床意义的遗传变异体对于更好地了解对汞及其不良影响的易感性至关重要。目前,针对更广泛的汞污染的土著人群体基因组特征(尤其是来自亚马逊地区的人群)的研究还很缺乏。因此,本研究旨在评估与汞吸收、分布、代谢和排泄过程相关的基因组特征,研究对象是来自巴西亚马逊地区的 64 名土著个体。我们旨在确定这些个体是否表现出对汞暴露的更高敏感性。我们的研究确定了三个具有高影响的变异体(GSTA1 rs1051775、GSTM1 rs1183423000 和 rs1241704212),后两者在研究人群中的出现频率高于全球人群。此外,我们还发现了七个具有修饰作用的新变异体和与全球人群不同的基因组特征。这些遗传变异体可能使研究人群比全球人群更容易受到更有害的汞暴露。作为第一项分析巴西亚马逊地区美洲印第安人汞代谢途径更广泛基因组的研究,我们强调,我们的研究旨在通过利用基因组研究作为一种方法来识别对汞暴露更敏感的人群,为公共政策做出贡献。

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