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重新审视遗传因素对人类汞暴露及中毒的影响:一项范围综述

Revisiting Genetic Influence on Mercury Exposure and Intoxication in Humans: A Scoping Review.

作者信息

Crespo-Lopez Maria Elena, Barthelemy Jean Ludger, Lopes-Araújo Amanda, Santos-Sacramento Leticia, Leal-Nazaré Caio Gustavo, Soares-Silva Isabela, Macchi Barbarella M, do Nascimento José Luiz M, Arrifano Gabriela de Paula, Augusto-Oliveira Marcus

机构信息

Laboratório de Farmacologia Molecular, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém 66075-110, PA, Brazil.

Laboratório de Neuroquímica Molecular e Celular, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém 66075-110, PA, Brazil.

出版信息

Toxics. 2023 Nov 29;11(12):967. doi: 10.3390/toxics11120967.

Abstract

Human intoxication to mercury is a worldwide health problem. In addition to the type and length of exposure, the genetic background plays an important role in mercury poisoning. However, reviews on the genetic influence in mercury toxicity are scarce and not systematic. Therefore, this review aimed to systematically overview the most recent evidence on the genetic influence (using single nucleotide polymorphisms, SNPs) on human mercury poisoning. Three different databases (PubMed/Medline, Web of Science and Scopus) were searched, and 380 studies were found that were published from 2015 to 2022. After applying inclusion/exclusion criteria, 29 studies were selected and data on characteristics (year, country, profile of participants) and results (mercury biomarkers and quantitation, SNPs, main findings) were extracted and analyzed. The largest number of studies was performed in Brazil, mainly involving traditional populations of the Tapajós River basin. Most studies evaluated the influence of the SNPs related to genes of the glutathione system (GST, GPx, etc.), the ATP-binding cassette transporters and the metallothionein proteins. The recent findings regarding other SNPs, such as those of apolipoprotein E and brain-derived neurotrophic factor genes, are also highlighted. The importance of the exposure level is discussed considering the possible biphasic behavior of the genetic modulation phenomena that could explain some SNP associations. Overall, recommendations are provided for future studies based on the analysis obtained in this scoping review.

摘要

人类汞中毒是一个全球性的健康问题。除了接触汞的类型和时长外,遗传背景在汞中毒中也起着重要作用。然而,关于遗传因素对汞毒性影响的综述稀缺且缺乏系统性。因此,本综述旨在系统地概述有关遗传因素(使用单核苷酸多态性,即SNPs)对人类汞中毒影响的最新证据。检索了三个不同的数据库(PubMed/Medline、Web of Science和Scopus),共找到2015年至2022年发表的380项研究。在应用纳入/排除标准后,选取了29项研究,并提取和分析了有关特征(年份、国家、参与者概况)和结果(汞生物标志物及定量、SNPs、主要发现)的数据。研究数量最多的是在巴西进行的,主要涉及塔帕若斯河流域的传统人群。大多数研究评估了与谷胱甘肽系统(GST、GPx等)、ATP结合盒转运蛋白和金属硫蛋白相关基因的SNPs的影响。还强调了关于其他SNPs的最新发现,如载脂蛋白E和脑源性神经营养因子基因的SNPs。考虑到可能解释某些SNP关联的遗传调节现象的双相行为,讨论了接触水平的重要性。总体而言,基于本范围综述获得的分析结果,为未来研究提供了建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215f/10747380/5a9399c630da/toxics-11-00967-g001.jpg

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