Analysis of polymorphic loci of candidate genes in patients with occupational diseases

Q4 Medicine
Y. Chernyak, A. P. Merinova
{"title":"Analysis of polymorphic loci of candidate genes in patients with occupational diseases","authors":"Y. Chernyak, A. P. Merinova","doi":"10.47470/0016-9900-2023-102-7-689-694","DOIUrl":null,"url":null,"abstract":"Introduction. Development and progress features of vibration syndrome (VS) and noise-induced hearing loss (NIHL) are determined by genetic factors to a certain extent. The latter define the relevance of the search for individual approaches to  prevention and medical support of patients with these occupational diseases. \nThe aim of the study was to investigate the genotypes distribution of polymorphic loci of candidate genes in patients with occupational diseases caused by vibration and noise impact. \nMaterials and methods. Polymorphic variants of the HSPA1B (rs1061581), IL17A (rs2275913), IL10 (rs1800872), and TNF-α (rs1800629) genes of three hundred ninety eight males were studied using PCR-RFLP and real-time PCR methods, including 268  patients with VS divided into two groups: VShtv (n = 117) and VScomb (n = 151), in which VS was caused by exposure to hand-transmitted vibration (HTV) or combined exposure to HTV and whole-body vibration (COMB), respectively. The study also involved 96 patients with occupational NIHL diagnosis and 34 individuals of the comparison group without occupational contact with physical factors. \nResults. The increase in GG-HSPA1B (1267A/G) genotype frequency  (p=0.058) was found in VScomb patients compared with those from the VShtv group. There was a significant difference in carriers of the C/C genotype of the IL10 (rs1800872) polymorphic locus in the group of NIHL patients relative to the comparison group (p=0.036). The results of regression analysis indicate the carriage of the A allele to reduce the risk of NIHL development. \nLimitations. The limitations include the number of examined cases in all groups, especially in comparison group and the lack of groups of workers with no occupational exposure to a physical factor.   \nConclusion. The obtained results expand the understanding of the genetic features able to determine sensitivity to the physical factors exposure that define the development of occupational pathology and the issues to be resolved at the next stage of research.","PeriodicalId":12550,"journal":{"name":"Gigiena i sanitariia","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gigiena i sanitariia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47470/0016-9900-2023-102-7-689-694","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction. Development and progress features of vibration syndrome (VS) and noise-induced hearing loss (NIHL) are determined by genetic factors to a certain extent. The latter define the relevance of the search for individual approaches to  prevention and medical support of patients with these occupational diseases. The aim of the study was to investigate the genotypes distribution of polymorphic loci of candidate genes in patients with occupational diseases caused by vibration and noise impact. Materials and methods. Polymorphic variants of the HSPA1B (rs1061581), IL17A (rs2275913), IL10 (rs1800872), and TNF-α (rs1800629) genes of three hundred ninety eight males were studied using PCR-RFLP and real-time PCR methods, including 268  patients with VS divided into two groups: VShtv (n = 117) and VScomb (n = 151), in which VS was caused by exposure to hand-transmitted vibration (HTV) or combined exposure to HTV and whole-body vibration (COMB), respectively. The study also involved 96 patients with occupational NIHL diagnosis and 34 individuals of the comparison group without occupational contact with physical factors. Results. The increase in GG-HSPA1B (1267A/G) genotype frequency  (p=0.058) was found in VScomb patients compared with those from the VShtv group. There was a significant difference in carriers of the C/C genotype of the IL10 (rs1800872) polymorphic locus in the group of NIHL patients relative to the comparison group (p=0.036). The results of regression analysis indicate the carriage of the A allele to reduce the risk of NIHL development. Limitations. The limitations include the number of examined cases in all groups, especially in comparison group and the lack of groups of workers with no occupational exposure to a physical factor.   Conclusion. The obtained results expand the understanding of the genetic features able to determine sensitivity to the physical factors exposure that define the development of occupational pathology and the issues to be resolved at the next stage of research.
职业病患者候选基因多态性位点分析
介绍。振动综合征(VS)和噪声性听力损失(NIHL)的发生发展特点在一定程度上由遗传因素决定。后者界定了为这些职业病患者寻求预防和医疗支助的个别办法的相关性。本研究旨在探讨振动和噪声影响下职业病患者候选基因多态性位点的基因型分布。材料和方法。采用PCR- rflp和real-time PCR方法,对338例男性VS患者的HSPA1B (rs1061581)、IL17A (rs2275913)、IL10 (rs1800872)和TNF-α (rs1800629)基因多态性变异进行了研究,将268例VS患者分为VShtv组(n = 117)和VScomb组(n = 151),其中VS分别由暴露于手传播振动(HTV)或暴露于HTV和全身振动(COMB)联合引起。本研究还包括96例职业性NIHL诊断患者和34例没有职业性接触物理因素的对照组。结果。与VShtv组相比,VScomb组GG-HSPA1B (1267A/G)基因型频率升高(p=0.058)。NIHL患者组IL10 (rs1800872)多态性位点C/C基因型携带者与对照组比较差异有统计学意义(p=0.036)。回归分析结果表明,携带A等位基因可降低NIHL发生的风险。的局限性。局限性包括在所有组中检查病例的数量,特别是在对照组中,以及缺乏没有职业接触物理因素的工人组。结论。所获得的结果扩大了对遗传特征的理解,这些特征能够决定对确定职业病理学发展的物理因素暴露的敏感性,以及下一阶段研究需要解决的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Gigiena i sanitariia
Gigiena i sanitariia Environmental Science-Pollution
CiteScore
0.80
自引率
0.00%
发文量
192
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信