<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen TH</submitter><funding>Ministry of Science and Technology, Taiwan</funding><funding>Kaohsiung Medical University Hospital</funding><pagination>E4079</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6862333</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(21)</volume><pubmed_abstract>Health of the metal industrial workers should be a noteworthy issue due to the hazard ofchronic exposure to metals or toxic elements. The interactions among multiple elements aresophisticated and may differ from person to person. Tumor necrosis factor-α (TNF-α) genepolymorphisms were supposed to be involved with the interactions because TNF-α plays animportant role in inflammation, a mechanism by which toxic elements cause threats to humanhealth. This research aimed to analyze the influence of TNF-αgene polymorphisms and multielementson serum TNF-α level. Blood multi-elements concentrations (lead, cadmium, arsenic,selenium, cobalt, copper, and zinc), serum TNF-α level, and TNF-α single nucleotidepolymorphisms (SNPs), including -238G > A (rs361525), -308G > A (rs1800629), -857C > T(rs1799724), -863C > A (rs1800630), and -1031T > C (rs1799964), were measured in 462 metalindustrial workers. We applied mixed-effect models to analyze the interactions among multielementsand TNF-α SNPs. Blood concentration of all elements were positively associated withserum TNF-α level, and the effects may be modified by TNF-α gene polymorphisms. Our studyrevealed that TNF-α -308A/A and -1031C/C may be susceptible genotypes, and thus we suggestthat those workers should take preventive measures against metal toxicity.</pubmed_abstract><journal>International journal of environmental research and public health</journal><pubmed_title>The Association of Serum TNF-α Levels and Blood Multi-Elements Modified by TNF-α Gene Polymorphisms in Metal Industrial Workers.</pubmed_title><pmcid>PMC6862333</pmcid><funding_grant_id>MOST 105-2314-B-037-018-MY3</funding_grant_id><funding_grant_id>KMUH107-7R85</funding_grant_id><pubmed_authors>Sun HY</pubmed_authors><pubmed_authors>Huang JJ</pubmed_authors><pubmed_authors>Chuang HY</pubmed_authors><pubmed_authors>Lee SS</pubmed_authors><pubmed_authors>Chen TH</pubmed_authors><pubmed_authors>Kung WS</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Association of Serum TNF-α Levels and Blood Multi-Elements Modified by TNF-α Gene Polymorphisms in Metal Industrial Workers.</name><description>Health of the metal industrial workers should be a noteworthy issue due to the hazard ofchronic exposure to metals or toxic elements. The interactions among multiple elements aresophisticated and may differ from person to person. Tumor necrosis factor-α (TNF-α) genepolymorphisms were supposed to be involved with the interactions because TNF-α plays animportant role in inflammation, a mechanism by which toxic elements cause threats to humanhealth. This research aimed to analyze the influence of TNF-αgene polymorphisms and multielementson serum TNF-α level. Blood multi-elements concentrations (lead, cadmium, arsenic,selenium, cobalt, copper, and zinc), serum TNF-α level, and TNF-α single nucleotidepolymorphisms (SNPs), including -238G > A (rs361525), -308G > A (rs1800629), -857C > T(rs1799724), -863C > A (rs1800630), and -1031T > C (rs1799964), were measured in 462 metalindustrial workers. We applied mixed-effect models to analyze the interactions among multielementsand TNF-α SNPs. Blood concentration of all elements were positively associated withserum TNF-α level, and the effects may be modified by TNF-α gene polymorphisms. Our studyrevealed that TNF-α -308A/A and -1031C/C may be susceptible genotypes, and thus we suggestthat those workers should take preventive measures against metal toxicity.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2024-11-19T15:27:29.296Z</modification><creation>2020-05-21T21:09:12Z</creation></dates><accession>S-EPMC6862333</accession><cross_references><pubmed>31652851</pubmed><doi>10.3390/ijerph16214079</doi></cross_references></HashMap>