Associated Effect of SLC40A1 and TMPRSS6 Polymorphisms on Iron Overload
Mutations in the ferroportin (FPN) gene SLC40A1 alter iron recycling and cause disturbances in iron homeostasis. The variants of TMPRSS6 contribute to the development of iron deficiencies. In this study, we determined the role of FPN and TMPRSS6 gene polymorphisms in the modulation of iron homeostas...
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Published in: | Metabolites Vol. 12; no. 10; p. 919 |
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Abstract | Mutations in the ferroportin (FPN) gene SLC40A1 alter iron recycling and cause disturbances in iron homeostasis. The variants of TMPRSS6 contribute to the development of iron deficiencies. In this study, we determined the role of FPN and TMPRSS6 gene polymorphisms in the modulation of iron homeostasis based on biochemical parameters. PCR analysis and sequencing were performed to determine the single nucleotide polymorphisms (SNPs) SLC40A1 c.44−24G>C (rs1439816), SLC40A1 c.663T>C (rs2304704), and TMPRSS6 c.2207T>C (rs855791). Hemoglobin concentration and iron status were determined by standard procedures. We studied 79 iron-loaded individuals for SLC40A1 polymorphisms. Interestingly, 35/79 individuals with SLC40A1 SNPs also carried a TMPRSS6 c.2207T>C polymorphism. The biochemical values of the iron overloaded individuals were compared to those of the individuals carrying TMPRSS6 SNPs and the healthy individuals (wild-type group). The ferritin concentration, transferrin saturation % (TS%), and hemoglobin concentration were significantly higher in the participants with FPN SNPs than in the other three groups. The ferritin concentration and TS% were higher in participants with both SLC40A1 and TMPRSS6 SNPs than in the TMPRSS6 and wild-type groups, while hemoglobin concentration was significantly higher than that in the TMPRSS6 SNP group only. The participants with TMPRSS6 SNPs had significantly lower ferritin concentration, TS%, and hemoglobin concentration than all the other groups. SLC40A1 and TMPRSS6 SNPs might act in the opposite direction, preventing the development of severe iron overload, and the modulation of the iron status by TMPRSS6 SNPs might provide protection. |
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AbstractList | Mutations in the ferroportin (FPN) gene SLC40A1 alter iron recycling and cause disturbances in iron homeostasis. The variants of TMPRSS6 contribute to the development of iron deficiencies. In this study, we determined the role of FPN and TMPRSS6 gene polymorphisms in the modulation of iron homeostasis based on biochemical parameters. PCR analysis and sequencing were performed to determine the single nucleotide polymorphisms (SNPs) SLC40A1 c.44–24G>C (rs1439816), SLC40A1 c.663T>C (rs2304704), and TMPRSS6 c.2207T>C (rs855791). Hemoglobin concentration and iron status were determined by standard procedures. We studied 79 iron-loaded individuals for SLC40A1 polymorphisms. Interestingly, 35/79 individuals with SLC40A1 SNPs also carried a TMPRSS6 c.2207T>C polymorphism. The biochemical values of the iron overloaded individuals were compared to those of the individuals carrying TMPRSS6 SNPs and the healthy individuals (wild-type group). The ferritin concentration, transferrin saturation % (TS%), and hemoglobin concentration were significantly higher in the participants with FPN SNPs than in the other three groups. The ferritin concentration and TS% were higher in participants with both SLC40A1 and TMPRSS6 SNPs than in the TMPRSS6 and wild-type groups, while hemoglobin concentration was significantly higher than that in the TMPRSS6 SNP group only. The participants with TMPRSS6 SNPs had significantly lower ferritin concentration, TS%, and hemoglobin concentration than all the other groups. SLC40A1 and TMPRSS6 SNPs might act in the opposite direction, preventing the development of severe iron overload, and the modulation of the iron status by TMPRSS6 SNPs might provide protection. Mutations in the ferroportin (FPN) gene SLC40A1 alter iron recycling and cause disturbances in iron homeostasis. The variants of TMPRSS6 contribute to the development of iron deficiencies. In this study, we determined the role of FPN and TMPRSS6 gene polymorphisms in the modulation of iron homeostasis based on biochemical parameters. PCR analysis and sequencing were performed to determine the single nucleotide polymorphisms (SNPs) SLC40A1 c.44–24G>C (rs1439816), SLC40A1 c.663T>C (rs2304704), and TMPRSS6 c.2207T>C (rs855791). Hemoglobin concentration and iron status were determined by standard procedures. We studied 79 iron-loaded individuals for SLC40A1 polymorphisms. Interestingly, 35/79 individuals with SLC40A1 SNPs also carried a TMPRSS6 c.2207T>C polymorphism. The biochemical values of the iron overloaded individuals were compared to those of the individuals carrying TMPRSS6 SNPs and the healthy individuals (wild-type group). The ferritin concentration, transferrin saturation % (TS%), and hemoglobin concentration were significantly higher in the participants with FPN SNPs than in the other three groups. The ferritin concentration and TS% were higher in participants with both SLC40A1 and TMPRSS6 SNPs than in the TMPRSS6 and wild-type groups, while hemoglobin concentration was significantly higher than that in the TMPRSS6 SNP group only. The participants with TMPRSS6 SNPs had significantly lower ferritin concentration, TS%, and hemoglobin concentration than all the other groups. SLC40A1 and TMPRSS6 SNPs might act in the opposite direction, preventing the development of severe iron overload, and the modulation of the iron status by TMPRSS6 SNPs might provide protection. Mutations in the ferroportin (FPN) gene SLC40A1 alter iron recycling and cause disturbances in iron homeostasis. The variants of TMPRSS6 contribute to the development of iron deficiencies. In this study, we determined the role of FPN and TMPRSS6 gene polymorphisms in the modulation of iron homeostasis based on biochemical parameters. PCR analysis and sequencing were performed to determine the single nucleotide polymorphisms (SNPs) SLC40A1 c.44−24G>C (rs1439816), SLC40A1 c.663T>C (rs2304704), and TMPRSS6 c.2207T>C (rs855791). Hemoglobin concentration and iron status were determined by standard procedures. We studied 79 iron-loaded individuals for SLC40A1 polymorphisms. Interestingly, 35/79 individuals with SLC40A1 SNPs also carried a TMPRSS6 c.2207T>C polymorphism. The biochemical values of the iron overloaded individuals were compared to those of the individuals carrying TMPRSS6 SNPs and the healthy individuals (wild-type group). The ferritin concentration, transferrin saturation % (TS%), and hemoglobin concentration were significantly higher in the participants with FPN SNPs than in the other three groups. The ferritin concentration and TS% were higher in participants with both SLC40A1 and TMPRSS6 SNPs than in the TMPRSS6 and wild-type groups, while hemoglobin concentration was significantly higher than that in the TMPRSS6 SNP group only. The participants with TMPRSS6 SNPs had significantly lower ferritin concentration, TS%, and hemoglobin concentration than all the other groups. SLC40A1 and TMPRSS6 SNPs might act in the opposite direction, preventing the development of severe iron overload, and the modulation of the iron status by TMPRSS6 SNPs might provide protection. |
Author | Granata, Francesca Brancaleoni, Valentina Graziadei, Giovanna Di Pierro, Elena Duca, Lorena Nava, Isabella |
AuthorAffiliation | Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, U.O.C. Medicina Generale, 20122 Milano, Italy |
AuthorAffiliation_xml | – name: Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, U.O.C. Medicina Generale, 20122 Milano, Italy |
Author_xml | – sequence: 1 givenname: Lorena orcidid: 0000-0002-2008-3187 surname: Duca fullname: Duca, Lorena organization: Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, U.O.C. Medicina Generale, 20122 Milano, Italy – sequence: 2 givenname: Francesca orcidid: 0000-0002-1115-3374 surname: Granata fullname: Granata, Francesca organization: Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, U.O.C. Medicina Generale, 20122 Milano, Italy – sequence: 3 givenname: Elena orcidid: 0000-0002-1413-1349 surname: Di Pierro fullname: Di Pierro, Elena organization: Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, U.O.C. Medicina Generale, 20122 Milano, Italy – sequence: 4 givenname: Valentina orcidid: 0000-0003-1521-3319 surname: Brancaleoni fullname: Brancaleoni, Valentina organization: Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, U.O.C. Medicina Generale, 20122 Milano, Italy – sequence: 5 givenname: Giovanna orcidid: 0000-0002-6801-5730 surname: Graziadei fullname: Graziadei, Giovanna organization: Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, U.O.C. Medicina Generale, 20122 Milano, Italy – sequence: 6 givenname: Isabella orcidid: 0000-0003-4106-0088 surname: Nava fullname: Nava, Isabella organization: Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, U.O.C. Medicina Generale, 20122 Milano, Italy |
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Cites_doi | 10.1038/ng.130 10.1074/jbc.M110.173096 10.1007/s00439-004-1166-y 10.1002/ajh.21465 10.1038/ng.462 10.1016/j.bcmd.2003.08.003 10.1016/j.gene.2020.144767 10.1371/journal.pone.0082127 10.1007/s12263-014-0442-2 10.1007/s00277-008-0590-9 10.1002/ajh.23929 10.1111/j.1365-2141.2010.08306.x 10.1038/ng.456 10.1016/j.beha.2004.08.025 10.1016/j.jmb.2008.12.063 10.1093/hmg/dds028 10.1016/j.sjbs.2020.11.004 10.1053/j.seminhematol.2009.06.006 10.1111/j.1365-2141.2012.09198.x 10.1016/S1097-2765(00)80425-6 10.1016/j.cmet.2005.01.003 10.1016/j.bcmd.2007.07.009 10.1111/j.1600-0609.2009.01340.x 10.1053/beha.2002.0207 10.1182/blood-2011-04-348698 10.1016/j.cmet.2015.09.006 10.3324/haematol.2019.232124 10.1182/blood-2010-06-287292 10.1515/hsz-2011-0221 10.1101/475467 10.1016/j.bcmd.2015.04.001 |
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Keywords | transferrin saturation iron overload ferritin TMPRSS6 SLC40A1 iron ferroportin iron deficiency matriptase-2 hemoglobin |
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Snippet | Mutations in the ferroportin (FPN) gene SLC40A1 alter iron recycling and cause disturbances in iron homeostasis. The variants of TMPRSS6 contribute to the... Mutations in the ferroportin (FPN) gene SLC40A1 alter iron recycling and cause disturbances in iron homeostasis. The variants of TMPRSS6 contribute to the... |
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StartPage | 919 |
SubjectTerms | Amino acids Anemia Blood & organ donations Ferritin ferroportin Gene polymorphism Genes Hemoglobin Homeostasis Iron iron overload Liver diseases matriptase-2 Metabolic disorders Mutation Polymorphism Proteins Single-nucleotide polymorphism SLC40A1 TMPRSS6 Transferrin |
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Title | Associated Effect of SLC40A1 and TMPRSS6 Polymorphisms on Iron Overload |
URI | https://www.ncbi.nlm.nih.gov/pubmed/36295822 https://www.proquest.com/docview/2728495183 https://search.proquest.com/docview/2729521817 https://pubmed.ncbi.nlm.nih.gov/PMC9612384 https://doaj.org/article/630ba60cbe4e47e7b3cc42fd2d622d47 |
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