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Association between SOD1, CAT, GSHPX1 polymorphisms and the risk of inflammatory bowel disease in the Polish population

PURPOSE: The main aim of this study was investigate the association between the genetic polymorphism of antioxidant enzyme genes: SOD1, CAT and GSHPX1 and the risk of inflammatory bowel disease (IBD), including Crohn’s disease and ulcerative colitis in the Polish population. METHODS: A total of 445...

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Autores principales: Mrowicka, Malgorzata, Mrowicki, Jerzy, Mik, Michal, Wojtczak, Radoslaw, Dziki, Lukasz, Dziki, Adam, Majsterek, Ireneusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752524/
https://www.ncbi.nlm.nih.gov/pubmed/29312611
http://dx.doi.org/10.18632/oncotarget.22675
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author Mrowicka, Malgorzata
Mrowicki, Jerzy
Mik, Michal
Wojtczak, Radoslaw
Dziki, Lukasz
Dziki, Adam
Majsterek, Ireneusz
author_facet Mrowicka, Malgorzata
Mrowicki, Jerzy
Mik, Michal
Wojtczak, Radoslaw
Dziki, Lukasz
Dziki, Adam
Majsterek, Ireneusz
author_sort Mrowicka, Malgorzata
collection PubMed
description PURPOSE: The main aim of this study was investigate the association between the genetic polymorphism of antioxidant enzyme genes: SOD1, CAT and GSHPX1 and the risk of inflammatory bowel disease (IBD), including Crohn’s disease and ulcerative colitis in the Polish population. METHODS: A total of 445 subjects including 200 patients with IBD and 245 controls were allowed in this study. We determined activity of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx1) and examination their association with the SNPs of respective genes (SOD1 +35A/C, CAT C-262T and GSHPX1 Pro197Leu). RFLP technique was used to determine the selected genes polymorphisms. Antioxidant enzymes activity were evaluated in erythrocyte hemolysate of 23 patients with non-active IBD and 30 healthy participants. RESULTS: The A/C genotype and the C allele frequencies of A/C polymorphism of SOD1 gene were significantly associated with the reduced risk of IBD (OR=0.43; 95% CI 0.23; 0.83). Alike, C/T (OR=0.45; 95% CI= 0.29; 0.70) and T/T genotype (OR=0.43; 95% CI= 0.21; 0.87) of GSHPX1 gene polymorphism diminished the susceptibility to IBD. A significant decrease of CAT (P=0.028) and increase of GPx1 (P=0.025) enzyme activities were seen in IBD patients compared to control. CONCLUSIONS: Our data confirm dysregulated antioxidant capacity in patients suffering from IBD. Both, the SOD1 A/C genotype as well as GSHPX1 C/T and T/T genotypes may be associated with a reduction risk of IBD in the Polish population.
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spelling pubmed-57525242018-01-08 Association between SOD1, CAT, GSHPX1 polymorphisms and the risk of inflammatory bowel disease in the Polish population Mrowicka, Malgorzata Mrowicki, Jerzy Mik, Michal Wojtczak, Radoslaw Dziki, Lukasz Dziki, Adam Majsterek, Ireneusz Oncotarget Research Paper PURPOSE: The main aim of this study was investigate the association between the genetic polymorphism of antioxidant enzyme genes: SOD1, CAT and GSHPX1 and the risk of inflammatory bowel disease (IBD), including Crohn’s disease and ulcerative colitis in the Polish population. METHODS: A total of 445 subjects including 200 patients with IBD and 245 controls were allowed in this study. We determined activity of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx1) and examination their association with the SNPs of respective genes (SOD1 +35A/C, CAT C-262T and GSHPX1 Pro197Leu). RFLP technique was used to determine the selected genes polymorphisms. Antioxidant enzymes activity were evaluated in erythrocyte hemolysate of 23 patients with non-active IBD and 30 healthy participants. RESULTS: The A/C genotype and the C allele frequencies of A/C polymorphism of SOD1 gene were significantly associated with the reduced risk of IBD (OR=0.43; 95% CI 0.23; 0.83). Alike, C/T (OR=0.45; 95% CI= 0.29; 0.70) and T/T genotype (OR=0.43; 95% CI= 0.21; 0.87) of GSHPX1 gene polymorphism diminished the susceptibility to IBD. A significant decrease of CAT (P=0.028) and increase of GPx1 (P=0.025) enzyme activities were seen in IBD patients compared to control. CONCLUSIONS: Our data confirm dysregulated antioxidant capacity in patients suffering from IBD. Both, the SOD1 A/C genotype as well as GSHPX1 C/T and T/T genotypes may be associated with a reduction risk of IBD in the Polish population. Impact Journals LLC 2017-11-27 /pmc/articles/PMC5752524/ /pubmed/29312611 http://dx.doi.org/10.18632/oncotarget.22675 Text en Copyright: © 2017 Mrowicka et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Mrowicka, Malgorzata
Mrowicki, Jerzy
Mik, Michal
Wojtczak, Radoslaw
Dziki, Lukasz
Dziki, Adam
Majsterek, Ireneusz
Association between SOD1, CAT, GSHPX1 polymorphisms and the risk of inflammatory bowel disease in the Polish population
title Association between SOD1, CAT, GSHPX1 polymorphisms and the risk of inflammatory bowel disease in the Polish population
title_full Association between SOD1, CAT, GSHPX1 polymorphisms and the risk of inflammatory bowel disease in the Polish population
title_fullStr Association between SOD1, CAT, GSHPX1 polymorphisms and the risk of inflammatory bowel disease in the Polish population
title_full_unstemmed Association between SOD1, CAT, GSHPX1 polymorphisms and the risk of inflammatory bowel disease in the Polish population
title_short Association between SOD1, CAT, GSHPX1 polymorphisms and the risk of inflammatory bowel disease in the Polish population
title_sort association between sod1, cat, gshpx1 polymorphisms and the risk of inflammatory bowel disease in the polish population
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752524/
https://www.ncbi.nlm.nih.gov/pubmed/29312611
http://dx.doi.org/10.18632/oncotarget.22675
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