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The Genetic Variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) as Possible Risk Factors of Psoriasis Development

Advances in genotypic technologies enable identification of possible associations between genetic variants of certain genes and increased risk of developing plaque psoriasis or psoriatic arthritis. The aim of the study was to analyze the NOTCH3 (6746T>C) (rs1044009) and PSMA6 (-8C>G) (rs104899...

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Autores principales: Bartosińska, Joanna, Zmorzyński, Szymon, Sarecka-Hujar, Beata, Raczkiewicz, Dorota, Wojcierowska-Litwin, Magdalena, Korszeń-Pilecka, Iwona, Michalak-Stoma, Anna, Kowal, Małgorzata, Bartosiński, Jarosław, Filip, Agata, Krasowska, Dorota, Chodorowska, Grażyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467108/
https://www.ncbi.nlm.nih.gov/pubmed/34575036
http://dx.doi.org/10.3390/life11090887
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author Bartosińska, Joanna
Zmorzyński, Szymon
Sarecka-Hujar, Beata
Raczkiewicz, Dorota
Wojcierowska-Litwin, Magdalena
Korszeń-Pilecka, Iwona
Michalak-Stoma, Anna
Kowal, Małgorzata
Bartosiński, Jarosław
Filip, Agata
Krasowska, Dorota
Chodorowska, Grażyna
author_facet Bartosińska, Joanna
Zmorzyński, Szymon
Sarecka-Hujar, Beata
Raczkiewicz, Dorota
Wojcierowska-Litwin, Magdalena
Korszeń-Pilecka, Iwona
Michalak-Stoma, Anna
Kowal, Małgorzata
Bartosiński, Jarosław
Filip, Agata
Krasowska, Dorota
Chodorowska, Grażyna
author_sort Bartosińska, Joanna
collection PubMed
description Advances in genotypic technologies enable identification of possible associations between genetic variants of certain genes and increased risk of developing plaque psoriasis or psoriatic arthritis. The aim of the study was to analyze the NOTCH3 (6746T>C) (rs1044009) and PSMA6 (-8C>G) (rs1048990) polymorphisms and their role in genetic susceptibility to psoriasis. The study included 158 psoriatic patients and 100 healthy controls. The frequencies of the NOTCH3 genotypes differed between the psoriatic patients and healthy controls (p = 0.050). No differences were found in the distribution of PSMA6 genotypes and alleles between the psoriatic patients and healthy controls. The studied psoriatic patients presented a higher frequency of the CC genotype of PSMA6 compared to the healthy controls (8.8% vs. 2%, respectively). Psoriatic arthritis was more frequent among patients with the CC genotype of PSMA6 (p = 0.059). CC homozygosity of NOTCH3 was more commonly observed in the studied psoriatic patients than in the healthy controls (OR = 4.76, p = 0.032). The obtained data suggest that genetic variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) genes may play significant roles in psoriatic patients. Further studies are necessary to unequivocally determine their role as genetic risk factors of psoriasis development.
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spelling pubmed-84671082021-09-27 The Genetic Variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) as Possible Risk Factors of Psoriasis Development Bartosińska, Joanna Zmorzyński, Szymon Sarecka-Hujar, Beata Raczkiewicz, Dorota Wojcierowska-Litwin, Magdalena Korszeń-Pilecka, Iwona Michalak-Stoma, Anna Kowal, Małgorzata Bartosiński, Jarosław Filip, Agata Krasowska, Dorota Chodorowska, Grażyna Life (Basel) Article Advances in genotypic technologies enable identification of possible associations between genetic variants of certain genes and increased risk of developing plaque psoriasis or psoriatic arthritis. The aim of the study was to analyze the NOTCH3 (6746T>C) (rs1044009) and PSMA6 (-8C>G) (rs1048990) polymorphisms and their role in genetic susceptibility to psoriasis. The study included 158 psoriatic patients and 100 healthy controls. The frequencies of the NOTCH3 genotypes differed between the psoriatic patients and healthy controls (p = 0.050). No differences were found in the distribution of PSMA6 genotypes and alleles between the psoriatic patients and healthy controls. The studied psoriatic patients presented a higher frequency of the CC genotype of PSMA6 compared to the healthy controls (8.8% vs. 2%, respectively). Psoriatic arthritis was more frequent among patients with the CC genotype of PSMA6 (p = 0.059). CC homozygosity of NOTCH3 was more commonly observed in the studied psoriatic patients than in the healthy controls (OR = 4.76, p = 0.032). The obtained data suggest that genetic variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) genes may play significant roles in psoriatic patients. Further studies are necessary to unequivocally determine their role as genetic risk factors of psoriasis development. MDPI 2021-08-28 /pmc/articles/PMC8467108/ /pubmed/34575036 http://dx.doi.org/10.3390/life11090887 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bartosińska, Joanna
Zmorzyński, Szymon
Sarecka-Hujar, Beata
Raczkiewicz, Dorota
Wojcierowska-Litwin, Magdalena
Korszeń-Pilecka, Iwona
Michalak-Stoma, Anna
Kowal, Małgorzata
Bartosiński, Jarosław
Filip, Agata
Krasowska, Dorota
Chodorowska, Grażyna
The Genetic Variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) as Possible Risk Factors of Psoriasis Development
title The Genetic Variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) as Possible Risk Factors of Psoriasis Development
title_full The Genetic Variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) as Possible Risk Factors of Psoriasis Development
title_fullStr The Genetic Variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) as Possible Risk Factors of Psoriasis Development
title_full_unstemmed The Genetic Variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) as Possible Risk Factors of Psoriasis Development
title_short The Genetic Variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) as Possible Risk Factors of Psoriasis Development
title_sort genetic variants of notch3 (6746t>c) and psma6 (-8c>g) as possible risk factors of psoriasis development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467108/
https://www.ncbi.nlm.nih.gov/pubmed/34575036
http://dx.doi.org/10.3390/life11090887
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