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Absence of GSTT1 and polymorphisms in GSTP1 and TP53 are associated with the incidence of acne vulgaris
BACKGROUNDS: Acne vulgaris is a chronic inflammatory skin disease of the pilosebaceous unit affecting most teenagers and numerous adults throughout the world. The present study was designed to assess the association of the presence or absence of GSTM1, GSTT1, and single nucleotide polymorphisms rs16...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234175/ https://www.ncbi.nlm.nih.gov/pubmed/37113088 http://dx.doi.org/10.1111/srt.13333 |
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author | Ullah, Rehmat Afgan, Sher Akhtar, Mariyam Asif, Muhammad Latif, Muhammad Mehmood, Rashid Naeem, Muhammad Zahra, Kiran Farooq, Muhammad Ben Said, Mourad Iqbal, Furhan |
author_facet | Ullah, Rehmat Afgan, Sher Akhtar, Mariyam Asif, Muhammad Latif, Muhammad Mehmood, Rashid Naeem, Muhammad Zahra, Kiran Farooq, Muhammad Ben Said, Mourad Iqbal, Furhan |
author_sort | Ullah, Rehmat |
collection | PubMed |
description | BACKGROUNDS: Acne vulgaris is a chronic inflammatory skin disease of the pilosebaceous unit affecting most teenagers and numerous adults throughout the world. The present study was designed to assess the association of the presence or absence of GSTM1, GSTT1, and single nucleotide polymorphisms rs1695 in GSTP1 and rs1042522 in TP53 gene with acne vulgaris. METHODS: The cross‐sectional case–control study was conducted at the Institute of Zoology from May 2020 to March 2021 and included acne vulgaris patients (N = 100) and controls (N = 100) enrolled in Dera Ghazi Khan district, Pakistan. Multiplex and tetra‐primer amplification refractory mutation system‐polymerase chain reactions were applied to investigate the genotype in analyzed genes. The association of rs1695 and rs1042522 with acne vulgaris was studied either individually or in various combinations with GATM1 and T1. RESULTS: A significant association of absence of GSTT1 and mutant genotype at rs1695 (GG) and at rs1042522 (CC) in GSTP1 and TP53, respectively, was found to be associated with acne vulgaris in enrolled subjects. Subjects aged 10–25 years and smokers were more susceptible to acne vulgaris. CONCLUSION: Our results suggest that genotypes of glutathione S‐transferases (GSTs) and TP53 are involved in protection against oxidative stress and may influence disease progression in acne vulgaris. |
format | Online Article Text |
id | pubmed-10234175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102341752023-08-11 Absence of GSTT1 and polymorphisms in GSTP1 and TP53 are associated with the incidence of acne vulgaris Ullah, Rehmat Afgan, Sher Akhtar, Mariyam Asif, Muhammad Latif, Muhammad Mehmood, Rashid Naeem, Muhammad Zahra, Kiran Farooq, Muhammad Ben Said, Mourad Iqbal, Furhan Skin Res Technol Original Articles BACKGROUNDS: Acne vulgaris is a chronic inflammatory skin disease of the pilosebaceous unit affecting most teenagers and numerous adults throughout the world. The present study was designed to assess the association of the presence or absence of GSTM1, GSTT1, and single nucleotide polymorphisms rs1695 in GSTP1 and rs1042522 in TP53 gene with acne vulgaris. METHODS: The cross‐sectional case–control study was conducted at the Institute of Zoology from May 2020 to March 2021 and included acne vulgaris patients (N = 100) and controls (N = 100) enrolled in Dera Ghazi Khan district, Pakistan. Multiplex and tetra‐primer amplification refractory mutation system‐polymerase chain reactions were applied to investigate the genotype in analyzed genes. The association of rs1695 and rs1042522 with acne vulgaris was studied either individually or in various combinations with GATM1 and T1. RESULTS: A significant association of absence of GSTT1 and mutant genotype at rs1695 (GG) and at rs1042522 (CC) in GSTP1 and TP53, respectively, was found to be associated with acne vulgaris in enrolled subjects. Subjects aged 10–25 years and smokers were more susceptible to acne vulgaris. CONCLUSION: Our results suggest that genotypes of glutathione S‐transferases (GSTs) and TP53 are involved in protection against oxidative stress and may influence disease progression in acne vulgaris. John Wiley and Sons Inc. 2023-04-22 /pmc/articles/PMC10234175/ /pubmed/37113088 http://dx.doi.org/10.1111/srt.13333 Text en © 2023 The Authors. Skin Research and Technology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Ullah, Rehmat Afgan, Sher Akhtar, Mariyam Asif, Muhammad Latif, Muhammad Mehmood, Rashid Naeem, Muhammad Zahra, Kiran Farooq, Muhammad Ben Said, Mourad Iqbal, Furhan Absence of GSTT1 and polymorphisms in GSTP1 and TP53 are associated with the incidence of acne vulgaris |
title | Absence of GSTT1 and polymorphisms in GSTP1 and TP53 are associated with the incidence of acne vulgaris |
title_full | Absence of GSTT1 and polymorphisms in GSTP1 and TP53 are associated with the incidence of acne vulgaris |
title_fullStr | Absence of GSTT1 and polymorphisms in GSTP1 and TP53 are associated with the incidence of acne vulgaris |
title_full_unstemmed | Absence of GSTT1 and polymorphisms in GSTP1 and TP53 are associated with the incidence of acne vulgaris |
title_short | Absence of GSTT1 and polymorphisms in GSTP1 and TP53 are associated with the incidence of acne vulgaris |
title_sort | absence of gstt1 and polymorphisms in gstp1 and tp53 are associated with the incidence of acne vulgaris |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234175/ https://www.ncbi.nlm.nih.gov/pubmed/37113088 http://dx.doi.org/10.1111/srt.13333 |
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