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Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population

INTRODUCTION: Several studies have reported that the V89L and TA repeat polymorphisms [(TA)n] of the SRD5A2 gene were associated with SRD5A2 activity. The activity of dihydrotestosterone, which is converted from testosterone by SRD5A2, is responsible for sebum secretion and the formation of acne. We...

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Autores principales: Hu, Xue, Ding, Wei, Jin, Xinye, Wang, Jia, Zou, Dajin, Chen, Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872244/
https://www.ncbi.nlm.nih.gov/pubmed/29610568
http://dx.doi.org/10.5114/ada.2018.73162
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author Hu, Xue
Ding, Wei
Jin, Xinye
Wang, Jia
Zou, Dajin
Chen, Yue
author_facet Hu, Xue
Ding, Wei
Jin, Xinye
Wang, Jia
Zou, Dajin
Chen, Yue
author_sort Hu, Xue
collection PubMed
description INTRODUCTION: Several studies have reported that the V89L and TA repeat polymorphisms [(TA)n] of the SRD5A2 gene were associated with SRD5A2 activity. The activity of dihydrotestosterone, which is converted from testosterone by SRD5A2, is responsible for sebum secretion and the formation of acne. We hypothesized that abnormalities in SRD5A2 action could contribute to the formation of acne. AIM: To study whether the structural change of the SRD5A2 gene may affect the risk of acne in patients with normal serum testosterone levels. MATERIAL AND METHODS: Genotyping of rs523349 and (TA)n of SRD5A2 was performed in 49 Chinese acne patients with significant improvements with SRD5A2 inhibitor-finasteride but normal serum testosterone levels, and in 50 healthy Chinese age-matched controls without acne. RESULTS: There was no significant difference between the two groups in the frequencies of V and L alleles and VV, VL, and LL genotypes of V89L (χ(2) test, p > 0.5). (TA)n polymorphic repeat sites are 5 alleles (TA0, TA3, TA6, TA9, TA12) in our population. The differences in S and L allele frequencies between the two groups were statistically significant (p < 0.005). People with a longer (n ≥ 6) allele of the (TA)n repeat polymorphism had a higher risk of having acne than those with a shorter (n < 6) allele (OR = 3.52, 95% CI: 1.73–7.16). CONCLUSIONS: This study suggests that SRD5A2 polymorphisms might be associated with acne risk. This is the first report focusing on the Chinese population according to our knowledge. Further large sample studies may be required to confirm the association and to assess any interactions with environmental factors.
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spelling pubmed-58722442018-04-02 Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population Hu, Xue Ding, Wei Jin, Xinye Wang, Jia Zou, Dajin Chen, Yue Postepy Dermatol Alergol Original Paper INTRODUCTION: Several studies have reported that the V89L and TA repeat polymorphisms [(TA)n] of the SRD5A2 gene were associated with SRD5A2 activity. The activity of dihydrotestosterone, which is converted from testosterone by SRD5A2, is responsible for sebum secretion and the formation of acne. We hypothesized that abnormalities in SRD5A2 action could contribute to the formation of acne. AIM: To study whether the structural change of the SRD5A2 gene may affect the risk of acne in patients with normal serum testosterone levels. MATERIAL AND METHODS: Genotyping of rs523349 and (TA)n of SRD5A2 was performed in 49 Chinese acne patients with significant improvements with SRD5A2 inhibitor-finasteride but normal serum testosterone levels, and in 50 healthy Chinese age-matched controls without acne. RESULTS: There was no significant difference between the two groups in the frequencies of V and L alleles and VV, VL, and LL genotypes of V89L (χ(2) test, p > 0.5). (TA)n polymorphic repeat sites are 5 alleles (TA0, TA3, TA6, TA9, TA12) in our population. The differences in S and L allele frequencies between the two groups were statistically significant (p < 0.005). People with a longer (n ≥ 6) allele of the (TA)n repeat polymorphism had a higher risk of having acne than those with a shorter (n < 6) allele (OR = 3.52, 95% CI: 1.73–7.16). CONCLUSIONS: This study suggests that SRD5A2 polymorphisms might be associated with acne risk. This is the first report focusing on the Chinese population according to our knowledge. Further large sample studies may be required to confirm the association and to assess any interactions with environmental factors. Termedia Publishing House 2018-02-20 2018-02 /pmc/articles/PMC5872244/ /pubmed/29610568 http://dx.doi.org/10.5114/ada.2018.73162 Text en Copyright: © 2018 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Hu, Xue
Ding, Wei
Jin, Xinye
Wang, Jia
Zou, Dajin
Chen, Yue
Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
title Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
title_full Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
title_fullStr Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
title_full_unstemmed Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
title_short Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
title_sort longer ta repeat but not v89l polymorphisms in the srd5a2 gene may confer acne risk in the chinese population
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872244/
https://www.ncbi.nlm.nih.gov/pubmed/29610568
http://dx.doi.org/10.5114/ada.2018.73162
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