Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia.

Dutasteride, a dual inhibitor of both type I and II 5α-reductases, is used to treat male pattern hair loss (MPHL). However, patient response to dutasteride varies in each individual, the cause of which is yet to be identified. To identify genetic variants associated with response to dutasteride trea...

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Main Authors: Arang Rhie, Ho-Young Son, Soo Jung Kwak, Seungbok Lee, Dong Young Kim, Bark-Lynn Lew, Woo-Young Sim, Jeong-Sun Seo, Ohsang Kwon, Jong-Il Kim, Seong Jin Jo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0222533
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spelling doaj-02ec6ec71a8f41a0918bd856e5de29292021-03-03T20:31:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01149e022253310.1371/journal.pone.0222533Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia.Arang RhieHo-Young SonSoo Jung KwakSeungbok LeeDong Young KimBark-Lynn LewWoo-Young SimJeong-Sun SeoOhsang KwonJong-Il KimSeong Jin JoDutasteride, a dual inhibitor of both type I and II 5α-reductases, is used to treat male pattern hair loss (MPHL). However, patient response to dutasteride varies in each individual, the cause of which is yet to be identified. To identify genetic variants associated with response to dutasteride treatment for MPHL, a total of 42 men with moderate MPHL who had been treated with dutasteride for 6 months were genotyped and analysed by quantitative linear regression, case-control association tests, and Fisher's exact test. The synonymous single nucleotide polymorphism (SNP) rs72623193 in DHRS9 was most significantly associated with response to dutasteride, followed by the non-synonymous SNP rs2241057 in CYP26B1. Additionally, variants in ESR1, SRD5A1, CYP19A1, and RXRG are suggested to be associated with response to dutasteride. Cumulative effect and interaction among these SNPs were presented in both additive and non-additive models.https://doi.org/10.1371/journal.pone.0222533
collection DOAJ
language English
format Article
sources DOAJ
author Arang Rhie
Ho-Young Son
Soo Jung Kwak
Seungbok Lee
Dong Young Kim
Bark-Lynn Lew
Woo-Young Sim
Jeong-Sun Seo
Ohsang Kwon
Jong-Il Kim
Seong Jin Jo
spellingShingle Arang Rhie
Ho-Young Son
Soo Jung Kwak
Seungbok Lee
Dong Young Kim
Bark-Lynn Lew
Woo-Young Sim
Jeong-Sun Seo
Ohsang Kwon
Jong-Il Kim
Seong Jin Jo
Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia.
PLoS ONE
author_facet Arang Rhie
Ho-Young Son
Soo Jung Kwak
Seungbok Lee
Dong Young Kim
Bark-Lynn Lew
Woo-Young Sim
Jeong-Sun Seo
Ohsang Kwon
Jong-Il Kim
Seong Jin Jo
author_sort Arang Rhie
title Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia.
title_short Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia.
title_full Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia.
title_fullStr Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia.
title_full_unstemmed Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia.
title_sort genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Dutasteride, a dual inhibitor of both type I and II 5α-reductases, is used to treat male pattern hair loss (MPHL). However, patient response to dutasteride varies in each individual, the cause of which is yet to be identified. To identify genetic variants associated with response to dutasteride treatment for MPHL, a total of 42 men with moderate MPHL who had been treated with dutasteride for 6 months were genotyped and analysed by quantitative linear regression, case-control association tests, and Fisher's exact test. The synonymous single nucleotide polymorphism (SNP) rs72623193 in DHRS9 was most significantly associated with response to dutasteride, followed by the non-synonymous SNP rs2241057 in CYP26B1. Additionally, variants in ESR1, SRD5A1, CYP19A1, and RXRG are suggested to be associated with response to dutasteride. Cumulative effect and interaction among these SNPs were presented in both additive and non-additive models.
url https://doi.org/10.1371/journal.pone.0222533
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