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

被引:6
|
作者
Rhie, Arang [1 ,2 ]
Son, Ho-Young [1 ,3 ,4 ]
Kwak, Soo Jung [1 ,3 ,4 ]
Lee, Seungbok [1 ,3 ,4 ]
Kim, Dong Young [5 ,6 ,7 ]
Lew, Bark-Lynn [8 ]
Sim, Woo-Young [8 ]
Seo, Jeong-Sun [1 ,3 ,4 ]
Kwon, Ohsang [5 ,6 ,7 ]
Kim, Jong-Il [1 ,3 ,4 ]
Jo, Seong Jin [5 ,6 ,7 ]
机构
[1] Seoul Natl Univ, Med Res Ctr, Genom Med Inst GMI, Seoul, South Korea
[2] NHGRI, Genome Informat Sect, Computat & Stat Genom Branch, NIH, Bethesda, MD 20892 USA
[3] Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea
[4] Seoul Natl Univ, Dept Biochem & Mol Biol, Coll Med, Seoul, South Korea
[5] Seoul Natl Univ, Dept Dermatol, Coll Med, Seoul, South Korea
[6] Seoul Natl Univ Hosp, Biomed Res Inst, Lab Cutaneous Aging & Hair Res, Seoul, South Korea
[7] Seoul Natl Univ, Med Res Ctr, Inst Human Environm Interface Biol, Coll Med, Seoul, South Korea
[8] Kyung Hee Univ, Coll Med, Dept Dermatol, Seoul, South Korea
来源
PLOS ONE | 2019年 / 14卷 / 09期
关键词
MALE-PATTERN BALDNESS; TRANS-RETINOIC ACID; BINDING-PROTEINS; PROSTATE-CANCER; HAIR FOLLICLE; RECEPTOR GENE; EXPRESSION; METABOLISM; ENZYMES; CYTOCHROME-P450;
D O I
10.1371/journal.pone.0222533
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dutasteride, a dual inhibitor of both type I and II 5 alpha-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.
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页数:13
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