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SRD5A 1 and SRD5A2 are Associated with Treatment for Benign Prostatic Hyperplasia with the Combination of 5α-Reductase Inhibitors and α-Adrenergic Receptor Antagonists.

Authors :
Xin Gu
Rong Ha
Tao Huang
Li Wang
Sha Tao
Lu Tian
Zhuo Chen
Yang Jiao
Jian Kang
Siqun Zheng
Jianfeng Xu
Jielin Sun
Jun Qi
Source :
Journal of Urology; Aug2013, Vol. 190 Issue 2, p615-619, 5p
Publication Year :
2013

Abstract

Purpose: Common treatments for benign prostatic hyperplasia include 5α-reductase inhibitors and a-adrenergic receptor antagonists. However, these treatments can only partially decrease the risk of benign prostatic hyperplasia progression. SRD5A1 and SRD5A2 are 5β-reductase inhibitor targets. We investigated the association between drug efficacy and single nucleotide polymorphisms in the SRD5A1 and SRD5A2 genes in a Chinese population. Materials and Methods: We genotyped 11 tagging single nucleotide polymorphisms in the SRD5A1 and SRD5A2 genes in a total of 426 benign prostatic hyperplasia cases and 1,008 controls from Xinhua Hospital, Shanghai, People's Republic of China. Cases were treated with type II 5α-reductase inhibitors and β-adrenergic receptor antagonists. We tested the association of tagging single nucleotide polymorphisms with benign prostatic hyperplasia risk/progression, clinical characteristics at baseline, including the I-PSS (International Prostate Symptom Score) and total prostate volume, and changes in clinical characteristics after treatment. Results: The 11 tagging single nucleotide polymorphisms were not significantly associated with benign prostatic hyperplasia risk or progression (each p >0.05). In the SRD5A1 gene rs6884552 and rs3797177 were significantly associated with baseline I-PSS (p = 0.04 and 0.003, respectively). In the SRD5A2 gene rs523349 (V89L) and rs9332975 were significantly associated with baseline total prostate volume (p = 0.01 and 0.001, respectively). In SRD5A1 rs166050 was significantly associated with the posttreatment change in total prostate volume (p = 0.04). In SRD5A2 rs523349 and rs612224 were significantly associated with the posttreatment I-PSS change (p = 0.03 and 0.009, respectively). Conclusions: SRD5A1 and SRD5A2 single nucleotide polymorphisms are significantly associated with the clinical characteristics of benign prostatic hyperplasia and the efficacy of benign prostatic hyperplasia treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00225347
Volume :
190
Issue :
2
Database :
Supplemental Index
Journal :
Journal of Urology
Publication Type :
Academic Journal
Accession number :
89016294
Full Text :
https://doi.org/10.1016/j.juro.2013.03.024