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5-α还原酶抑制剂在良性前列腺增生治疗中的应用。

The use of 5-alpha reductase inhibitors in the treatment of benign prostatic hyperplasia.

作者信息

Kim Eric H, Brockman John A, Andriole Gerald L

机构信息

Division of Urologic Surgery, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Asian J Urol. 2018 Jan;5(1):28-32. doi: 10.1016/j.ajur.2017.11.005. Epub 2017 Nov 26.

DOI:10.1016/j.ajur.2017.11.005
PMID:29379733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5780290/
Abstract

Benign prostatic hyperplasia (BPH) is characterized by an enlarged prostate, lower urinary tract symptoms (LUTS), and a decreased urinary flow rate. Common in older men, BPH is a progressive disease that can eventually lead to complications including acute urinary retention (AUR) and the need for BPH-related surgery. Both normal and abnormal prostate growth is driven by the androgen dihydrotestosterone (DHT), which is formed from testosterone under the influence of 5-alpha reductase. Thus, 5-alpha reductase inhibitors (5-ARIs) effectively reduce the serum and intraprostatic concentration of DHT, causing an involution of prostate tissue. Two 5-ARIs are currently available for the treatment of BPH-finasteride and dutasteride. Both have been demonstrated to decrease prostate volume, improve LUTS and urinary flow rates, which ultimately reduces the risk of AUR and BPH-related surgery. Therefore, either alone or in combination with other BPH medications, 5-ARIs are a mainstay of BPH management.

摘要

良性前列腺增生(BPH)的特征是前列腺增大、下尿路症状(LUTS)以及尿流率降低。BPH在老年男性中很常见,是一种渐进性疾病,最终可能导致包括急性尿潴留(AUR)和BPH相关手术需求在内的并发症。正常和异常的前列腺生长均由雄激素双氢睾酮(DHT)驱动,DHT是在5α还原酶的影响下由睾酮形成的。因此,5α还原酶抑制剂(5-ARIs)可有效降低血清和前列腺内DHT的浓度,导致前列腺组织 involution(此处involution可能有误,推测应为“退化”之类意思)。目前有两种5-ARIs可用于治疗BPH——非那雄胺和度他雄胺。两者均已被证明可减小前列腺体积、改善LUTS和尿流率,最终降低AUR和BPH相关手术的风险。因此,5-ARIs单独使用或与其他BPH药物联合使用,都是BPH治疗的主要手段。

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EAU guidelines on the treatment and follow-up of non-neurogenic male lower urinary tract symptoms including benign prostatic obstruction.EAU 指南:非神经原性男性下尿路症状(包括良性前列腺梗阻)的治疗和随访。
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