• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

5α-还原酶抑制剂在治疗下尿路症状和良性前列腺增生中的应用现状。

Current status of 5alpha-reductase inhibitors in the management of lower urinary tract symptoms and BPH.

机构信息

Department of Urology, University of Thessaly, 6-8, Feidiou Street, 41221 Larissa, Greece.

出版信息

World J Urol. 2010 Feb;28(1):9-15. doi: 10.1007/s00345-009-0493-y. Epub 2009 Dec 3.

DOI:10.1007/s00345-009-0493-y
PMID:19956956
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2809314/
Abstract

PURPOSE

Benign prostatic hyperplasia (BPH) is a progressive disease that is commonly associated with bothersome lower urinary tract symptoms (LUTS) and might result in complications, such as acute urinary retention and BPH-related surgery. Therefore, the goals of therapy for BPH are not only to improve LUTS in terms of symptoms and urinary flow, but also to identify those patients at a risk of unfavorable disease progression and to optimize their management. This article reviews the current status of therapy with 5alpha-reductase inhibitors (5ARIs), namely fiasteride and dutasteride, for men with LUTS and BPH.

METHOD

Data from key randomized controlled trials (Oxford level 1b) on the use of 5ARIs are analyzed.

RESULTS

The efficacy of 5ARIs either as monotherapy or in combination with alpha(1)-adrenoceptor antagonists in the management of LUTS and the impact of monotherapy and combined therapy on BPH progression are discussed. Further promises, including the withdrawal of the alpha-blocker from the combined medical treatment and the potential clinical implications from the use of 5ARIs for prostate cancer chemoprevention in patients receiving 5ARIs for symptomatic BPH are highlighted.

CONCLUSIONS

Current evidence shows that 5ARIs are effective in treating LUTS and preventing disease progression and represent a recommended option in treatment guidelines for men who have moderate to severe LUTS and enlarged prostates.

摘要

目的

良性前列腺增生(BPH)是一种进行性疾病,常伴有恼人的下尿路症状(LUTS),并可能导致并发症,如急性尿潴留和与 BPH 相关的手术。因此,BPH 治疗的目标不仅是改善 LUTS 的症状和尿流,还要识别那些有不利疾病进展风险的患者,并优化其管理。本文综述了 5α-还原酶抑制剂(5ARIs),即非那雄胺和度他雄胺,在治疗有 LUTS 和 BPH 的男性中的治疗现状。

方法

分析了关键的随机对照试验(牛津水平 1b)中关于使用 5ARIs 的数据。

结果

讨论了 5ARIs 作为单一疗法或与 α1-肾上腺素能受体拮抗剂联合治疗 LUTS 的疗效,以及单一疗法和联合疗法对 BPH 进展的影响。强调了进一步的前景,包括从联合药物治疗中撤出 α-阻滞剂,以及在接受 5ARIs 治疗有症状的 BPH 的患者中使用 5ARIs 进行前列腺癌化学预防的潜在临床意义。

结论

现有证据表明,5ARIs 可有效治疗 LUTS 和预防疾病进展,是治疗有中度至重度 LUTS 和前列腺增大的男性的推荐选择。

相似文献

1
Current status of 5alpha-reductase inhibitors in the management of lower urinary tract symptoms and BPH.5α-还原酶抑制剂在治疗下尿路症状和良性前列腺增生中的应用现状。
World J Urol. 2010 Feb;28(1):9-15. doi: 10.1007/s00345-009-0493-y. Epub 2009 Dec 3.
2
BPH progression: concept and key learning from MTOPS, ALTESS, COMBAT, and ALF-ONE.良性前列腺增生进展:来自MTOPS、ALTESS、COMBAT和ALF-ONE的概念及关键认识。
BJU Int. 2008 Mar;101 Suppl 3:17-21. doi: 10.1111/j.1464-410X.2008.07497.x.
3
Current role for combination therapy in male LUTS.联合治疗在男性下尿路症状中的当前作用。
Arch Esp Urol. 2010 Jun;63(5):323-32.
4
Progression, risk factors and subsequent medical management of symptomatic benign prostatic hyperplasia.有症状的良性前列腺增生的进展、危险因素及后续医学管理
Arch Ital Urol Androl. 2009 Mar;81(1):1-8.
5
Influence of baseline variables on changes in International Prostate Symptom Score after combined therapy with dutasteride plus tamsulosin or either monotherapy in patients with benign prostatic hyperplasia and lower urinary tract symptoms: 4-year results of the CombAT study.度他雄胺联合坦索罗辛或单药治疗良性前列腺增生伴下尿路症状患者后国际前列腺症状评分变化的基线变量影响:CombAT 研究 4 年结果。
BJU Int. 2014 Apr;113(4):623-35. doi: 10.1111/bju.12500. Epub 2014 Jan 9.
6
Inhibitors of 5alpha-reductase in the treatment of benign prostatic hyperplasia.5α-还原酶抑制剂在良性前列腺增生治疗中的应用
Curr Pharm Des. 2006;12(7):775-83. doi: 10.2174/138161206776056010.
7
Drug Insight: 5alpha-reductase inhibitors for the treatment of benign prostatic hyperplasia.药物洞察:用于治疗良性前列腺增生的5α还原酶抑制剂
Nat Clin Pract Urol. 2006 Sep;3(9):495-503. doi: 10.1038/ncpuro0577.
8
Combination therapy for the pharmacological management of benign prostatic hyperplasia: rationale and treatment options.良性前列腺增生症药物治疗的联合疗法:理论依据与治疗选择
Drugs Aging. 2005;22(11):901-12. doi: 10.2165/00002512-200522110-00002.
9
Managing the progression of lower urinary tract symptoms/benign prostatic hyperplasia: therapeutic options for the man at risk.管理下尿路症状/良性前列腺增生的进展:高危男性的治疗选择。
BJU Int. 2007 Aug;100(2):249-53. doi: 10.1111/j.1464-410X.2007.07056.x.
10
Effect of discontinuation of 5alpha-reductase inhibitors on prostate volume and symptoms in men with BPH: a prospective study.5α-还原酶抑制剂停用对良性前列腺增生男性患者前列腺体积和症状的影响:一项前瞻性研究。
Urology. 2009 Apr;73(4):802-6. doi: 10.1016/j.urology.2008.10.046. Epub 2009 Feb 3.

引用本文的文献

1
Bunge Ameliorates Benign Prostatic Hyperplasia through Regulation of Oxidative Stress via Nrf-2/HO-1 Activation.Bunge 通过激活 Nrf-2/HO-1 来调节氧化应激改善良性前列腺增生。
J Microbiol Biotechnol. 2024 May 28;34(5):1059-1072. doi: 10.4014/jmb.2308.08053. Epub 2023 Oct 31.
2
and Mixture Improves Benign Prostatic Hyperplasia in Rats by Regulating Androgen Receptor Signaling and Apoptosis.并且混合物通过调节雄激素受体信号和细胞凋亡改善大鼠的良性前列腺增生。
Nutrients. 2023 Feb 5;15(4):818. doi: 10.3390/nu15040818.
3
Administration of Seed Extracts Ameliorates Testosterone-Induced Benign Prostatic Hyperplasia (BPH) in Male Wistar Rats.给予种子提取物可改善雄性Wistar大鼠睾酮诱导的良性前列腺增生(BPH)。
Res Rep Urol. 2022 May 26;14:225-239. doi: 10.2147/RRU.S365598. eCollection 2022.
4
Ethanol Extract of Inhibits the Development of Benign Prostatic Hyperplasia by Exhibiting Anti-oxidant and Anti-inflammatory Effects.[提取物名称]的乙醇提取物通过展现抗氧化和抗炎作用抑制良性前列腺增生的发展。
J Cancer Prev. 2022 Mar 30;27(1):42-49. doi: 10.15430/JCP.2022.27.1.42.
5
Protective effects of combination of Stauntonia hexaphylla and Cornus officinalis on testosterone-induced benign prostatic hyperplasia through inhibition of 5α- reductase type 2 and induced cell apoptosis.野木瓜和山茱萸组合对睾酮诱导的良性前列腺增生的保护作用:通过抑制2型5α-还原酶和诱导细胞凋亡
PLoS One. 2020 Aug 13;15(8):e0236879. doi: 10.1371/journal.pone.0236879. eCollection 2020.
6
Aconiti Lateralis Radix Preparata, the Dried Root of Debx., Improves Benign Prostatic Hyperplasia via Suppressing 5-Alpha Reductase and Inducing Prostate Cell Apoptosis.附子,毛茛科植物乌头的干燥根,通过抑制5α-还原酶和诱导前列腺细胞凋亡改善良性前列腺增生。
Evid Based Complement Alternat Med. 2019 Jul 31;2019:6369132. doi: 10.1155/2019/6369132. eCollection 2019.
7
Cost Comparison of Benign Prostatic Hyperplasia Treatment Options.良性前列腺增生治疗方案的成本比较
Curr Urol Rep. 2019 Jun 19;20(8):45. doi: 10.1007/s11934-019-0907-3.
8
Impact of disease progression on individual IPSS trajectories and consequences of immediate versus delayed start of treatment in patients with moderate or severe LUTS associated with BPH.疾病进展对中重度 BPH 相关下尿路症状患者个体 IPSS 轨迹的影响,以及即刻治疗与延迟治疗开始的后果。
World J Urol. 2020 Feb;38(2):463-472. doi: 10.1007/s00345-019-02783-x. Epub 2019 May 11.
9
Histomorphological effects of the oil extract of seed on benign prostatic hyperplasia induced by exogenous testosterone and estradiol in adult Wistar rats.种子油提取物对成年Wistar大鼠外源性睾酮和雌二醇诱导的良性前列腺增生的组织形态学影响。
Avicenna J Phytomed. 2019 Jan-Feb;9(1):21-33.
10
Effects of Lespedeza Cuneata aqueous extract on testosterone-induced prostatic hyperplasia.雀舌草水提物对睾酮诱导的前列腺增生的影响。
Pharm Biol. 2019 Dec;57(1):90-98. doi: 10.1080/13880209.2018.1564929.

本文引用的文献

1
The effects of combination therapy with dutasteride and tamsulosin on clinical outcomes in men with symptomatic benign prostatic hyperplasia: 4-year results from the CombAT study.度他雄胺和坦索罗辛联合治疗对有症状的良性前列腺增生症男性临床结局的影响:来自 CombAT 研究的 4 年结果。
Eur Urol. 2010 Jan;57(1):123-31. doi: 10.1016/j.eururo.2009.09.035. Epub 2009 Sep 19.
2
Finasteride in the treatment of patients with benign prostatic hyperplasia: a review.非那雄胺治疗良性前列腺增生症患者:综述。
Ther Clin Risk Manag. 2009 Jun;5(3):535-45. doi: 10.2147/tcrm.s6195. Epub 2009 Jul 12.
3
A broader role for 5ARIs in prostate disease? Existing evidence and emerging benefits.5α还原酶抑制剂在前列腺疾病中作用范围更广?现有证据及新出现的益处。
Prostate. 2009 Jun 1;69(8):895-907. doi: 10.1002/pros.20939.
4
Use of 5alpha-reductase inhibitors for prostate cancer chemoprevention: American Society of Clinical Oncology/American Urological Association 2008 Clinical Practice Guideline.5α-还原酶抑制剂用于前列腺癌化学预防:美国临床肿瘤学会/美国泌尿外科学会2008年临床实践指南
J Urol. 2009 Apr;181(4):1642-57. doi: 10.1016/j.juro.2009.01.071. Epub 2009 Feb 26.
5
The influence of baseline parameters on changes in international prostate symptom score with dutasteride, tamsulosin, and combination therapy among men with symptomatic benign prostatic hyperplasia and an enlarged prostate: 2-year data from the CombAT study.基线参数对有症状的良性前列腺增生和前列腺肿大男性使用度他雄胺、坦索罗辛及联合治疗后国际前列腺症状评分变化的影响:CombAT研究的2年数据
Eur Urol. 2009 Feb;55(2):461-71. doi: 10.1016/j.eururo.2008.10.037. Epub 2008 Nov 6.
6
Comparative analysis of alpha-blocker utilization in combination with 5-alpha reductase inhibitors for enlarged prostate in a managed care setting among Medicare-aged men.在医保覆盖年龄的男性群体的管理式医疗环境中,α受体阻滞剂与5-α还原酶抑制剂联合用于治疗前列腺增生的对比分析。
Am J Manag Care. 2008 May;14(5 Suppl 2):S160-6.
7
Finasteride monotherapy maintains stable lower urinary tract symptoms in men with benign prostatic hyperplasia following cessation of alpha blockers.非那雄胺单药治疗可使良性前列腺增生男性在停用α受体阻滞剂后维持稳定的下尿路症状。
Can Urol Assoc J. 2008 Feb;2(1):16-21. doi: 10.5489/cuaj.520.
8
Benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management.良性前列腺增生作为一种进行性疾病:风险因素及药物治疗选择指南
Int J Clin Pract. 2008 Jul;62(7):1076-86. doi: 10.1111/j.1742-1241.2008.01785.x. Epub 2008 May 8.
9
Dutasteride: a review of its use in the management of prostate disorders.度他雄胺:其在前列腺疾病管理中的应用综述
Drugs. 2008;68(4):463-85. doi: 10.2165/00003495-200868040-00008.
10
The effects of dutasteride, tamsulosin and combination therapy on lower urinary tract symptoms in men with benign prostatic hyperplasia and prostatic enlargement: 2-year results from the CombAT study.度他雄胺、坦索罗辛及联合治疗对良性前列腺增生和前列腺肿大男性下尿路症状的影响:CombAT研究的2年结果
J Urol. 2008 Feb;179(2):616-21; discussion 621. doi: 10.1016/j.juro.2007.09.084. Epub 2007 Dec 21.