Silodosin in the treatment of benign prostatic hyperplasia

被引:45
|
作者
Rossi, Maxime [1 ]
Roumeguere, Thierry [1 ]
机构
[1] ULB, Erasme Hosp, Dept Urol, Univ Clin Brussels, B-1070 Brussels, Belgium
来源
关键词
silodosin; alpha(1A)-blockers; lower urinary tract symptoms; benign prostatic hyperplasia; uroselectivity; SUBTYPE MESSENGER-RNAS; URINARY-TRACT SYMPTOMS; FLOPPY-IRIS-SYNDROME; ALPHA(1A)-ADRENOCEPTOR-SELECTIVE ANTAGONIST; ALPHA(1)-ADRENOCEPTOR SUBTYPES; KMD-3213; QUANTIFICATION; ADRENOCEPTORS; SELECTIVITY; INHIBITORS;
D O I
10.2147/DDDT.S10428
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Benign prostatic hyperplasia (BPH)-associated lower urinary tract symptoms (LUTS) are highly prevalent in older men. Medical therapy is the first-line treatment for LUTS due to BPH. Alpha-adrenergic receptor blockers remain one of the mainstays in the treatment of male LUTS and clinical BPH. They exhibit early onset of efficacy with regard to both symptoms and flow rate improvement, and this is clearly demonstrated in placebo-controlled trials with extensions out to five years. These agents have been shown to prevent symptomatic progression of the disease. The aim of this article is to offer a critical review of the current literature on silodosin, formerly known as KMD-3213, a novel alpha-blocker with unprecedented selectivity for alpha(1A)-adrenergic receptors, as compared with both alpha(1B)- and alpha(1D)-adrenoceptors, exceeding the selectivity of all currently used alpha(1)-blockers, and with clinically promising effects.
引用
收藏
页码:291 / 297
页数:7
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