1. Pathophysiology of Benign Prostatic Hyperplasia and Benign Prostatic Enlargement: A Mini-Review.
- Author
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Madersbacher S, Sampson N, and Culig Z
- Subjects
- 3-Oxo-5-alpha-Steroid 4-Dehydrogenase metabolism, 5-alpha Reductase Inhibitors therapeutic use, Aging immunology, Diabetes Mellitus epidemiology, Diabetes Mellitus metabolism, Dihydrotestosterone metabolism, Dutasteride therapeutic use, Dyslipidemias epidemiology, Dyslipidemias metabolism, Finasteride therapeutic use, Humans, Inflammation immunology, Lower Urinary Tract Symptoms drug therapy, Lower Urinary Tract Symptoms epidemiology, Lower Urinary Tract Symptoms immunology, Male, Metabolic Syndrome epidemiology, Metabolic Syndrome metabolism, Prostatic Hyperplasia drug therapy, Prostatic Hyperplasia epidemiology, Prostatic Hyperplasia immunology, Receptors, Androgen metabolism, Aging metabolism, Lower Urinary Tract Symptoms metabolism, Prostatic Hyperplasia metabolism
- Abstract
Benign prostatic hyperplasia (BPH), benign prostatic enlargement (BPE) and lower urinary tract symptoms (LUTS) belong to the most frequent diseases in ageing men. Beyond the 6th decade of life, more than 30% of men suffer from moderate to severe LUTS requiring intervention. The pathophysiology of BPH/BPE is still incompletely understood. The dominant role of the androgen system and the androgen receptor is well defined. Androgen receptors are expressed in BPH tissue in which they are activated by the potent androgen dihydrotestosterone. Synthesis of dihydrotestosterone is under control of the 5α-reductase enzyme, activity of which is antagonized by finasteride and dutasteride. More recently, the impact of prostatic inflammation and metabolic parameters particularly for the development of BPE and LUTS has increasingly been recognized. A better understanding of the pathophysiology is a prerequisite for the development of novel, more effective medical treatment options., (© 2019 S. Karger AG, Basel.)
- Published
- 2019
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