Future Direction in Pharmacotherapy for Non-neurogenic Male Lower Urinary Tract Symptoms

• Tipo: Outra Publicação em Revista Científica Internacional
• Data: 2013

Autores

Soler, R (Autor) Outra; Andersson, KE (Autor) Outra; Chancellor, MB (Autor) Outra; Chapple, CR (Autor) Outra; de Groat, WC (Autor) Outra; Drake, MJ (Autor) Outra; Gratzke, C (Autor) Outra; Lee, R (Autor) Outra; Francisco Cruz (Autor) FMUP

Revista

Título: European Urology

Vol. 64

Páginas: 610-621

ISSN: 0302-2838

Editora: Elsevier

Indexação

ISI Web of Knowledge - 49 Citações

Scopus - 56 Citações

Outras Informações

ID Authenticus: P-006-74B

DOI: 10.1016/j.eururo.2013.04.042

Abstract (EN): Background: The pathophysiology of male lower urinary tract symptoms (LUTS) is highly complex and multifactorial. The shift in perception that LUTS are not sex or organ specific has not been followed by significant innovations regarding the available drug classes. Objective: To review pathophysiologic mechanisms and clinical and experimental data related to the development of new pharmacologic treatments for male LUTS. Evidence acquisition: The PubMed database was used to identify articles describing experimental and clinical studies of pathophysiologic mechanisms contributing to male LUTS and, supported by them, new pharmacotherapies with clinical or experimental evidence in the field. Evidence synthesis: Several pathologic processes (eg, androgen signaling, inflammation, and metabolic factors) and targets (eg, the urothelium, prostate, interstitial cells, detrusor, neurotransmitters, neuromodulators, and receptors) have been implicated in male LUTS. Some newly introduced drugs, such as phosphodiesterase type 5 inhibitors and beta 3-adrenergic agonists, have just started broad use in clinical practice. Drugs with potential benefit, such as vitamin D3 receptor analogs, gonadotropin-releasing hormone antagonists, cannabinoids, and drugs injected into the prostate, have been evaluated in experimental studies and have progressed to clinical trials. However, safety and efficacy data for these drugs are still scarce. Some compounds with interesting profiles have only been tested in experimental settings (eg, transient receptor potential channel blockers, Rho-kinase inhibitors, purinergic receptor blockers, and endothelin-converting enzyme inhibitors). Conclusions: New pathophysiologic mechanisms of male LUTS are described that lead to the continuous development of new pharmacotherapies. To date, few drugs have been added to the current armamentarium, and several are in various phases of clinical or experimental investigation.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 12