PMID- 21718399 OWN - NLM STAT- MEDLINE DCOM- 20120507 LR - 20171116 IS - 1742-1241 (Electronic) IS - 1368-5031 (Linking) VI - 65 IP - 9 DP - 2011 Sep TI - Current benign prostatic hyperplasia treatment: impact on sexual function and management of related sexual adverse events. PG - 1005-13 LID - 10.1111/j.1742-1241.2011.02731.x [doi] AB - Benign prostatic hyperplasia (BPH) is a common disease in older men that can lead to lower urinary tract symptoms (LUTS). Male sexual dysfunction is also an age-related condition. Epidemiological studies have confirmed an association between BPH/LUTS and sexual dysfunction in ageing men that is independent of the effects of age, other co-morbidities and lifestyle factors. Proposed pathophysiological mechanisms for BPH/LUTS-associated sexual dysfunction include the nitric oxide/cyclic guanosine monophosphate (NO/cGMP) pathway, rho-kinase and endothelin-1 activity, autonomic nervous system overactivity and the metabolic syndrome, and pelvic organ atherosclerosis. Both BPH/LUTS and sexual dysfunction can have a substantial negative impact on a man's quality of life. However, urologists and primary care physicians appear to under-recognise sexual dysfunction in men with BPH/LUTS. Current guidelines recommend alpha-blockers and 5-alpha reductase inhibitors, either alone or in combination, among appropriate medical treatment options for BPH/LUTS. Randomised, controlled trials demonstrate that these therapies can be associated with sexual adverse effects (AEs) such as loss of libido, erectile dysfunction and ejaculatory disorders. Sexual dysfunction should be fully evaluated in men requiring treatment for BPH/LUTS using validated questionnaires. Management of sexual dysfunction in men treated for BPH/LUTS should involve assessment of co-morbidities and concomitant medications, consideration of lifestyle interventions such as weight loss and increased physical activity to improve risk factors and, if necessary, introduction of pharmacotherapies. In addition, physicians should provide patients with proper counselling on the possible sexual AEs of medical therapies for BPH/LUTS and their impact on sexual satisfaction, while being aware of the possibility that counselling in itself is likely to influence reported rates of sexual dysfunction. CI - (c) 2011 Blackwell Publishing Ltd. FAU - Mirone, V AU - Mirone V AD - Department of Urology, University Federico II of Naples, Naples, Italy. mirone@unina.it FAU - Sessa, A AU - Sessa A FAU - Giuliano, F AU - Giuliano F FAU - Berges, R AU - Berges R FAU - Kirby, M AU - Kirby M FAU - Moncada, I AU - Moncada I LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Review DEP - 20110701 PL - India TA - Int J Clin Pract JT - International journal of clinical practice JID - 9712381 RN - 0 (5-alpha Reductase Inhibitors) RN - 0 (Adrenergic alpha-Antagonists) RN - 0 (Drug Combinations) RN - 0 (Endothelin-1) RN - 31C4KY9ESH (Nitric Oxide) RN - EC 2.7.11.1 (rho-Associated Kinases) RN - H2D2X058MU (Cyclic GMP) SB - IM MH - 5-alpha Reductase Inhibitors/therapeutic use MH - Adrenergic alpha-Antagonists/therapeutic use MH - Adult MH - Aged MH - Atherosclerosis/complications MH - Autonomic Nervous System Diseases/complications MH - Cyclic GMP/metabolism MH - Drug Combinations MH - Endothelin-1/metabolism MH - Humans MH - Male MH - Metabolic Syndrome/complications MH - Middle Aged MH - Nitric Oxide/metabolism MH - Prostatic Hyperplasia/complications/*drug therapy MH - Prostatism/*etiology MH - Sexual Dysfunction, Physiological/diagnosis/*etiology/therapy MH - rho-Associated Kinases/metabolism EDAT- 2011/07/02 06:00 MHDA- 2012/05/09 06:00 CRDT- 2011/07/02 06:00 PHST- 2011/07/02 06:00 [entrez] PHST- 2011/07/02 06:00 [pubmed] PHST- 2012/05/09 06:00 [medline] AID - 10.1111/j.1742-1241.2011.02731.x [doi] PST - ppublish SO - Int J Clin Pract. 2011 Sep;65(9):1005-13. doi: 10.1111/j.1742-1241.2011.02731.x. Epub 2011 Jul 1.