Uticaj farmakološke terapije benigne hiperplazije prostate na volumen prostate i slobodni testosteron i, posledično, na urinarne parametre i seksualnu želju muškaraca

  • Nebojša A Stojanović Department of Urology Military Hospital, Niš, Serbia
  • Nebojša Đenić urgical Department, Military Hospital, Niš, Serbia
  • Dragan Bogdanović Department of Biochemical and Medical Sciences, The State University of Novi Pazar, Novi Pazar, Serbia
  • Konstansa Lazarević Department of Biochemical and Medical Sciences, The State University of Novi Pazar, Novi Pazar, Serbia
Ključne reči: prostatic hyperplasia||, ||prostata, hipertrofija, drug therapy||, ||lečenje lekovima, urination disorders||, ||mokrenje, poremećaji, sexual dysfunction, physiological||, ||seksualni poremećaji, quality of life||, ||kvalitet života,

Sažetak


Uvod/Cilj. Farmakološka terapija benigne hiperplazije prostate (BHP) ublažava progresiju bolesti i utiče na androgeni hormonski status. Opadanje nivoa slobodnog testosterona (slobodniT) unutar ukupnog testosterona (ukupniT) dovodi do simptoma seksualne disfunkcije. Cilj rada bio je da se prikažu rezultati uticaja farmakološke terapije BHP u toku 6 meseci korišćenja na volumen prostate (VP) i nivo slobodnogT kao i efekat na urianarne parametre i seksualnu želju muškaraca. Metode. Ova klinička prospektivna studija obuhvatila je 156 bolesnika sa BHP, sa umerenim simptomima poremećaja mokrenja – internacionalni prostata simptom skor (IPSS) < 19,VP > 30 mL i vrednošću prostata specifičnog antigena (PSA) < 4 ng/mL. Prosečna starost bolesnika bila je 61,16 ± 2,97 god. Rađene su analize krvi sa određivanjem tumorskih markera (PSA, slobodni PSA), hormona (ukupniT, slobodniT, odnos slobodniT/ukupniT), transabdominalna ultrasonografija i urofloumetrija. Simptomi poremećenog mokrenja mereni su upitnicima za IPSS i kvalitet života (Quality of Life – QoL), a promene seksualne želje upitnikom Internacionalni indeks erektilne funkcije (IIEF). Formirane su četiri grupe sa po 39 bolesnika. Prva grupa dobijala je alfa1-blokator (AB) tamsulosin, druga grupa inhibitor 5alfa-reduktaze (5-ARI) finasterid, treća grupa kombinovanu terapiju (tamsulosin i finasterid) i četvrta, kontrolna grupa, bila je bez terapije. Kontrole su rađene na tri i šest meseci tokom terapije. Rezultati. Značajno je smanjen VP kod bolesnika sa kombinovanom terapijom (-6,95 ± 2,00; p < 0,001) i finasteridom (-6,67 3,35). U grupi sa finasteridom značajno je smanjen slobodniT (-4,23 ± 5,20; p < 0,001) i odnos slobodniT/ukupniT (-0,12 ± 0,08; p < 0,001), kao i u grupi sa kombinovanom terapijom [slobodniT (-2,64 ± 7,81) i odnos slobodniT/ukupniT (-0,09 ± 0,13)]. Urofloumetrija je pokazala značajno poboljšanje svih urinarnih parametara u svim terapijskim grupama. Kombinovanom terapijom postignuto je najveće poboljšanje maksimalnog protoka (Qmax)(+4,06 1,75; p < 0,001) i simptoma poremećenog mokrenja (-10,95 ± 3,19). Seksualna želja kod bolesnika sa tamsulosinom bla je značajno poboljšana (+0,78 1,00; p < 0,001), dok je u grupi sa finasteridom registrovano blago pogoršanje, ali bez statističke značajnosti. Zaključak. Hormonska komponenta farmakološke terapije za BHP najefikasnije smanjuje VP i nivo slobodnogT, poboljšava simptome poremećenog mokrenja sa blagim pogoršanjem seksualne želje muškaraca lečenih samo finasteridom.

Biografije autora

Nebojša A Stojanović, Department of Urology Military Hospital, Niš, Serbia
Načelnik Odseka za Urologiju,Vojna bolnica Niš
Nebojša Đenić, urgical Department, Military Hospital, Niš, Serbia

Doc dr sci med

Surgical  Department

Military Hospital Nis

Dragan Bogdanović, Department of Biochemical and Medical Sciences, The State University of Novi Pazar, Novi Pazar, Serbia

Doc dr sci med

Department of Biochemical and Medical Sciences

The State University of Novi Pazar

 

Konstansa Lazarević, Department of Biochemical and Medical Sciences, The State University of Novi Pazar, Novi Pazar, Serbia

Doc dr sci med

Department of Biochemical and Medical Sciences

The State University of Novi Pazar

Reference

Patel ND, Parsons JK. Epidemiology and etiology of benign prostatic hyperplasia and bladder outlet obstruction. Indian J Urol 2014; 30(2): 170−6.

Kirby R. Improving lower urinary tract symptoms in BPH. Practitioner 2011; 255(1739): 15−9, 2.

Cooper LA, Page ST. Androgens and prostate disease. Asian J Androl 2014; 16(2): 248−55.

Buvat J, Maggi M, Guay A, Torres LO. Testosterone deficiency in men: systematic Review and standard operating procedures for diagnosis and treatment. J Sex Med 2013; 10: 245−84.

Maggi M, Buvat J, Corona G, Guay A, Torres LO. Hormonal causes of male sexual dysfunctions and their management (hy-perprolactinemia, thyroid disorders, GH disorders, and DHEA). J Sex Med 2013; 10: 661−77.

Seisen T, Rouprêt M, Gallais JL, Costa P. Relevant clinical and bi-ological criteria for the diagnosis of androgen deficiency in the aging male (ADAM). Prog Urol 2012; 22(Suppl 1): S21−6. (French)

Russo A1, La Croce G, Capogrosso P, Ventimiglia E, Colicchia M, Serino A, et al. Latest pharmacotherapy options for benign prostatic hyperplasia. Expert Opin Pharmacother 2014; 15(16): 2319−28.

Osman NI, Mangera A, Chapple CR. Non-Hormonal treatment of BPH/BOO. Indian J Urol 2014; 30(2): 194−201.

Azzouni F, Mohler J. Role of 5α-reductase inhibitors in benign prostatic diseases. Prostate Cancer Prostatic Dis 2012; 15(3): 222−30.

Rick FG, Saadat SH, Szalontay L, Block NL, Kazzazi A, Djavan B, et al. Hormonal manipulation of benign prostatic hyperplas-ia. Curr Opin Urol 2013; 23(1): 17−24.

Giuliano F. Questionnaires in sexual medicine. Prog Urol 2013; 23(9): 811−21.

Paick S, Meehan A, Lee M, Penson D, Wessells H. The relationship among lower urinary tract symptoms, prostate specific antigen and erectile dysfunction in men with benign prostatic hyperplasia: results from the proscar long-term efficacy and safety study. J Urol 2005; 173(3): 903−7.

Kaplan SA, Lee JY, Meehan AG, Kusek JW, MTOPS Research Group. Long-term treatment with finasteride improves clinical progression of benign prostatic hyperplasia in men with an enlarged versus a smaller prostate: Data from the MTOPS trial. J Urol 2011; 185(4): 1369−73.

Zabkowski T. Evaluation of the clinical indications, adverse drug reactions, and finasteride use in patients with benign prostatic hyperplasia in Poland. Pharmacol Rep 2014; 66(4): 565−9.

Kaplan SA, Chung DE, Lee RK, Scofield S, Te AE. A 5-year ret-rospective analysis of 5alpha-reductase inhibitors in men with benign prostatic hyperplasia: Finasteride has comparable uri-nary symptom efficacy and prostate volume reduction, but less sexual side effects and breast complications than dut. Int J Clin Pract 2012; 66(11): 1052−55.

Favilla V, Cimino S, Castelli T, Madonia M, Barbagallo I, Morgia G. Relationship between lower urinary tract symptoms and serum levels of sex hormones in men with symptomatic benign prostatic hyperplasia. BJU Int 2010; 106(11): 1700−3.

Park DS, Hong JY, Hong YK, Lee SR, Hwang JH, Kang MH, et al. Correlation between serum prostate specific antigen level and prostate volume in a community-based cohort: large-scale screening of 35, 223 Korean men. Urology 2013; 82(6): 1394−9.

Welliver C, Butcher M, Potini Y, McVary KT. Impact of alpha blockers, 5-alpha reductase inhibitors and combination therapy on sexual function. Curr Urol Rep 2014; 15(10): 441.

Gur S, Kadowitz PJ, Hellstrom WJ. Effects of 5-alpha reductase inhibitors on erectile function, sexual desire and ejaculation. Expert Opin Drug Saf 2013; 12(1): 81−90.

Gacci M, Eardley I, Giuliano F, Hatzichristou D, Kaplan SA, Maggi M, et al. Critical Analysis of the Relationship Between Sexual Dysfunctions and Lower Urinary Tract Symptoms Due to Be-nign Prostatic Hyperplasia. Eur Urol 2011; 60(4): 809−25.

Irwig MS. Persistent sexual side effects of finasteride: Could they be permanent. J Sex Med 2012; 9(11): 2927−32.

Trost L, Saitz TR, Hellstrom WJ. Side effects of 5-alpha reduc-tase inhibitors A comprehensive review. Sex Med Rev 2013; 1: 24−41.

Lee JH, Kim Y, Park YW, Lee DG. Relationship between be-nign prostatic hyperplasia/lower urinary tract symptoms and total serum testosterone level in healthy middle-aged eugonad-al men. J Sex Med 2014; 11(5): 1309−15.

Kim MK, Zhao C, Kim SD, Kim DG, Park JK. Relationship of sex hormones and nocturia in lower urinary tract symptoms induced by benign prostatic hyperplasia. Aging Male 2012; 15(2): 90−5.

Joo KJ, Sung WS, Park SH, Yang WJ, Kim TH. Comparison of α-blocker monotherapy and α-blocker plus 5α-reductase inhibitor combination therapy based on prostate volume for treatment of benign prostatic hyperplasia. J Int Med Res 2012; 40(3): 899−908.

Son H, Cho SY, Park S, Kang JY, Kim CS, Kim HG. A retrospec-tive study of clinical outcomes of α-blocker or finasteride monotherapy followed by combination therapy: determination of the period of combination therapy of α-blocker and finas-teride. Int J Clin Pract 2013; 67(4): 351−5.

Bechis SK, Otsetov AG, Ge R, Olumi AF. Personalized Medicine for the Management of Benign Prostatic Hyperplasia. J Urol 2014; 192(1): 16−23.

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2017/06/02
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