Impact of pharmacologic therapy for benign prostatic hyperplasia on prostate volume and free testosterone and consequently on urinary parameters and sexual desire in men
2017
Background/Aim. Pharmacologic therapy for benign prostatic hyperplasia (BPH)
relieves disease progression and affects the androgen hormone status. A
decrease in the level of free testosterone (freeT) within total testosterone
(totalT) leads to symptoms of sexual dysfunction. The aim of the present
paper is to show the impact of pharmacological treatment for BPH on prostate
volume (PV) and levels of freeT and the effects on urinary parameters and
sexual desire in menduring 6 months of administration. Methods. A clinical
prospective study including 156 BPH patients with moderate urinary symptoms -
International Prostate Symptom Score (IPSS) 30 mL and prostate
specific antigen (PSA) value <4 ng/mL. The average age of patients was 61.16
± 2.97 years. The performed tests included determination of tumor markers
(PSA, free PSA), hormones (totalT, freeT, freeT/totalTratio), transabdominal
ultrasonography and uroflowmetry. Urinary symptoms were measured by IPSS and
the Quality of Life (QoL) questionnaire while the changes in sexual desire
were measured using the International Index of Erectile Function (IIEF)
questionnaire. Four groups were formed, 39 patients each. Group 1 received
alpha1-blocker (AB) tamsulosine, group 2 5alpha-reductase inhibitor (5-ARI)
finasteride, group 3 combined therapy (tamsulosin and finasteride), while the
control group had no therapy. Follow-ups were performed every three and six
months during therapy administration. Results. Prostate volume significantly
decreased in patients on combined therapy(-6.95 ± 2.00; p<0.001)and
finasteride (-6.67 ± 3.35). In the finasteride group, levels of freeT (-4.23
± 5.2; p<0.001)and freeT/totalT ratio (-0.12 ± 0.08; p<0.001)significantly
decreased as did the freeT(-2.64 ± 7.81) and freeT/totalT ratio (-0.09 ±
0.13) in the combined therapy group. Uroflowmetry showed significant
improvement in all parameters across all therapy groups. Combined therapy
provided the greatest improvement in maximum flow rate (Qmax) (+4.06 ± 1.75;
p<0.001) and urinary symptoms (-10.95 ± 3.19). Significant improvement of
sexual desire occurred in patients on tamsulosin (+0.78 ± 1.00; p<0.001),
with slight deterioration in the finasteride group, but without statistical
significance. Conclusion. Hormonal component of pharmacologic therapy for BPH
most effectively reduces PV and freeT levels, improves urinary symptoms with
slight decline of sexual desire in men on finasteride monotherapy.
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