Abstract

In the present study, we investigated the relationship between potency of oxidative stress and BPH and this may assist to contribute to the realistic explanation of the ethiopathogenesis of BPH. Seventy four newly diagnosed men with BPH (mean age: 54+/-11.2), who had not undergone any previous treatment for BPH, and 62 healthy volunteers (mean age: 55+/-14) were enrolled in the present study. To determine the antioxidative status of plasma, total antioxidant capacity (TAC) was calculated, and to determine the oxidative status of plasma (TOS) total peroxide levels were measured. The ratio of TAC to total peroxide was accepted as an indicator of oxidative stress (OSI). Data are presented as mean SD +/- unless specified. Student t-test and correlation analyses were used to evaluate the statistical significance differences in the median values recorded for all parameters between BPH and control group. Plasma TAC TOS were found in patients and controls (1.70 +/- 0.32, 1.68 +/- 0.19 micromol Trolox Equiv./L), (12.48 +/- 1.98, 12.40 +/- 1.14 micromol / L) respectively. OSI was calculated as 7.57 +/- 1.91, 7.48 +/- 1.33, respectively. Plasma TAC, TOS and OSI levels were not found to be significantly difference between patients and control subjects (p>0.05, p>0.05, p>0.05). The present study has shown that there were not relationship between potency of oxidative stress and BPH. Further well designed studies should be planned to find out whether the oxidative stress-related parameters play role in BPH as an interesting pathology in regard of the etiopathogenesis.

Highlights

  • In the present study, we investigated the relationship between potency of oxidative stress and Benign prostatic hyperplasia (BPH) and this may assist to contribute to the realistic explanation of the ethiopathogenesis of BPH

  • We investigated the relationship between potency of oxidative stress and BPH and this may assist to contribute to the realistic explanation of the ethiopathogenesis of BPH

  • Total PSA and f-PSA levels were significantly higher in patients than control subjects (P=0,001) (Table 2)

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Summary

Introduction

Essential for normal prostate growth and development, play a prominent role. Savas et al Oxidative Stress in BPH disturbances may promote prostate hyperplasia and BPH pathogenesis. Reactive oxygen species (ROS) are produced in metabolic and physiological processes, and harmful oxidative reactions may occur in organisms which remove ROS via enzymatic and nonenzymatic antioxidative mechanisms. Oxidative stress, which has been implicated in over 100 disorders, develops in consequence.[2,3] To our knowledge, there has been no report involving the oxidative/antioxidative status of plasma in the BPH.

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