Morphological changes in prostatic tissue of patients with benign prostatic hyperplasia treated with permixon®


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Abstract

A pilot trial has been performed to assess effects of permixon on
prostatic tissue in patients with benign prostatic hyperplasia (BPH).
A total of 49 BPH and control patients entered the trial. 36 patients
of the study group were randomized into 3 subgroups of 12 patients
each. Permixon was taken in a standard dose of 320 mg/day for 3, 6
and 12 months, respectively. Mean duration of BPH was 3.7 years
(0-8 years). Mean value of PCA was 6.0 ng/ml. The control group of
13 patients were not given permixon. Multifocal prostatic biopsy was
performed in all the patients before and after the treatment or follow-up.
Stromal-parenchymatous correlation in the study group significantly
increased (by 59%) - from 3.28 (0.25-9.61) to 5.22 (1.20-10.67)
(p = 0.0002). For the control group this correlation was insignificant.
Permixon-treated patients demonstrated inhibition of prostatic epithelium
proliferative activity by 32% (p = 0.0001) and a rise in the
stage of proliferative centers development from stage II-III to IV-V.
Intensity of inflammation in prostatic tissue decreased by 53% in the
study group and insignificantly in the control group. Thus, permixon
treatment of BPH leads to a significant rise in stromal-parenchymatous
correlation due to inhibition of proliferative activity of prostatic
epithelium and attenuation of inflammation.

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