Dutasteride, a 5 alpha reductase inhibitor, could be associated with the exacerbation of inflammation in patients with benign prostatic hyperplasia.

IPSS alpha‐1 blocker chronic prostatic inflammation dihydrotestosterone dutasteride high endothelial venule‐like vessel

Journal

International journal of urology : official journal of the Japanese Urological Association
ISSN: 1442-2042
Titre abrégé: Int J Urol
Pays: Australia
ID NLM: 9440237

Informations de publication

Date de publication:
23 Oct 2024
Historique:
received: 26 05 2024
accepted: 03 10 2024
medline: 23 10 2024
pubmed: 23 10 2024
entrez: 23 10 2024
Statut: aheadofprint

Résumé

α-1 blockers and dutasteride are widely used as agents to treat benign prostatic hyperplasia (BPH); the impact of these drugs on prostatic inflammation is still unclear. Herein, we investigated the impact of α-1 blockers and dutasteride treatment of BPH in terms of the degree of prostatic inflammation. Tissue specimens were obtained from 143 BPH patients who were administered α-1 blockers up until their operation. Thirty-three of the patients had also been treated with dutasteride before the procedure. The degree of prostatic inflammation was quantified histologically by the ratio of high endothelial venule (HEV)-like vessels. We divided this retrospective cohort into α-1 blocker monotherapy and combination therapy (α-1 blockers + dutasteride) groups and evaluated clinical parameters of the two groups in relation to the degree of chronic prostatic inflammation. At the same time, we assessed factors exacerbating chronic prostatic inflammation. Comparison of the monotherapy and combination therapy groups showed no significant differences in the parameters of the urodynamic study or degree of chronic prostatic inflammation, whereas the IPSS total score, voiding subscore, nocturia, intermittency, weak stream, and straining were significantly lower in the combination than the monotherapy group. The duration of α-1 blockers administration was not correlated with the ratio of HEV-like vessels, while that of dutasteride was strongly correlated (correlation coefficient = 0.595; p < 0.001). Multiple regression analysis demonstrated that the duration of dutasteride administration was a key factor exacerbating the degree of chronic prostatic inflammation. The present study showed that despite their ameliorating effect on prostatic hyperplasia, dutasteride contributed significantly to chronic prostatic inflammation.

Sections du résumé

BACKGROUND BACKGROUND
α-1 blockers and dutasteride are widely used as agents to treat benign prostatic hyperplasia (BPH); the impact of these drugs on prostatic inflammation is still unclear. Herein, we investigated the impact of α-1 blockers and dutasteride treatment of BPH in terms of the degree of prostatic inflammation.
MATERIALS AND METHODS METHODS
Tissue specimens were obtained from 143 BPH patients who were administered α-1 blockers up until their operation. Thirty-three of the patients had also been treated with dutasteride before the procedure. The degree of prostatic inflammation was quantified histologically by the ratio of high endothelial venule (HEV)-like vessels. We divided this retrospective cohort into α-1 blocker monotherapy and combination therapy (α-1 blockers + dutasteride) groups and evaluated clinical parameters of the two groups in relation to the degree of chronic prostatic inflammation. At the same time, we assessed factors exacerbating chronic prostatic inflammation.
RESULTS RESULTS
Comparison of the monotherapy and combination therapy groups showed no significant differences in the parameters of the urodynamic study or degree of chronic prostatic inflammation, whereas the IPSS total score, voiding subscore, nocturia, intermittency, weak stream, and straining were significantly lower in the combination than the monotherapy group. The duration of α-1 blockers administration was not correlated with the ratio of HEV-like vessels, while that of dutasteride was strongly correlated (correlation coefficient = 0.595; p < 0.001). Multiple regression analysis demonstrated that the duration of dutasteride administration was a key factor exacerbating the degree of chronic prostatic inflammation.
CONCLUSIONS CONCLUSIONS
The present study showed that despite their ameliorating effect on prostatic hyperplasia, dutasteride contributed significantly to chronic prostatic inflammation.

Identifiants

pubmed: 39441013
doi: 10.1111/iju.15612
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Author(s). International Journal of Urology published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Urological Association.

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Auteurs

So Inamura (S)

Department of Urology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Yusuke Fukiage (Y)

Department of Urology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Hisato Kobayashi (H)

Department of Urology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Manami Tsutsumiuchi (M)

Department of Urology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Masaya Seki (M)

Department of Urology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Minekatsu Taga (M)

Department of Urology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Masato Fukushima (M)

Department of Urology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Motohiro Kobayashi (M)

Department of Tumor Pathology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Osamu Yokoyama (O)

Department of Urology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Naoki Terada (N)

Department of Urology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.

Classifications MeSH