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Pathogenetic approach to the treatment of patients with benign prostatic hyperplasia and chronic prostatitis: modern strategies. A review

A. Al-Shukri, Maria K. Frantsishevskaya, Vladislav Ya. Dubinsky, S. Al-Shukri

Consilium Medicum, 2026

Abstract

The recent increase in the global incidence of benign prostatic hyperplasia (BPH) over the past three decades, combined with the anticipated aging of the population, underscores the urgent need for effective and pathogenetically grounded non-surgical treatment methods. Research has established that chronic inflammation is not merely an accompanying factor but a critical component in the pathogenesis of BPH. Specifically, inflammatory cells and the pro-inflammatory cytokines they produce initiate a series of pathological responses, including tissue remodeling and fibrosis, while also promoting the proliferation of both stromal and epithelial cells within the prostate. Furthermore, inflammatory cytokines have been shown to disrupt hormonal balance in the prostate gland, fostering tissue remodeling and hyperplastic growth. This inflammatory response in BPH often leads to a state of relative hypoxia, driven by the increased oxygen demands of proliferating cells. An additional insult is oxidative stress; the interplay of reduced antioxidant capacity, excessive reactive oxygen species, and chronic inflammation creates a vicious cycle that exacerbates hyperplastic changes. Standard therapies currently employed for BPH primarily focus on symptom relief without directly addressing oxidative stress or inflammation. Given the significant role chronic inflammation plays in BPH pathogenesis, an anti-inflammatory treatment strategy is particularly relevant. One promising approach involves…

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