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The association between local atherosclerosis of the prostatic artery and benign prostatic enlargement in humans: Putative mechanism of chronic ischemia for prostatic enlargement
Author(s) -
Haga Nobuhiro,
Akaihata Hidenori,
Hata Junya,
Aikawa Ken,
Yanagida Tomohiko,
Matsuoka Kanako,
Koguchi Tomoyuki,
Hoshi Seiji,
Ogawa Soichiro,
Kataoka Masao,
Sato Yuichi,
Ishibashi Kei,
Suzuki Osamu,
Hashimoto Yuko,
Kojima Yoshiyuki
Publication year - 2018
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.23658
Subject(s) - medicine , prostatectomy , urology , hyperplasia , prostate , prostate cancer , pathology , cancer
Background To investigate the possible pathogenesis of the benign prostatic enlargement (BPE) induced by local atherosclerosis, the association between local atherosclerosis and prostatic enlargement was investigated, and molecular biological analyses were performed using human prostatectomy specimens. Methods A total of 69 consecutive patients who underwent robot‐assisted radical prostatectomy (RARP) participated in this prospective study. To evaluate actual local atherosclerosis, prostatic arteries were removed during RARP. Microscopic assessment of local atherosclerosis was classified as one of three degrees of narrowing (minimal, moderate, and severe) according to the degree of obstruction of the inner cavity of the prostatic artery. The expressions of several mediators related to chronic ischemia and cell proliferation of the prostate were investigated by immunohistochemistry. Results The median age of the present cohort was 68 (range: 55‐75) years. Although there was no relationship between local atherosclerosis and lower urinary symptoms evaluated by questionnaires, local atherosclerosis was significantly more severe in patients who had a history of treatment for benign prostatic hyperplasia ( P = 0.02). Prostate size was significantly larger in the severe local atherosclerosis group than in the minimal and moderate local atherosclerosis groups ( P < 0.001 and P = 0.03, respectively). Thepositive expression rates of hypoxia‐inducible factor (HIF)‐1α, malondialdehyde (MDA), transforming growth factor (TGF)‐β 1 , and basic fibroblast growth factor (bFGF) in the prostate were significantly higher in patients with local atherosclerosis than in patients without local atherosclerosis (all P < 0.01, respectively). Conclusions In human surgical specimens, there is evidence that local atherosclerosis of the prostatic artery is significantly associated with prostate size. Given the molecular evidence provided in this study, the putative mechanism for this relationship is that chronic ischemia induced upregulation of oxidative stress pathways, leading to BPE.