Development and validation of a clinical nomogram to predict prostatic inflammation in men with lower urinary tract symptoms

医学 下尿路症状 列线图 国际前列腺症状评分 泌尿科 前列腺 前列腺炎 前列腺活检 糖尿病 前列腺癌 逻辑回归 活检 内科学 泌尿系统 癌症 内分泌学
作者
Stavros Gravas,Cosimo De Nunzio,Luís Campos Pinheiro,Javier Ponce de León,Konstantinos Skriapas,Ziad Milad,Riccardo Lombardo,Mariana Medeiros,Pantelis Makrides,Michael Samarinas,Mauro Gacci
出处
期刊:Prostate Cancer and Prostatic Diseases [Springer Nature]
被引量:1
标识
DOI:10.1038/s41391-024-00857-5
摘要

Abstract Background Prostatic inflammation is an important etiological component of benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS). The Prostatic Inflammation Nomogram Study (PINS) aimed to develop and validate a nomogram for predicting the presence of prostatic inflammation in men with LUTS. Methods This non-interventional, cross-sectional, prospective study was conducted in six secondary/tertiary centers across Cyprus, Greece, Italy, Portugal, and Spain. Men (≥40 years) with BPH/LUTS scheduled to undergo prostatic surgery or transrectal ultrasound-guided (TRUS) prostate biopsy were included. Fifteen demographic and clinical participant characteristics were selected as possible predictors of prostatic inflammation. The presence of inflammation (according to Irani score) in the prostatic tissue samples obtained from surgery/TRUS biopsy was determined. The effect of each characteristic on the likelihood a prostate specimen demonstrated inflammation (classified by Irani score into two categories, 0–2 [no/minimal inflammation] or 3–6 [moderate/severe inflammation]) was assessed using multiple logistic regression. A nomogram was developed and its discriminatory ability and validity were assessed. Results In total, 423 patients (mean age 68.9 years) were recruited. Prostate volume ultrasound (PVUS) > 50 mL, history of urinary tract infection (UTI) treatment, presence of diabetes, and International Prostate Symptom Score (IPPS) Storage score were statistically significant predictors of Irani classification. Logistic regression demonstrated a statistically significant effect for leucocytes detected via urine dipstick, presence of diabetes, PVUS > 50 mL, history of UTIs, and higher IPSS Storage score for the odds of an inflammatory score category of 3–6 versus 0–2. The nomogram had a concordance index of 0.71, and good internal validity. Conclusions The nomogram developed from PINS had good predictive ability and identified various characteristics to be predictors of prostatic inflammation. Use of the nomogram may aid in individualizing treatment for LUTS, by identifying individuals who are candidates for therapies targeting prostatic inflammation.
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