Biomarkers Implicated in Lower Urinary Tract Symptoms: Systematic Review and Pathway Analyses

医学 泌尿系统 生物标志物 膀胱过度活动 下尿路症状 混淆 生物标志物发现 间质性膀胱炎 生物信息学 肿瘤科 内科学 病理 蛋白质组学 前列腺 化学 替代医学 癌症 基因 生物 生物化学
作者
Nazema Y. Siddiqui,Brian T. Helfand,Victor P. Andreev,Joseph T. Kowalski,Megan Bradley,H. Henry Lai,Mitchell B. Berger,Margaret Mueller,Jennifer A. Bickhaus,Vignesh T. Packiam,Dee E. Fenner,Brenda W Gillispie,Ziya Kırkalı
出处
期刊:The Journal of Urology [Ovid Technologies (Wolters Kluwer)]
卷期号:202 (5): 880-889 被引量:27
标识
DOI:10.1097/ju.0000000000000257
摘要

Lower urinary tract symptoms are prevalent and burdensome, yet methods to enhance diagnosis and appropriately guide therapies are lacking. We systematically reviewed the literature for human studies of biomarkers associated with lower urinary tract symptoms.PubMed®, EMBASE® and Web of Science® were searched from inception to February 13, 2018. Articles were included if they were in English, performed in benign urological populations without neurological disorders or interstitial cystitis/bladder pain syndrome, and assessed a biomarker's association with or ability to predict specific lower urinary tract symptoms or urological conditions. Bioinformatic pathway analyses were conducted to determine whether individual biomarkers associated with symptoms are present in unifying pathways.Of 6,150 citations identified 125 met the inclusion criteria. Most studies (93.6%) assessed biomarkers at 1 time point and were cross-sectional in nature. Few studies adjusted for potentially confounding clinical variables or assessed biomarkers in an individual over time. No individual biomarkers are currently validated as diagnostic tools for lower urinary tract symptoms. Compared to controls, pathway analyses identified multiple immune response pathways that were enriched in overactive bladder syndrome and cell migration/cytoskeleton remodeling pathways that were enriched in female stress incontinence.Major deficiencies in the existing biomarker literature include poor reproducibility of laboratory data, unclear classification of patients with lower urinary tract symptoms and lack of adjustment for clinical covariates. Despite these limitations we identified multiple putative pathways in which panels of biological markers need further research.
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