Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/30095
Title: Exploring biomarkers in the overactive bladder: Alterations in miRNA levels of a panel of genes in patients with OAB
Authors: Fırat, Elif
Aybek, Zafer
Akgün, Ş.
Küçüker, Kürşat
Akça, Hakan
Aybek, Hülya
Keywords: biomarkers
microRNA
overactive bladder
microRNA 139
microRNA 142
microRNA 200c
microRNA 92a
microRNA 98
unclassified drug
biological marker
adult
aged
area under the curve
Article
blood analysis
controlled study
correlation analysis
diagnostic accuracy
diagnostic test accuracy study
diagnostic value
disease marker
down regulation
female
human
major clinical study
middle aged
OAB V8 questionnaire
pathogenesis
pathophysiology
polymerase chain reaction
protein expression
receiver operating characteristic
scoring system
sensitivity and specificity
upregulation
urinary tract disease assessment
very elderly
young adult
blood
gene expression profiling
genetics
metabolism
Adult
Aged
Aged, 80 and over
Biomarkers
Female
Gene Expression Profiling
Humans
MicroRNAs
Middle Aged
Urinary Bladder, Overactive
Young Adult
Publisher: John Wiley and Sons Inc.
Abstract: Aims: It has been demonstrated that there are abundant stable microRNAs (miRNAs) in plasma, which is potentially disease-specific. Adrenergic and muscarinic pathways play an important role in voiding physiology. Alterations in the levels of miRNAs are thought to influence the regulation of these pathways at the molecular level. The aim of this study was to investigate the relationship of miRNAs with overactive bladder pathogenesis and to provide a new perspective to treatment approaches. Methods: This study included patients with an overactive bladder (OAB) diagnosis and a healthy control group. All patients completed a validated OAB-V8 questionnaire. The relative expression levels of 12 miRNAs were examined in plasma by PCR. Receiver operating characteristic (ROC) curves were generated to evaluate the diagnostic qualification of miRNAs. Results: The relative expression levels of let-7b-5p, miR-92a-3p, miR-98-5p, miR-142-3p, and miR-200c-3p were significantly upregulated and miR-139-5p was significantly downregulated in patients with OAB and no correlation was determined between the levels of miRNAs with OAB symptom score. Among the miRNAs, miR-98-5p provided the highest diagnostic accuracy alone (area under curve [AUC] = 0.79) in ROC analysis. The combination of miR-98-5p + miR-139-5p was seen to be a good indicator (AUC = 0.839). Conclusions: These results suggest that alteration of the miRNA levels can be used as auxiliary parameters to explain the pathophysiology of OAB syndrome and could shed light on new treatment options. © 2019 Wiley Periodicals, Inc.
URI: https://hdl.handle.net/11499/30095
https://doi.org/10.1002/nau.24065
ISSN: 0733-2467
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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