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Machine Learning-Based Classification of Transcriptome Signatures of Non-Ulcerative Bladder Pain Syndrome.
Akshay, Akshay; Besic, Mustafa; Kuhn, Annette; Burkhard, Fiona C; Bigger-Allen, Alex; Adam, Rosalyn M; Monastyrskaya, Katia; Hashemi Gheinani, Ali.
Afiliação
  • Akshay A; Functional Urology Research Laboratory, Department for BioMedical Research DBMR, University of Bern, 3008 Bern, Switzerland.
  • Besic M; Graduate School for Cellular and Biomedical Sciences, University of Bern, 3012 Bern, Switzerland.
  • Kuhn A; Functional Urology Research Laboratory, Department for BioMedical Research DBMR, University of Bern, 3008 Bern, Switzerland.
  • Burkhard FC; Department of Gynaecology, Inselspital University Hospital, 3010 Bern, Switzerland.
  • Bigger-Allen A; Functional Urology Research Laboratory, Department for BioMedical Research DBMR, University of Bern, 3008 Bern, Switzerland.
  • Adam RM; Department of Urology, Inselspital University Hospital, University of Bern, 3012 Bern, Switzerland.
  • Monastyrskaya K; Urological Diseases Research Center, Boston Children's Hospital, Boston, MA 02115, USA.
  • Hashemi Gheinani A; Department of Surgery, Harvard Medical School, Boston, MA 02114, USA.
Int J Mol Sci ; 25(3)2024 Jan 26.
Article em En | MEDLINE | ID: mdl-38338847
ABSTRACT
Lower urinary tract dysfunction (LUTD) presents a global health challenge with symptoms impacting a substantial percentage of the population. The absence of reliable biomarkers complicates the accurate classification of LUTD subtypes with shared symptoms such as non-ulcerative Bladder Pain Syndrome (BPS) and overactive bladder caused by bladder outlet obstruction with Detrusor Overactivity (DO). This study introduces a machine learning (ML)-based approach for the identification of mRNA signatures specific to non-ulcerative BPS. Using next-generation sequencing (NGS) transcriptome data from bladder biopsies of patients with BPS, benign prostatic obstruction with DO, and controls, our statistical approach successfully identified 13 candidate genes capable of discerning BPS from control and DO patients. This set was validated using Quantitative Polymerase Chain Reaction (QPCR) in a larger patient cohort. To confirm our findings, we applied both supervised and unsupervised ML approaches to the QPCR dataset. A three-mRNA signature TPPP3, FAT1, and NCALD, emerged as a robust classifier for non-ulcerative BPS. The ML-based framework used to define BPS classifiers establishes a solid foundation for comprehending the gene expression changes in the bladder during BPS and serves as a valuable resource and methodology for advancing signature identification in other fields. The proposed ML pipeline demonstrates its efficacy in handling challenges associated with limited sample sizes, offering a promising avenue for applications in similar domains.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cistite Intersticial / Bexiga Urinária Hiperativa Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cistite Intersticial / Bexiga Urinária Hiperativa Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article