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An artificial neural network model to diagnose non-obstructive azoospermia based on RNA-binding protein-related genes

Non-obstructive azoospermia (NOA) is a severe form of male infertility, but its pathological mechanisms and diagnostic biomarkers remain obscure. Since the dysregulation of RNA-binding proteins (RBPs) had nonnegligible effects on spermatogenesis, we aimed to investigate the functions and diagnosis v...

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Autores principales: Peng, Fan, Muhuitijiang, Bahaerguli, Zhou, Jiawei, Liang, Haoyu, Zhang, Yu, Zhou, Ranran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188335/
https://www.ncbi.nlm.nih.gov/pubmed/37116198
http://dx.doi.org/10.18632/aging.204674
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author Peng, Fan
Muhuitijiang, Bahaerguli
Zhou, Jiawei
Liang, Haoyu
Zhang, Yu
Zhou, Ranran
author_facet Peng, Fan
Muhuitijiang, Bahaerguli
Zhou, Jiawei
Liang, Haoyu
Zhang, Yu
Zhou, Ranran
author_sort Peng, Fan
collection PubMed
description Non-obstructive azoospermia (NOA) is a severe form of male infertility, but its pathological mechanisms and diagnostic biomarkers remain obscure. Since the dysregulation of RNA-binding proteins (RBPs) had nonnegligible effects on spermatogenesis, we aimed to investigate the functions and diagnosis values of RBPs in NOA. 58 testicular samples (control = 11, NOA = 47) from Gene Expression Omnibus (GEO) were set as the training cohort. Three public datasets, containing GSE45885 (control = 4, NOA = 27), GSE45887 (control = 4, NOA = 16), and GSE145467 (control = 10, NOA = 10), and 44 clinical samples from the local hospital (control = 27, NOA = 17) were used for validation. Through a series of bioinformatical analyses and machine learning algorithms, including genomic difference detection, protein-protein interaction network analysis, LASSO, SVM-RFE, and Boruta, DDX20 and NCBP2 were determined as significant predictors of NOA. Single-cell RNA sequencing of 432 testicular cell samples from NOA patients indicated that DDX20 and NCBP2 were associated with spermatogenesis (false discovery rate < 0.05). Based on the transcriptome expressions of DDX20 and NCBP2, we constructed multiple diagnosis models using logistic regression, random forest, and artificial neural network (ANN). The ANN model exhibited the most reliable predictive performance in the training cohort (AUC = 0.840), GSE45885 (AUC = 0.731), GSE45887 (AUC = 0.781), GSE145467 (AUC = 0.850), and local cohort (AUC = 0.623). Totally, an ANN diagnosis model based on RBP DDX20 and NCBP2 was developed and externally validated in NOA, functioning as a promising tool in clinical practice.
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spelling pubmed-101883352023-05-18 An artificial neural network model to diagnose non-obstructive azoospermia based on RNA-binding protein-related genes Peng, Fan Muhuitijiang, Bahaerguli Zhou, Jiawei Liang, Haoyu Zhang, Yu Zhou, Ranran Aging (Albany NY) Research Paper Non-obstructive azoospermia (NOA) is a severe form of male infertility, but its pathological mechanisms and diagnostic biomarkers remain obscure. Since the dysregulation of RNA-binding proteins (RBPs) had nonnegligible effects on spermatogenesis, we aimed to investigate the functions and diagnosis values of RBPs in NOA. 58 testicular samples (control = 11, NOA = 47) from Gene Expression Omnibus (GEO) were set as the training cohort. Three public datasets, containing GSE45885 (control = 4, NOA = 27), GSE45887 (control = 4, NOA = 16), and GSE145467 (control = 10, NOA = 10), and 44 clinical samples from the local hospital (control = 27, NOA = 17) were used for validation. Through a series of bioinformatical analyses and machine learning algorithms, including genomic difference detection, protein-protein interaction network analysis, LASSO, SVM-RFE, and Boruta, DDX20 and NCBP2 were determined as significant predictors of NOA. Single-cell RNA sequencing of 432 testicular cell samples from NOA patients indicated that DDX20 and NCBP2 were associated with spermatogenesis (false discovery rate < 0.05). Based on the transcriptome expressions of DDX20 and NCBP2, we constructed multiple diagnosis models using logistic regression, random forest, and artificial neural network (ANN). The ANN model exhibited the most reliable predictive performance in the training cohort (AUC = 0.840), GSE45885 (AUC = 0.731), GSE45887 (AUC = 0.781), GSE145467 (AUC = 0.850), and local cohort (AUC = 0.623). Totally, an ANN diagnosis model based on RBP DDX20 and NCBP2 was developed and externally validated in NOA, functioning as a promising tool in clinical practice. Impact Journals 2023-04-24 /pmc/articles/PMC10188335/ /pubmed/37116198 http://dx.doi.org/10.18632/aging.204674 Text en Copyright: © 2023 Peng et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Peng, Fan
Muhuitijiang, Bahaerguli
Zhou, Jiawei
Liang, Haoyu
Zhang, Yu
Zhou, Ranran
An artificial neural network model to diagnose non-obstructive azoospermia based on RNA-binding protein-related genes
title An artificial neural network model to diagnose non-obstructive azoospermia based on RNA-binding protein-related genes
title_full An artificial neural network model to diagnose non-obstructive azoospermia based on RNA-binding protein-related genes
title_fullStr An artificial neural network model to diagnose non-obstructive azoospermia based on RNA-binding protein-related genes
title_full_unstemmed An artificial neural network model to diagnose non-obstructive azoospermia based on RNA-binding protein-related genes
title_short An artificial neural network model to diagnose non-obstructive azoospermia based on RNA-binding protein-related genes
title_sort artificial neural network model to diagnose non-obstructive azoospermia based on rna-binding protein-related genes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188335/
https://www.ncbi.nlm.nih.gov/pubmed/37116198
http://dx.doi.org/10.18632/aging.204674
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