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Discovery of Urinary Proteomic Signature for Differential Diagnosis of Acute Appendicitis
Acute appendicitis is one of the most common acute abdomens, but the confident preoperative diagnosis is still a challenge. In order to profile noninvasive urinary biomarkers that could discriminate acute appendicitis from other acute abdomens, we carried out mass spectrometric experiments on urine...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7165319/ https://www.ncbi.nlm.nih.gov/pubmed/32337245 http://dx.doi.org/10.1155/2020/3896263 |
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author | Zhao, Yinghua Yang, Lianying Sun, Changqing Li, Yang He, Yangzhige Zhang, Li Shi, Tieliu Wang, Guangshun Men, Xuebo Sun, Wei He, Fuchu Qin, Jun |
author_facet | Zhao, Yinghua Yang, Lianying Sun, Changqing Li, Yang He, Yangzhige Zhang, Li Shi, Tieliu Wang, Guangshun Men, Xuebo Sun, Wei He, Fuchu Qin, Jun |
author_sort | Zhao, Yinghua |
collection | PubMed |
description | Acute appendicitis is one of the most common acute abdomens, but the confident preoperative diagnosis is still a challenge. In order to profile noninvasive urinary biomarkers that could discriminate acute appendicitis from other acute abdomens, we carried out mass spectrometric experiments on urine samples from patients with different acute abdomens and evaluated diagnostic potential of urinary proteins with various machine-learning models. Firstly, outlier protein pools of acute appendicitis and controls were constructed using the discovery dataset (32 acute appendicitis and 41 control acute abdomens) against a reference set of 495 normal urine samples. Ten outlier proteins were then selected by feature selection algorithm and were applied in construction of machine-learning models using naïve Bayes, support vector machine, and random forest algorithms. The models were assessed in the discovery dataset by leave-one-out cross validation and were verified in the validation dataset (16 acute appendicitis and 45 control acute abdomens). Among the three models, random forest model achieved the best performance: the accuracy was 84.9% in the leave-one-out cross validation of discovery dataset and 83.6% (sensitivity: 81.2%, specificity: 84.4%) in the validation dataset. In conclusion, we developed a 10-protein diagnostic panel by the random forest model that was able to distinguish acute appendicitis from confusable acute abdomens with high specificity, which indicated the clinical application potential of noninvasive urinary markers in disease diagnosis. |
format | Online Article Text |
id | pubmed-7165319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-71653192020-04-24 Discovery of Urinary Proteomic Signature for Differential Diagnosis of Acute Appendicitis Zhao, Yinghua Yang, Lianying Sun, Changqing Li, Yang He, Yangzhige Zhang, Li Shi, Tieliu Wang, Guangshun Men, Xuebo Sun, Wei He, Fuchu Qin, Jun Biomed Res Int Research Article Acute appendicitis is one of the most common acute abdomens, but the confident preoperative diagnosis is still a challenge. In order to profile noninvasive urinary biomarkers that could discriminate acute appendicitis from other acute abdomens, we carried out mass spectrometric experiments on urine samples from patients with different acute abdomens and evaluated diagnostic potential of urinary proteins with various machine-learning models. Firstly, outlier protein pools of acute appendicitis and controls were constructed using the discovery dataset (32 acute appendicitis and 41 control acute abdomens) against a reference set of 495 normal urine samples. Ten outlier proteins were then selected by feature selection algorithm and were applied in construction of machine-learning models using naïve Bayes, support vector machine, and random forest algorithms. The models were assessed in the discovery dataset by leave-one-out cross validation and were verified in the validation dataset (16 acute appendicitis and 45 control acute abdomens). Among the three models, random forest model achieved the best performance: the accuracy was 84.9% in the leave-one-out cross validation of discovery dataset and 83.6% (sensitivity: 81.2%, specificity: 84.4%) in the validation dataset. In conclusion, we developed a 10-protein diagnostic panel by the random forest model that was able to distinguish acute appendicitis from confusable acute abdomens with high specificity, which indicated the clinical application potential of noninvasive urinary markers in disease diagnosis. Hindawi 2020-04-04 /pmc/articles/PMC7165319/ /pubmed/32337245 http://dx.doi.org/10.1155/2020/3896263 Text en Copyright © 2020 Yinghua Zhao et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhao, Yinghua Yang, Lianying Sun, Changqing Li, Yang He, Yangzhige Zhang, Li Shi, Tieliu Wang, Guangshun Men, Xuebo Sun, Wei He, Fuchu Qin, Jun Discovery of Urinary Proteomic Signature for Differential Diagnosis of Acute Appendicitis |
title | Discovery of Urinary Proteomic Signature for Differential Diagnosis of Acute Appendicitis |
title_full | Discovery of Urinary Proteomic Signature for Differential Diagnosis of Acute Appendicitis |
title_fullStr | Discovery of Urinary Proteomic Signature for Differential Diagnosis of Acute Appendicitis |
title_full_unstemmed | Discovery of Urinary Proteomic Signature for Differential Diagnosis of Acute Appendicitis |
title_short | Discovery of Urinary Proteomic Signature for Differential Diagnosis of Acute Appendicitis |
title_sort | discovery of urinary proteomic signature for differential diagnosis of acute appendicitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7165319/ https://www.ncbi.nlm.nih.gov/pubmed/32337245 http://dx.doi.org/10.1155/2020/3896263 |
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