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Prediction of disease severity using serum biomarkers in patients with mild-moderate Atopic Dermatitis: A pilot study
Atopic dermatitis (AD) is an inflammatory skin condition that relies largely on subjective evaluation of clinical signs and symptoms for diagnosis and severity assessment. Using multivariate data, we attempted to construct prediction models that can diagnose the disease and assess its severity. We c...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621918/ https://www.ncbi.nlm.nih.gov/pubmed/37917786 http://dx.doi.org/10.1371/journal.pone.0293332 |
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author | Lee, In-Seon Yeom, Mijung Kim, Kyuseok Hahm, Dae-Hyun Kang, SeHyun Park, Hi-Joon |
author_facet | Lee, In-Seon Yeom, Mijung Kim, Kyuseok Hahm, Dae-Hyun Kang, SeHyun Park, Hi-Joon |
author_sort | Lee, In-Seon |
collection | PubMed |
description | Atopic dermatitis (AD) is an inflammatory skin condition that relies largely on subjective evaluation of clinical signs and symptoms for diagnosis and severity assessment. Using multivariate data, we attempted to construct prediction models that can diagnose the disease and assess its severity. We combined data from 28 mild-moderate AD patients and 20 healthy controls (HC) to create random forest models for classification (AD vs. HC) and regression analysis to predict symptom severities. The classification model outperformed the random permutation model significantly (area under the curve: 0.85 ± 0.10 vs. 0.50 ± 0.15; balanced accuracy: 0.81 ± 0.15 vs. 0.50 ± 0.15). Correlation analysis revealed a significant positive correlation between measured and predicted total SCORing Atopic Dermatitis score (SCORAD; r = 0.43), objective SCORAD (r = 0.53), eczema area and severity index scores (r = 0.58, each p < 0.001), but not between measured and predicted itch ratings (r = 0.21, p = 0.18). We developed and tested multivariate prediction models and identified important features using a variety of serum biomarkers, implying that discovering the deep-branching relationships between clinical measurements and serum measurements in mild-moderate AD patients may be possible using a multivariate machine learning method. We also suggest future methods for utilizing machine learning algorithms to enhance drug target selection, diagnosis, prognosis, and customized treatment in AD. |
format | Online Article Text |
id | pubmed-10621918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-106219182023-11-03 Prediction of disease severity using serum biomarkers in patients with mild-moderate Atopic Dermatitis: A pilot study Lee, In-Seon Yeom, Mijung Kim, Kyuseok Hahm, Dae-Hyun Kang, SeHyun Park, Hi-Joon PLoS One Research Article Atopic dermatitis (AD) is an inflammatory skin condition that relies largely on subjective evaluation of clinical signs and symptoms for diagnosis and severity assessment. Using multivariate data, we attempted to construct prediction models that can diagnose the disease and assess its severity. We combined data from 28 mild-moderate AD patients and 20 healthy controls (HC) to create random forest models for classification (AD vs. HC) and regression analysis to predict symptom severities. The classification model outperformed the random permutation model significantly (area under the curve: 0.85 ± 0.10 vs. 0.50 ± 0.15; balanced accuracy: 0.81 ± 0.15 vs. 0.50 ± 0.15). Correlation analysis revealed a significant positive correlation between measured and predicted total SCORing Atopic Dermatitis score (SCORAD; r = 0.43), objective SCORAD (r = 0.53), eczema area and severity index scores (r = 0.58, each p < 0.001), but not between measured and predicted itch ratings (r = 0.21, p = 0.18). We developed and tested multivariate prediction models and identified important features using a variety of serum biomarkers, implying that discovering the deep-branching relationships between clinical measurements and serum measurements in mild-moderate AD patients may be possible using a multivariate machine learning method. We also suggest future methods for utilizing machine learning algorithms to enhance drug target selection, diagnosis, prognosis, and customized treatment in AD. Public Library of Science 2023-11-02 /pmc/articles/PMC10621918/ /pubmed/37917786 http://dx.doi.org/10.1371/journal.pone.0293332 Text en © 2023 Lee et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lee, In-Seon Yeom, Mijung Kim, Kyuseok Hahm, Dae-Hyun Kang, SeHyun Park, Hi-Joon Prediction of disease severity using serum biomarkers in patients with mild-moderate Atopic Dermatitis: A pilot study |
title | Prediction of disease severity using serum biomarkers in patients with mild-moderate Atopic Dermatitis: A pilot study |
title_full | Prediction of disease severity using serum biomarkers in patients with mild-moderate Atopic Dermatitis: A pilot study |
title_fullStr | Prediction of disease severity using serum biomarkers in patients with mild-moderate Atopic Dermatitis: A pilot study |
title_full_unstemmed | Prediction of disease severity using serum biomarkers in patients with mild-moderate Atopic Dermatitis: A pilot study |
title_short | Prediction of disease severity using serum biomarkers in patients with mild-moderate Atopic Dermatitis: A pilot study |
title_sort | prediction of disease severity using serum biomarkers in patients with mild-moderate atopic dermatitis: a pilot study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621918/ https://www.ncbi.nlm.nih.gov/pubmed/37917786 http://dx.doi.org/10.1371/journal.pone.0293332 |
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