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Can serum biomarkers predict the outcome of systemic immunosuppressive therapy in adult atopic dermatitis patients?

BACKGROUND: Atopic dermatitis (AD or eczema) is a most common chronic skin disease. Designing personalised treatment strategies for AD based on patient stratification is of high clinical relevance, given a considerable variation in the clinical phenotype and responses to treatments among patients. I...

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Autores principales: Hurault, G., Roekevisch, E., Schram, M. E., Szegedi, K., Kezic, S., Middelkamp‐Hup, M. A., Spuls, P. I., Tanaka, R. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060148/
https://www.ncbi.nlm.nih.gov/pubmed/35665204
http://dx.doi.org/10.1002/ski2.77
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author Hurault, G.
Roekevisch, E.
Schram, M. E.
Szegedi, K.
Kezic, S.
Middelkamp‐Hup, M. A.
Spuls, P. I.
Tanaka, R. J.
author_facet Hurault, G.
Roekevisch, E.
Schram, M. E.
Szegedi, K.
Kezic, S.
Middelkamp‐Hup, M. A.
Spuls, P. I.
Tanaka, R. J.
author_sort Hurault, G.
collection PubMed
description BACKGROUND: Atopic dermatitis (AD or eczema) is a most common chronic skin disease. Designing personalised treatment strategies for AD based on patient stratification is of high clinical relevance, given a considerable variation in the clinical phenotype and responses to treatments among patients. It has been hypothesised that the measurement of biomarkers could help predict therapeutic responses for individual patients. OBJECTIVE: We aim to assess whether serum biomarkers can predict the outcome of systemic immunosuppressive therapy in adult AD patients. METHODS: We developed a statistical machine learning model using the data of an already published longitudinal study of 42 patients who received azathioprine or methotrexate for over 24 weeks. The data contained 26 serum cytokines and chemokines measured before the therapy. The model described the dynamic evolution of the latent disease severity and measurement errors to predict AD severity scores (Eczema Area and Severity Index, (o)SCORing of AD and Patient Oriented Eczema Measure) two‐weeks ahead. We conducted feature selection to identify the most important biomarkers for the prediction of AD severity scores. RESULTS: We validated our model in a forward chaining setting and confirmed that it outperformed standard time‐series forecasting models. Adding biomarkers did not improve predictive performance. CONCLUSIONS: In this study, biomarkers had a negligible and non‐significant effect for predicting the future AD severity scores and the outcome of the systemic therapy.
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spelling pubmed-90601482022-06-04 Can serum biomarkers predict the outcome of systemic immunosuppressive therapy in adult atopic dermatitis patients? Hurault, G. Roekevisch, E. Schram, M. E. Szegedi, K. Kezic, S. Middelkamp‐Hup, M. A. Spuls, P. I. Tanaka, R. J. Skin Health Dis Original Articles BACKGROUND: Atopic dermatitis (AD or eczema) is a most common chronic skin disease. Designing personalised treatment strategies for AD based on patient stratification is of high clinical relevance, given a considerable variation in the clinical phenotype and responses to treatments among patients. It has been hypothesised that the measurement of biomarkers could help predict therapeutic responses for individual patients. OBJECTIVE: We aim to assess whether serum biomarkers can predict the outcome of systemic immunosuppressive therapy in adult AD patients. METHODS: We developed a statistical machine learning model using the data of an already published longitudinal study of 42 patients who received azathioprine or methotrexate for over 24 weeks. The data contained 26 serum cytokines and chemokines measured before the therapy. The model described the dynamic evolution of the latent disease severity and measurement errors to predict AD severity scores (Eczema Area and Severity Index, (o)SCORing of AD and Patient Oriented Eczema Measure) two‐weeks ahead. We conducted feature selection to identify the most important biomarkers for the prediction of AD severity scores. RESULTS: We validated our model in a forward chaining setting and confirmed that it outperformed standard time‐series forecasting models. Adding biomarkers did not improve predictive performance. CONCLUSIONS: In this study, biomarkers had a negligible and non‐significant effect for predicting the future AD severity scores and the outcome of the systemic therapy. John Wiley and Sons Inc. 2022-01-07 /pmc/articles/PMC9060148/ /pubmed/35665204 http://dx.doi.org/10.1002/ski2.77 Text en © 2021 The Authors. Skin Health and Disease published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Hurault, G.
Roekevisch, E.
Schram, M. E.
Szegedi, K.
Kezic, S.
Middelkamp‐Hup, M. A.
Spuls, P. I.
Tanaka, R. J.
Can serum biomarkers predict the outcome of systemic immunosuppressive therapy in adult atopic dermatitis patients?
title Can serum biomarkers predict the outcome of systemic immunosuppressive therapy in adult atopic dermatitis patients?
title_full Can serum biomarkers predict the outcome of systemic immunosuppressive therapy in adult atopic dermatitis patients?
title_fullStr Can serum biomarkers predict the outcome of systemic immunosuppressive therapy in adult atopic dermatitis patients?
title_full_unstemmed Can serum biomarkers predict the outcome of systemic immunosuppressive therapy in adult atopic dermatitis patients?
title_short Can serum biomarkers predict the outcome of systemic immunosuppressive therapy in adult atopic dermatitis patients?
title_sort can serum biomarkers predict the outcome of systemic immunosuppressive therapy in adult atopic dermatitis patients?
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060148/
https://www.ncbi.nlm.nih.gov/pubmed/35665204
http://dx.doi.org/10.1002/ski2.77
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