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Coupling sparse Cox models with clustering of longitudinal transcriptomics data for trauma prognosis
BACKGROUND: Longitudinal gene expression analysis and survival modeling have been proved to add valuable biological and clinical knowledge. This study proposes a novel framework to discover gene signatures and patterns in a high-dimensional time series transcriptomics data and to assess their associ...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048345/ https://www.ncbi.nlm.nih.gov/pubmed/33853663 http://dx.doi.org/10.1186/s13040-021-00257-8 |
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author | Constantino, Cláudia S. Carvalho, Alexandra M. Vinga, Susana |
author_facet | Constantino, Cláudia S. Carvalho, Alexandra M. Vinga, Susana |
author_sort | Constantino, Cláudia S. |
collection | PubMed |
description | BACKGROUND: Longitudinal gene expression analysis and survival modeling have been proved to add valuable biological and clinical knowledge. This study proposes a novel framework to discover gene signatures and patterns in a high-dimensional time series transcriptomics data and to assess their association with hospital length of stay. METHODS: We investigated a longitudinal and high-dimensional gene expression dataset from 168 blunt-force trauma patients followed during the first 28 days after injury. To model the length of stay, an initial dimensionality reduction step was performed by applying Cox regression with elastic net regularization using gene expression data from the first hospitalization days. Also, a novel methodology to impute missing values to the genes selected previously was proposed. We then applied multivariate time series (MTS) clustering to analyse gene expression over time and to stratify patients with similar trajectories. The validation of the patients’ partitions obtained by MTS clustering was performed using Kaplan-Meier curves and log-rank tests. RESULTS: We were able to unravel 22 genes strongly associated with hospital’s discharge. Their expression values in the first days after trauma showed to be good predictors of the length of stay. The proposed mixed imputation method allowed to achieve a complete dataset of short time series with a minimum loss of information for the 28 days of follow-up. MTS clustering enabled to group patients with similar genes trajectories and, notably, with similar discharge days from the hospital. Patients within each cluster have comparable genes’ trajectories and may have an analogous response to injury. CONCLUSION: The proposed framework was able to tackle the joint analysis of time-to-event information with longitudinal multivariate high-dimensional data. The application to length of stay and transcriptomics data revealed a strong relationship between gene expression trajectory and patients’ recovery, which may improve trauma patient’s management by healthcare systems. The proposed methodology can be easily adapted to other medical data, towards more effective clinical decision support systems for health applications. |
format | Online Article Text |
id | pubmed-8048345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80483452021-04-15 Coupling sparse Cox models with clustering of longitudinal transcriptomics data for trauma prognosis Constantino, Cláudia S. Carvalho, Alexandra M. Vinga, Susana BioData Min Methodology BACKGROUND: Longitudinal gene expression analysis and survival modeling have been proved to add valuable biological and clinical knowledge. This study proposes a novel framework to discover gene signatures and patterns in a high-dimensional time series transcriptomics data and to assess their association with hospital length of stay. METHODS: We investigated a longitudinal and high-dimensional gene expression dataset from 168 blunt-force trauma patients followed during the first 28 days after injury. To model the length of stay, an initial dimensionality reduction step was performed by applying Cox regression with elastic net regularization using gene expression data from the first hospitalization days. Also, a novel methodology to impute missing values to the genes selected previously was proposed. We then applied multivariate time series (MTS) clustering to analyse gene expression over time and to stratify patients with similar trajectories. The validation of the patients’ partitions obtained by MTS clustering was performed using Kaplan-Meier curves and log-rank tests. RESULTS: We were able to unravel 22 genes strongly associated with hospital’s discharge. Their expression values in the first days after trauma showed to be good predictors of the length of stay. The proposed mixed imputation method allowed to achieve a complete dataset of short time series with a minimum loss of information for the 28 days of follow-up. MTS clustering enabled to group patients with similar genes trajectories and, notably, with similar discharge days from the hospital. Patients within each cluster have comparable genes’ trajectories and may have an analogous response to injury. CONCLUSION: The proposed framework was able to tackle the joint analysis of time-to-event information with longitudinal multivariate high-dimensional data. The application to length of stay and transcriptomics data revealed a strong relationship between gene expression trajectory and patients’ recovery, which may improve trauma patient’s management by healthcare systems. The proposed methodology can be easily adapted to other medical data, towards more effective clinical decision support systems for health applications. BioMed Central 2021-04-14 /pmc/articles/PMC8048345/ /pubmed/33853663 http://dx.doi.org/10.1186/s13040-021-00257-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Constantino, Cláudia S. Carvalho, Alexandra M. Vinga, Susana Coupling sparse Cox models with clustering of longitudinal transcriptomics data for trauma prognosis |
title | Coupling sparse Cox models with clustering of longitudinal transcriptomics data for trauma prognosis |
title_full | Coupling sparse Cox models with clustering of longitudinal transcriptomics data for trauma prognosis |
title_fullStr | Coupling sparse Cox models with clustering of longitudinal transcriptomics data for trauma prognosis |
title_full_unstemmed | Coupling sparse Cox models with clustering of longitudinal transcriptomics data for trauma prognosis |
title_short | Coupling sparse Cox models with clustering of longitudinal transcriptomics data for trauma prognosis |
title_sort | coupling sparse cox models with clustering of longitudinal transcriptomics data for trauma prognosis |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048345/ https://www.ncbi.nlm.nih.gov/pubmed/33853663 http://dx.doi.org/10.1186/s13040-021-00257-8 |
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