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Data-driven patient stratification of UK Biobank cohort suggests five endotypes of multimorbidity

Multimorbidity generally refers to concurrent occurrence of multiple chronic conditions. These patients are inherently at high risk and often lead a poor quality of life due to delayed treatments. With the emergence of personalized medicine and stratified healthcare, there is a need to stratify pati...

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Autores principales: Prasad, Bodhayan, Bjourson, Anthony J, Shukla, Priyank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9677496/
https://www.ncbi.nlm.nih.gov/pubmed/36209412
http://dx.doi.org/10.1093/bib/bbac410
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author Prasad, Bodhayan
Bjourson, Anthony J
Shukla, Priyank
author_facet Prasad, Bodhayan
Bjourson, Anthony J
Shukla, Priyank
author_sort Prasad, Bodhayan
collection PubMed
description Multimorbidity generally refers to concurrent occurrence of multiple chronic conditions. These patients are inherently at high risk and often lead a poor quality of life due to delayed treatments. With the emergence of personalized medicine and stratified healthcare, there is a need to stratify patients right at the primary care setting. Here we developed multimorbidity analysis pipeline (MulMorPip), which can stratify patients into multimorbid subgroups or endotypes based on their lifetime disease diagnosis and characterize them based on demographic features and underlying disease–disease interaction networks. By implementing MulMorPip on UK Biobank cohort, we report five distinct molecular subclasses or endotypes of multimorbidity. For each patient, we calculated the existence of broad disease classes defined by Charlson's comorbidity classification using the International Classification of Diseases-10 encoding. We then applied multiple correspondence analysis in 77 524 patients from UK Biobank, who had multimorbidity of more than one disease, which resulted in five multimorbid clusters. We further validated these clusters using machine learning and were able to classify 20% model-blind test set patients with an accuracy of 97% and an average Jaccard similarity of 84%. This was followed by demographic characterization and development of interlinking disease network for each cluster to understand disease–disease interactions. Our identified five endotypes of multimorbidity draw attention to dementia, stroke and paralysis as important drivers of multimorbidity stratification. Inclusion of such patient stratification at the primary care setting can help general practitioners to better observe patients’ multiple chronic conditions, their risk stratification and personalization of treatment strategies.
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spelling pubmed-96774962022-11-21 Data-driven patient stratification of UK Biobank cohort suggests five endotypes of multimorbidity Prasad, Bodhayan Bjourson, Anthony J Shukla, Priyank Brief Bioinform Case Study Multimorbidity generally refers to concurrent occurrence of multiple chronic conditions. These patients are inherently at high risk and often lead a poor quality of life due to delayed treatments. With the emergence of personalized medicine and stratified healthcare, there is a need to stratify patients right at the primary care setting. Here we developed multimorbidity analysis pipeline (MulMorPip), which can stratify patients into multimorbid subgroups or endotypes based on their lifetime disease diagnosis and characterize them based on demographic features and underlying disease–disease interaction networks. By implementing MulMorPip on UK Biobank cohort, we report five distinct molecular subclasses or endotypes of multimorbidity. For each patient, we calculated the existence of broad disease classes defined by Charlson's comorbidity classification using the International Classification of Diseases-10 encoding. We then applied multiple correspondence analysis in 77 524 patients from UK Biobank, who had multimorbidity of more than one disease, which resulted in five multimorbid clusters. We further validated these clusters using machine learning and were able to classify 20% model-blind test set patients with an accuracy of 97% and an average Jaccard similarity of 84%. This was followed by demographic characterization and development of interlinking disease network for each cluster to understand disease–disease interactions. Our identified five endotypes of multimorbidity draw attention to dementia, stroke and paralysis as important drivers of multimorbidity stratification. Inclusion of such patient stratification at the primary care setting can help general practitioners to better observe patients’ multiple chronic conditions, their risk stratification and personalization of treatment strategies. Oxford University Press 2022-10-08 /pmc/articles/PMC9677496/ /pubmed/36209412 http://dx.doi.org/10.1093/bib/bbac410 Text en © The Author(s) 2022. Published by Oxford University Press. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Study
Prasad, Bodhayan
Bjourson, Anthony J
Shukla, Priyank
Data-driven patient stratification of UK Biobank cohort suggests five endotypes of multimorbidity
title Data-driven patient stratification of UK Biobank cohort suggests five endotypes of multimorbidity
title_full Data-driven patient stratification of UK Biobank cohort suggests five endotypes of multimorbidity
title_fullStr Data-driven patient stratification of UK Biobank cohort suggests five endotypes of multimorbidity
title_full_unstemmed Data-driven patient stratification of UK Biobank cohort suggests five endotypes of multimorbidity
title_short Data-driven patient stratification of UK Biobank cohort suggests five endotypes of multimorbidity
title_sort data-driven patient stratification of uk biobank cohort suggests five endotypes of multimorbidity
topic Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9677496/
https://www.ncbi.nlm.nih.gov/pubmed/36209412
http://dx.doi.org/10.1093/bib/bbac410
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