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Data-driven comorbidity analysis of 100 common disorders reveals patient subgroups with differing mortality risks and laboratory correlates

Authors :
Miika Koskinen
Jani K. Salmi
Anu Loukola
Mika J. Mäkelä
Juha Sinisalo
Olli Carpén
Risto Renkonen
HUSLAB
Medicum
University of Helsinki
Research Programs Unit
Bio Bank
Precision Cancer Pathology
HUS Inflammation Center
Department of Dermatology, Allergology and Venereology
Clinicum
HUS Heart and Lung Center
Department of Medicine
Department of Pathology
Olli Mikael Carpen / Principal Investigator
HUS Diagnostic Center
Department of Bacteriology and Immunology
Risto Renkonen / Principal Investigator
Infection Biology Research Program
Source :
Scientific reports. 12(1)
Publication Year :
2022

Abstract

The populational heterogeneity of a disease, in part due to comorbidity, poses several complexities. Individual comorbidity profiles, on the other hand, contain useful information to refine phenotyping, prognostication, and risk assessment, and they provide clues to underlying biology. Nevertheless, the spectrum and the implications of the diagnosis profiles remain largely uncharted. Here we mapped comorbidity patterns in 100 common diseases using 4-year retrospective data from 526,779 patients and developed an online tool to visualize the results. Our analysis exposed disease-specific patient subgroups with distinctive diagnosis patterns, survival functions, and laboratory correlates. Computational modeling and real-world data shed light on the structure, variation, and relevance of populational comorbidity patterns, paving the way for improved diagnostics, risk assessment, and individualization of care. Variation in outcomes and biological correlates of a disease emphasizes the importance of evaluating the generalizability of current treatment strategies, as well as considering the limitations that selective inclusion criteria pose on clinical trials.

Details

ISSN :
20452322
Volume :
12
Issue :
1
Database :
OpenAIRE
Journal :
Scientific reports
Accession number :
edsair.doi.dedup.....e34a86b0f962b9d6cb4889cde9fb7dc7