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| Main Authors: | , , , , , , , , , |
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| Format: | Preprint |
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2025
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2506.22136 |
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| _version_ | 1866916813061750784 |
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| author | Gardinazzi, Yuri March, Roger Gonzaléz Kalahasti, Suprabhath Ramirez, Andrea Montaño Neri, Matteo Nguyen, Cicely Palermo, Giovanni Weis, Erik Ledebur, Katharina Dervić, Elma |
| author_facet | Gardinazzi, Yuri March, Roger Gonzaléz Kalahasti, Suprabhath Ramirez, Andrea Montaño Neri, Matteo Nguyen, Cicely Palermo, Giovanni Weis, Erik Ledebur, Katharina Dervić, Elma |
| contents | Comorbidity networks, which capture disease-disease co-occurrence usually based on electronic health records, reveal structured patterns in how diseases cluster and progress across individuals. However, how these networks evolve across different age groups and how this evolution relates to properties like disease prevalence and mortality remains understudied. To address these issues, we used publicly available comorbidity networks extracted from a comprehensive dataset of 45 million Austrian hospital stays from 1997 to 2014, covering 8.9 million patients. These networks grow and become denser with age. We identified groups of diseases that exhibit similar patterns of structural centrality throughout the lifespan, revealing three dominant age-related components with peaks in early childhood, midlife, and late life. To uncover the drivers of this structural change, we examined the relationship between prevalence and degree. This allowed us to identify conditions that were disproportionately connected to other diseases. Using betweenness centrality in combination with mortality data, we further identified high-mortality bridging diseases. Several diseases show high connectivity relative to their prevalence, such as iron deficiency anemia (D50) in children, nicotine dependence (F17), and lipoprotein metabolism disorders (E78) in adults. We also highlight structurally central diseases with high mortality that emerge at different life stages, including cancers (C group), liver cirrhosis (K74), subarachnoid hemorrhage (I60), and chronic kidney disease (N18). These findings underscore the importance of targeting age-specific, network-central conditions with high mortality for prevention and integrated care. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2506_22136 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Characterization Of Diseases In Temporal Comorbidity Networks Gardinazzi, Yuri March, Roger Gonzaléz Kalahasti, Suprabhath Ramirez, Andrea Montaño Neri, Matteo Nguyen, Cicely Palermo, Giovanni Weis, Erik Ledebur, Katharina Dervić, Elma Physics and Society Social and Information Networks Medical Physics Comorbidity networks, which capture disease-disease co-occurrence usually based on electronic health records, reveal structured patterns in how diseases cluster and progress across individuals. However, how these networks evolve across different age groups and how this evolution relates to properties like disease prevalence and mortality remains understudied. To address these issues, we used publicly available comorbidity networks extracted from a comprehensive dataset of 45 million Austrian hospital stays from 1997 to 2014, covering 8.9 million patients. These networks grow and become denser with age. We identified groups of diseases that exhibit similar patterns of structural centrality throughout the lifespan, revealing three dominant age-related components with peaks in early childhood, midlife, and late life. To uncover the drivers of this structural change, we examined the relationship between prevalence and degree. This allowed us to identify conditions that were disproportionately connected to other diseases. Using betweenness centrality in combination with mortality data, we further identified high-mortality bridging diseases. Several diseases show high connectivity relative to their prevalence, such as iron deficiency anemia (D50) in children, nicotine dependence (F17), and lipoprotein metabolism disorders (E78) in adults. We also highlight structurally central diseases with high mortality that emerge at different life stages, including cancers (C group), liver cirrhosis (K74), subarachnoid hemorrhage (I60), and chronic kidney disease (N18). These findings underscore the importance of targeting age-specific, network-central conditions with high mortality for prevention and integrated care. |
| title | Characterization Of Diseases In Temporal Comorbidity Networks |
| topic | Physics and Society Social and Information Networks Medical Physics |
| url | https://arxiv.org/abs/2506.22136 |