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Published on: May 11, 2015
Learning a Comorbidity-Driven Taxonomy of Pediatric Pulmonary Hypertension
Mei-Sing Ong1, Mary P Mullen2, Eric D Austin2
1From the Computational Health Informatics Program (M.-S.O., M.D.N., A.G., S.W.K., K.D.M.), Department of Cardiology (M.P.M.), Division of Critical Care Medicine, Department of Anesthesiology, Perioperative, and Pain Medicine (A.G.), and Department of Anesthesia (A.G.), Harvard School of Medicine, Boston Children's Hospital, MA; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN (E.D.A.); Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge (P.S.); Department of Pediatrics, Massachusetts General Hospital, Boston (M.D.N.); and Department of Biostatistics, Harvard School of Public Health, Boston, MA. (T.C.). mei-sing_ong@hms.harvard.edu.
Insights
Network science analysis of pediatric pulmonary hypertension (PH) comorbidities identified known and rare disease subtypes. This approach aids in refining PH classification and understanding its diverse manifestations in children.
Area of Science:
- Pediatric Pulmonology
- Computational Biology
- Network Science
Background:
- Pediatric pulmonary hypertension (PH) is a complex condition with varied clinical presentations and treatment responses.
- Accurate classification of pediatric PH subtypes is essential for personalized patient care.
- Current understanding of the full spectrum of pediatric PH remains incomplete.
Purpose of the Study:
- To investigate the clinical manifestations of PH in children.
- To evaluate the utility of a network-based approach for identifying PH subtypes using comorbidity data.
- To enhance the classification of pediatric PH.
Main Methods:
- Retrospective cohort study of 6,943,263 children in the US (2010-2013).
- Identified 1583 children with PH and analyzed associated comorbidities.
- Constructed a Bayesian comorbidity network and applied clustering analysis to derive disease subtypes.
Main Results:
- 186 comorbidities were significantly associated with pediatric PH.
- Network analysis successfully identified established PH subtypes based on WHO and Panama classifications.
- The study uncovered rare PH subtypes linked to genetic syndromes, previously identified only in limited case studies.
Conclusions:
- Network science offers a powerful method for discovering disease subtypes from longitudinal comorbidity data.
- This validated approach successfully identified known PH subtypes and revealed rare ones.
- The findings provide a basis for further research to enrich existing pediatric PH classifications.
Rationale:
Pediatric pulmonary hypertension (PH) is a heterogeneous condition with varying natural history and therapeutic response. Precise classification of PH subtypes is, therefore, crucial for individualizing care. However, gaps remain in our understanding of the spectrum of PH in children.
Objective:
We seek to study the manifestations of PH in children and to assess the feasibility of applying a network-based approach to discern disease subtypes from comorbidity data recorded in longitudinal data sets.
Methods And Results:
A retrospective cohort study comprising 6 943 263 children (<18 years of age) enrolled in a commercial health insurance plan in the United States, between January 2010 and May 2013. A total of 1583 (0.02%) children met the criteria for PH. We identified comorbidities significantly associated with PH compared with the general population of children without PH. A Bayesian comorbidity network was constructed to model the interdependencies of these comorbidities, and network-clustering analysis was applied to derive disease subtypes comprising subgraphs of highly connected comorbid conditions. A total of 186 comorbidities were found to be significantly associated with PH. Network analysis of comorbidity patterns captured most of the major PH subtypes with known pathological basis defined by the World Health Organization and Panama classifications. The analysis further identified many subtypes documented in only a few case studies, including rare subtypes associated with several well-described genetic syndromes.
Conclusions:
Application of network science to model comorbidity patterns recorded in longitudinal data sets can facilitate the discovery of disease subtypes. Our analysis relearned established subtypes, thus validating the approach, and identified rare subtypes that are difficult to discern through clinical observations, providing impetus for deeper investigation of the disease subtypes that will enrich current disease classifications.
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