Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Background: Asthma is a heterogeneous disease with a diverse array of phenotypes that differ in inflammatory characteristics and severity. Identifying and classifying phenotypes in the real world could provide a foundation to improve and personalize asthma management. Leveraging machine learning in analyzing electronic health records (EHRs) provides an opportunity to identify real-world asthma phenotypes.
Objective: We utilized machine-learning techniques applied to EHRs to detect and predict real-world severe asthma (SA) phenotypes and improve the precision of asthma severity diagnoses.
Methods: Data from 31,795 asthma patients were extracted from a health care system's EHR, with 1,112 patients meeting inclusion criteria for analysis. Principal component analysis (PCA) and a Gaussian mixture model classified patients into subject clusters (SCs). Asthma severity was assessed using two predictive models, one based on the American Thoracic Society (ATS) definition and the other a supervised model trained on 50 randomly selected patients whose disease severity was predetermined by 2 independent physicians.
Results: Three principal components (PCs) emerged, reflecting lung function (PC1), blood inflammatory markers (PC2), and systemic corticosteroid receipt (PC3). PCA identified 5 distinct asthma phenotypes with significant clinical, physiologic, and inflammatory differences. A supervised model, trained on 50 randomly selected patients, predicted SA with 92% precision and 85% accuracy. SC3 was classified as an inflammatory, SA phenotype, making it highly suitable for biologic therapy.
Conclusion: Integrating machine learning with EHRs successfully classified and identified real-world asthma phenotypes, demonstrating the potential of this approach to identify SA for appropriate management and/or clinical studies.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12139413 | PMC |
http://dx.doi.org/10.1016/j.jacig.2025.100473 | DOI Listing |