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Developing a prediction model of children asthma risk using population-based family history health records
Amani F Hamad1, Lin Yan1, Mohammad Jafari Jozani2
1Department of Community Health Sciences, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Insights
Predicting childhood asthma risk is improved by including parental and child comorbidities. This enhances early intervention strategies for better asthma management in children.
Area of Science:
- Pediatric Medicine
- Epidemiology
- Computational Biology
Background:
- Asthma is a significant pediatric respiratory condition.
- Early identification of high-risk children is crucial for effective prevention and management.
- Existing prediction models may not fully capture the complexity of asthma development.
Purpose of the Study:
- To develop and validate a prediction model for childhood asthma risk.
- To assess the impact of incorporating comorbidities in children and parents into the prediction model.
- To identify key predictors of asthma development in children.
Main Methods:
- Retrospective population-based cohort study using administrative data.
- Inclusion of children born between 1974 and 2000 with parental linkages.
- Application of machine learning models (LASSO logistic regression and random forest) to identify predictors.
Main Results:
- The base model showed limited predictive performance.
- Incorporating children's comorbidities significantly improved sensitivity (0.71).
- Further improvements were observed with the inclusion of parental comorbidities (sensitivity 0.72).
- Key predictors included children's menstrual and mood/anxiety disorders, and parental lipid metabolism disorders and asthma.
Conclusions:
- Children's and parental comorbidities enhance the accuracy of asthma prediction models.
- The findings support the integration of comprehensive comorbidity data for improved childhood asthma risk assessment.
- This approach can aid in targeted preventive strategies and early asthma management.
Background:
Identifying children at high risk of developing asthma can facilitate prevention and early management strategies. We developed a prediction model of children's asthma risk using objectively collected population-based children and parental histories of comorbidities.
Methods:
We conducted a retrospective population-based cohort study using administrative data from Manitoba, Canada, and included children born from 1974 to 2000 with linkages to ≥1 parent. We identified asthma and prior comorbid condition diagnoses from hospital and outpatient records. We used two machine-learning models: least absolute shrinkage and selection operator (LASSO) logistic regression (LR) and random forest (RF) to identify important predictors. The predictors in the base model included children's demographics, allergic conditions, respiratory infections, and parental asthma. Subsequent models included additional multiple comorbidities for children and parents.
Results:
The cohort included 195,666 children: 51.3% were males and 17.7% had asthma diagnosis. The base LR model achieved a low predictive performance with sensitivity of 0.47, 95% confidence interval (0.45-0.48), and specificity of 0.67 (0.66-0.67) using a predicted probability threshold of 0.20. Sensitivity significantly improved when children's comorbidities were included using LASSO LR: 0.71 (0.69-0.72). Predictive performance further improved by including parental comorbidities (sensitivity = 0.72 [0.70-0.73], specificity = 0.69 [0.69-0.70]). We observed similar results for the RF models. Children's menstrual disorders and mood and anxiety disorders, parental lipid metabolism disorders and asthma were among the most important variables that predicted asthma risk.
Conclusion:
Including children and parental comorbidities to children's asthma prediction models improves their accuracy.
Related Concept Videos
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Asthma-II: Pathophysiology and Classification
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Critical processes in asthma pathophysiology include:
Statistical Methods for Analyzing Epidemiological Data
Asthma-IV: Diagnostic and Management
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Mechanistic Models: Compartment Models in Individual and Population Analysis

