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Developing a prediction model of children asthma risk using population-based family history health records.
Hamad, Amani F; Yan, Lin; Jafari Jozani, Mohammad; Hu, Pingzhao; Delaney, Joseph A; Lix, Lisa M.
Affiliation
  • Hamad AF; Department of Community Health Sciences, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Yan L; Department of Community Health Sciences, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Jafari Jozani M; Department of Statistics, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Hu P; Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada.
  • Delaney JA; College of Pharmacy, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Lix LM; Department of Epidemiology, University of Washington, Seattle, Washington, USA.
Pediatr Allergy Immunol ; 34(10): e14032, 2023 10.
Article in En | MEDLINE | ID: mdl-37877849
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Asthma Limits: Child / Female / Humans / Male Country/Region as subject: America do norte Language: En Journal: Pediatr Allergy Immunol Journal subject: ALERGIA E IMUNOLOGIA / PEDIATRIA Year: 2023 Type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Asthma Limits: Child / Female / Humans / Male Country/Region as subject: America do norte Language: En Journal: Pediatr Allergy Immunol Journal subject: ALERGIA E IMUNOLOGIA / PEDIATRIA Year: 2023 Type: Article Affiliation country: Canada