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Novel Machine Learning Identifies 5 Asthma Phenotypes Using Cluster Analysis of Real-World Data.
Wu, Chao-Ping; Sleiman, Joelle; Fakhry, Battoul; Chedraoui, Celine; Attaway, Amy; Bhattacharyya, Anirban; Bleecker, Eugene R; Erdemir, Ahmet; Hu, Bo; Kethireddy, Shravan; Meyers, Deborah A; Rashidi, Hooman H; Zein, Joe G.
Affiliation
  • Wu CP; Respiratory Institute, Cleveland Clinic, Cleveland, Ohio.
  • Sleiman J; Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
  • Fakhry B; Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
  • Chedraoui C; Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
  • Attaway A; Respiratory Institute, Cleveland Clinic, Cleveland, Ohio; Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
  • Bhattacharyya A; Department of Medicine, Mayo Clinic, Jacksonville, Fla.
  • Bleecker ER; Department of Medicine, Division of Pulmonary Medicine, Mayo Clinic, Scottsdale, Ariz.
  • Erdemir A; Respiratory Institute, Cleveland Clinic, Cleveland, Ohio.
  • Hu B; Respiratory Institute, Cleveland Clinic, Cleveland, Ohio.
  • Kethireddy S; Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
  • Meyers DA; Department of Medicine, Division of Pulmonary Medicine, Mayo Clinic, Scottsdale, Ariz.
  • Rashidi HH; Pathology and Laboratory Medicine Institute, Cleveland Clinic, Ohio.
  • Zein JG; Department of Medicine, Division of Pulmonary Medicine, Mayo Clinic, Scottsdale, Ariz. Electronic address: Zein.Joe@mayo.edu.
Article de En | MEDLINE | ID: mdl-38685479
ABSTRACT

BACKGROUND:

Asthma classification into different subphenotypes is important to guide personalized therapy and improve outcomes.

OBJECTIVES:

To further explore asthma heterogeneity through determination of multiple patient groups by using novel machine learning (ML) approaches and large-scale real-world data.

METHODS:

We used electronic health records of patients with asthma followed at the Cleveland Clinic between 2010 and 2021. We used k-prototype unsupervised ML to develop a clustering model where predictors were age, sex, race, body mass index, prebronchodilator and postbronchodilator spirometry measurements, and the usage of inhaled/systemic steroids. We applied elbow and silhouette plots to select the optimal number of clusters. These clusters were then evaluated through LightGBM's supervised ML approach on their cross-validated F1 score to support their distinctiveness.

RESULTS:

Data from 13,498 patients with asthma with available postbronchodilator spirometry measurements were extracted to identify 5 stable clusters. Cluster 1 included a young nonsevere asthma population with normal lung function and higher frequency of acute exacerbation (0.8 /patient-year). Cluster 2 had the highest body mass index (mean ± SD, 44.44 ± 7.83 kg/m2), and the highest proportion of females (77.5%) and Blacks (28.9%). Cluster 3 comprised patients with normal lung function. Cluster 4 included patients with lower percent of predicted FEV1 of 77.03 (12.79) and poor response to bronchodilators. Cluster 5 had the lowest percent of predicted FEV1 of 68.08 (15.02), the highest postbronchodilator reversibility, and the highest proportion of severe asthma (44.9%) and blood eosinophilia (>300 cells/µL) (34.8%).

CONCLUSIONS:

Using real-world data and unsupervised ML, we classified asthma into 5 clinically important subphenotypes where group-specific asthma treatment and management strategies can be designed and deployed.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Allergy Clin Immunol Pract Année: 2024 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Allergy Clin Immunol Pract Année: 2024 Type de document: Article