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Published on: November 4, 2010
Treatment outcome clustering patterns correspond to discrete asthma phenotypes in children
Ivana Banić1, Mario Lovrić2,3, Gerald Cuder4
1Srebrnjak Children's Hospital, Srebrnjak 100, 10000, Zagreb, Croatia.
Insights
Machine learning identified four pediatric asthma clusters with distinct treatment responses. Some clusters showed better outcomes, linked to atopy and specific genes, while others had poorer success due to inflammation type and comorbidities.
Area of Science:
- Pediatric pulmonology
- Computational biology
- Precision medicine
Background:
- Childhood asthma remains difficult to control despite standard therapies.
- Asthma heterogeneity necessitates personalized treatment approaches.
Purpose of the Study:
- To identify distinct pediatric asthma clusters using machine learning.
- To correlate these clusters with treatment outcomes and specific phenotypes.
Main Methods:
- Applied machine learning algorithms to a pediatric asthma cohort.
- Assessed treatment outcome prediction accuracy.
- Analyzed lung function (FEV1, MEF50), airway inflammation (FENO), and disease control.
Main Results:
- Identified 4 distinct pediatric asthma clusters with varied treatment outcomes.
- Clusters 1 and 3 showed better outcomes, associated with atopy and GLCCI1 gene variants.
- Clusters 2 and 4 had poorer outcomes, linked to inflammation type, obesity, and systemic inflammation markers.
Conclusions:
- Asthma management requires personalized strategies beyond generalized approaches.
- Distinct phenotypes within pediatric asthma influence treatment success.
- Machine learning can aid in identifying patient subgroups for tailored therapies.
Abstract:
Despite widely and regularly used therapy asthma in children is not fully controlled. Recognizing the complexity of asthma phenotypes and endotypes imposed the concept of precision medicine in asthma treatment. By applying machine learning algorithms assessed with respect to their accuracy in predicting treatment outcome, we have successfully identified 4 distinct clusters in a pediatric asthma cohort with specific treatment outcome patterns according to changes in lung function (FEV1 and MEF50), airway inflammation (FENO) and disease control likely affected by discrete phenotypes at initial disease presentation, differing in the type and level of inflammation, age of onset, comorbidities, certain genetic and other physiologic traits. The smallest and the largest of the 4 clusters- 1 (N = 58) and 3 (N = 138) had better treatment outcomes compared to clusters 2 and 4 and were characterized by more prominent atopic markers and a predominant allelic (A allele) effect for rs37973 in the GLCCI1 gene previously associated with positive treatment outcomes in asthmatics. These patients also had a relatively later onset of disease (6 + yrs). Clusters 2 (N = 87) and 4 (N = 64) had poorer treatment success, but varied in the type of inflammation (predominantly neutrophilic for cluster 4 and likely mixed-type for cluster 2), comorbidities (obesity for cluster 2), level of systemic inflammation (highest hsCRP for cluster 2) and platelet count (lowest for cluster 4). The results of this study emphasize the issues in asthma management due to the overgeneralized approach to the disease, not taking into account specific disease phenotypes.
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