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Updated: Jan 13, 2026

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
Published on: June 21, 2018
The IL-4 rs2070874 polymorphism may be associated with the severity of recurrent viral-induced wheeze
Flore Amat1,2,3,4, Malek Louha5, Marta Benet4,6,7
1Department of Allergology-Centre de l'Asthme et des Allergies, Hôpital d'Enfants Armand Trousseau, Assistance Publique-Hôpitaux de Paris, Paris, France.
Insights
Genetic variants in asthma candidate genes are linked to childhood wheezing phenotypes. The IL-4 rs2070874 polymorphism
Area of Science:
- Pediatric Pulmonology
- Genetics
- Immunology
Background:
- Childhood recurrent wheezing presents diverse phenotypes, often leading to asthma.
- Identifying genetic links to these phenotypes is crucial for early diagnosis and management.
Purpose of the Study:
- To investigate the association between genetic variants of asthma candidate genes and specific phenotypes of early-onset wheezing in children.
- To explore the role of genetic polymorphisms in differentiating wheezing phenotypes.
Main Methods:
- Recruited young children with recurrent wheezing, assessing wheezing severity, atopic comorbidities, and biomarkers.
- Genotyped 16 single nucleotide polymorphisms (SNPs) associated with asthma or atopy.
- Utilized hierarchical clustering for phenotype grouping and multinomial logistic regression for SNP association analysis.
Main Results:
- Three distinct wheezing phenotypes were identified: nonatopic uncontrolled severe wheeze (n=207), atopic multiple trigger wheeze (n=61), and episodic viral wheeze (n=49).
- The TT-genotype of the IL-4 rs2070874 polymorphism showed a significant association with the severe, nonatopic wheeze phenotype compared to episodic viral wheeze (OR 7.9; P=0.001).
Conclusions:
- The IL-4 rs2070874 polymorphism's association with severe viral-induced wheeze highlights the role of IL-4 in inflammatory pathways.
- This finding contributes to understanding the genetic underpinnings of severe wheezing phenotypes in children.
Background:
Childhood recurrent wheezing and consequently asthma corresponds to various phenotypes. Our aim was to link genetic variants of asthma candidate genes to the phenotypes of early onset wheezing.
Study Design:
We included very young consecutive children presenting with recurrent wheezing who had been evaluated for the severity of wheezing, associated atopic comorbidities, and tested for biomarkers of atopy and inflammation. All were genotyped for 16 single nucleotide polymorphisms (SNPs) linked with asthma or atopy. An unsupervised hierarchical bottom-up method was used for clustering the phenotypes and a multinomial logistic regression was performed for each individual SNP.
Results:
We replicated the three phenotypes previously described Trousseau Asthma Program in 317 children aged 21.5 ± 7.9 months: cluster 1 (nonatopic uncontrolled severe wheeze), n = 207, a severe viral-induced wheeze, cluster 2 (atopic multiple trigger wheeze), n = 61, with multiple allergic comorbidities, and cluster 3 (episodic viral wheeze), n = 49, a mild viral-induced wheeze. The TT-genotype of the IL-4 rs2070874 polymorphism was significantly associated with the nonatopic uncontrolled severe wheeze compared to the episodic viral wheeze (OR 7.9; CI95% [2.5-25.3]; P = 0.001).
Conclusion:
Association between the TT-genotype of IL-4 rs2070874 polymorphism and a severe phenotype of viral-induced wheeze further underlines the role IL-4 plays in the inflammation pathway leading to viral respiratory infections.
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