Aspirin-Exacerbated Respiratory Disease Polymorphisms; a review study
Aida Fathollahpour1, Fahimeh Abdi Abyaneh2, Behzad Darabi3
1Iran Universuty of Medical Science, Tehran, Iran.
Genetic factors influencing Aspirin Exacerbated Respiratory Disease (AERD) are complex. Identifying common gene variants may aid in diagnosing and treating AERD, a condition linked to asthma and NSAID sensitivity.
Area of Science:
- Genetics
- Immunology
- Respiratory Medicine
Background:
- Aspirin Exacerbated Respiratory Disease (AERD) involves bronchoconstriction after NSAID use in asthma patients.
- The genetic underpinnings of AERD remain largely unknown.
- Human genome analysis offers insights into genetic polymorphisms and disease susceptibility.
Purpose of the Study:
- To identify genetic factors influencing Aspirin Exacerbated Respiratory Disease (AERD).
- To explore the association between gene polymorphisms and AERD.
- To provide a basis for improved AERD diagnosis and treatment.
Main Methods:
- Systematic review of research studies, letters, comments, editorials, eBooks, and reviews.
- Searches conducted in PubMed/MEDLINE, Web of Sciences, Cochrane Library, and Scopus.
- Keywords included polymorphisms, aspirin-exacerbated respiratory disease, asthma, and allergy.
Main Results:
- Thirty-eight studies were included in the analysis.
- AERD complications were associated with polymorphisms in numerous genes, including ALOX15, EP2, ADRB2, and various HLA types.
- Significant heterogeneity in gene polymorphisms complicates the identification of specific causative genetic changes.
Conclusions:
- AERD is linked to a complex interplay of gene polymorphisms.
- The heterogeneity observed makes pinpointing single genetic factors challenging.
- Examining common gene variants associated with AERD may facilitate diagnosis and treatment strategies.
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