Single-nucleotide polymorphism in chronic rhinosinusitis: A systematic review
Autor: | Stefani Stefania, Maniaci Antonino, Musso Nicolò, Cocuzza Salvatore, Viglianisi Chiara, Christian Calvo-Henriquez, Merlino Federico, Lechien Jerome Renee, Stracquadanio Stefano, Bonanno Antonio, Santagati Maria, Ignazio La Mantia |
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Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: |
medicine.medical_specialty
Chronic rhinosinusitis SNP Single-nucleotide polymorphism Comorbidity Polymorphism Single Nucleotide polymorphism Atopy Pathogenesis Polymorphism (computer science) Internal medicine medicine Eosinophilia Humans Genetic Predisposition to Disease Sinusitis Asthma Rhinitis metagenomics business.industry chronic rhinosinusitis sequencing medicine.disease Otorhinolaryngology Chronic Disease medicine.symptom business |
Popis: | Objectives We performed a systematic review on single nucleotide polymorphisms and risk-related chronic rhinosinusitis. Design and setting A comprehensive review of the last 20 years' English language literature regarding chronic rhinosinusitis and single nucleotide polymorphisms was performed. We included in the synthesis all the papers reporting gene variation implicated in the pathogenesis of chronic inflammation and polyps. Results We found 12 papers with 9,127 patients, of which 2,739 CRS cases and 6388 controls. The major comorbidities reported related to chronic rhinosinusitis were Atopy in 4,555 (49.9%), Asthma in 4594 (50.33%), Samter Triad in 448 (4.9%), and Eosinophilia in 391 subjects (4.28%). Conclusion Our systematic review revealed the major SNPs significantly associated with chronic rhinosinusitis and the specific pathways involved. Given the presence of different extraction methods and samples sequencing, further studies with larger courts are necessary to identify significative single nucleotide polymorphisms. |
Databáze: | OpenAIRE |
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