Literature DB >> 12680831

Clinical characteristics and genotype analysis of patients with cystic fibrosis and nasal polyposis.

M Cimmino1, M Cavaliere, M Nardone, A Plantulli, A Orefice, V Esposito, V Raia.   

Abstract

The prevalence of nasal polyps in a group of paediatric patients with cystic fibrosis was prospectively studied in comparison with a control group with cystic fibrosis but without polyps. Clinical variables, including pulmonary function tests, skin testing and mucociliary transport, were carried out in both groups, as well as genotype analysis. Endoscopic intranasal evaluation identified polyps in 29 of 89 patients (33%). Statistical analysis revealed that patients with nasal polyposis had better pulmonary function, a higher rate of Pseudomonas aeruginosa colonization, more hospitalizations, and more prevalence of allergy to Aspergillus fumigatus than did the comparison group. We found no statistically different genotype distribution between the polyposis and the control group. However, it can be emphasized that the prevalence of the compound heterozygous genotype is higher in the nasal polyposis group than in controls. Our observations suggest that other genetic and environmental factors could play an important role in the development of nasal polyposis.

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Year:  2003        PMID: 12680831     DOI: 10.1046/j.1365-2273.2003.00677.x

Source DB:  PubMed          Journal:  Clin Otolaryngol Allied Sci        ISSN: 0307-7772


  12 in total

1.  Analysis of most common CFTR mutations in patients affected by nasal polyps.

Authors:  Marzena Kostuch; Janusz Klatka; Andrzej Semczuk; Jacek Wojcierowski; Lucas Kulczycki; Jan Oleszczuk
Journal:  Eur Arch Otorhinolaryngol       Date:  2005-06-17       Impact factor: 2.503

2.  Environmental allergies and respiratory morbidities in cystic fibrosis.

Authors:  Joseph M Collaco; Christopher B Morrow; Deanna M Green; Garry R Cutting; Peter J Mogayzel
Journal:  Pediatr Pulmonol       Date:  2012-11-09

3.  Sinonasal characteristics and quality of life by SNOT-22 in adult patients with cystic fibrosis.

Authors:  Suzie Hyeona Kang; Camila Degen Meotti; Karine Bombardelli; Otávio Bejzman Piltcher; Paulo de Tarso Roth Dalcin
Journal:  Eur Arch Otorhinolaryngol       Date:  2016-12-18       Impact factor: 2.503

Review 4.  Pathogenesis and management of nasal polyposis in cystic fibrosis.

Authors:  Jochen G Mainz; Assen Koitschev
Journal:  Curr Allergy Asthma Rep       Date:  2012-04       Impact factor: 4.806

Review 5.  Sinus bacteriology in patients with cystic fibrosis or primary ciliary dyskinesia: A systematic review.

Authors:  Maria E Møller; Mikkel C Alanin; Christian Grønhøj; Kasper Aanæs; Niels Høiby; Christian von Buchwald
Journal:  Am J Rhinol Allergy       Date:  2017-09-01       Impact factor: 2.467

Review 6.  Perspectives on the etiology of chronic rhinosinusitis: an immune barrier hypothesis.

Authors:  Robert C Kern; David B Conley; William Walsh; Rakesh Chandra; Atsushi Kato; Anju Tripathi-Peters; Leslie C Grammer; Robert P Schleimer
Journal:  Am J Rhinol       Date:  2008-09-10

7.  Cystic Fibrosis: Brazilian ENT Experience.

Authors:  Tania Sih; Ricardo Godinho; Leticia Paiva Franco; Otávio Piltcher
Journal:  Int J Otolaryngol       Date:  2012-05-06

Review 8.  Chronic rhinosinusitis and nasal polyposis in cystic fibrosis: update on diagnosis and treatment.

Authors:  Suzie Hyeona Kang; Paulo de Tarso Roth Dalcin; Otavio Bejzman Piltcher; Raphaella de Oliveira Migliavacca
Journal:  J Bras Pneumol       Date:  2015 Jan-Feb       Impact factor: 2.624

Review 9.  Epidemiology of chronic rhinosinusitis, selected risk factors, comorbidities, and economic burden.

Authors:  Achim Beule
Journal:  GMS Curr Top Otorhinolaryngol Head Neck Surg       Date:  2015-12-22

10.  Incidence and evolution of nasal polyps in children and adolescents with cystic fibrosis.

Authors:  Silke Anna Thereza Weber; Giesela Fleischer Ferrari
Journal:  Braz J Otorhinolaryngol       Date:  2008 Jan-Feb
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