Literature DB >> 24791677

Effect of the F508del genotype on outcomes of endoscopic sinus surgery in children with cystic fibrosis.

Bao Anh Julie Do1, Larry C Lands2, Christine Saint-Martin3, Marco A Mascarella1, John J Manoukian4, Sam J Daniel4, Lily H P Nguyen5.   

Abstract

OBJECTIVE: Numerous authors have sought to describe genotype-phenotype correlations in cystic fibrosis (CF), notably to pancreatic insufficiency and lung disease. However, few studies have focused on the association between the F508del genotype and response to sinus surgery. The objective of this study is to assess the effect of the F508del genotype on sinonasal disease severity and outcomes following functional endoscopic sinus surgery (FESS) in a pediatric population.
METHODS: A retrospective chart review of 153 children with CF seen at a tertiary care pediatric hospital from 1995 to 2008 was performed. Patients were classified into one of three groups according to F508del genotype, either as homozygous, heterozygous or not carrying a F508del mutation. The sinonasal disease phenotype of the three groups was compared based on clinical and radiological findings, extent of endoscopic sinus surgery and rate of revision surgery.
RESULTS: The relationship between the F508del genotype and pancreatic insufficiency was confirmed (p<0.05). There was no association between the F508del genotype and increased need for FESS (p=0.75). Moreover, no association was established between F508del homozygosity and presence of nasal polyps, Lund-Mackay score, extent of surgery or length of postoperative hospitalization. The rates of revision surgery did not differ significantly among the three genotypes analyzed (p=0.59).
CONCLUSION: There is no clear association between the F508del genotype and an increased need for FESS, extent of surgery, or revision surgery. Given the phenotypic variability of sinonasal disease in patients with CF, a prospective study is needed to better understand outcomes following FESS and the contribution of gene modifiers to this effect.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Cystic fibrosis; F508del genotype; Functional endoscopic sinus surgery

Mesh:

Year:  2014        PMID: 24791677     DOI: 10.1016/j.ijporl.2014.04.030

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  4 in total

1.  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

2.  Cystic fibrosis transmembrane conductance regulator function, not TAS2R38 gene haplotypes, predict sinus surgery in children and young adults with cystic fibrosis.

Authors:  Nicholas M Dalesio; Melis A Aksit; Kwangmi Ahn; Karen S Raraigh; Joseph M Collaco; Sharon McGrath-Morrow; Pamela L Zeitlin; Steven S An; Garry R Cutting
Journal:  Int Forum Allergy Rhinol       Date:  2020-04-13       Impact factor: 3.858

3.  Predictors of sinonasal disease onset, progression, and severity in pediatric cystic fibrosis patients.

Authors:  Michael S Weinstock; Amber D Shaffer; Amanda L Stapleton
Journal:  Am J Otolaryngol       Date:  2021-03-31       Impact factor: 2.873

4.  Pediatric allergic fungal rhinosinusitis with extensive intracranial extension - Case report and literature review.

Authors:  Haifa Lafi Alenzi; Ali Al Momen; Fadel Molani
Journal:  Int J Surg Case Rep       Date:  2020-09-12
  4 in total

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