Literature DB >> 29100868

Lung function decline is delayed but not decreased in patients with cystic fibrosis and the R117H gene mutation.

Jeffrey S Wagener1, Stefanie J Millar2, Nicole Mayer-Hamblett3, Gregory S Sawicki4, Edward F McKone5, Christopher H Goss6, Michael W Konstan7, Wayne J Morgan8, David J Pasta2, Richard B Moss9.   

Abstract

BACKGROUND: Patients with cystic fibrosis (CF) experience variable lung disease phenotypes. The R117H mutation is often associated with preserved lung function. Our objective was to compare the rate of lung function decline in patients with the R117H mutation and patients homozygous for the F508del mutation.
METHODS: Rate of decline in percentage-of-predicted FEV1 (ppFEV1) was analyzed using the 2006-2010 US CF Foundation Patient Registry.
RESULTS: 4-year rate of decline was slower in 156 R117H patients compared with 6251 F508del patients (-0.61 vs -2.03 ppFEV1/year, P<0.001). Rates of decline in children were slower in R117H vs F508del patients (6-12-year-olds: +0.73 vs -1.91 ppFEV1/year, P<0.001 and 13-17-year-olds: -1.55 vs -2.66 ppFEV1/year, P=0.046), whereas rates in adults were not significantly different (18-24-year-olds: -1.52 vs -2.12, P=0.26 and ≥25-year-olds: -1.17 vs -1.40, P=0.33).
CONCLUSIONS: These findings are consistent with a delayed onset, but ultimately similar progression, of lung disease in R117H compared with homozygous F508del patients.
Copyright © 2017 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cystic fibrosis; F508del; Lung function; Lung function decline; R117H

Mesh:

Substances:

Year:  2017        PMID: 29100868      PMCID: PMC6547371          DOI: 10.1016/j.jcf.2017.10.003

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  19 in total

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Authors:  Clement L Ren; Harsh Desai; Mary Platt; Marissa Dixon
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4.  Diagnosis of Cystic Fibrosis in Screened Populations.

Authors:  Philip M Farrell; Terry B White; Michelle S Howenstine; Anne Munck; Richard B Parad; Margaret Rosenfeld; Olaf Sommerburg; Frank J Accurso; Jane C Davies; Michael J Rock; Don B Sanders; Michael Wilschanski; Isabelle Sermet-Gaudelus; Hannah Blau; Silvia Gartner; Susanna A McColley
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5.  Severity of chest disease in cystic fibrosis patients in relation to their genotypes.

Authors:  L N al-Jader; A L Meredith; H C Ryley; J P Cheadle; S Maguire; G Owen; M C Goodchild; P S Harper
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

6.  A mutation in CFTR produces different phenotypes depending on chromosomal background.

Authors:  S Kiesewetter; M Macek; C Davis; S M Curristin; C S Chu; C Graham; A E Shrimpton; S M Cashman; L C Tsui; J Mickle
Journal:  Nat Genet       Date:  1993-11       Impact factor: 38.330

7.  Genetic determination of exocrine pancreatic function in cystic fibrosis.

Authors:  P Kristidis; D Bozon; M Corey; D Markiewicz; J Rommens; L C Tsui; P Durie
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8.  Bronchoalveolar lavage findings in cystic fibrosis patients with stable, clinically mild lung disease suggest ongoing infection and inflammation.

Authors:  M W Konstan; K A Hilliard; T M Norvell; M Berger
Journal:  Am J Respir Crit Care Med       Date:  1994-08       Impact factor: 21.405

9.  Risk factors for rate of decline in FEV1 in adults with cystic fibrosis.

Authors:  Michael W Konstan; Jeffrey S Wagener; Donald R Vandevanter; David J Pasta; Ashley Yegin; Lawrence Rasouliyan; Wayne J Morgan
Journal:  J Cyst Fibros       Date:  2012-05-05       Impact factor: 5.482

10.  On the mechanism of gating defects caused by the R117H mutation in cystic fibrosis transmembrane conductance regulator.

Authors:  Ying-Chun Yu; Yoshiro Sohma; Tzyh-Chang Hwang
Journal:  J Physiol       Date:  2016-03-23       Impact factor: 5.182

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2.  Ivacaftor in People with Cystic Fibrosis and a 3849+10kb CT or D1152H Residual Function Mutation.

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  2 in total

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