Your browser doesn't support javascript.
loading
Effect of lumacaftor-ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis: Results from the PROSPECT MCC sub-study.
Donaldson, Scott H; Laube, Beth L; Mogayzel, Peter; Corcoran, Timothy E; Pilewski, Joseph M; Ceppe, Agathe; Wu, Jihong; Bhambhvani, Pradeep G; Ratjen, Felix; Sagel, Scott D; Clancy, J P; Rowe, Steven M; Bennett, William D.
Affiliation
  • Donaldson SH; Department of Medicine and the Marsico Lung Institute, University of North Carolina at Chapel Hill, 2204 Marsico Hall, CB#7248, 125 Mason Farm Road, Chapel Hill, NC 27514, United States. Electronic address: Scott_Donaldson@med.unc.edu.
  • Laube BL; Department of Pediatrics, Johns Hopkins University, Baltimore, MD, United States.
  • Mogayzel P; Department of Pediatrics, Johns Hopkins University, Baltimore, MD, United States.
  • Corcoran TE; Department of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
  • Pilewski JM; Department of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
  • Ceppe A; Department of Medicine and the Marsico Lung Institute, University of North Carolina at Chapel Hill, 2204 Marsico Hall, CB#7248, 125 Mason Farm Road, Chapel Hill, NC 27514, United States.
  • Wu J; Department of Medicine and the Marsico Lung Institute, University of North Carolina at Chapel Hill, 2204 Marsico Hall, CB#7248, 125 Mason Farm Road, Chapel Hill, NC 27514, United States.
  • Bhambhvani PG; Department of Medicine and the Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, AL, United States.
  • Ratjen F; Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Sagel SD; Department of Pediatrics, Children's Hospital Colorado and University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
  • Clancy JP; Cystic Fibrosis Foundation, Bethesda, MD, United States.
  • Rowe SM; Department of Medicine and the Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, AL, United States.
  • Bennett WD; Department of Medicine and the Marsico Lung Institute, University of North Carolina at Chapel Hill, 2204 Marsico Hall, CB#7248, 125 Mason Farm Road, Chapel Hill, NC 27514, United States.
J Cyst Fibros ; 21(1): 143-145, 2022 01.
Article in En | MEDLINE | ID: mdl-34083123
CFTR function is required for normal mucociliary clearance (MCC) and cough-assisted clearance (CC). Lumacaftor-ivacaftor is approved for use in people with cystic fibrosis (CF) carrying two copies of F508del-CFTR. In this observational study performed at four study sites, we characterized the effect of lumacaftor-ivacaftor on mucociliary and cough clearance and related this to other clinical and research endpoints after one month of treatment. Twenty-five adolescents and adults were enrolled. No effect on whole lung MCC was observed, but CC was significantly increased. Sweat chloride improved by 18 mEq/L in this group, indicating a modest restoration of CFTR activity, but no demonstrable change in FEV1 or lung clearance index was observed. We speculate that the modest effect of lumacaftor-ivacaftor on CFTR function was insufficient to yield an improvement in MCC.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mucociliary Clearance / Quinolones / Cystic Fibrosis / Benzodioxoles / Aminophenols / Aminopyridines Type of study: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: J Cyst Fibros Year: 2022 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mucociliary Clearance / Quinolones / Cystic Fibrosis / Benzodioxoles / Aminophenols / Aminopyridines Type of study: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: J Cyst Fibros Year: 2022 Document type: Article Country of publication: