| Literature DB >> 34083123 |
Scott H Donaldson1, Beth L Laube2, Peter Mogayzel2, Timothy E Corcoran3, Joseph M Pilewski3, Agathe Ceppe4, Jihong Wu4, Pradeep G Bhambhvani5, Felix Ratjen6, Scott D Sagel7, J P Clancy8, Steven M Rowe5, William D Bennett4.
Abstract
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.Entities:
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Year: 2021 PMID: 34083123 PMCID: PMC8630086 DOI: 10.1016/j.jcf.2021.05.004
Source DB: PubMed Journal: J Cyst Fibros ISSN: 1569-1993 Impact factor: 5.482