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      Concentration of fractional excretion of nitric oxide (FENO): A potential airway biomarker of restored CFTR function.

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          Abstract

          Lower airway biomarkers of restored cystic fibrosis transmembrane conductance regulator (CFTR) function are limited. We hypothesized that fractional excretion of nitric oxide (FENO), typically low in CF patients, would demonstrate reproducibility during CFTR-independent therapies, and increase during CFTR-specific intervention (ivacaftor) in patients with CFTR gating mutations.

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          Author and article information

          Journal
          J. Cyst. Fibros.
          Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
          Elsevier BV
          1873-5010
          1569-1993
          Nov 2015
          : 14
          : 6
          Affiliations
          [1 ] Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, United States.
          [2 ] Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
          [3 ] Department of Mathematical Sciences, University of Cincinnati, Cincinnati, OH, United States.
          [4 ] Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States. Electronic address: john.clancy@cchmc.org.
          Article
          S1569-1993(15)00164-2
          10.1016/j.jcf.2015.07.002
          26210165
          2224c804-0d3e-4671-8e9f-cc7f4819932c
          History

          Cystic fibrosis,Nitric oxide,CFTR biomarker,CFTR modulator,FENO

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