Literature DB >> 31699569

Insights into the variability of nasal potential difference, a biomarker of CFTR activity.

Spyridoula Kyrilli1, Theophraste Henry2, Michael Wilschanski3, Isabelle Fajac4, Jane C Davies5, Jean-Philippe Jais6, Isabelle Sermet-Gaudelus7.   

Abstract

BACKGROUND: Nasal potential difference (NPD) is used to evaluate CFTR function in vivo. We aimed to evaluate the intrasubject and intersubject variability of NPD measurements.
METHODS: We reviewed NPD tracings of 116 patients with CF enrolled in the placebo arm of a multicenter study. Patients carried at least one nonsense mutation and underwent repeated NPD tests every 16 weeks. NPD parameters included basal potential difference (basal PD), inhibition of sodium absorption by amilorideAmiloride), chloride (Cl-) transport in response to a Cl--free solution (Δ Low Cl-), isoproterenolIsoproterenol), the sum of Δ Low Cl- and Δ Isoproterenol (Δ Low Cl--Isoproterenol) and ATPATP).
RESULTS: Basal PD and Δ Amiloride displayed the highest variabilities, mainly stemming from intercenter and intrasubject effect. Δ Low Cl-, Δ Isoproterenol and Δ Low Cl--Isoproterenol demonstrated a large intrasubject variability but a smaller intersubject variability. The intrasubject measurement variability for Δ Low Cl--Isoproterenol, was within ± 7.2 mV with 95% probability. It was greater in patients reporting ongoing pulmonary exacerbations.
CONCLUSIONS: The large intercenter variability of basal PD and Δ Amiloride highlights the operator-dependent aspect of these measurements. A difference greater than 7.2 mV in Δ Low Cl--Isoproterenol in a given patient on CFTR modulator can be attributed, with 95% probability, to a treatment effect rather than to the variability inherent in the measurement.
Copyright © 2019. Published by Elsevier B.V.

Entities:  

Keywords:  Biomarker; Cystic Fibrosis; Nasal potential difference

Year:  2019        PMID: 31699569     DOI: 10.1016/j.jcf.2019.09.015

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


  4 in total

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Review 4.  Advances in Preclinical In Vitro Models for the Translation of Precision Medicine for Cystic Fibrosis.

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  4 in total

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