Literature DB >> 20472865

An international randomized multicenter comparison of nasal potential difference techniques.

George M Solomon1, Michael W Konstan, Michael Wilschanski, Joanne Billings, Isabelle Sermet-Gaudelus, Frank Accurso, François Vermeulen, Elina Levin, Heather Hathorne, Ginger Reeves, Gina Sabbatini, Aubrey Hill, Nicole Mayer-Hamblett, Melissa Ashlock, John Paul Clancy, Steven M Rowe.   

Abstract

BACKGROUND: The transepithelial nasal potential difference (NPD) is used to assess cystic fibrosis transmembrane conductance regulator (CFTR) activity. Unreliability, excessive artifacts, and lack of standardization of current testing systems can compromise its use as a diagnostic test and outcome measure for clinical trials.
METHODS: To determine whether a nonperfusing (agar gel) nasal catheter for NPD measurement is more reliable and less susceptible to artifacts than a continuously perfusing nasal catheter, we performed a multicenter, randomized, crossover trial comparing a standardized NPD protocol using an agar nasal catheter with the same protocol using a continuously perfusing catheter. The data capture technique was identical in both protocols. A total of 26 normal adult subjects underwent NPD testing at six different centers.
RESULTS: Artifact frequency was reduced by 75% (P < .001), and duration was less pronounced using the agar catheter. The measurement of sodium conductance was similar between the two catheter methods, but the agar catheter demonstrated significantly greater CFTR-dependent hyperpolarization, because Δ zero Cl- + isoproterenol measurements were significantly more hyperpolarized with the agar catheter (224.2 ± 12.9 mV with agar vs 18.2 ± 9.1 mV with perfusion, P < .05).
CONCLUSIONS: The agar nasal catheter approach demonstrates superior reliability compared with the perfusion nasal catheter method for measurement of NPD. This nonperfusion catheter method should be considered for adoption as a standardized protocol to monitor CFTR activity in clinical trials.

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Year:  2010        PMID: 20472865      PMCID: PMC2951758          DOI: 10.1378/chest.10-0179

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  21 in total

1.  Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosis.

Authors:  P G Noone; K W Hohneker; Z Zhou; L G Johnson; C Foy; C Gipson; K Jones; T L Noah; M W Leigh; C Schwartzbach; J Efthimiou; R Pearlman; R C Boucher; M R Knowles
Journal:  Mol Ther       Date:  2000-01       Impact factor: 11.454

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Journal:  J Pediatr       Date:  1998-04       Impact factor: 4.406

3.  Protocols for in vivo measurement of the ion transport defects in cystic fibrosis nasal epithelium.

Authors:  P G Middleton; D M Geddes; E W Alton
Journal:  Eur Respir J       Date:  1994-11       Impact factor: 16.671

4.  In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis.

Authors:  M R Knowles; A M Paradiso; R C Boucher
Journal:  Hum Gene Ther       Date:  1995-04       Impact factor: 5.695

5.  Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice.

Authors:  E W Alton; P G Middleton; N J Caplen; S N Smith; D M Steel; F M Munkonge; P K Jeffery; D M Geddes; S L Hart; R Williamson
Journal:  Nat Genet       Date:  1993-10       Impact factor: 38.330

6.  Relative ion permeability of normal and cystic fibrosis nasal epithelium.

Authors:  M Knowles; J Gatzy; R Boucher
Journal:  J Clin Invest       Date:  1983-05       Impact factor: 14.808

7.  Standardized procedure for measurement of nasal potential difference: an outcome measure in multicenter cystic fibrosis clinical trials.

Authors:  Thomas A Standaert; Louis Boitano; Julia Emerson; Laura J H Milgram; Michael W Konstan; Janice Hunter; Pierre-Yves Berclaz; Lois Brass; Pamela L Zeitlin; Keith Hammond; Zoe Davies; Carla Foy; Peadar G Noone; Michael R Knowles
Journal:  Pediatr Pulmonol       Date:  2004-05

8.  Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis.

Authors:  C Goubau; M Wilschanski; V Skalická; P Lebecque; K W Southern; I Sermet; A Munck; N Derichs; P G Middleton; L Hjelte; R Padoan; M Vasar; K De Boeck
Journal:  Thorax       Date:  2009-03-23       Impact factor: 9.139

9.  Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations.

Authors:  Michael Wilschanski; Yaacov Yahav; Yasmin Yaacov; Hannah Blau; Lea Bentur; Joseph Rivlin; Micha Aviram; Tali Bdolah-Abram; Zsuzsa Bebok; Liat Shushi; Batsheva Kerem; Eitan Kerem
Journal:  N Engl J Med       Date:  2003-10-09       Impact factor: 91.245

10.  Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis.

Authors:  M Knowles; J Gatzy; R Boucher
Journal:  N Engl J Med       Date:  1981-12-17       Impact factor: 91.245

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  22 in total

1.  Repurposing tromethamine as inhaled therapy to treat CF airway disease.

Authors:  Mahmoud H Abou Alaiwa; Janice L Launspach; Kelsey A Sheets; Jade A Rivera; Nicholas D Gansemer; Peter J Taft; Peter S Thorne; Michael J Welsh; David A Stoltz; Joseph Zabner
Journal:  JCI Insight       Date:  2016-06-02

Review 2.  Biomarkers for cystic fibrosis drug development.

Authors:  Marianne S Muhlebach; J P Clancy; Sonya L Heltshe; Assem Ziady; Tom Kelley; Frank Accurso; Joseph Pilewski; Nicole Mayer-Hamblett; Elizabeth Joseloff; Scott D Sagel
Journal:  J Cyst Fibros       Date:  2016-10-27       Impact factor: 5.482

3.  Resveratrol ameliorates abnormalities of fluid and electrolyte secretion in a hypoxia-Induced model of acquired CFTR deficiency.

Authors:  Bradford A Woodworth
Journal:  Laryngoscope       Date:  2015-05-06       Impact factor: 3.325

4.  Moderate intensity exercise mediates comparable increases in exhaled chloride as albuterol in individuals with cystic fibrosis.

Authors:  Courtney M Wheatley; Sarah E Baker; Mary A Morgan; Marina G Martinez; Bo Liu; Steven M Rowe; Wayne J Morgan; Eric C Wong; Stephen R Karpen; Eric M Snyder
Journal:  Respir Med       Date:  2015-05-23       Impact factor: 3.415

Review 5.  Nasal potential difference to detect Na+ channel dysfunction in acute lung injury.

Authors:  R Mac Sweeney; H Fischer; D F McAuley
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2010-11-26       Impact factor: 5.464

6.  Chloride Conductance, Nasal Potential Difference and Cystic Fibrosis Pathophysiology.

Authors:  Elenara da Fonseca Andrade Procianoy; Fernando Antônio de Abreu E Silva; Paulo José Cauduro Maróstica; Paul M Quinton
Journal:  Lung       Date:  2019-11-16       Impact factor: 2.584

7.  A multiple reader scoring system for Nasal Potential Difference parameters.

Authors:  George M Solomon; Bo Liu; Isabelle Sermet-Gaudelus; Isabelle Fajac; Michael Wilschanski; Francois Vermeulen; Steven M Rowe
Journal:  J Cyst Fibros       Date:  2017-04-29       Impact factor: 5.482

8.  Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD).

Authors:  George M Solomon; Inez Bronsveld; Kathryn Hayes; Michael Wilschanski; Paola Melotti; Steven M Rowe; Isabelle Sermet-Gaudelus
Journal:  J Vis Exp       Date:  2018-09-13       Impact factor: 1.355

9.  Acquired cystic fibrosis transmembrane conductance regulator dysfunction in the lower airways in COPD.

Authors:  Mark T Dransfield; Andrew M Wilhelm; Brian Flanagan; Clifford Courville; Sherry L Tidwell; S Vamsee Raju; Amit Gaggar; Chad Steele; Li Ping Tang; Bo Liu; Steven M Rowe
Journal:  Chest       Date:  2013-08       Impact factor: 9.410

10.  Progress in cystic fibrosis and the CF Therapeutics Development Network.

Authors:  Steven M Rowe; Drucy S Borowitz; Jane L Burns; John P Clancy; Scott H Donaldson; George Retsch-Bogart; Scott D Sagel; Bonnie W Ramsey
Journal:  Thorax       Date:  2012-10       Impact factor: 9.139

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