Literature DB >> 24660233

Sweat chloride as a biomarker of CFTR activity: proof of concept and ivacaftor clinical trial data.

Frank J Accurso, Fredrick Van Goor, Jiuhong Zha, Anne J Stone, Qunming Dong, Claudia L Ordonez, Steven M Rowe, John Paul Clancy, Michael W Konstan, Heather E Hoch, Sonya L Heltshe, Bonnie W Ramsey, Preston W Campbell, Melissa A Ashlock.   

Abstract

BACKGROUND: We examined data from a Phase 2 trial {NCT00457821} of ivacaftor, a CFTR potentiator, in cystic fibrosis (CF) patients with aG551D mutation to evaluate standardized approaches to sweat chloride measurement and to explore the use of sweat chloride and nasal potential difference (NPD) to estimate CFTR activity.
METHODS: Sweat chloride and NPD were secondary endpoints in this placebo-controlled, multicenter trial. Standardization of sweat collection, processing,and analysis was employed for the first time. Sweat chloride and chloride ion transport (NPD) were integrated into a model of CFTR activity.
RESULTS: Within-patient sweat chloride determinations showed sufficient precision to detect differences between dose-groups and assess ivacaftor treatment effects. Analysis of changes in sweat chloride and NPD demonstrated that patients treated with ivacaftor achieved CFTR activity equivalent to approximately 35%–40% of normal.
CONCLUSIONS: Sweat chloride is useful in multicenter trials as a biomarker of CFTR activity and to test the effect of CFTR potentiators.

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Year:  2014        PMID: 24660233      PMCID: PMC4102431          DOI: 10.1016/j.jcf.2013.09.007

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.527


  28 in total

1.  Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis: a double-blind placebo-controlled trial.

Authors:  E W Alton; M Stern; R Farley; A Jaffe; S L Chadwick; J Phillips; J Davies; S N Smith; J Browning; M G Davies; M E Hodson; S R Durham; D Li; P K Jeffery; M Scallan; R Balfour; S J Eastman; S H Cheng; A E Smith; D Meeker; D M Geddes
Journal:  Lancet       Date:  1999-03-20       Impact factor: 79.321

2.  Change in sweat chloride as a clinical end point in cystic fibrosis clinical trials: the ivacaftor experience.

Authors:  Anthony G Durmowicz; Kimberly A Witzmann; Curtis J Rosebraugh; Badrul A Chowdhury
Journal:  Chest       Date:  2013-01       Impact factor: 9.410

3.  Assessment of sweat-testing practices for the diagnosis of cystic fibrosis.

Authors:  V A LeGrys
Journal:  Arch Pathol Lab Med       Date:  2001-11       Impact factor: 5.534

4.  The predictive potential of the sweat chloride test in cystic fibrosis patients with the G551D mutation.

Authors:  Verena I Seliger; David Rodman; Fredrick Van Goor; Andreas Schmelz; Peter Mueller
Journal:  J Cyst Fibros       Date:  2013-04-28       Impact factor: 5.482

5.  A CFTR potentiator in patients with cystic fibrosis and the G551D mutation.

Authors:  Bonnie W Ramsey; Jane Davies; N Gerard McElvaney; Elizabeth Tullis; Scott C Bell; Pavel Dřevínek; Matthias Griese; Edward F McKone; Claire E Wainwright; Michael W Konstan; Richard Moss; Felix Ratjen; Isabelle Sermet-Gaudelus; Steven M Rowe; Qunming Dong; Sally Rodriguez; Karl Yen; Claudia Ordoñez; J Stuart Elborn
Journal:  N Engl J Med       Date:  2011-11-03       Impact factor: 91.245

6.  Relationship between airway ion transport and a mild pulmonary disease mutation in CFTR.

Authors:  L C Walker; C J Venglarik; G Aubin; M R Weatherly; N A McCarty; B Lesnick; F Ruiz; J P Clancy; E J Sorscher
Journal:  Am J Respir Crit Care Med       Date:  1997-05       Impact factor: 21.405

7.  The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis.

Authors:  Michele D Bishop; Steven D Freedman; Julian Zielenski; Najma Ahmed; Annie Dupuis; Sheelagh Martin; Lynda Ellis; Julie Shea; Isobel Hopper; Mary Corey; Paul Kortan; Gregory Haber; Christine Ross; John Tzountzouris; Leslie Steele; Peter N Ray; Lap-Chee Tsui; Peter R Durie
Journal:  Hum Genet       Date:  2005-09-29       Impact factor: 4.132

8.  [French guidelines for sweat test practice and interpretation for cystic fibrosis neonatal screening].

Authors:  I Sermet-Gaudelus; A Munck; M Rota; M Roussey; D Feldmann; T Nguyen-Khoa
Journal:  Arch Pediatr       Date:  2010-08-16       Impact factor: 1.180

9.  Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein.

Authors:  B Illek; L Zhang; N C Lewis; R B Moss; J Y Dong; H Fischer
Journal:  Am J Physiol       Date:  1999-10

10.  Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770.

Authors:  Fredrick Van Goor; Sabine Hadida; Peter D J Grootenhuis; Bill Burton; Dong Cao; Tim Neuberger; Amanda Turnbull; Ashvani Singh; John Joubran; Anna Hazlewood; Jinglan Zhou; Jason McCartney; Vijayalaksmi Arumugam; Caroline Decker; Jennifer Yang; Chris Young; Eric R Olson; Jeffery J Wine; Raymond A Frizzell; Melissa Ashlock; Paul Negulescu
Journal:  Proc Natl Acad Sci U S A       Date:  2009-10-21       Impact factor: 11.205

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  44 in total

1.  Multiprobe Nuclear Imaging of the Cystic Fibrosis Lung as a Biomarker of Therapeutic Effect.

Authors:  Timothy E Corcoran; Alex S Huber; Michael M Myerburg; Daniel J Weiner; Landon W Locke; Ryan T Lacy; Lawrence Weber; Michael R Czachowski; Darragh J Johnston; Ashok Muthukrishnan; Alison T Lennox; Joseph M Pilewski
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2019-04-10       Impact factor: 2.849

2.  PharmGKB summary: ivacaftor pathway, pharmacokinetics/pharmacodynamics.

Authors:  Alison E Fohner; Ellen M McDonagh; John P Clancy; Michelle Whirl Carrillo; Russ B Altman; Teri E Klein
Journal:  Pharmacogenet Genomics       Date:  2017-01       Impact factor: 2.089

3.  Current Status and Future Opportunities in Lung Precision Medicine Research with a Focus on Biomarkers. An American Thoracic Society/National Heart, Lung, and Blood Institute Research Statement.

Authors:  Ann Chen Wu; James P Kiley; Patricia J Noel; Shashi Amur; Esteban G Burchard; John P Clancy; Joshua Galanter; Maki Inada; Tiffanie K Jones; Jonathan A Kropski; James E Loyd; Lawrence M Nogee; Benjamin A Raby; Angela J Rogers; David A Schwartz; Don D Sin; Avrum Spira; Scott T Weiss; Lisa R Young; Blanca E Himes
Journal:  Am J Respir Crit Care Med       Date:  2018-12-15       Impact factor: 21.405

4.  Correlating Cystic Fibrosis Transmembrane Conductance Regulator Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis.

Authors:  Allison F McCague; Karen S Raraigh; Matthew J Pellicore; Emily F Davis-Marcisak; Taylor A Evans; Sangwoo T Han; Zhongzhou Lu; Anya T Joynt; Neeraj Sharma; Carlo Castellani; Joseph M Collaco; Mary Corey; Michelle H Lewis; Chris M Penland; Johanna M Rommens; Anne L Stephenson; Patrick R Sosnay; Garry R Cutting
Journal:  Am J Respir Crit Care Med       Date:  2019-05-01       Impact factor: 21.405

5.  In vivo and in vitro ivacaftor response in cystic fibrosis patients with residual CFTR function: N-of-1 studies.

Authors:  Meghan E McGarry; Beate Illek; Ngoc P Ly; Lorna Zlock; Sabrina Olshansky; Courtney Moreno; Walter E Finkbeiner; Dennis W Nielson
Journal:  Pediatr Pulmonol       Date:  2017-01-09

Review 6.  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

Review 7.  Cystic fibrosis genetics: from molecular understanding to clinical application.

Authors:  Garry R Cutting
Journal:  Nat Rev Genet       Date:  2014-11-18       Impact factor: 53.242

8.  Effectiveness of ivacaftor in cystic fibrosis patients with non-G551D gating mutations.

Authors:  Jennifer Guimbellot; George M Solomon; Arthur Baines; Sonya L Heltshe; Jill VanDalfsen; Elizabeth Joseloff; Scott D Sagel; Steven M Rowe
Journal:  J Cyst Fibros       Date:  2018-04-21       Impact factor: 5.482

Review 9.  Ion Channel Modulators in Cystic Fibrosis.

Authors:  Martina Gentzsch; Marcus A Mall
Journal:  Chest       Date:  2018-05-08       Impact factor: 9.410

10.  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

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