Nasal potential difference (NPD) is used as a biomarker of the cystic fibrosis transmembrane conductance regulator (CFTR) and epithelial sodium channel (ENaC) activity. We evaluated methods to detect changes in chloride and sodium transport by NPD based on a secondary analysis of a Phase II CFTR-modulator study. Thirty-nine subjects with CF who also had the G551D-CFTR mutation were randomized to receive ivacaftor (Kalydeco™; also known as VX-770) in four doses or placebo twice daily for at least 14 days. All data were analyzed by a single investigator who was blinded to treatment assignment. We compared three analysis methods to determine the best approach to quantify changes in chloride and sodium transport: (1) the average of both nostrils; (2) the most-polarized nostril at each visit; and (3) the most-polarized nostril at screening carried forward. Parameters of ion transport included the PD change with zero chloride plus isoproterenol (CFTR activity), the basal PD, Ringer's PD, and change in PD with amiloride (measurements of ENaC activity), and the delta NPD (measuring CFTR and ENaC activity). The average and most-polarized nostril at each visit were most sensitive to changes in chloride and sodium transport, whereas the most-polarized nostril at screening carried forward was less discriminatory. Based on our findings, NPD studies should assess both nostrils rather than a single nostril. We also found that changes in CFTR activity were more readily detected than changes in ENaC activity, and that rigorous standardization was associated with relatively good within-subject reproducibility in placebo-treated subjects (±2.8 mV). Therefore, we have confirmed an assay of reasonable reproducibility for detecting chloride-transport improvements in response to CFTR modulation.
Citation: Rowe SM, Liu B, Hill A, Hathorne H, Cohen M, Beamer JR, et al. (2013) Optimizing Nasal Potential Difference Analysis for CFTR Modulator Development: Assessment of Ivacaftor in CF Subjects with the G551D-CFTR Mutation. PLoS ONE 8(7): e66955. doi:10.1371/journal.pone.0066955
Editor: Prosper N. Boyaka, The Ohio State University, United States of America
Received: March 6, 2013; Accepted: May 13, 2013; Published: July 26, 2013
Copyright: © 2013 Rowe et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported by the National Institutes of Health (grant NIH K23 DK075788 to SMR) and the Cystic Fibrosis Foundation and Cystic Fibrosis Foundation Therapeutics (grant CLANCY05Y0 to SMR and JPC). No additional external funding received for this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: Several authors on this manuscript are (or were) employees of Vertex Pharmaceuticals (QD, CLO, AJS, and ERO), Drs. JPC, FJA, and SMR were site investigators for the primary study of interest that was funded by Vertex Pharmaceuticals, and Dr. JPC has served as a consultant for Vertex Pharmaceuticals (member of the CF Global Scientific Advisory Board). This does not alter the authors' adherence to all of the PLOS ONE policies on sharing data and materials.
Cystic fibrosis (CF) is a common genetic disorder resulting from mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene . In the airways, the CFTR protein channel transports chloride (Cl−) and bicarbonate and regulates other ion-transport pathways including alternate Cl− channels and the epithelial sodium (Na+) channel (ENaC) –. CFTR dysfunction interrupts the normal regulation of salt and water transport leading to desiccated airway secretions, mucus stasis, infection, and inflammation, which culminate in bronchiectasis and respiratory failure.
CFTR activity can be measured in vivo using nasal potential difference (NPD) and sweat Cl− analysis . NPD is unique because it isolates both ENaC and CFTR Cl− channel function independent of other ion transport processes, providing a real-time estimate of CFTR and ENaC activity. NPD measurements correlate with the CF clinical phenotype in retrospective studies ,  and are frequently used in clinical trials to detect rescue of CFTR activity in humans –. However, due to lack of consensus regarding optimal methodology, it remains unclear as to what methods are superior , .
Ivacaftor (Kalydeco™; also known as VX-770) is a CFTR potentiator approved for the treatment of CF caused by the G551D mutation (in patients ≥6 years of age) by increasing gating and anion channel activity of G551D-CFTR (found in approximately 4% of patients ). A Phase II clinical trial of ivacaftor demonstrated dose-dependent improvements in CFTR biomarkers (including NPD and sweat Cl− along with clinical efficacy measures) in subjects with the G551D-CFTR mutation . This was the first published study employing the latest NPD standardization across centers in the United States, and provided a unique opportunity to optimize NPD parameters to detect modulator activity. In this secondary analysis of data from the Phase II trial, we evaluated three methods for determining NPD and the capacity of each to detect changes in various NPD parameters.
The details of the clinical trial have been previously published . This study was performed at 12 participating sites across the United States. Institutional review board (IRB) approval at each participating center and written informed consent were obtained for all enrolled study subjects for a two-part, randomized, placebo-controlled trial examining different doses of ivacaftor in subjects with the G551D-CFTR mutation on at least one allele. The NCT number is NCT00457821, and the study title is ‘A Phase 2a, Randomized, Double-Blind, Placebo-Controlled Study of VX-770 to Evaluate Safety, Pharmacokinetics, and Biomarkers of CFTR Activity in Cystic Fibrosis (CF) Subjects with Genotype G551D’, URL http://clinicaltrials.gov/ct2/show/NCT00457821.
Subjects were enrolled based on a diagnosis of CF, age >18 years, lung function >40% of the predicted value for age, sex, and height, and genotype for the G511D-CFTR mutation. Since >90% of CF patients are White, the vast majority of enrolled study subjects were White. The study had insufficient numbers of subjects for conclusions to be made regarding gender effects, but gender is included for descriptive purposes.
Subjects were randomized to receive placebo (n = 12) or ivacaftor in doses of 25 mg (n = 8), 75 mg (n = 16), 150 mg (n = 16), or 250 mg (n = 7) that were administered orally every 12 hours for 14–28 days. The analysis in this report combined Day 14 values from Parts 1 and 2 of the study. In addition, similar NPD data (difference between Day 1 and Day 14 values) from placebo subjects in a subsequent Phase II study of the putative F508del-CFTR corrector lumacaftor (also known as VX-809) (n = 13 subjects, all F508del-CFTR homozygous) were included in aggregate analysis . IRB approval at each participating center and written informed consent were obtained for all enrolled study subjects in the lumacaftor trial.
Several NPD parameters were assessed (difference from pretreatment values through Day 14) including: (1) zero Cl− plus isoproterenol (a direct measure of CFTR activity); (2) average basal PD (five sites in the inferior meatus), (3) maximal basal PD, (4) Ringer's basal PD, (5) change in PD with amiloride, and (6) percent change in PD with amiloride [(2) through (6) are all measurements of Na+ transport); and (7) the delta NPD (the change in PD from end of Ringer's perfusion to end of zero Cl− plus isoproterenol perfusion – a combined measure of both CFTR and ENaC activity).
Three NPD methods were compared: (1) the average of both nostrils; (2) the most-polarized nostril at each visit; and (3) the most-polarized nostril at screening carried forward for the subsequent measurements. NPD analysis and statistical analysis methods are included in Methods S1 in File S1.
Study Subject Demographic Information, Safety, and Tolerability
The baseline characteristics of study subjects have been summarized in a separate publication  and are shown in Table 1. The safety and tolerability profile of ivacaftor in this study also have been described previously .
Stability of NPD Solutions
Stability of NPD solutions is summarized in Table S1 in File S1. The concentrations of Na+, Cl−, amiloride, and pH remained within 10% of initial values over 12 months under refrigerated (2°–8°C) conditions.
Changes in CFTR-Dependent Cl− Transport
We applied the three NPD analysis methods to examine the change in zero Cl− plus isoproterenol, the principle measure of CFTR-dependent Cl− activity (Figure 1). Significant improvements in Cl− activity were observed at the 75-mg, 150-mg, and 250-mg dose groups for all three methods, including both within-subject and placebo comparisons. The magnitude of change in Cl− activity was smaller with the most-polarized nostril at screening carried forward compared to the other two analysis methods (without a reduction in variance), suggesting this method was inferior for detecting a change in PD produced by an efficacious CFTR modulator. Each method exhibited a significant linear test for trend (P≤0.01).
Data are shown for the analysis of the average of both nostrils, the most-polarized nostril at screening carried forward, and the most-polarized nostril at each visit. The dose-dependent linear trends were statistically significant for all three analyses (P<0.02).
Changes in Na+ Transport
Figure 2 summarizes the change in average basal PD for the three analysis methods. Both the average of both nostrils and the most-polarized nostril at each visit methods demonstrated dose-dependent improvements in baseline hyperpolarization with treatment. In contrast, the most-polarized nostril at screening carried forward analysis demonstrated only minimal improvement with ivacaftor treatment, and this analysis method had the widest confidence interval among patients treated with placebo. As opposed to Cl− transport, the treatment effect for Na+ transport was not significant at the 250-mg dose.
Data are shown for the analysis of the average of both nostrils, the most-polarized nostril at screening carried forward, and the most-polarized nostril at each visit. Significant dose-dependent linear trends were demonstrated for the average of both nostrils and the most-polarized nostril at each visit (P<0.02).
Figure 3 shows the change in maximal basal PD for the three analysis methods. Significant, dose-dependent reductions in hyperpolarization were noted for the average of both nostrils and the most-polarized nostril at each visit, which extended to the 150-mg and 250-mg dose groups, compared with placebo. In contrast, the most-polarized nostril at screening carried forward did not demonstrate significant changes at 75, 150, or 250 mg (within-subject or vs placebo). The change in Ringer's PD for each analytic method exhibited similar findings to that seen with the average basal PD and the maximal basal PD parameters (Figure S1 in File S1). Only the average of both nostrils demonstrated statistically significant changes at 75, 150, and 250 mg (vs placebo).
Data are shown for the analysis of the average of both nostrils, the most-polarized nostril at screening carried forward, and the most-polarized nostril at each visit. The dose-dependent linear trends were statistically significant for all three analyses (P<0.05).
The change in PD with amiloride for the three analysis methods is shown in Figure S2 in File S1. Dose-dependent effects were observed for the average of both nostrils and the most-polarized nostril at each visit, but results with this parameter were less clear and consistent than with the basal PD and Ringer's PD estimates of ENaC activity. The percent change in amiloride was particularly difficult to interpret with no clear dose effects seen (Figure S3 in File S1).
Changes in delta NPD
The change in delta NPD has not been used commonly in clinical trials of CFTR modulators or in gene replacement studies, but two recent cross-sectional studies provided evidence that this measurement correlates with disease phenotype , . Similar to sweat Cl−, delta NPD incorporates both Na+ and Cl− transport (ENaC and CFTR activity) into a single measurement, potentially reflecting the balance of Na+ absorption and Cl− secretion in the epithelium. Changes in the delta NPD parameter are shown in Figure 4; ivacaftor produced dose-dependent improvements based on all three analysis methods (P<0.02), with diminished effects at the 250-mg dose as was observed with sweat Cl− testing in this population. None of the NPD measures (Na+, Cl−, or the delta NPD) correlated with changes in lung function (FEV1, FVC, or FEF25%–75%).
Data are shown for the analysis of the average of both nostrils, the most-polarized nostril at screening carried forward, and the most-polarized nostril at each visit. The dose-dependent linear trends were statistically significant for all three analyses (P<0.02).
These data provide an evidence-basis for the design of future trials using NPD. We derived sample-size data from NPD effects seen with the 150-mg ivacaftor dose, because it included the largest number of study subjects and demonstrated evidence of bioactivity based on Cl−, Na+, and delta NPD measurements (Tables 2, 3, 4). For each table, we illustrate sample sizes required to provide 80% and 90% power for the average of both nostrils and the most-polarized nostril at each visit; the most-polarized nostril at screening carried forward method was inferior in each case and therefore not included. A large number of subjects are required to demonstrate a statistically significant change in CFTR activity (zero Cl− plus isoproterenol) between groups, regardless of the analysis method (Table 2A). For within-subject analysis, sample sizes are reasonable for Phase II trial designs in CF (Table 2B). As few as 10 subjects per group would be sufficient to detect a 5 mV treatment effect (the postulated effect size to indicate a meaningful difference in clinical phenotype prior to this trial and a criterion previously used to define responders in CF modulator studies , ).
Sample-size estimates also were examined for ENaC activity based on average basal PD, maximal basal PD, and Ringer's PD (Figures 2 and 3, Figure S2 in File S1). For the change in average basal PD, sample sizes for the average of both nostrils and the most-polarized nostril at each visit are shown with 80% and 90% power for between-group (Table 3A) and within-group (Table 3B) assessment methods. For the average basal PD, the average of both nostrils and the most-polarized nostril at each visit demonstrated the smallest sample sizes required to show a significant within-group effect (Table 3). Within-group and between-group variances for maximal basal PD and Ringer's PD were identical, thus the sample size estimates from these parameters were the same and are shown together in Table S2 in File S1.
Sample-size estimates for the delta NPD (both ENaC and CFTR activity) using the three analyses are shown in Table 4 and were similar to that observed for Cl− transport. To detect a change of −15 mV (approximating the mean effect magnitude in subjects with CF treated with 150 mg of ivacaftor), seven to nine subjects are required for within-group comparisons with 80% power. Together, these results suggest that the greatest sensitivity to detect a change in PD in patients with CF exposed to a CFTR modulator is achieved by directly measuring CFTR activity, or jointly estimating CFTR and ENaC activity by the delta NPD.
Consistency of NPD Parameters in Placebo-Treated Subjects Across Modulator Trials
Based on the results and experience in the Phase II ivacaftor study, the NPD protocol was modified for the subsequent placebo-controlled, Phase II lumacaftor trial, including the institution of electronic data capture and use of an agar probe electrode as previously described . The two study groups were generally similar, enrolling only adult subjects with two known CFTR mutations and FEV1>40% predicted , . Using a combined placebo dataset derived from both trials (n = 25 subjects, average of both nostrils), the mean difference (± standard deviation [SD]) from screening to Day 14 in PD parameters were consistent with the ivacaftor-only trial, including (1) zero Cl− plus isoproterenol (CFTR activity) = 0.21 mV (±4.15 SD); (2) average basal PD (ENaC activity) = 1.75 mV (±9.80 SD); and (3) delta NPD (CFTR and ENaC activity) = 0.15 mV (±9.75 SD).
The NPD is a CFTR biomarker capable of isolating CFTR activity, segregates patients based on CFTR function, is a recognized diagnostic test for CF, and has been a critical endpoint in early phase clinical trials of CFTR modulators –. In the current report, we provide a comprehensive analysis of NPD endpoints from a successful multicenter CFTR modulator clinical trial comprising 39 subjects. This was the largest placebo-controlled study evaluating an efficacious CFTR modulator completed to date, and the first multicenter trial to use centralized solutions and other standardization procedures to improve NPD testing consistency. The Phase III studies of ivacaftor in patients did not include the NPD, and the Phase II study of VX-809 monotherapy in CF patients with two F508del CFTR mutations did not demonstrate improvement in the NPD or in clinical efficacy measures , . The positive and consistent findings in both CFTR biomarkers and clinical outcome measures from the Phase II study of ivacaftor in G551D-CF patients provided a unique opportunity to determine the optimal measures for quantifying CFTR activity and inform future decisions in NPD analysis. The average of both nostrils and the most-polarized nostril at each visit achieved robust statistical significance for most parameters, including changes in Cl− transport, change in Na+ transport (average basal PD, maximal basal PD, Ringer's PD, and change in PD with amiloride), and a combined measure of ion transport (delta NPD). In contrast, analysis based on the most-polarized nostril at screening carried forward was less robust, with greater variability and smaller treatment effects observed (particularly for the parameters measuring ENaC activity; see Figures 2, 3, 4 and Figures S2, S3 in File S1). These results support the conclusion that performance of NPD should include both nostrils in clinical trials.
NPD has historically been a challenging assay requiring rigorous conduct to ensure consistent and valid results. Despite significant expansion of the number of participating centers and operators in the trial described here, the within-subject variability of CFTR activity [change in zero Cl− plus isoproterenol (SD = ±2.8 mV for placebo-treated subjects using the average of both nostrils and ±2.7 mV for the most-polarized nostril at each visit)] was lower than in previous multicenter trials that used a smaller number of experienced centers and topical agents (±5.1 mV)  or systemic drugs (±5.2 mV) . This also compares favorably with reproducibility of this measurement from single-center studies , . The rigorous standardization of the NPD procedure conducted prior to the start of this trial may have contributed to the consistent within-subject variance, despite the addition of several new centers to the NPD network. Included among these were the use of a standard operating procedure, qualification procedures for NPD operators to demonstrate proficiency (including hands-on supervision and training), use of centralized NPD solutions (with accompanying quality assurance), and centralized NPD interpretation (including a strict blinding process). Attributing the consistent within-subject variance to rigorous standardization of the procedure is further supported by the fact that >85% of tracings were deemed acceptable for review (based on tracing stability at solution changes and absence of tracing artifact). This was confirmed in the Phase II lumacaftor study in which the placebo cohort showed consistency across key NPD parameters despite the addition of seven study sites.
The Na+ transport (ENaC) parameters that best detected changes following ivacaftor treatment included average basal PD, maximal basal PD, and Ringer's PD, with no single Na+ transport parameter clearly outperforming the other two (Figures 2, 3, and Figure S2 in File S1). In contrast, the absolute change and percent change in amiloride response were less consistent and generally failed to demonstrate clear treatment effects (Figures S3, S4 in File S1). While this may be due to the fact that the effects on ENaC activity with ivacaftor are indirect, we speculate that the parameters measuring ENaC activity, particularly changes in PD with amiloride, may be relatively dependent upon catheter placement since the resting PD can vary greatly when separated by small distances within the inferior meatus. The CFTR activity measurement, in contrast, may be less dependent upon placement since the prominent effects of ENaC are eliminated by amiloride perfusion.
We observed discordant findings when examining ENaC and CFTR activity in the highest ivacaftor dose cohort (Figures 1, 2, 3, Figures S2, S3, S4 in File S1), with continued improvements in CFTR activity accompanied by no further improvements in ENaC activity. The delta NPD dose-response curve (Figure 4) was qualitatively similar to that previously reported for sweat Cl−, which also exhibited the greatest bioactivity in the 150-mg dose group. The results support the notion that, like sweat Cl−, delta NPD provides an aggregate measure of CFTR and ENaC activity .
Power analyses indicate that sample sizes needed to detect a −3 mV change in CFTR activity (zero Cl− plus isoproterenol; n = 20 for average of both nostrils, n = 18 for the most-polarized nostril at each visit) based on within-group analysis and 80% power should be sufficient to detect modest changes in ENaC activty (+10 mV for the average basal PD, average of both nostrils or the most-polarized nostril at each visit; Table 3). Although this example would be underpowered to detect differences between treatment group and placebo, we recommend including a placebo arm to help preserve the integrity of the analysis by a blinded interpreter.
The results of our study indicate that both nostrils should be included when performing the NPD as part of interventional trials, since this allows measurement of the average PD from both nostrils and the most-polarized nostril at each visit. Measurements dependent on both nostrils were superior to using a single nostril (i.e., the most-polarized nostril at screening carried forward), an inference that previously has been suggested . Since the average of both nostrils tended to be less variable compared with the other methods assessing CFTR and ENaC activity, we recommend this as the principle method used for NPD testing. The current dataset provides guidance for NPD use in future modulator trials and confirms the value of rigorous standardization on assay performance.
Includes Methods S1, Figure Legends S1–S4, Figures S1, S2, S3, S4, Tables S1 and S2, and References S1 sections.
The members of the VX06-770-101 study group are: Moira L. Aitken, University of Washington, Seattle, WA; Melissa A. Ashlock, Cystic Fibrosis Foundation Therapeutics, Inc., Bethesda, MD; Michael P. Boyle, Johns Hopkins Medical Institutions, Baltimore, MD; Preston W. Campbell, Cystic Fibrosis Foundation Therapeutics, Inc., Bethesda, MD; Scott H. Donaldson, University of North Carolina at Chapel Hill, Chapel Hill, NC; Jordan Dunitz, University of Minnesota, Minneapolis, MN; Peter R. Durie, The Hospital for Sick Children and the University of Toronto, Toronto, Canada; Scott D. Freedman, Beth Israel Deaconess Medical Center, Boston, MA; Douglas B. Hornick, University of Iowa, Iowa City, IA; Michael W. Konstan, Case Western Reserve University and Rainbow Babies and Children's Hospital, Cleveland, OH; Richard B. Moss, Stanford University School of Medicine, Palo Alto, CA; Joseph M. Pilewski, University of Pittsburgh, Pittsburgh, PA; Bonnie W. Ramsey, Seattle Children's Hospital, Seattle, WA; Ronald C. Rubenstein, The Children's Hospital of Philadelphia (CHOP), Philadelphia, PA; Scott D. Sagel, University of Colorado Denver, Aurora, CO; Ahmet Z. Uluer, Children's Hospital of Boston, Boston, MA.
Churee Pardee, BSN, MSN, and Lisa Monchil, RRT (University of Colorado Denver); Heather Young, MAE, RRT, CCRC, Ginger Reeves, BS, RRT and Gina Sabbatini, BS (University of Alabama at Birmingham); Lois Brass, RN and Kelvin MacDonald, MD (Johns Hopkins); Brooke Noren, BSN, Cynthia Williams, CRTT, RCP, and Dale Carlquist (University of Minnesota); Julie Avolio, BScN (Hospital for Sick Children, Toronto); Myra Slutsky, HonBA (St. Michael's Hospital, Toronto); Cheri Lux, Janice Launspach, RN, CCRC and Mary Teresi, PharmD (University of Iowa Carver School of Medicine); Roberta Ksenich, RN, CCRC and Timothy R. Myers, BS, RRT (Case Western Reserve University); Carol Barlow, RN, Nadia Bendahmane and Caroline O'Connor (University of North Carolina at Chapel Hill); Colleen Dunn, RRT, CCRC and Zoe Davies, PNP (Stanford University); Elizabeth Hartigan, RN, MPH, Sandra Hurban, RN and Adrienne Horn, RN (University of Pittsburgh); Christina Kubrak, RRT, NPS, CCRC (Children's Hospital of Philadelphia); Erin M. Leone, MPH, CCRC (Children's Hospital Boston); Alan Genatossio, RN and Sharon McNamara, RN (Seattle Children's Hospital); Louis J. Boitano MSc, RRT (University of Washington, Seattle).
The authors would like to acknowledge the following employees from Vertex Pharmaceuticals Incorporated; Barry Lubarsky and Adrienne Aiello for medical writing and coordination support. The authors are grateful to J. Denise Wetzel, CCHMC Medical Writer, for critical review of the manuscript.
Conceived and designed the experiments: SMR MC JB FJA CLO ERO JPC. Performed the experiments: SMR HH MC FJA JPC. Analyzed the data: SMR BL AH QD AJS JPC. Contributed reagents/materials/analysis tools: BL AH. Wrote the paper: SMR FJA QD JPC.
- 1. Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, et al. (1989) Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 245: 1066–1073. doi: 10.1126/science.2475911
- 2. Rowe SM, Miller S, Sorscher EJ (2005) Cystic fibrosis. N Engl J Med 352: 1992–2001. doi: 10.1056/nejmra043184
- 3. Boucher RC (2007) Airway surface dehydration in cystic fibrosis: pathogenesis and therapy. Annu Rev Med 58: 157–170. doi: 10.1146/annurev.med.58.071905.105316
- 4. Donaldson SH, Boucher RC (2007) Sodium channels and cystic fibrosis. Chest 132: 1631–1636. doi: 10.1378/chest.07-0288
- 5. Thelin WR, Boucher RC (2007) The epithelium as a target for therapy in cystic fibrosis. Curr Opin Pharmacol 7: 290–295. doi: 10.1016/j.coph.2007.01.004
- 6. Knowles MR, Paradiso AM, Boucher RC (1995) In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis. Hum Gene Ther 6: 445–455. doi: 10.1089/hum.1995.6.4-445
- 7. Leal T, Fajac A, Wallace HL, Lebecque P, Lebacq J, et al. (2008) Airway ion transport impacts on disease presentation and severity in cystic fibrosis. Clin Biochem 41: 764–772. doi: 10.1016/j.clinbiochem.2008.03.013
- 8. Wilschanski M, Dupuis A, Ellis L, Jarvi K, Zielenski J, et al. (2006) Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials. Am J Respir Crit Care Med 174: 787–794. doi: 10.1164/rccm.200509-1377oc
- 9. Ahrens RC, Standaert TA, Launspach J, Han SH, Teresi ME, et al. (2002) Use of nasal potential difference and sweat chloride as outcome measures in multicenter clinical trials in subjects with cystic fibrosis. Pediatr Pulmonol 33: 142–150. doi: 10.1002/ppul.10043
- 10. Clancy JP, Bebok Z, Ruiz F, King C, Jones J, et al. (2001) Evidence that systemic gentamicin suppresses premature stop mutations in patients with cystic fibrosis. Am J Respir Crit Care Med 163: 1683–1692. doi: 10.1164/ajrccm.163.7.2004001
- 11. Hentchel-Franks K, Lozano D, Eubanks-Tarn V, Cobb B, Fan L, et al. (2004) Activation of airway cl- secretion in human subjects by adenosine. Am J Respir Cell Mol Biol 31: 140–146. doi: 10.1165/rcmb.2004-0012oc
- 12. Yaakov Y, Kerem E, Yahav Y, Rivlin J, Blau H, et al. (2007) Reproducibility of nasal potential difference measurements in cystic fibrosis. Chest 132: 1219–1226. doi: 10.1378/chest.06-2975
- 13. Wilschanski M, Yahav Y, Yaacov Y, Blau H, Bentur L, et al. (2003) Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations. N Engl J Med 349: 1433–1441. doi: 10.1056/nejmoa022170
- 14. Wilschanski M, Famini H, Strauss-Leviatan N, Rivlin J, Blau H, et al. (2001) Nasal potential difference measurements in patients with atypical cystic fibrosis. Eur Respir J 17: 1208–1215. doi: 10.1183/09031936.01.00092501
- 15. Wilschanski M, Famini H, Blau H, Rivlin J, Augarten A, et al. (2000) A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutations. Am J Respir Crit Care Med 161: 860–865. doi: 10.1164/ajrccm.161.3.9904116
- 16. Wilschanski M (2010) Small molecules to treat cystic fibrosis. Proc Am Thorac Soc 7: 399–403. doi: 10.1513/pats.201001-012aw
- 17. Solomon GM, Konstan MW, Wilschanski M, Billings J, Sermet-Gaudelus I, et al. (2010) An international randomized multicenter comparison of nasal potential difference techniques. Chest 138: 919–928. doi: 10.1378/chest.10-0179
- 18. Segal I, Yaakov Y, Adler SN, Blau H, Broide E, et al. (2008) Cystic fibrosis transmembrane conductance regulator ion channel function testing in recurrent acute pancreatitis. J Clin Gastroenterol 42: 810–814. doi: 10.1097/mcg.0b013e318156617c
- 19. Linde L, Boelz S, Nissim-Rafinia M, Oren YS, Wilschanski M, et al. (2007) Nonsense-mediated mRNA decay affects nonsense transcript levels and governs response of cystic fibrosis patients to gentamicin. J Clin Invest 117: 683–692. doi: 10.1172/jci28523
- 20. Kerem E, Hirawat S, Armoni S, Yaakov Y, Shoseyov D, et al. (2008) Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial. Lancet 372: 719–727. doi: 10.1016/s0140-6736(08)61168-x
- 21. Jaron R, Yaakov Y, Rivlin J, Blau H, Bentur L, et al. (2008) Nasal potential difference in non-classic cystic fibrosis-long term follow up. Pediatr Pulmonol 43: 545–549. doi: 10.1002/ppul.20807
- 22. Accurso FJ, Rowe SM, Clancy JP, Boyle MP, Dunitz JM, et al. (2010) Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation. N Engl J Med 363: 1991–2003. doi: 10.1056/nejmoa0909825
- 23. Rowe SM, Accurso FJ, Clancy JP (2007) Detection of cystic fibrosis transmembrane conductance regulator activity in early-phase clinical trials. Proc Am Thorac Soc 4: 387–398. doi: 10.1513/pats.200703-043br
- 24. Clancy JP, Rowe SM, Bebok Z, Aitken ML, Gibson R, et al. (2007) No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations. Am J Respir Cell Mol Biol 37: 57–66. doi: 10.1165/rcmb.2006-0173oc
- 25. LeGrys VA (2000) Sweat analysis proficiency testing for cystic fibrosis. Pediatr Pulmonol 30: 476–480. doi: 10.1002/1099-0496(200012)30:6<476::aid-ppul7>3.0.co;2-o
- 26. Clancy JP, Rowe SM, Accurso FJ, Aitken ML, Amin R, et al. (2011) Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation. Thorax doi: 10.1016/j.ypdi.2012.02.015
- 27. Cantin AM, Hanrahan JW, Bilodeau G, Ellis L, Dupuis A, et al. (2006) Cystic fibrosis transmembrane conductance regulator function is suppressed in cigarette smokers. Am J Respir Crit Care Med 173: 1139–1144. doi: 10.1164/rccm.200508-1330oc
- 28. Sermet-Gaudelus I, Girodon E, Sands D, Stremmler N, Vavrova V, et al. (2010) Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport. Am J Respir Crit Care Med 182: 929–936. doi: 10.1164/rccm.201003-0382oc
- 29. Clancy JP, Rowe SM, Accurso FJ, Aitken ML, Amin RS, et al. (2012) Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation. Thorax 67: 12–18. doi: 10.1136/thoraxjnl-2011-200393
- 30. Ramsey BW, Davies J, McElvaney NG, Tullis E, Bell SC, et al. (2011) A CFTR potentiator in patients with cystic fibrosis and the G551D mutation. N Engl J Med 365: 1663–1672. doi: 10.1056/nejmoa1105185
- 31. Clancy JP, Rowe SR, Young H (2006) Alternate Analyses of Nasal Potential Difference Measurements to Assess Ion Transport in Human Subjects [abstract]. Pediatr Pulmonol Suppl 41: 301.
- 32. Noone PG, Hohneker KW, Zhou Z, Johnson LG, Foy C, et al. (2000) Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosis. Mol Ther 1: 105–114. doi: 10.1006/mthe.1999.0009