Long-term gas exchange characteristics as markers of deterioration in patients with cystic fibrosis
© Kraemer et al. 2009
Received: 04 August 2009
Accepted: 12 November 2009
Published: 12 November 2009
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© Kraemer et al. 2009
Received: 04 August 2009
Accepted: 12 November 2009
Published: 12 November 2009
In patients with cystic fibrosis (CF) the architecture of the developing lungs and the ventilation of lung units are progressively affected, influencing intrapulmonary gas mixing and gas exchange. We examined the long-term course of blood gas measurements in relation to characteristics of lung function and the influence of different CFTR genotype upon this process.
Serial annual measurements of PaO2 and PaCO2 assessed in relation to lung function, providing functional residual capacity (FRCpleth), lung clearance index (LCI), trapped gas (VTG), airway resistance (sReff), and forced expiratory indices (FEV1, FEF50), were collected in 178 children (88 males; 90 females) with CF, over an age range of 5 to 18 years. Linear mixed model analysis and binary logistic regression analysis were used to define predominant lung function parameters influencing oxygenation and carbon dioxide elimination.
PaO2 decreased linearly from age 5 to 18 years, and was mainly associated with FRCpleth, (p < 0.0001), FEV1 (p < 0.001), FEF50 (p < 0.002), and LCI (p < 0.002), indicating that oxygenation was associated with the degree of pulmonary hyperinflation, ventilation inhomogeneities and impeded airway function. PaCO2 showed a transitory phase of low PaCO2 values, mainly during the age range of 5 to 12 years. Both PaO2 and PaCO2 presented with different progression slopes within specific CFTR genotypes.
In the long-term evaluation of gas exchange characteristics, an association with different lung function patterns was found and was closely related to specific genotypes. Early examination of blood gases may reveal hypocarbia, presumably reflecting compensatory mechanisms to improve oxygenation.
Mixing of inspired gas is a prerequisite for effective respiration and is dependent upon the architecture of the lung. In children with cystic fibrosis (CF), the architecture of the developing lungs and the ventilation of peripheral lung units are progressively affected, influencing the efficiency of gas mixing and gas exchange. We have previously reported observations that inequalities in ventilation occur significantly earlier in the course of lung function decline than changes in other functional characteristics . Moreover, we have recently demonstrated in this Journal, that pulmonary hyperinflation and development of trapped gas represent major functional features of disease progression in children with CF . In agreement with several author groups, airway dysfunction and pulmonary deterioration in CF is thought to be expressed by ventilation inhomogeneities [1–6], pulmonary hyperinflation [2, 7] and gas trapping [2, 8, 9] occurring very early in life [5, 10, 11]. The different patterns of functional derangements stress the need to include a range of lung function tests including gas exchange characteristics and to investigate whether the CFTR genotype has an impact upon these processes in CF patients, as has been previously reported [12–14].
Limited knowledge exists as to whether gas exchange parameters measured under resting conditions are helpful in defining progression of lung disease in children with CF. A correlation between survival and adequacy of gas exchange, and the hypothesis that carbon dioxide retention may be a predictor of survival, was initially published by Wagener et al. in 1980 . Mechanisms of impaired gas exchange and their influence on ventilation-perfusion inequality through shunts have recently been studied by Soni et al. . A previous study of ours performed in a limited number of children with advanced stages of CF showed the interdependence of oxygenation, ventilation inhomogeneities and trapped gas assemblage .
The aim of this prospectively acquired cohort study was to evaluate the onset and course of deterioration of gas exchange in relation to changes in lung volume, ventilation distribution, trapped gas and airway obstruction, as well as the influence of specific genotypes in CF patients, from the 5th to the 18th year of life. Following up on our recent work published in this Journal, we looked at the long-term course of gas exchange characteristics in relation to different facettes of lung function [1, 2].
Patients were recruited from the Bernese Cystic Fibrosis Patient Data Registry, prospectively developed as an extension of the American Cystic Fibrosis Patient Registry founded by Warwick in 1966 . Standard clinical and biomedical parameters, as well as gas exchange characteristics and lung function data of a total of 204 CF patients regularly seen at the outpatient clinic between 1978 and 2008 are documented in the registry. The inclusion criteria for the present study were: (i) CF diagnosis based on the presence of characteristic phenotypic features , (ii) confirmed by a duplicate quantitative pilocarpine iontophoresis sweat test measuring both Na and Cl values > 60 mEq/L as well as by (iii) genotype identification using extended mutation screening of both alleles [19, 20], and (iv) complete documentation of a minimum of 3 blood gas analyses with concomitantly measured lung function parameters performed annually between the ages of 5 to18 yrs, investigated during clinical stability. Twenty of the 204 patients (9.8%) were younger than 6 years of age (blood gas analysis and lung function data not available), and in 6 CF patients (2.9%), fewer than 3 annual measurements were available. Some of lung function data in the database have been reported previously with respect to the phenomenon of ventilation inhomogeneities  and pulmonary hyperinflation , and the sensitization against Aspergillus fumigatus . There is no overlap with previous publications with respect to the major topic of the present report dealing with gas exchange characteristics. This study protocol was approved by the Departmental Ethics Committee of the University Children's Hospital Berne and by the Government Ethics Committee of the State of Berne, Switzerland.
Whole-body plethysmography and the multibreath nitrogen washout (MBNW) technique provided data pertaining to functional residual capacity (FRCpleth, FRCMBNW), lung clearance index (LCI), volume of trapped gas (VTG), effective specific airway resistance (sReff), and forced expiratory indices (FEV1, FEF50). Measurement techniques have been described in detail in previous papers [1, 2, 21]. All values were expressed by z-transformation in standard deviation scores (SDS), based on gender- and age-specific regression equation [22–25], specifically calculated for each lung function device as previously presented [1, 2]. Full details concerning lung function techniques, calculation of SDS, and the statistical methods are given in the additional file 1.
In children, the preferred technique for routine blood gas analysis is the sampling of arterialized capillary blood from the earlobe [8, 26, 27], a technique that has been established for clinical use and applied in various long-term studies [28–31]. The accuracy of this technique depends upon careful preparation of the earlobe , puncture technique [26, 27] and immediate analysis. Several author groups have validated the accuracy of this particular technique for clinical and long-term evaluation of gas exchange [26, 27, 32–34], provided certain important methodological conditions are fulfilled. Therefore, oxygen (PaO2) and carbon dioxide (PaCO2) tensions were measured in arterialized blood collected from the ear lobe [8, 26, 27, 33] using a Radiometer ABL5, Copenhagen, Denmark.
Blood gas sampling was performed after whole-body plethysmography and before the multibreath nitrogen washout measurements. The procedure was done in a quiet atmosphere and our patients were familiar with the process. The ear lobe was prepared according to the technique initially described [26, 27], and previously established in our laboratory . Vasodilatation of the earlobe was achieved by rubbing the lobe with a nicotinate paste (Finalgon) [26, 27, 32, 33] for at least 10 minutes and heating with an infrared lamp. During quiet breathing, the arterialized blood was collected from a drop on the inferior aspect of the earlobe, from which it was drawn into 3 thin heparinized glass capillary tubes by surface tension under the guidance of a gloved finger over the open end of the tube. The capillary tubes were then kept on ice until aspiration into the gas analyzer, which was carried out immediately after the blood draw.
Details of the blood gas analysis performed by earlobe puncture technique [8, 26, 27], and information on reproducibility are given in the additional file 1. Most definitions of hypoxemia are related to arterial blood gas values obtained during exercise testing predominantly performed in adult patients. There is no clearly defined cut-off indicating gas exchange impairment at rest in children with lung disease. Lamarre et al. , as well as Stokes et al.  defined hypoxemia at rest in children as a PaO2 <80 mmHg. Gaultier et al. suggested defining hypoxemia in children as less than 90% of predicted values [27, 37]. We re-calculated the original data of Gaultier et al. using a power function based on age in years and taking the 90 % level of confidence of Gautier's predicted values. Accordingly, the lower limit would be 78.3 mmHg for children aged 6 years, and 81.9 mmHg for children aged 8 years [27, 37]. We therefore took a PaO2 level of 80 mmHg as the lowest limit defining sufficient oxygen uptake .
Heights and weights were measured by experienced nurses, using a Harpenden stadiometer and according to recommended procedures . The computation of longitudinal weight and height data was based on calculation of age- and gender-corrected body mass index (BMI) expressed as z-scores, using the method and values for children reported by Cole et al .
All patients were genotyped by a SSCP/HD scanning method followed by direct sequencing of the variants, thus permitting rapid and sensitive detection of 97-98 % of known and novel (newly identified) CF mutations, as previously described [19, 40]. Genomic DNA was extracted from EDTA blood samples using the QIAamp Maxi Kit (Qiagen) according to the manufacturer's recommendations and quantified by spectrophotometry. In addition, a non-invasive method of buccal cell brushing  was used to obtain DNA from premature infants, recipients of previous blood transfusions and infants with me meconium ileus. Mutation screening of the entire coding sequences of the CFTR gene (including the 27 exons and exon/intron boundaries, intron 11 and 19, as well as the promoter region) was performed in each patient using a well-established single strand conformation polymorphism/heteroduplex (SSCP/HD) analysis.
Repeated serial measurements of lung function data, acquired annually, were calculated as annual mean ± SEM changes for presentation, and the statistical analysis included procedures such as univariate regression procedures, linear mixed model (LMM) analysis , and binary logistic regression analysis, using SPSS (version 17, SPSS Inc., Chicago, USA). Graphical presentation was completed using Prism software (version 4.0, GraphPad Software, Inc., San Diego, USA). In order to avoid potential confounding factors such as age at diagnosis, improvement of management and/or treatment over the years of observation as described by Soni et al , we assessed the influence of these potential confounders by 3 characteristics such as "year at birth", "year at diagnosis" and the "year at testing". The "year at test" proved to be the principal confounder influencing the course of PaO2 significantly (t = 2.831; p = 0.005). Consequently, "year at test" was taken as a covariate in all statistical analyses.
The application of linear mixed model analysis evaluating repeated measurements has several advantages. In contrast to General Linear Models (GLM), the time points at which measurements are obtained need not be equal for all subjects, and therefore, subjects with missing data are not dropped from the analysis. In addition LMM analysis features a single model for a repeated measurement approach (i) assessing influences of various effects, (ii) estimating these effects at each time point, and (iii) comparing them correctly against a background of between-patient variation. There is no need to calculate mean values across all time points (to obtain the overall effect influences), or to analyze time points separately (to obtain specific effects at each time point). Standard errors for effects at individual time points are calculated using information from all time points and are, therefore, more robust than standard errors calculated from separate time points. Finally, the covariance pattern of the repeated measurements can be determined and taken into account (e.g. the model can figure out whether measurements are correlated across all time points, or whether they show more complex pattern over time) . These are important advantages especially for observational studies, where people often miss regularly scheduled clinic appointments or experimental sessions. In addition, LMM analysis offers the possibility to select the best variance-covariance structure for repeated measurement data, and interactions of interest can be specified . More details to the discussion LMM versus GLM analysis are given in the additional file 1, under the heading "Options of Statistical Modeling".
Patient cohort (A), data base characteristics (B), and distribution of CFTR mutations (C) taken from the Bernese CF Registry (n = 178, 87.3% of a total number of 204 CF patients)
Patient cohort follow-up statistics
Gender distribution of patients
Blood gas tests within age periods
5 to 8 y
9 to 14 y
15 to 18 y
From entire database, 26 patients (12.7%) excluded because of insufficient number of tests, (6) or age < 6 years (20)
Blood gas test and lung function measurement follow-up statistics
Number of blood gas tests median (range)
Blood gas tests per year of observation
Total of tests
1987 to 1993
1994 to 2000
per year of observation
2001 to 2008
Distribution of CFTR mutations
Equal distribution of CFTR genotypes over age range and over years of observation
All patients except 3 suffered from pancreatic insufficiency. P. aeruginosa infection was present in 111 patients (67.7 %), with a mean age at onset of 5.7 years (range 0.1 to 20.5 years). Twenty-three patients were intermittently colonized and 30 remained free from P. aeruginosa colonization. Five patients underwent lung transplantation and in 2 the liver was transplanted. Within this study cohort of patients, a total of 1457 tests were performed representing a median (range) of 8.1 (3-15) test sets per child, or 68.2 (37-90) test sets per year of observation. Gender was equally distributed. According to the frequencies in our population-specific CFTR genotype distribution, the patients were stratified into 6 groups consisting of (a) F508del homozygotes F508del[2| (inframe/inframe): n = 103 (57.9%), (b) R553X, G542X, Q525X and E585X compound heterozygotes with F508del (inframe/nonsense mutations): n = 22, (12.4%), (c) 3905insT compound heterozygotes 3905insT/F508del (frameshift/F508del): n = 19, (10.7%), (d) 3905insT compound heterozygotes with other than F508del (frameshift/non-F508del): n = 12, (6.7%), (e) 1717-1G>A, 621+1G<T and 4005+1G>A compound heterozygotes with F508del (inframe/splicesite): n = 7 (3.9%), and (f) miscellaneous genotypes n = 15, (8.4%). The genotypes were equally distributed over the age-range studied and the years of observation.
Hypoxemia. Overall PaO2 presented with a linear decline from a mean ± SEM of 80.7 ± 1.9 mmHg at 5 years of age to a mean of 69.9 ± 1.6 mmHg at age 18 years. As FEV1 is the most commonly used lung function parameter internationally, the figure additionally shows the PaO2 decline within 2 subgroups stratified according to normal FEV1 (z-score > -2 SDS) or abnormal FEV1 (z-score < -2 SDS). The measurements within the 2 subgroups were equally distributed over the age range studied. Unpaired t-test with Welch' correction compared PaO2 measurements with normal FEV1 (46.8%) presenting a mean ± SEM oxygenation of 76.9 ± 0.62 mmHg versus PaO2 measurements with a FEV1 <-2 SDS with a mean oxygenation of 70.2 ± 0.70 mmHg This significant difference in PaO2 decline was mainly due to a mean difference of 6.7 ± 0.94 mmHg between the FEV1-subgroups (p < 0.0001) and not to a difference in their slopes.
The annual changes in PaCO2 demonstrated a more complex course. The mean PaCO2 of 33.2 ± 0.45 mmHg at 5 years of age showed a transient stagnation in a large proportion of patients before rising to a mean of 36.1 ± 0.47 mmHg at the age of 18 years. This phenomenon of low PaCO2 measurements was observed in 103 of the 164 patients (62.8%), mainly associated with a FEV1 > -2SDS, and occurred over an age range of 5.8 to 15.8 years. An unpaired t-test with Welch' correction comparing PaCO2 measurements with a mean PaCO2 of 33.7 ± 0.32 mmHg for blood gas measurements associated with normal FEV1 versus a mean PaCO2 of 35.1 ± 0.29 mmHg in association with abnormal FEV1 also revealed a significantly different PaCO2 course with a mean difference of 2.4 ± 0.6 mmHg between the FEV1-subgroups (p = 0.0002).
Hypercapnia, defined as a PaCO2 >45 mmHg at rest, was observed only in a few patients in our collective. In contrast, we were surprised by some very low PaCO2 values occurring during the course between ages 5 to 12 years (Figure 1).
Hypocarbia, and especially a lower level for PaCO2 at rest in children has not yet been defined internationally. Using three different statistical techniques (binary logistic regression, ROC and discriminant analysis) explained in detail in the additional file 1, hypocarbia was defined as a PaCO2 less than or equal to 34 mmHg.
Univariate and multivariate linear mixed model (LMM) analysis evaluating lung function parameters as explanatory variables of PaO2, including adjustment by "year at testing"
LMM univariate analysis adjusted for age and test year
95 % CI
-1.907 to -1.376
-0.403 to -0.272
-1.471 to -0.947
-0.599 to -0.434
0.991 to 1.261
0.507 to 0.664
0.922 to 1.825
LMM multivariate analysis with backward elimination procedure*
95 % CI
-1.180 to -0.5555
-0.191 to -0.058
-0.225 to -0.021
0.284 to 0.738
0.0412 to 0.281
The present observational study illustrates the complexity of gas exchange in children with cystic fibrosis, especially with reference to the age-related changes in oxygenation. The age-related deterioration of oxygenation has not yet been well described, presumably due to the fact that gas exchange characteristics are not routinely evaluated over a period of a substantial number of years. Our study, performed in a representative number of cases and followed-up over a consistent number of years demonstrates that oxygenation is specifically influenced by different lung function deficits and CF genotypes. There are several major findings of this study: First, (i) a linear decline in oxygenation could be demonstrated over the age range 5 to 18 years, which was closely and independently related to the degree of pulmonary hyperinflation (FRCpleth), the degree of flow and volume limitation (FEV1, FEF50), and ventilation inhomogeneities (LCI). Secondly, (ii) as reported for several lung function parameters [1, 2], the decline in PaO2 is representative of an overall deterioration of lung disease, reflecting that factors such as the degree of pulmonary hyperinflation, ventilation inhomogeneities and impeded airway function are involved in the long-term course of gas exchange characteristics. Most importantly, however, (iii) in more than half the patients with hypoxemia, FEV1 was within the range of normal values, and hence with functional deficits not detectable by spirometric lung function testing alone. Furthermore, (iv) an association could be found between oxygenation and the genotype. The so called "Swiss-Type" (3905insT/F508del), presented with the worst PaO2 values already detectable at the age of 5 years and the subgroup R553X/F508del showed the worst deterioration (steepest slope) over the age range studied. Interestingly, some special subgroups of genotypes (inframe/splicesite, 3905insT/non-F508del) showed only discrete changes in gas exchange over the years. It follows that PaO2 may serve as a sensitive marker of lung function deterioration in CF.
The present study demonstrates that the preservation of airway function and hence an intact static recoil of the lungs over years is essential, as has been shown by Zapletal . It was reported by Hart et al. that if FEV1 declines in children and young adults with CF, there is an increase in the elastic load and work of breathing, resulting in a rapid shallow breathing pattern, that is associated with further impairment of gas exchange . Pulmonary hyperinflation and ventilation inhomogeneities are further pathophysiologic characteristics, which have to be taken into consideration regarding progression in CF, as reported previously by our group [1, 2].
A detailed discussion about blood gas measurements in children, the stratification into genetic subgroups, limitations in the interpretation of extensive lung function tests and the different options for statistical modeling are given in the additional file 1. An important limitation of this type of data resides in the ability to obtain repeated measurements of lung function annually over a substantial period of time. Noteworthy therefore, we were able to obtain serial annual measurements over a 10-year period in 62 % of the patients. Although the technique of blood gas measurements from the arterialized earlobe is well established and routinely used in several laboratories [26, 27, 32–34], in the following some technical aspects have to be mentioned. Finally, limitation of collected functional data over a wide range of years may include confounders related to changes in the technical set-up. As proposed by Soni et al , we assessed the influence of these potential confounders by 3 characteristics such as "year at birth", "year at diagnosis" and the "year at testing". The "year at test" proved to be the principal confounder influencing the course of PaO2. Most important finally, the variances of lung function over age are specific for each lung function parameter. Therefore, values of lung function data have to be expressed by z-scores, calculated from age- and gender-specific equations for value prediction for each lung function parameter, and in particular also for each lung function device as previously presented [1, 2].
Currently direct arterial catheterization of the radial artery is the widely accepted gold standard technique for obtaining the most accurate assessment of pulmonary gas exchange, especially in adult medicine. However, this technique is painful and not suitable for use in children for long-term evaluation. Alternative non-invasive methods have been proposed such as pulse oxymetry, which is used to assess arterial oxyhemoglobin saturation. However, obtained values correlated poorly with arterial PaO2 values . Pulse oxymetry is a poor predictor of PaO2 because of the sigmoidal shape of the oxyhemoglobin dissociation curve and because the curve can be shifted under various clinical and physiological conditions. Therefore, capillary arterialized blood gas analysis is a very convenient technique especially suitable for children and for repeated measurements. Comparisons between earlobe capillary PaO2 and radial arterial PaO2 were performed by Godfrey et al.  and Gaultier et al. . The former author group compared earlobe and arterial values in 8 adult subjects (age range of 26 to 63 years) at rest and on exercise, showing that the mean difference between arterial and earlobe samples for PaO2 at rest was 2.09 ± 2.48 mmHg and for PaCO2 0.65 ± 1.2. Gaultier et al.  studied these differences in 70 infants or children suffering from cardiac or pulmonary disease and demonstrated significant differences in PaO2 of 1.86 ± 0.60 mmHg only in children younger than 8 years. It was concluded that sampling blood from the earlobe is appropriate as a substitute for arterial PaO2, provided certain important methodological conditions such as sampling site and optimal vasodilatation are fulfilled. In a study examining PaO2 measurements over a long period of time, it would be preferable to validate the results periodically using arterial samples. It is, however, difficult to justify arterial blood sampling in a collective of CF children with no or only minor pulmonary function impairments. In a meta-analysis performed by Zavorsky et al. , it was shown that capillary blood gases accurately reflect arterial blood samples and that sampling blood from the earlobe is appropriate as an alternative to arterial PaO2. However, the discrepancy between capillary and arterial PaO2 increased with increasing PaO2. Reproducibility of earlobe blood gas measurements was assessed by Godfrey et al.  and Gaultier et al. .
There is only limited knowledge about the relationship between oxygenation and factors such as the degree of pulmonary hyperinflation, ventilation inhomogeneities and/or airway function under resting conditions in CF. Moreover, hypocarbia in CF is poorly described in the literature and the correlation of gas exchange characteristics with lung function is unknown. There is only one report in which the association between hypocarbia and hypercapnia and the matching of ventilation has been studied in dogs . The present report focuses on the decline of oxygenation in CF. As demonstrated in Table 2, oxygenation is significantly associated with the degree of flow limitation given by the FEV1. This finding is in line with Hirsch et al., who could demonstrate a higher ventilatory equivalent in CF patients in comparison with control subjects, suggesting increased work of breathing due to airflow obstruction and dead space ventilation. Ventilation appears mechanically inefficient but necessary to keep arterial PaCO2 from rising and oxygen saturation from falling at rest . Moreover, Hart et al. showed that in children and young adults with advanced stable pulmonary CF disease, falling FEV1 induced an increase in the respiratory muscle load, predominately by a decrease in lung compliance (CLdyn) rather than an increase in total lung resistance (RL). Other physiologic studies have demonstrated an increase in tidal volume (VT) with a reduction in respiratory rate (RR) in association with impairment of gas exchange . The present study indicates that oxygenation at rest is significantly associated with LCI and with FRCpleth and reduced forced expiratory volume (FEV1) as an indirect parameter of airflow limitation.
To date, a relationship between CFTR genotypes and severity of pulmonary disease has proven difficult to determine . The present study, however, clearly demonstrates an association between gas exchange characteristics (especially oxygenation) and genotypes. These findings are in line with previous work obtained in infants  and children [1, 2] with CF. Schaedel et al. used FEV1 in terms of % predicted of normal, to demonstrate a slower rate of decline in patients with missense mutations compared with F508del homozygotes . Since these patients generally had a sufficient level of pancreatic function, it was concluded that CFTR genotypes associated with long-term pancreatic sufficiency have more benign lung disease and better pulmonary function [12, 14]. With the exception of one patient with a missense mutation, all patients in our study collective presented with pancreatic insufficiency, requiring continuous supplementation with pancreatic enzymes and high caloric nutritional support. The major new finding in the present study is an allocation of specific genotypes to (i) sufficient oxygenation combined with low PaCO2 levels, and (ii) insufficient oxygenation combined with normocarbia, reflecting different phenotypes of disease progression. Inframe/splicesite and non-F508del/frameshift mutations seem to have a significant better gas exchange pattern than the other groups. The different progression between F508del/frameshift and non-F508del/frameshift is especially striking. Based on recent findings  showing complete lack of CFTR protein at the apical membrane in F508del/3905insT compound heterozygous patients, we hypothesize that there may be an interaction between the plasma membrane resulting in a more severe phenotype. However, further experiments are needed to elucidate the fate of the 3905insT protein in the cell after its biosynthesis.
In conclusion, the linear decline of PaO2 over the years was closely associated with the degree of pulmonary hyperinflation, ventilation inhomogeneities, and parameters of airway function on the one hand and with genotypes on the other hand. We found that gas exchange characteristics (PaO2, PaCO2) are very sensitive parameters of deterioration in CF lung disease. Since the assessment of factors influencing the overall estimate of gas exchange is of major interest to understand functional deficits influencing progression not only in quantitative, but also in qualitative terms, classification into certain functional risk groups may have implications for therapeutical intervention. However, further studies are needed to demonstrate whether changes in PaCO2 in relation to PaO2 are potential predictors of exacerbation or of the long-term clinical outcome. We keep in mind, that the ability of blood gas measurements to serve as outcome measures in interventional studies largely depends from the knowledge to what extent changes recorded during a short-term study will be out of the variability of the measurement changes established by the present long term approach over years.
body mass index
body temperature and pressure saturated
Cystic Fibrosis Transmembrane conductance Regulator
Forced Expiratory Volume in One second
Forced expiratory flow at 50 percent FVC
Functional residual capacity (plethysmographically determined)
Functional residual capacity (determined by MBNW)
Forced Vital Capacity
Lung clearance index
Linear mixed model
Multibreath nitrogen washout
partial carbon monoxide pressure
partial oxygen pressure
Standard deviation score obtained by z-transformation
Standard error of the mean
specific effective airway resistance
single strand confirmation polymorphism/heteroduplex
Total Lung Capacity
volume of trapped gas
The study was supported by grants of the Swiss National Research Foundation (SNF 32-040681.94_SG, SNF 32-040562.95_RK, 32-055697.98 _SG, 32-066767.02_SG, and SNF 32-112652.06_SG) as well as the Foundation Telethon Action Switzerland. The authors are indebted to Prof. Martin H. Schöni, M.D., Dr. Anna Rüdeberg, M.D., Dr. Carmen Casaulta-Aebischer, M.D., and the entire nursing staff of the Bernese Cystic Fibrosis Clinic for their contribution in the registration of the clinical data and in obtaining the samples for genotype analysis. The authors also thank Ms. Gisela Wirz for performing the lung function tests and taking care of the data base, as well as Dr. Jane McDougall for reviewing the manuscript.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.