Scholarly article on topic 'Airways resistance and specific conductance for the diagnosis of obstructive airways diseases'

Airways resistance and specific conductance for the diagnosis of obstructive airways diseases Academic research paper on "Clinical medicine"

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Academic research paper on topic "Airways resistance and specific conductance for the diagnosis of obstructive airways diseases"

Topalovic et al. Respiratory Research (2015) 16:88 DOI 10.1186/s12931-015-0252-0

RESPIRATORY RESEARCH

RESEARCH

Open Access

Airways resistance and specific conductance® for the diagnosis of obstructive airways diseases

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Marko Topalovic1, Eric Derom2, Christian R. Osadnik3,4, Thierry Troosters1,3, Marc Decramer1, Wim Janssens1 and on behalf of the Belgian Pulmonary Function Study Investigators

Abstract

Background: Airway resistance (RAW) and specific airway conductance (sGAW) are measures that reflect the patency of airways. Little is known of the variability of these measures between different lung diseases. This study investigated the contribution of RAW and sGAW to a diagnosis of obstructive airways disease and their role in differentiating asthma from COPD.

Methods: 976 subjects admitted for the first time to a pulmonary practice in Belgium were included. Clinical diagnoses were based on complete pulmonary function tests and supported by investigations of physicians' discretion. 651 subjects had a final diagnosis of obstructive diseases, 168 had another respiratory disease and 157 subjects had no respiratory disease (healthy controls).

Results: RAW and sGAW were significantly different (p < 0.0001) between obstructive and other groups. Abnormal Raw and sGAW were found in 39 % and 18 % of the population, respectively, in which 81 % and 90 % had diagnosed airway obstruction. Multiple regression revealed sGAW to be a significant and independent predictor of an obstructive disorder. To differentiate asthma from COPD, RAW was found to be more relevant and statistically significant. In asthma patients with normal FEV1/FVC ratio, both RAW and sGAW were more specific than sensitive diagnostic tests in differentiating asthma from healthy subjects.

Conclusions: RAW and sGAW are significant factors that contribute to the diagnosis and differentiation of obstructive airways diseases.

Keywords: Body-plethysmography, Airway resistance, Pulmonary function tests, Chronic obstructive pulmonary disease, Asthma

Background

Whole-body plethysmography is an increasingly frequent and important component of comprehensive pulmonary function testing in respiratory medicine, and an integral diagnostic procedure to evaluate static lung volumes and airway resistance [1, 2]. To determine airways resistance, plethysmography applies the gas law of Boyle-Mariotte [3] to evaluate the difference in the pressure of the closed box (in which the subject is breathing) in conjunction with flows measured at the subject's mouth by breathing out of the box [4, 5].

* Correspondence: Wim.Janssens@uzleuven.be

department of Clinicaland ExperimentalMedicine, Laboratory of

Respiratory Diseases, University Hospital Leuven, KULEUVEN University of

Leuven, Herestraat 49, 3000 Leuven, Belgium

Fulllist of author information is available at the end of the article

Bio Med Central

The two most commonly used resistive parameters are airway resistance (RAW) and specific airway conductance (sGAW). Raw reflects changes in alveolar pressure over changes in flow [6] representing true resistance of the airways. RAW is determined by airway narrowing and is therefore considered a good parameter for the diagnosis of airflow obstruction [6]. As the manoeuvre to determine airway resistance is dependent on thoracic gas volume (with larger volumes resulting in opened airways), specific airway resistance (sRAW) is divided by thoracic gas volume to obtain RAW. Mathematically, sRAW does not represent resistance but the flow-standardized work that one needs to perform in order to complete the manoeuvre [4]. SGAW is the inverse of sRAW and therefore reflects the conductance of the airways independent of lung volumes.

© 2015 Topalovic et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http:// creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Despite a large body of physiological evidence, clinicians have lost their interest in measures of resistance which are generally perceived as useless in the work-up of clinical problems. A strong case for the use of such measures in clinical practice recently emerged from a large multicentre study in Belgium (the Belgian Pulmonary Function Study). This study demonstrated that regular measurement of airway resistance (both RAW and sGAW), one of four most commonly used pulmonary function tests (PFTs), significantly contributes to a reduction in the number of differential diagnoses and accuracy of final diagnosis [7]. Nevertheless, it is not yet clear how such parameters vary between different lung disease groups and the extent to which they may contribute to differentiation between asthma, COPD and healthy subjects. The aims of the study were to a) explore the variability of resistance parameters between established diagnoses of respiratory diseases in a general patient sample, and b) investigate whether measures of resistance can differentiate between the obstructive diseases and further refine the diagnosis of asthma or COPD.

Methods

Study subjects

In total 976 subjects were included from the Belgian Pulmonary Function Study. This prospective cohort study includes all successive new subjects from the periods of June 6th till September 12th 2011, and January 16th till June 12th 2012 across 33 hospitals in Belgium. Details on the protocol can be found in the corresponding publication [7]. All subjects were of Caucasian race aged 18 to 75 years with a history of respiratory complaints (dyspnea, cough, sputum, wheezing etc.). All performed complete PFTs at cohort entry including post-bronchodilator spirometry, measurement of diffusion capacity and body-plethysmography including measures of lung volumes, airway resistance (RAW) and conductance (sGAW, only available in 778 subjects). Pulmonologists performed additional tests such as imaging, ECG and other PFTs to determine diagnosis, where necessary. All final diagnoses for each included subject were validated by local Belgian focus groups of 20 to 25 pulmonologists who jointly evaluated all test outcomes. A final diagnosis was selected from a predefined list of 13 diseases covering the wide spectrum of respiratory diseases that are potentially diagnosed by pulmonary function: asthma, COPD, other obstructive diseases, upper airway obstruction, neuromuscular disease, thoracic or pleural disease, obesity, interstitial lung disease, systemic sclerosis or vascular disease, cardiac failure, hyperventilation, no primary pulmonary abnormality, and others (lung cancer, rhinosi-nusitis, etc.). The study was registered on clinicaltrials.gov (identifier: NCT01297881).

Pulmonary function tests

All PFTs were performed according to the ATS/ERS criteria [8] using standardized equipment available in the participating pulmonary function laboratory (including: Sensormedics Whole Body Plethysmograph, Care fusion, Belgium; Masterscreen Jaeger, Care fusion, Belgium; Medisoft boybox 5500, Belgium; Ganshoren-Medisoft Hyp'air compact, Belgium). Spirometry data are post-bronchodilator measures and expressed, together with airway resistance and lung volume measurements as percent predicted of normal reference values [9, 10]. SGAW was calculated by implementing a least-squared fit of the line through the specific resistance loop at a defined fixed flow of ±0.5 L/s [5, 11]. Diffusing capacity (DL,CO) was measured by the single-breath carbon monoxide gas transfer method and expressed as percent predicted of reference values [12].

Initial inspection of resistance values (expressed as % predicted) from healthy subjects (no primary pulmonary disease) revealed slightly different resistance values than anticipated. This may be due to limited setting where existing reference values for resistive parameters were developed. We therefore established new upper and lower limits of normality for RAW and sGAW based on a 90 % reference interval from our large healthy reference population (N = 157). The new proposed upper limit of normality for RAW was 0.38 (kPa/L/s), corresponding to 173 % of the median healthy population reference value. The new lower limit of normality for sGAW was 0.63 (1/ kPa*sec) corresponding to 74 % of the reference value. As with existing reference equations on RAW (median value 0.22) and sGAW (median value 0.85), no gender separation was made as no influence on median resistive values of our healthy reference population was observed.

To explore independency of RAW and sGAW on an individual patient level, we compared it with other lung function parameters indicative of the presence of airflow obstruction. These included: FEVi/FVC ratio, MMEF, RV, TLC and FRC. If one of the latter was out of the predicted normal range, it was considered to be disturbed. Increases in the number of disturbed measures were associated with increased probability of the presence of 'true' airflow obstruction.

Statistical analysis

Statistical Analysis System (SAS) version 9.3, (SAS Institute, Cary, USA) was used for all statistical analyses. A Shapiro-Wilk test was used to explore data normality of each group, and differences between two groups were analysed via unpaired t-tests or Mann-Whitney tests where normal or non-normal data distribution existed, respectively. Logistic-regression models were applied for analysis of binary variables using stepwise selection to identify the subset of variables with the strongest relation to the

presence of obstruction or specific disease diagnoses. The default criterion for variables entering or egressing the models was significance at the 0.15 level. Receiver operating characteristic (ROC) curve analysis was performed via GraphPad Prism version 5.01, (GraphPad Software, La Jolla, California, USA) to identify the best cut-off values of RAW and sGAW to distinguish between asthma and COPD diagnoses. New reference values were determined using MedCalc 14.8.1 (MedCalc Software bvba, Ostend, Belgium), with Tukey test applied to detect outliers.

Results

Baseline characteristics

Baseline characteristics of all included subjects are summarised in Table 1 according to three groups, based upon final diagnosis. The 'healthy' group included subjects without primary pulmonary abnormality; the 'obstruction' group included subjects with COPD, asthma, upper airway obstruction and other obstructive diseases (e.g. chronic bronchitis, bronchiolitis, small airways disease, bronchiectasis, cystic fibrosis); and the 'other pulmonary diseases' group comprised subjects with other, non-obstructive pulmonary diseases. Consistent with clinical practice, the 'obstruction' group was the most common diagnostic group (N = 651, 67 % of total sample), followed by 'other pulmonary diseases' (N = 168, 17 %) and 'healthy' (N = 157,16 %).

Value of resistance parameters for diagnosis of obstructive airways disease

Median RAW values were greater and median sGAW values lower in the group of obstructive patients compared to both the healthy controls and the group of

non-obstructive respiratory diseases (Table 1). These differences were highly statistically significant (both p < 0.0001). Expressed as a percentage of predicted values using the reference equation of Quanjer [10], the total study cohort proportion of disturbed RAW (defined as >150 % predicted of the fixed median value) was 39 % (N = 377), whilst for sGAW (defined as <50 % predicted) it was 9 % (N =73). Eighteen percent of healthy controls had an abnormal RAW and one had an abnormal sGAW. Implementation of the lower and upper limits of normal for RAW and sGAW developed from our own healthy population resulted in a significant change in the proportion of detected abnormalities. Increased RAW (0.38 kPa/L/s; >173 % predicted) was observed in only 30 % (N =290) of subjects, whilst reduced sGAW (0.63 1/kPa*sec; <74 % predicted) was observed in 22 % (N = 171) of subjects (Fig. 1). Independently of the cutoffs used, the group of patients with obstructive diseases had a significant higher proportion of increased RAW. In particular, 47 % of all subjects with obstructive airways disease (Panel A) or 37 % if using the less stringent cut-off (Panel B), presented with an increased resistance. A reduced sGAW (Panels C and D) had a high positive predictive value for obstructive diseases, as 92 % or 90 % (depending of cut-off) of all cases with low sGAW presented with such a diagnosis. This was confirmed in the multiple logistic regression analysis, which identified sGAW as a significant contributing factor to a diagnosis of obstructive lung disease (Table 2). To verify whether resistance parameters (expressed as percent predicted) are beneficial and additional to other PFT parameters to diagnose obstructive airflow disorders, we created different regression models comprising parameters of spirometry only, parameters from spirometry and body-plethysmography and by the combination of the former including diffusing

Table 1 Study population characteristics

Healthy Obstruction Other pulmonary diseases

Subjects, n 157 651 168

Age, years 53 (41 -64) 55 (42-65) 57 (44-67)

Smoking, pack yr. 0 (0-5) 0 (0-30) 0 (0-15)

BMI, kg/m2 25.3 (21.6-28.7) 25.2 (21.1 -29.7) 27.6 (23.1-32.0)

FEV1, %predicted 103.3 (91.5-114.7) 84.2 (67.0-97.7) 88.1 (74.4-103.8)

FVC, %predicted 106.6 (97.2-114.9) 97.7 (84.4-110.4) 92.1 (76.5-107.8)

DLCO, %predicted 86.4 (77.0-99.2) 78.7 (63.0-89.9) 70.3 (56.3-85.7)

RV, %predicted 106.9 (91.6-129.7) 131.6 (104.0-159.9) 101.8 (80.9-124.6)

TLC, %predicted 104.6 (95.7-112.1) 106.0 (94.8-117.1) 88.6 (79.7-103.4)

FRC, %predicted 105.1 (93.4-123.1) 119.4 (99.2-143.3) 95.7 (78.0-116.5)

Raw, kPa/L/s 0.24 (0.18-0.30) 0.32 (0.23-0.45) 0.25 (0.17-0.35)

sGAW, 1/ kPa*sec 1.21 (0.95-1.57) 0.84 (0.56-1.17) 1.28 (0.90-1.71)

Definition of abbreviations: BMI body mass index, DLCO carbon monoxide diffusing capacity, FEV1 forced expiratory volume in one second, FRC functional residual capacity, FVC forced vital capacity, RV residual volume, RAW airway resistance, sGAW specific airway conductance, TLC total lung capacity, Values are median and IQR

Fig. 1 Comparison of RAW and sGAW disturbance within each group of diseases and specific obstructive disease. Each panelis divided into three sections indicating group of diseases and levelof disturbance of parameters within each group. Obstructive group is additionally divided into three subsections representing specific obstructive diseases. Panels a and c/ RAW and sGAW using standard normality limit for disturbance (>150 %, < 50 % of predicted values); Panels b and d/ RAW and sGAW using statistically drawn limits of healthy subgroup for disturbance; Disturbance is indicated with the cross hatch in the figure; Data from N = 976 (RAW) and N = 778 (sGAW) subjects, respectively

capacity. Stepwise selection excluded RAW in all models, however sGAW contributed significantly to all lung function models.

The presence of abnormal RAW and sGAW values rarely occurred in isolation and was commonly observed in conjunction with disturbances of other PFT parameters indicative of obstruction (Table 3). This was particularly evident for sGAW where only few subjects had normal values of all other PFT parameters. Of the nine cases of isolated sGAW disturbance, two were diagnosed as healthy,

one had neuromuscular disease, one had another obstructive disease, and five had asthma. Additionally, most subjects who presented with isolated abnormally high RAW values had a diagnosis of asthma with normal lung function. Application of the classical cut-offs resulted in detection of 54 subjects with disturbed resistance, of which 28 had asthma, 11 were considered healthy, one had COPD, five presented with other obstructive diseases and nine had various other respiratory diseases. Our more restrictive cut-off threshold identified 29 instances of

Table 2 Relationship between pulmonary function parameters and the presence of obstruction in multiple logistic regression with stepwise selection

Table 4 Relationship between pulmonary function parameters and the presence of asthma in multiple logistic regression with stepwise selection (subjects with obstructive diseases only)

Variables Odds Ratio (95 % Confidence limit) p value Variables Odds Ratio (95 % Confidence limit) p value

1. sGAW, %predicted 0.99 6 (0.994-0.998) 0.0003 1. FEV1/FVC 1.043 (1.012-1.074) <0.0001

MEF75, %predicted 0.98 0 (0.972-0.988) <0.0001 MEF25, %predicted 1.024(1.010-1.038) 0.0024

FEV1/FVC 0.93 6 (0.912-0.960) <0.0001 PEF, %predicted 1.018 (1.006-1.030) 0.0088

2. Raw, %predicted 1.002 (1.000-1.004) 0.0320

TLC, %predicted 1.058 (1.043-1.075) <.0001 2.

sGAW, %predicted 0.99 7 (0.995-0.999) 0.0031 FEV1, %predicted 1.029 (1.013-1.046) <.0001

MMEF, %predicted 0.98 7 (0.978-0.996) 0.0108 MEF25, %predicted 1.022 (1.010-1.035) 0.0015

MEF75, %predicted 0.97 9 (0.969-0.988) <.0001 Raw, %predicted 1.002 (1.000-1.004) 0.0287

FEV1, %predicted 0.970 (0.955-0.986) <.0001 FRC, %predicted 0.981 (0.973-0.989) <.0001

1/Variables of spirometry and resistance (initial model1: FVC, %pred, FEV^ %pred, FEV,/FVC, MEF75, %pred, MEF50, %pred, MEF25, %pred, MMEF, %pred, PEF, %pred. Raw, %pred. and sGAW, %pred.); 2/ added variables of lung volumes (initial model2: model1, TLC, %pred, RV, %pred, FRC, %pred.); Adding variables of diffusion capacity (initial model3: model2, DLCO, %pred, KCO, %pred.) resulted in same values as model2

disturbed resistance, of which 18 had asthma, six were considered healthy and five had other respiratory diseases.

Value of resistance parameters for differentiating asthma from COPD in obstructive airways diseases

Due to the lack of available data for sGAW in some subjects, diagnostic groups differed in size from the principal analysis, but not in their proportion relative to each other. Median (IQR) RAW values for the asthma (N = 369) and COPD (N =221) groups were 0.30 kPa/L/s (0.22-0.42) and 0.39 kPa/L/s (0.26-0.53), respectively (p < 0.0001). For sGAW (N = 286 for asthma; N = 165 for COPD), these were 0.90 1/kPa*sec (0.69-1.22) and 0.60 1/kPa*sec (0.41-0.98), respectively (p < 0.0001).

When using the complete set of PFTs in the group of patients with obstructive diseases, application of multiple logarithmic regression with stepwise selection did not reveal an independent statistical role for RAW or sGAW in the differentiation between asthma and COPD. Although RAW was statistically significant in models involving spirometry and plethysmography parameters only, the better variable of differentiation was diffusion capacity (Table 4). When looking at the cumulative disturbances of other PFT parameters per diseased subject, in COPD, the presence of disturbed RAW or sGAW was

DLCO, %predicted FEV1/FVC TLC, %predicted FRC, %predicted

1.071 (1.051-1.090) 1.051 (1.024-1.078) 1.040 (1.014-1.067) 0.970 (0.956-0.984)

<.0001 <.0001 0.0021 0.0041

1/Variables of spirometry and resistance (initial model1: FVC, %pred, FEV^ %pred, FEV1/FVC, MEF75, %pred, MEF50, %pred, MEF25, %pred, MMEF, %pred, PEF, %pred. RAW, %pred. and sGAW, %pred.); 2/ added variables of lung volumes (initial model2: model1, TLC, %pred, RV, %pred, FRC, %pred.); 3/ added variables of diffusion capacity (initial model3: model2,DLCO, %pred, KCO, %pred.)

associated with abnormalities in several other PFT parameters. For those with asthma, increased RAW more commonly occurred in isolation (Table 5). The latter may suggest a more specific role of RAW in the diagnosis of asthma with a non-obstructive spirometry.

Resistance and specific conductance in non-obstructive asthma

In COPD, RAW and sGAW were never independently disturbed as significant changes always concurred with significant changes of other PFT measures, including the FEVi/FVC ratio by definition. In contrast, subjects with asthma, 28 of 112 (28 %) or 18 of 85 (21 %) presented with isolated RAW disturbance. To further examine this independent value of resistance in asthma, we focussed on the subgroup of asthmatics and healthy controls with normal FEV1/FVC ratio (above LLN) which resulted in a group of 285 subjects with available RAW data and 213 subjects with available sGAW data. When applying the maximal sum of sensitivity and specificity to select the

Table 3 Disturbed resistance in relation with the disturbance of other lung function parameters indicative of obstruction

Raw (>150 %pred.)

Raw (>173 %pred.)

sGaw (<50 %pred.)

sGaw (<74 %pred.)

Alone 54 (=20 %)

Together 218

Alone 29 (=14%)

Together 176

Alone 1 (=1.5 %)

Together 68

Alone 9 (=6 %)

Together 147

Alone: disturbance of only RAW or sGAW. Some patients excluded from analysis due to missing measurement data. Included parameters: FEV1/FVC, MMEF, RV, TLC and FRC

Table 5 Number of subjects with disturbance per disease (when resistance or specific conductance is already disturbed) stratified over total number of disturbed lung function parameters indicative of obstruction

Disturbance RAW (>150 %pred.) N = 204 RAW (>173 %pred.) N=162 sGAW (<50 %pred.) N = 61 sGAW (<74 %pred.) N=133

(=31%) (=25%) (=12%) (=26%)

Asthma (N=112) COPD(N = 92) Asthma (N = 85) COPD(N = 77) Asthma (N=16) COPD(N = 45) Asthma (N = 55) COPD(N = 78)

0 28 1 18 0 0 0 5 0

1 27 7 23 6 4 0 12 3

2 25 12 19 11 2 2 12 8

3 20 11 16 7 5 4 16 7

4 9 32 6 26 4 19 9 29

5 3 29 3 27 1 20 1 31

Some patients excluded from analysis due to missing measurement data. Proportions observed in a group of all subjects with obstructive diseases. Included parameters: FEV1/FVC, MMEF, RV, TLC and FRC

best RAW cut-off for asthma diagnosis in that particular subgroup, ROC curve identified an ideal cut-off value of 0.31 kPa/L/s, with a specificity of 76 %, sensitivity of 45 % and positive predictive value of 78 % (Table 6, panel A). For sGAW a cut-off value of 0.98 was identified with associated specificity of 74 %, sensitivity of 50 % and positive predictive value of 75 % (Table 6, panel B).

Discussion

Our study demonstrates measures of airway resistance and specific conductance have a valuable and potentially important role in the diagnosis of obstructive diseases. Specific conductance clearly contributes to diagnosis of obstructive airways diseases, whilst airway resistance can help differentiate between asthma and COPD. The presence of abnormal resistive parameters in isolation from other PFT measures may help differentiate between asthma with normal FEV1/FVC ratio and normal, good health.

Questions regarding the relevance of resistive parameters for diagnosing respiratory diseases are certainly not new. Prior to this study, it has been shown that specific resistance (reciprocal of specific conductance) may indicate bronchial reversibility in asthma, as it has a different physiological meaning than FEVi [13]. Most of its contribution, however, is demonstrated in children with asthma where measurement of specific resistance has been shown to improve diagnostic accuracy

Table 6 Value of resistance to differentiate between healthy subjects and asthma patients with normal FEV/FVC ratio

Asthma (N) Control (N) Total (N)

A Raw >0.31 129 37 166

Raw 2 0.31 156 120 276

Total(N) 285 157 442

B SGaw < 0.98 106 35 141

sGaw S 0.98 107 101 208

Total(N) 213 136 349

and decrease diagnostic delay [14-16]. Interestingly, it has also been shown that specific resistance has a better role in predicting asthma then airway resistance [17], and has higher sensitivity than FEV1 in terms of detecting lung function changes during methacholine challenges [18]. In COPD, both specific conductance and airway resistance are more sensitive for assessing short-acting bronchodilator effects than FEV1 [18,19]. Increased airway resistance and decreased specific conductance have also been detected as early features of mild COPD [20, 21]. Detailed analysis of computer tomography scans shows that increased airway resistance in COPD is correlated with the thickening of the airway walls [22]. Our data are in line with these earlier observations, but provide a more comprehensive overview of the role of resistance and specific conductance in a large unbiased sample of a routine respiratory practice in conjunction with other pulmonary function tests. Although resistance and specific conductance overlap with the disturbed pattern of pulmonary function tests in patients with a respiratory disorder, in some subtypes, they may reveal unique components to suggest a certain diagnosis. We demonstrate that both parameters have their specific characteristics which are not the leading but yet still significant contributors to respiratory disease diagnosis.

As expected, the highest frequency of abnormal resistance and specific conductance was found in patients with obstructive airways diseases, particularly COPD. RAW abnormalities were present in 50 % of subjects with mild COPD stages (former GOLD I and II, 75 % of all COPD cases), This proportion rose to 91 % in those with more severe disease (former GOLD III and IV). Whilst fewer subjects had disturbed sGAW, specific conductance appeared more useful than resistance in distinguishing obstructive diseases from non-obstructive, healthy or restrictive diseases. To some extent this may be explained by the fact that sGAW is independent of the thoracic gas volume [23] and may thus differentiate disturbed resistances of smaller airways at low lung volumes (e.g. interstitial lung

disease) from real intraluminal narrowing or collapse, in cases of asthma and COPD [24]. The observation that RAW pops up again when it comes to the further differentiation of asthma from COPD, may be explained by the fact that disproportionally low resistances (by high thoracic gas volumes) for the level of airflow limitation and FEV1 reduction, is a specific characteristic of COPD [25]. Moreover, our data demonstrate that an isolated increase of RAW might be associated with a diagnosis of asthma when airflow limitation on spirometry is not present. Mechanistically, disturbed FEV1 measures may be seen as a consequence of increased airway resistance from central and peripheral airways. However, FEV1 is obtained from the first second of forced expiration and therefore poorly representative of the small airways. The latter are better visualized at the end of a forced expiration or eventually, by direct measures of resistance during tidal breathing [26, 27].

The most appropriate predictive cut-off values to identify normality of resistive and conductive parameters are contentious. A thorough evaluation of our healthy subject population using the current recommended reference equations yielded unsatisfactory results and indicated that the current reference values may not be up to date [10, 28]. Evaluation of these data using the predicted median and 90 % confident intervals in our healthy reference population (which was considered healthy after an extensive evaluation including all necessary tests) showed the cut-offs for RAW to be too liberal and the cut-offs for sGAW too restrictive. Despite calls for revision of these reference equations from different authors, no official action has been taken yet [28, 29]. Solving this problem may lead to a more accurate and better usability of this test in clinical settings as current predictive values were not constituted in a large and healthy representative population.

An inherent limitation of our multi-centre study may lie in its design to measure pulmonary function using variety of equipment, since it can affect variability and consistency of obtained measurements. Weaknesses of airway resistance and specific conductance are also apparent within the analysis. For example, it is clear that both resistive parameters have large variability within core groups, making them weak independent factors for disease differentiation [30]. Another weakness lies in the estimation process for specific conductance, which affects estimation of airway resistance as well. Practically, the line fitted through the resistance loop to calculate sGAW does not always accurately reflect the entire loop pattern. Often, these differences can be visually detected (e.g. widening of the loop, club-shaped format, S pattern, etc. [4]) but may result in similar inclinations. Additional exploration specifically focused on the pattern of such resistive loops will increase the value of these

parameters and may result in a better description of certain phenotypes.

Taken together, airway resistance and specific conductance are certainly not the grand slam winning parameters of pulmonary function tests, however they can significantly contribute to the diagnosis of obstructive diseases and further disease differentiation. Our data also indicate that changing the upper limit of normality for Raw to 0.38 kPa/L/s and accepting a new lower limit of normality for sGAW (0.63 1/kPa*sec) may even improve their diagnostic value.

Competing interests

The authors declare that they have no competing interests. Authors' contributions

Study concept and design: MT, ED, MD, WJ; Analysis and interpretation of the data: MT, TT, WJ; Writing of the manuscript and criticalrevision: Allauthors. Allauthors read and approved the finalmanuscript.

Acknowledgements

We thank allthe pulmonologists, the pulmonary function technicians, the patients and the hospitals who participated in the study for providing data. We thank the Belgian Society of Pneumology for their financialand moral support. Finally, we thank Mrs. Kristien De Bent, Ms. Erica Balligand and Mr. Geert Celis for the provided technicalsupport.

The Belgian Pulmonary Function study investigators

R.Vanherreweghe (Algemeen Stedelijk Ziekenhuis, Aalst); R.Deman, S.Deryke, B.Ghesyens, M.Haerens, S.Maddens (AZ Groeninge, Kortijk); W.Bultynck, W.Temmerman, L.Van Zandweghe (AZ Sint Blasius, Dendermonde); R.De Pauw, C.Depuydt, C.Haenebalcke, V.Ringoet, D. Van Renterghem (AZ Sint Jan, Brugge); A.Carlier, D.Colle, C.De Cock, J.Lamont (AZ Maria Middelares, Gent); P.Brancaleone (CH Jolimont-Lobbes); M.Vander Stappen (CHR Haute Senne); R.Peché, Ph.Pierard, P.Quarré, A.Van Meerhaeghe (CHU, Charleroi); D.Cataldo, JL.Corhay, B.Duysinx, V.Heinen, M.Naldi, D.Nguyen, L.Renaud (CHU, Liège); M.Cotils, P.Duchatelet, A.Gocmen, C.Lenclud (Clinique Louis Caty-Baudour); Ph.Lebrun, J.Noel(Clinique Saint-Pierre, Ottignies); A.Frémault (Grand Hopital de Charleroi); Ph.Bertrand, B.Bouckaert, I.Demedts, P.Demuynck (Heilig Hart Ziekenhuis, Roeselare); E.Frans, A.Heremans, T.Lauwerier, J.Roelandts (Imelda, Bonheiden); G.Bral, I.Declercq, I.Malysse (Jan Ypermanziekenhuis, leper); V.Van Damme (St. Andries Ziekenhuis, Tielt); Dr.Martinot (St. Elisabeth, Namur); P.Vandenbrande (St. Maarten Duffel, Mechelen); M.Bruyneel, I.Muylle, V.Ninane, (St. Pierre, Bruxelles); Ph.Collard, G.Liistro, B.Mwenge Gimbada, Th.Pieters, C.Pilette, F.Pirson, D.Rodenstein (UCL, Bruxelles); L.Delaunois, E.Marchand, O.Vandenplas (UCL, Mont-Godinne); W.De Backer, P.Germonpre, AJanssens, A.Vrints (UZA, Antwerpen); M.Decramer, WJanssens, P.Van Bleyenbergh, G.Verleden, W.Wuyts (UZ Gasthuisberg, Leuven); G.Brusselle, E.Derom, G. Joos, K.Tournoy, K.Vermaelen (UZ, Gent); P.Alexander, C.Gysbrechts (Ziekenhuis Ronse); L.Bedert, Dr.Bomans, Dr.De Beukelaar, E.De Droogh, D.Galdermans, Dr.Ingelbrecht, Dr.Lefebure, H.Slabbynck, Dr.Van Mulders, Dr.Van Schaardenburg, Dr.Verbuyst (ZNA, Antwerpen); M.Daenen (ZOL Genk).

Funding

Astra Zeneca Chair 2012-2014. Belgian Society of Pneumology. WJ is supported by the Flemish Research Foundation (FWO).

Author details

''Department of Clinicaland ExperimentalMedicine, Laboratory of Respiratory Diseases, University Hospital Leuven, KULEUVEN University of Leuven, Herestraat 49, 3000 Leuven, Belgium. 2Respiratory Division, University HospitalGhent, University of Ghent, Ghent, Belgium. 3Department of Rehabilitation Sciences, Faculty of Kinesiology and Rehabilitation Sciences, KU Leuven, Leuven, Belgium. 4Department of Physiotherapy, Monash University, Victoria, Australia. institute for Breathing and Sleep, Victoria, Australia. 6Monash Health, Monash Lung and Sleep, Victoria, Australia.

Received: 18 March 2015 Accepted: 8 July 2015 Published online: 22 July 2015

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