Reference percentiles for FEV1 and BMI in European children and adults with cystic fibrosis
- Pierre-Yves Boëlle1, 2, 3,
- Laura Viviani4,
- Pierre-Francois Busson2,
- Hanne V Olesen5,
- Sophie Ravilly6,
- Martin Stern7,
- Baroukh M Assael8,
- Celeste Barreto9,
- Pavel Drevinek10,
- Muriel Thomas11,
- Uros Krivec12,
- Meir Mei-Zahav13,
- Jean-François Vibert1, 2, 3,
- Annick Clement1, 2, 3,
- Anil Mehta14 and
- Harriet Corvol1, 2, 3Email author
© Boelle et al.; licensee BioMed Central Ltd. 2012
Received: 6 July 2012
Accepted: 1 September 2012
Published: 7 September 2012
The clinical course of Cystic Fibrosis (CF) is usually measured using the percent predicted FEV1 and BMI Z-score referenced against a healthy population, since achieving normality is the ultimate goal of CF care. Referencing against age and sex matched CF peers may provide valuable information for patients and for comparison between CF centers or populations. Here, we used a large database of European CF patients to compute CF specific reference equations for FEV1 and BMI, derived CF-specific percentile charts and compared these European data to their nearest international equivalents.
34859 FEV1 and 40947 BMI observations were used to compute European CF specific percentiles. Quantile regression was applied to raw measurements as a function of sex, age and height. Results were compared with the North American equivalent for FEV1 and with the WHO 2007 normative values for BMI.
FEV1 and BMI percentiles illustrated the large variability between CF patients receiving the best current care. The European CF specific percentiles for FEV1 were significantly different from those in the USA from an earlier era, with higher lung function in Europe. The CF specific percentiles for BMI declined relative to the WHO standard in older children. Lung function and BMI were similar in the two largest contributing European Countries (France and Germany).
The CF specific percentile approach applied to FEV 1 and BMI allows referencing patients with respect to their peers. These data allow peer to peer and population comparisons in CF patients.
The outcome of cystic fibrosis (CF) patients has improved in recent decades, with mortality less than 5 percent during the first 10 years of life in patients treated with current multidisciplinary care. However, disease severity remains variable among children, adolescents and adults[2, 3]. In CF, severity is principally assessed by the decline in lung function because lung disease still remains the most common cause of death. Lung function in CF is almost universally calculated as percent predicted FEV1 referenced against a healthy population[4, 5]. This particular choice reflects a widely held opinion that achieving normality remains the ultimate goal of CF care. Irrespective of whether or not this aspiration is achievable, a limitation of the current ‘reference against the normal range’ approach is that it does not provide a ranking of an individual patient’s status relative to age and sex-matched CF peers. Similar considerations apply to nutrition, which must be adequate to maintain lung function, or surrogate markers of disease severity calculated from semi-quantitative screening scales such as the Chrispin Norman Score that measures lung damage from chest radiography.
There have been attempts to overcome such limitations. Kulich and coworkers converted the absolute FEV1 into percentiles calculated from a registry of lung function values in North American CF patients. In a related manner, McCormick and colleagues converted a chest x-ray severity score in childhood into population based percentiles. Such self-referencing approaches, despite their calculation from cross sectional data, provide a reference base that allows the longitudinal tracking of CF disease outcome and informs on the relative position of a given patient against his or her peers.
As of now, the CF FEV1 specific percentiles have of necessity been obtained from US CF patients. It remains to be established whether these data are appropriate for European patients with CF. Indeed, there are many differences not only in how CF care is organized (for example, coverage of neonatal screening, timely referral to reference centers, variation in standards of care) but also in the environment between EU nations and across the Atlantic. Furthermore Kulich analyzed data from 15 years ago (1994 to 2001) that would not account for recent progress in CF care. To mitigate against such issues, we combined data from the European Cystic Fibrosis Society Patient Registry (ECFSPR) and data from the current French CF Modifier Gene Study, to obtain CF reference percentile equations for lung function and body mass index that would apply to current European CF patients and would additionally provide the ranking of an individual patient’s status relative to age and sex-matched CF peers. As a second objective, we examined whether FEV1 and BMI in CF patients differed between European countries and across two continents, Europe and North America (USA).
We used the multinational ECFSPR as primary source of data and additional observations from the French CF Modifier Gene Study (MUCONAT). The former was set up to “measure, survey and compare CF aspects and treatments” in European countries[3, 10]. Fourteen countries contributed data to the present study (Austria, Belgium, Bulgaria, Czech Republic, Denmark, France, Germany, Greece, Israel, Italy, the Netherlands, Portugal, Slovenia, Sweden). The coverage of the study relative to the overall CF population in a given country was estimated using genetic prevalence estimates reported by Farrell et al., by Efrati et al. for Israel, and by the French CF national registry for France. Patients’ consent was obtained from every participating country and all the registry protocols were compliant with the relevant national data protection laws. ECFSPR data at a patient level were collected on a anonymous basis.
The MUCONAT project collects data on prevalent and incident CF cases. It was approved by the French ethical committee (CPP n°2004/15) and the information collection was approved by the CNIL (n°04.404). As for the ECFSPR, the MUCONAT data were collected on a strictly anonymous basis. The project is based on the participation of 38 out of the 49 French CF centers. Prospective data collection started in 2007 for all prevalent and incident cases.
The following information was extracted from both databases: FEV1 measurements (in L), country of residence, CFTR genotype, sex, height, weight and age, BMI. The ECFSPR covered the period 2004 to 2007, with one observation per year and per patient. Data for years 2008 to 2010 were obtained for French patients from the MUCONAT database, so that there was no overlap with the ECFSPR source. The same patient may have contributed data over several years; however the current ECFSPR did not allow reliable data linkage throughout the years for all the participating countries, so longitudinal aspects were not taken into account. Measurements in patients after lung transplantation were removed for all the analyses.
In data contributed to the ECFSPR, some countries reported the “best” annual FEV1 measurement, while others, including the 2 largest contributing countries (France and Germany), reported an unselected measurement. Using the best measurement for computation leads to overestimation in the CF specific percentile curves and limit its use to assess patients from unselected measurement. To limit such bias, we transformed “best” FEV1 values before calculation (see Additional file1). In short, the correction was computed as follows: using the French data, where a systematic longitudinal collection of all FEV1 values is carried out, we determined, by sex and age, the average difference between the “best” annual FEV1 and an unselected value of the same year. A corrected FEV1 measurement was then obtained by subtracting this value from the reported FEV1 value in countries reporting best values. As a sensitivity analysis, we also analyzed the data without correction. This correction was not required for BMI, as the reported data was not selected.
Quantile regression was used to estimate CF-specific reference equations for FEV1 and BMI. The q-quantile (or q-percentile) in a given distribution is the value below which the smallest q percent of the population is found: for example, the median is the 50th quantile. Quantile regression allows modeling of quantile values as a function of covariates, whereas standard regression only models the mean value. Here, we modeled quantiles of the FEV1 and BMI distribution according to age and height in European CF patients, separately in men and women. We used cubic B-splines to capture the non-linear dependence of FEV1 on age and height, using 6 nodes to avoid overfit. FEV1 percentiles from 1 to 99% were fitted as a function of age alone, height alone and of age and height together. BMI quantiles were estimated as a function of age. Confidence intervals for quantiles were obtained using the bootstrap.
The difference between the European and the USA FEV1 CF specific percentiles and between the CF-specific BMI percentiles and the WHO normative values was assessed by the difference in area under the curve with a bootstrap test. Inter country variation was assessed between the 2 countries contributing the most patients (France and Germany), one group consisting of smaller countries with large coverage (> 75%) of CF patients (Israel, Denmark, Belgium, the Netherlands, Slovenia and Czech Republic) and a 4th group with other countries (Bulgaria, Sweden, Portugal, Greece, Austria, Italy). Confidence intervals for the median percentile in each country was obtained using bootstrap and corrected for multiple comparisons by the Bonferroni rule (4 groups times 3 age classes). All analyses were done using the R software v2.14 (quantreg version 4.62).
Number of measurements
FEV1 percent predicted (%)***
Mean ± SD
Mean ± SD
ECFS Patient Registry (2004-2007)
16.7 [0 - 78.4]
74.4 ± 31.8
-0.63 ± 1.07
18.1 [0 - 68.2]
75.0 ± 31.6
-0.54 ± 1.09
High coverage countries
18.6 [0 - 77.4]
80.1 ± 28.4
-0.35 ± 1.08
Low coverage countries
18.3 [0 - 69.0]
81.32 ± 28.0
-0.21 ± 1.08
20.3 [6.0 - 40.0]
72.9 ± 31.2
-0.53 ± 1.00
18.0 [0 - 78.4]
75.7 ± 31.1
-0.52 ± 1.07
As shown in Figure1, we found differences between the European and the USA percentiles. For example, a 20 year old European male patient 170 cm of height, with an FEV1 of 3 liters ranked at the 65th percentile among US CF patients, but only at the 61st percentile among European CF patients. The CF percentiles values according to age or height were higher than those obtained in the US at the first, second and third quartiles (P < 0.001 for comparison at each quartile). However, the overall topography of the quantiles paralleled that of the US with an upwards offset. The correlation was excellent between the US- and the European-calculated age and height adjusted CF specific percentiles (r = 0.99, P < 0.001).
Differences between US and European percentiles were more pronounced in males (the median increased by 0.2 L on average) than in females (increased by 0.1 L). The difference in median FEV1 between Europe and the US was also larger in older patients: 0.1 L difference in the < 15 years old but 0.3 L in males > 15 years and 0.15 L in females. Finally, among the young patients (<15 years old), the difference was greater in the 10th percentile than in the 90th percentile: in the latter, the curves were almost the same between the EU and the US.
Nutritional outcome (BMI)
Achieving normality in lung function or nutritional status is the ultimate goal of CF care, even if the possibility of achieving this ideal remains a moot point given the multisystem nature of CF and the complexities of the variable genotype-phenotype relationship. Using a healthy population as a reference (as is universal with FEV1 pp) determines how far CF patients lie from normality. We propose here that additional information may be gleaned by referencing CF patients against age and sex matched CF peers. A large database of European cystic fibrosis patients was used to compute these reference percentiles and the software code is available from the authors on request.
As of today, such CF-specific reference- ranges have mainly been used for research purposes, for example to provide a quantitative phenotype for comparing patients. However, they could also be useful in a given clinic to either directly compare the performance between CF centers or to help homogenize patients for inclusion in clinical trials. This disease-referencing approach could also be useful to physicians and patients to help visualize the status of a single patient relative to his or her peers. For example, a longitudinal plot could highlight unusual worsening of clinical conditions within European CF framework and help the physician on the need for more aggressive therapies.
One may worry that referencing CF patients relative to their peers could lessen physicians’ efforts to improve CF patients’ health status, if they were satisfied with their patients’ progress referenced against their peers. In other words, care must be taken in interpretation such that the CF specific percentiles should not be interpreted as “normative” values, but, as discussed above, as a reference providing additional information. Reassuringly, there was no indication that the availability of such equations from US patients since 2005 negatively impacted CF care as also evidenced by the approach of McCormick and colleagues who calculated similar centiles for chest X-ray scores. Furthermore, our local patient representatives, as required by our consents and ethical practices on the use of such data, when shown the approach, spontaneously remarked that they would like to know how they were performing relative to others in Europe. Future studies will have to determine the impact of providing both types of reference information, for example in the case of specific CFTR variants such as G551D-CFTR which now has a new therapy.
Of necessity, it will be imperative to regularly update the CF specific reference equations to reflect CF care improvement. For example, it was reassuring that the European CF-specific FEV1 percentiles were greater than those computed a few years ago from US CF patients. This difference was more pronounced in the lower percentiles at all ages. It is unlikely that this difference results of differential mortality, as mortality curves are very similar for CF patients in large European countries and the US[20, 21]. Better organization of CF care over time may have led to a larger number of less severe patients included in registries, therefore leading to improved overall performance. However, it remains equally likely that changes in the efficacy of CF care over time is an explanation for the observed differences given that almost one decade passed between data collection in the US and the European studies. Significant improvement in the survival and clinical status of CF patients has been achieved during this time, by earlier CF diagnosis, better nutritional support and mucus drainage, and better diagnosis and treatment of CF-related complications. An argument in favor of the increased care efficacy is that the improvement was more pronounced in the patients with the poorest lung function. In addition, the median CF specific FEV1 percentile calculated in today’s North-American patients using the Kulich equations tends to be above the expected 50th percentile.
Using the ECFSPR data permitted analysis of a large number of measurements obtained from several European countries. Participation to the ECFSPR is on a voluntary basis, and the coverage (i.e. the proportion of CF living population actually included in the registry) ranges from 15% to >99%, with 9 countries having coverage greater than 50%. Little selection bias is expected in countries with large coverage, while it may be significant in countries where participation is limited to some voluntary CF centers. In the latter case, the extent to which the reported patients’ characteristics are biased relative to the whole country CF population is unpredictable. However, in our analysis, the estimates were not substantially affected when we excluded countries with small coverage.
We computed the CF specific equations so that unselected data could be referenced against these curves. The FEV1 values reported from countries where only the best measurement was provided were therefore corrected before analysis. Otherwise, it could have been the case that the reference curves overestimate the true status of the CF patients, as a consequence of analyzing mostly best measurements. However, additional analysis of the raw data, without corrections, yielded identical results, showing that the impact was overall small (see supplemental material). Thus the common assumption that selective reporting of best lung function can confound data interpretation is not supported by our findings.
One other result of this study is that the European CF BMI percentiles were in good agreement with the normative WHO 2007 curves up to age 7 but lower thereafter. Despite recommendations to achieve greater fat and calorie intake, CF children and teenagers typically consume similar nutritional amounts as their healthy peers[23, 24]. A positive association has been observed between a better nutritional status and a higher pulmonary function, with an inverse relation to morbidity and mortality[6, 25]. The BMI of CF females remained closer to the WHO reference charts, while it has been reported that they experience steeper trajectories of health decline[26, 27].
In the inter-country comparison, we conjoined countries with a small number of patients and large coverage, and all countries with low coverage. This was done to limit the effect of chance variation that could arise from small populations. The outcomes in FEV1 were somewhat larger in countries with small coverage. As it is not possible to rule out selection bias such as a survivor effect coupled to under diagnosis in these countries, this result should not be taken as evidence of better outcomes. The BMI inter-country comparison was less affected by coverage.
Although the FEV1 CF specific percentiles provide a useful approach for comparing CF patients to their peers, they do not correct for attrition due to mortality. For example, the population median CF percentile is 50% at all ages, but it is obvious that ranking 50th among 8 years old CF patients is different from ranking 50th at age 40. The use of “survival adjusted” CF specific percentiles has been proposed to measure severity as a quantitative trait irrespective of age. More data will be required to fully adapt this method to the European situation which should become easier as neonatal screening takes hold across Europe thus significantly reducing ascertainment bias. In the meantime, the excellent correlation of the percentiles found from the European and the US analyses will in future allow cross comparison with US derived “common” phenotype in international studies involving North-America and Europe. This was indeed a critical limiting factor in earlier analyses[28, 29].
To conclude, although achieving normality is the ultimate goal of CF care, separately referencing against age and sex matched CF peers provides additional information to compare CF populations and better illustrates the range of variability between patients. These new reference equations also provide tools for computing quantitative traits for use in genome wide analyses. Ours is only a first step towards the possibility to a fair comparison of European CF patients and health system performance. With the future availability of large phenotypic databases, it might be possible to apply our approach in other rare diseases, an emerging priority across the globe.
The ECFSPR was funded by an unrestricted grant from Chiesi Farmaceutici, Italy. Institut National de la Santé et de la Recherche Médicale. Assistance Publique-Hôpitaux de Paris. Université Pierre et Marie Curie Paris. Agence Nationale de la Recherche. DGS, Association Vaincre La Mucoviscidose. Chancellerie des Universités (Legs Poix). Association Agir Informer Contre la Mucoviscidose. GIS-Institut des Maladies Rares. Société Française de la Mucoviscidose. In addition to the authors, we would like to thank European Registry Working Group Members; Austria: ELLEMUNTER. H. Medizinische Universität. Innsbruck. Austria. Bulgaria: GALEVA. I., Pediatric Clinic. Alexansdrovsky University Hospital. Sofia. Bulgaria. France: Lydie Lemonnier. Vaincre la Mucoviscidose. Paris. France. Greece: HATZIAGOROU. E., Cystic Fibrosis Center of the Aristotelian University of Thessaloniki. Thessaloniki. Greece. Hungary: UJHELYI, R. Cystic Fibrosis Outpatient Care Centre. Heim Pál Hospital for Children. Budapest. Hungary. Ireland: FLETCHER, G. The Cystic Fibrosis Registry of Ireland. Ireland. The Netherlands: GULMANS. V. Dutch Cystic Fibrosis Foundation (NCFS). The Netherlands. Russia: KASHIRSKAYA. N., Research Centre for Medical Genetics. Russian Academy of Medical Sciences. Moscow. Russia. Sweden: LINDBLAD. A., Department of Pediatrics. Queen Silvia Childrens Hospital. Sahgrenska University Hospital. Gothenburg. Sweden. The authors would like to thank the computer specialists and the clinical research assistants involved in the data collection. namely: Sandrine Larroude, Alexandra Blondel and Pauline Touche. We would like to especially thank the patients and families who participated in this study and the contributing French CF Centers and Principal Investigators. ABELY,M., American Memorial Hospital. Reims/BASSINET,L., Centre Hospitalier Intercommunal de Créteil, Créteil/BELLEGUIC,C., Hôpital Pontchaillou. Rennes/BELLON,G. Hôpital Femme Mère Enfant, Bron/BESSACI,K., American Memorial Hospital, Reims/BONNEL,A.S., Hôpital André Mignot. Le Chesnay/BRÉMONT,F. Hôpital des Enfants de Toulouse. Toulouse/BROUARD,J. Centre Hospitalier Universitaire de Caen. Caen/BUI,S. Hôpital Des Enfants Groupe Pellegrin Bordeaux/CHIRON,R. Hôpital Arnaud de Villeneuve. Montpellier/CHUMBI-FLORES,R. Hôpital de la Tronche. Grenoble/CLEMENT,A. Hôpital Armand Trousseau. Paris/CORVOL,H., Hôpital Armand Trousseau, Paris/DALPHIN,J.C. CNRS-UFC,UMR 6249 Chrono-environnement. Hôpital Jean Minjoz, Besançon/DALPHIN,M.L. Centre Hospitalier Universitaire de Besançon. Besançon/DAVID,V. Hôpital Mère-Enfant Nantes/DE MIRANDA,S. Hôpital Foch, Suresnes/DERELLE,J. Hôpital d’Enfants. Vandoeuvre les Nancy/DOMBLIDES,P. Hôpital Haut Lévêque Pessac/DOMINIQUE,S. Centre Hospitalier Universitaire Charles Nicolle. Rouen/DUBUS,J.C. Hôpital d’Enfants de la Timone. Marseille/DURIEU,I. UCBL1. Groupe Hospitalier Lyon Sud. Hospices Civils de Lyon. Pierre Bénite/DURY,S. Hôpital Maison Blanche. Reims/ELLAFFI,M. Centre Hospitalier Universitaire de Caen. Caen/EPAUD,R. Centre Hospitalier Intercommunal de Créteil, Créteil/FANTON,A., Hôpital d’Enfants du Bocage, Dijon/FAYON,M., Hôpital Des Enfants Groupe Pellegrin. Bordeaux/FLEURENCE,E. Hôpital d’Enfants, Saint-Denis de la Réunion/FOUCAUD,P., Hôpital André Mignot, Le Chesnay/GINIES,J.L. Centre Hospitalier Universitaire d’Angers. Angers/GODBERT,B. Hôpital de Brabois. Vandoeuvre les Nancy/GRENET,D. Hôpital Foch Suresnes/GUILLOT,M. Centre Hospitalier Robert Bisson. Lisieux/HÉRAUD,M. C. Centre Hospitalier Estaing. Clermont-Ferrand/HOUSSET,B. Centre Hospitalier Intercommunal de Créteil. Créteil/HUBERT,D. Hôpital Cochin. Paris/HUET,F. Hôpital d’Enfants du Bocage. Dijon/KESSLER,R. Hôpital Civil. Strasbourg/LABBÉ,A. Centre Hospitalier Estaing. Clermont-Ferrand/LAURANS,M. Centre Hospitalier Universitaire de Caen. Caen/LE BOURGEOIS,M. Necker Hôpital d’Enfants Malades. Paris/LE ROUX,P. Hôpital Jacques Monod. Montivilliers/LLERENA,C. Hôpital de la Tronche. Grenoble/LOEUILLE,G.A. Centre Hospitalier de Dunkerque. Dunkerque/MARGUET,C. Centre Hospitalier Universitaire Charles Nicolle. Rouen/MELY,L., Hôpital Renée Sabran. Giens/MOISAN-PETIT,V. Centre Hospitalier Bretagne Atlantique. Vannes/MUNCK,A. Hôpital Robert Debré. Paris/MURRIS-ESPIN,M., Hôpital Larrey. Toulouse/NOVE JOSSERAND,R. Groupe Hospitalier Lyon Sud. Hospices Civils de Lyon. Pierre Bénite/PAUTARD,J.C., Hôpital Nord. Amiens/PIN,I. INSERM U823 Université Joseph Fourier. Hôpital de la Tronche. Grenoble/PRAMIL,S. Centre Hospitalier Universitaire Charles Nicolle. Rouen/PREVOTAT,A. Hôpital Calmette Lille/RAMES,C. Hôpital Nord. Amiens/RAULT,G. Centre de Perharidy. Roscoff/REIX,P. Hôpital Femme Mère Enfant. Bron/REMUS,N. Centre Hospitalier Intercommunal de Créteil. Créteil/RENOUIL,M., Groupe Hospitalier Sud Réunion. Saint-Pierre de la Réunion/REYNAUD-GAUBERT,M., Hôpital Nord. Marseille/RICHAUD THIRIEZ,B. Hôpital Jean Minjoz, Besançon/ROUSSEY,M. Université de Rennes 1. Hôpital Sud Annexe Pédiatrique. Rennes/SERMET-GAUDELUS,I. Necker Hôpital d’Enfants Malades. Paris/STREMLER,N. Hôpital d’Enfants de la Timone. Marseille/UFFREDI,M.L. Centre Hospitalier Bretagne Atlantique. Vannes/URBAN,T. Centre Hospitalier Universitaire d’Angers. Angers/VIGNERON,P. Centre Hospitalier Bretagne Sud Lorient/WALLAERT,B. Hôpital Calmette. Lille/WEISS,L. Hôpital de Hautepierre, Strasbourg/WIZLA,N., Hôpital Jeanne de Flandre, Lille.
- Dodge JA, Morison S, Lewis PA, Coles EC, Geddes D, Russell G, Littlewood JM, Scott MT: Incidence, population, and survival of cystic fibrosis in the uk, 1968-95. uk cystic fibrosis survey management committee. Arch Dis Child. 1997, 77: 493-496. 10.1136/adc.77.6.493.PubMed CentralView ArticlePubMedGoogle Scholar
- Mehta G, Macek M Jr, Mehta A: Cystic fibrosis across europe: eurocarecf analysis of demographic data from 35 countries. J Cyst Fibros. 2010, 9 (Suppl 2): S5-S21.View ArticlePubMedGoogle Scholar
- McCormick J, Mehta G, Olesen HV, Viviani L, Macek M Jr, Mehta A: Comparative demographics of the european cystic fibrosis population: a cross-sectional database analysis. Lancet. 2010, 375: 1007-1013. 10.1016/S0140-6736(09)62161-9.View ArticlePubMedGoogle Scholar
- Hankinson JL, Odencrantz JR, Fedan KB: Spirometric reference values from a sample of the general U.S. population. Am J Respir Crit Care Med. 1999, 159: 179-187.View ArticlePubMedGoogle Scholar
- Knudson RJ, Lebowitz MD, Holberg CJ, Burrows B: Changes in the normal maximal expiratory flow-volume curve with growth and aging. Am Rev Respir Dis. 1983, 127: 725-734.PubMedGoogle Scholar
- Kastner-Cole D, Palmer CN, Ogston SA, Mehta A, Mukhopadhyay S: Overweight and obesity in deltaF508 homozygous cystic fibrosis. J Pediatr. 2005, 147: 402-404. 10.1016/j.jpeds.2005.06.003.View ArticlePubMedGoogle Scholar
- Matthew DJ, Warner JO, Chrispin AR, Norman AP: The relationship between chest radiographic scores and respiratory function tests in children with cystic fibrosis. Pediatr Radiol. 1977, 5: 198-200. 10.1007/BF00972175.View ArticlePubMedGoogle Scholar
- Kulich M, Rosenfeld M, Campbell J, Kronmal R, Gibson RL, Goss CH, Ramsey B: Disease-specific reference equations for lung function in patients with cystic fibrosis. Am J Respir Crit Care Med. 2005, 172: 885-891. 10.1164/rccm.200410-1335OC.View ArticlePubMedGoogle Scholar
- McCormick J, Conway SP, Mehta A: Paediatric northern score centile charts for the chest radiograph in cystic fibrosis. Clin Radiol. 2007, 62: 78-81. 10.1016/j.crad.2006.09.011.View ArticlePubMedGoogle Scholar
- ECFS: ECFS Patient Registry. http://www.ecfs.eu/projects/ecfs-patient-registry/intro
- Farrell PM: The prevalence of cystic fibrosis in the European Union. J Cyst Fibros. 2008, 7: 450-453. 10.1016/j.jcf.2008.03.007.View ArticlePubMedGoogle Scholar
- Efrati O, Nir J, Fraser D, Cohen-Cymberknoh M, Shoseyov D, Vilozni D, Modan-Moses D, Levy R, Szeinberg A, Kerem E, Rivlin J: Meconium ileus in patients with cystic fibrosis is not a risk factor for clinical deterioration and survival: the israeli multicenter study. J Pediatr Gastroenterol Nutr. 2010, 50: 173-178. 10.1097/MPG.0b013e3181a3bfdd.View ArticlePubMedGoogle Scholar
- de Onis M, Onyango AW, Borghi E, Siyam A, Nishida C, Siekmann J: Development of a WHO growth reference for school-aged children and adolescents. Bulletin of the World Health Organization. 2007, 85: 660-667. 10.2471/BLT.07.043497.PubMed CentralView ArticlePubMedGoogle Scholar
- Wei Y, Pere A, Koenker R, He X: Quantile regression methods for reference growth charts. Stat Med. 2006, 25: 1369-1382. 10.1002/sim.2271.View ArticlePubMedGoogle Scholar
- Lucotte G, Hazout S, De Braekeleer M: Complete map of cystic fibrosis mutation DF508 frequencies in Western Europe and correlation between mutation frequencies and incidence of disease. Hum Biol. 1995, 67: 797-803.PubMedGoogle Scholar
- de Onis M, Onyango AW, Borghi E, Siyam A, Nishida C, Siekmann J: Development of a who growth reference for school-aged children and adolescents. Bull World Health Organ. 2007, 85: 660-667. 10.2471/BLT.07.043497.PubMed CentralView ArticlePubMedGoogle Scholar
- Corvol H, Beucher J, Boelle PY, Busson PF, Muselet-Charlier C, Clement A, Ratjen F, Grasemann H, Laki J, Palmer CN: Ancestral haplotype 8.1 and lung disease severity in European cystic fibrosis patients. J Cyst Fibros. 2012, 11: 63-67. 10.1016/j.jcf.2011.09.006.View ArticlePubMedGoogle Scholar
- Taylor C, Commander CW, Collaco JM, Strug LJ, Li W, Wright FA, Webel AD, Pace RG, Stonebraker JR, Naughton K, et al: A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis Genetic modifier studies. Pediatr Pulmonol. 2011, 46: 857-869. 10.1002/ppul.21456.PubMed CentralView ArticlePubMedGoogle Scholar
- Ramsey BW, Davies J, McElvaney NG, Tullis E, Bell SC, Drevinek P, Griese M, McKone EF, Wainwright CE, Konstan MW, et al: A CFTR potentiator in patients with cystic fibrosis and the G551D mutation. N Engl J Med. 2011, 365: 1663-1672. 10.1056/NEJMoa1105185.PubMed CentralView ArticlePubMedGoogle Scholar
- Vaincre-la-Mucoviscidose, Ined: Bilan des données 2008. Registre Français de la Mucoviscidose. 2011, 1-20.Google Scholar
- Cystic Fibrosis Foundation: 2009 Annual Data Report. Patient Registry. 2009, 1-28.Google Scholar
- Cohen-Cymberknoh M, Shoseyov D, Kerem E: Managing cystic fibrosis: strategies that increase life expectancy and improve quality of life. Am J Respir Crit Care Med. 2011, 183: 1463-1471. 10.1164/rccm.201009-1478CI.View ArticlePubMedGoogle Scholar
- Stark LJ, Powers SW: Behavioral aspects of nutrition in children with cystic fibrosis. Curr Opin Pulm Med. 2005, 11: 539-542. 10.1097/01.mcp.0000183051.18611.e4.View ArticlePubMedGoogle Scholar
- Magoffin A, Allen JR, McCauley J, Gruca MA, Peat J, Van Asperen P, Gaskin K: Longitudinal analysis of resting energy expenditure in patients with cystic fibrosis. J Pediatr. 2008, 152: 703-708. 10.1016/j.jpeds.2007.10.021.View ArticlePubMedGoogle Scholar
- Michel SH, Maqbool A, Hanna MD, Mascarenhas M: Nutrition management of pediatric patients who have cystic fibrosis. Pediatr Clin North Am. 2009, 56: 1123-1141. 10.1016/j.pcl.2009.06.008.View ArticlePubMedGoogle Scholar
- Rosenfeld M, Davis R, FitzSimmons S, Pepe M, Ramsey B: Gender gap in cystic fibrosis mortality. Am J Epidemiol. 1997, 145: 794-803. 10.1093/oxfordjournals.aje.a009172.View ArticlePubMedGoogle Scholar
- Zemel BS, Jawad AF, FitzSimmons S, Stallings VA: Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry. J Pediatr. 2000, 137: 374-380. 10.1067/mpd.2000.107891.View ArticlePubMedGoogle Scholar
- McCormick J, Sims EJ, Green MW, Mehta G, Culross F, Mehta A: Comparative analysis of cystic fibrosis registry data from the uk with usa, france and australasia. J Cyst Fibros. 2005, 4: 115-122. 10.1016/j.jcf.2005.01.001.View ArticlePubMedGoogle Scholar
- Hodson ME, Simmonds NJ, Warwick WJ, Tullis E, Castellani C, Assael B, Dodge JA, Corey M: An international/multicentre report on patients with cystic fibrosis (CF) over the age of 40 years. J Cyst Fibros. 2008, 7: 537-542. 10.1016/j.jcf.2008.06.003.View ArticlePubMedGoogle Scholar
- Wright FA, Strug LJ, Doshi VK, Commander CW, Blackman SM, Sun L, Berthiaume Y, Cutler D, Cojocaru A, Collaco JM, et al: Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. Nat Genet. 2011, 43: 539-546. 10.1038/ng.838.PubMed CentralView ArticlePubMedGoogle Scholar
- Nathan N, Abou Taam R, Epaud R, Delacourt C, Deschildre A, Reix P, Chiron R, de Pontbriand U, Brouard J, Fayon M: A national internet-linked based database for pediatric interstitial lung diseases: the French network. Orphanet J Rare Dis. 2012, 7: 40-10.1186/1750-1172-7-40.PubMed CentralView ArticlePubMedGoogle Scholar
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