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Open Access Research article

Polymorphisms in ADRB2 gene can modulate the response to bronchodilators and the severity of cystic fibrosis

Fernando A L Marson1*, Carmen S Bertuzzo2, Antônio F Ribeiro1 and José D Ribeiro1

Author Affiliations

1 Department of Pediatrics, School of Medical Sciences, University of Campinas, 13081-970, P.O. Box: 6111, Campinas, SP, Brazil

2 Department of Genetics, Faculty of Medical Sciences, University of Campinas, 13081-970, P.O. Box: 6111, Campinas, SP, Brazil

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BMC Pulmonary Medicine 2012, 12:50  doi:10.1186/1471-2466-12-50

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2466/12/50


Received:10 April 2012
Accepted:31 August 2012
Published:5 September 2012

© 2012 Marson et al.; licensee 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.

Abstract

Background

The most common cystic fibrosis (CF) manifestation is the progressive chronic obstructive pulmonary disease caused by deficiency, dysfunction, or absence of the CFTR (Cystic Fibrosis Transmembrane Regulator) protein on the apical surface of the cells in the respiratory tract. The use of bronchodilators (BD), and inhaled corticosteroids (IC) have been suggested for the management of airway inflammation in CF. The effectiveness of BD and IC have been verified, proven in laboratory and in the clinical treatment for asthma patients. However, in CF, the effectiveness of these drugs is controversial. The extent of asthma’s response to BD depends on the presence of polymorphisms in the ADRB2 gene. In contrast, in CF, little is known about the response to the BD and the association of CF´s severity with the different polymorphisms in ADRB2 gene. In this context, our objective was to verify whether the Arg16Gly and Glu27Gln polymorphisms in ADRB2 gene are associated with severity and with the bronchodilator response in CF patients.

Method

Cross-sectional study of 122 CF patients subjected to analysis of mutations in the CFTR gene, polymorphisms in ADRB2 gene, along with clinical and laboratorial characteristics of severity.

Result

The Arg16Gly polymorphism in ADRB2 gene was associated with pancreatic insufficiency(p:0.009), Bhalla score(p:0.039), forced expiratory volume in the first second[FEV1(%)](p:0.003), forced expiratory flow between 25 and 75% of the forced vital capacity-FVC[FEF25-75(%)](p:0.008) and lower age at the first isolation of the Pseudomonas aeruginosa(p:0.012). The response to the BD spirometry was associated with clinical severity markers, FEV1(%)(p:0.011) and FEF25-75(%)(p:0.019), for the Arg16Gly polymorphism in the ADRB2 gene. The haplotype analysis showed association with the FEV1/FVC marker from the spirometry test, before and after using the BD, with higher values in the group with Gly/Gly and Glu/Glu, respectively, for the Arg16Gly and Gln27Glu polymorphisms. The analysis by MDR2.0 software, showed association with FEF25-75%; the response to Arg16Gly was respondent by 17.35% and Gln27Glu by 6.8% in variation found.

Conclusion

There was an association between the Arg16Gly and Gln27Glu polymorphisms in ADRB2 gene with CF´s severity and bronchodilator response.

Keywords:
Beta 2 adrenergic receptor; ADRB2 gene; Pulmonary function; Cystic fibrosis; Phenotype; Genotype

Background

Studies have confirmed the mechanisms though which cystic fibrosis (CF) patients with similar mutations show significantly different signs and symptoms [1-4]. Even among homozygous for classes I, II and/or III mutations, the disease's clinical expression may be very different. Explanations for these broad clinical variations included environmental factors [5], medical management [3], nutrient intake [6], psychological [7], economic situations [3], and classes of mutations and polymorphisms in modifier genes [2-4].

Unlike most patients with asthma, the inflammation in CF is predominantly neutrophilic [8], with an intense inflammatory component and lower rate of bronchial hyper responsiveness [9]. In contrast, inhaled bronchodilator (BD) has been used for the management of these two conditions [10]. In addition to the BD, β-agonists affect the other functions of the airways: they reduce inflammatory cells mediators release, cholinergic neurotransmission and vascular permeability, as well as increase the clearance mucociliary [11], features that justify its use in CF.

Studies regarding the BD asthma response have revealed different results, depending on the polymorphism in ADRB2 gene [12]. The physical and chemical characteristics of the β2 (β2-AR) receptors are found in scientific literature, and demonstrate its importance to many biological processes, including muscle relaxation in the lungs [13-15]. Among polymorphisms identified in coding region of the ADRB2 gene, the Arg16Gly (c.46A > G) and Gln27Glu (c.79C > G) are the most studied in asthma [12]. The Gln27Glu polymorphism confers resistance from the ADRB2 protein to BD action. The ADBR2*G allele is protective against asthma, reducing its risks by 27% [13]. ADBR2*G induces changes in receptor regulation, which occurs due to its increased susceptibility to the protein's degradation.

Haplotypes that include the ADBR2*A allele have better response to the inhaled β2 agonists. Presumably, better response to exogenous agonists reflects better response to endogenous agonists and a protective effect against asthma and other bronchial hyper responsiveness diseases [16]. Haplotypes with two Arg16Gly/Gln27Glu mutant receivers showed that the effects of the Arg16Gly predominate over the Gln27Glu. These receptors are subject to greater regulation by agonists than the normal allele from the β2-AR receptor [13].

The effectiveness of BD and IC have been attained and proven in both the laboratory and the clinical treatment for asthma patients. Nevertheless, with CF the effectiveness of these drugs is controversial. The effectiveness of asthma’s response to the BD is dependent on polymorphisms in ADRB2 gene. In contrast, with CF, little is known about the response to the BD and the CF´s severity in association with the different polymorphisms in ADRB2 gene [17-19]. Although previous studies had showed an association between bronchodilator response and the polymorphisms in the ADRB2 gene, these studies did not take into account secondary clinical variables that can provide extra information about the mechanism associated with action of the ADRB2 protein.

Recently, it was discovered that the regulation of CFTR activity is mediated by the activation of G-coupled receptors such as the β2-AR. CFTR and the β2-AR protein are associated in a large macromolecular complex [20-22]. Taouil and colleagues showed that the long-acting salmeterol treatment increased wild-type CFTR expression in primary human airway epithelial cells. They demonstrated that wild-type CFTR levels increased more than 2-fold during this treatment, while the mRNA levels were unaffected [21].

In this context, the aim of this study was to investigate the influence of the Arg16Gly and Glu27Gln polymorphisms from the ADRB2 gene on 26 clinical severity markers and the bronchodilator response in CF patients from a university referral center.

Methods

A cross-sectional study was conducted in a referral center for CF treatment, at the Campinas University Hospital (UNICAMP) in 2010 and 2011. A total of 122 patients were included, with at least seven years of age and who underwent pulmonary function tests before and after the use of inhaled Albuterol (400 mg) according to the American Thoracic Society (2011) [23]. The patients underwent two perspiration tests of chlorine and sodium with chlorine levels equal to or greater than 60 mEq/L, and/or identification of two mutations in CFTR gene [F508del, G542X, G551D, R553X, R1162X, I618T and N1303K]. The project was approved by the University Ethics Committee (#528/2008), all patients and/or their guardians signed an informed consent.

We clinically evaluated the patients according to the following clinical severity markers: clinical scores (Shwachman-Kulczycki, Kanga and Bhalla) [24]; body mass index (BMI) [for the patients older than 19 years the BMI = weight/(height)2 formula was used; for the remaining patients the WHO ANTHRO PLUS (children 7-19 years old) [25]; patient age (group: younger ≤ 24 months and older > than 24 months) and age at diagnosis (according to the sodium and chloride in altered perspiration - younger age group ≤ 24 months and older > than 24 months); first clinical symptoms [(digestive - younger age ≤ 3 months and older > than 3 months; pulmonary - younger age ≤ 6 months and older > than 6 months)]; the period up to 1st colonization by Pseudomonas aeruginosa (younger ≤ 31 months and older > than 31 months); presence of microorganisms in the sputum (P. aeruginosa mucoid and non mucoid, Achromobacter xylosoxidans, Burkolderea cepacia and Staphylococcus aureus); transcutaneous oxygen saturation; pulmonary function tests before and after BD use and CF´s co morbidities (nasal polyps, osteoporosis, meconium ileus, diabetes mellitus and pancreatic insufficiency).

The Spirometry proof was performed using a speedometer model CPFS/D (Med Graphics, Saint Paul, Minnesota, USA). Data were recorded by the BREEZE PF Version 3.8 B software for Windows 95/98/NT with inclusion of the following markers: forced vital capacity - FVC(%), forced expiratory volume in the first second - FEV1(%), ratio between the FEV1 and the FVC, and forced expiratory flow between 25-75% of the FVC (FEF25-75%). All patients underwent spirometry test before and after 15 minutes of the BD - albuterol (400 mg) administration. Patients receiving the BD therapy were instructed to stop the medication 8 hours prior to the short-acting beta agonist spirometry test and 48 hours prior to the long-acting beta agonist [23].

Genomic DNA was extracted using phenol-chloroform from venous blood samples. Polymorphism analysis in modifier genes was performed by the polymerase (PCR) allele specific (ARMS) reaction, according to Littlejohn et al. (2002) [26]. Four reactions were performed, (ARMS1a, ARMS2a, and ARMS1b ARMS2b), each containing a common primer and one specific allele. All four reactions were performed under the same conditions. Each consisting of a total of 10μL containing 1x4 PCR buffer, 200 μM dNTPs, 5.0nM MgCl2, 0.4U of Taq polymerase, 0.2 pMoles of each primer and 1.0μL (approximately 50 ng) of genomic DNA. The PCR amplification conditions consisted of 5 min at 94°C followed by 35 cycles of 94°C for 1 min, 60°C (46 A or G - 16 Arg or Gly), or 67°C (70°C or G - 27 Gln or Glu), 72°C for 1 minute and 72°C for 10 min. The amplicons were submitted to electrophoresis on 12% acryl amide gel and stained with ethidium bromide for visualization of the results.

Statistical analysis of the data

Statistical analysis was performed by the software SPSS v.17.0 (SPSS Inc., Chicago, IL, USA) [27], Epi Info v.6.0 [28] and R version 2.12 (Comprehensive R Archive Network, 2011). The statistical power calculation for the sample was performed by the GPOWER 3.0.5 software [29] demonstrating statistical power above 80% for the conducted analysis. Alpha = 0.05 was used in all data analyses.

Analysis of variance (ANOVA) and chi-squared (2) - Odds Ratio (OR) tests were performed for quantitative and categorical variables, respectively. Pulmonary function comparison data before and after the BD use was performed by the ANOVA test; subsequently, the different genotypes for the Arg16Gly and Gln27Glu polymorphisms in ADRB2 gene were analyzed by the Student’s t test. Supplementary analysis performed by MDR software 2.0 (Multifactor dimensionality Reduction - Norris-Cotton Cancer Center, 2008) and MDRPT 0.4.7 (Permutation Test Multifactor dimensionality Reduction - Norris-Cotton Cancer Center, 2008), to evaluate the influence of both polymorphisms with the variation in the spirometry values of the bronchospasm response. The analyses of subgroups by age were not possible in our population as subgroups had a small number of patients.

In order to avoid spurious data due to the multiple tests problematic [30], the significance level α was adjusted by the Bonferroni correction (α corrected = 0.05/number of tests).

Results

The frequencies of each genotype for the Arg16Gly polymorphism was: 23(18.85%), 54(44.26%) and 45(36.89%), respectively for the Arg/Arg, Arg/Gly and Gly/Gly. For the Gln27Glu polymorphism was 61(50.00%), 51(41.80%) and 10(8.20%), respectively for the Gln/Gln, Gln/Glu and Glu/Glu. The population is within the Hardy-Weinberg equilibrium (2 = 0.88, p > 0.05; 2 = 0.02; p > 0.05, respectively for the Arg16Gly and Gln27Glu polymorphisms in ADRB2 gene). The patients' characteristics included in the study are described in Table 1.

Table 1. Characteristics of patients included in the study (N = 122)1

The Arg16Gly polymorphism in ADRB2 gene, without the distribution by the CFTR gene genotype, was associated with the FEV1(%) (p = 0.003) and FEF25-75% (p = 0.008), the minor value was observed in patients with Arg/Arg genotype. Patients with no identified mutation in CFTR gene were associated with better value to FEF25-75% to Gly/Gly genotype (p = 0.008). The group with two mutations identified in CFTR gene was associated with bigger value to Bhalla score to Arg/Arg genotype (p = 0.04) (Figure 1). In this same patients’ group there was association with the pancreatic insufficiency, and the Arg/Arg genotype with an OR of 0.13 (95%CI = 0.03-0.86) and Gly/Gly with an OR of 8 (95%CI = 1.95-67.7) with the presence of co morbidity and with the first isolated P. aeruginosa, OR of 0.22 (95%CI = 0.05-0.99) for the Gly/Gly genotype.

thumbnailFigure 1. Bhalla score and spirometry values in Cystic Fibrosis patients modulated by polymorphism in ADRB2 gene. Association of the cystic fibrosis severity with polymorphism Arg16Gly in ADRB2 gene. A. Bloxplot of the Bhalla score in patients with two identified mutations in CFTR gene. The Bhalla score data is a gross value. # p:0.011; * p:0.779; ¥ p:0.007. B. Bloxplot of FEV1(%) in patients without taking CFTR mutation into account. # p:0.007; * p:0.277; ¥ p:0.003. C. Bloxplot of FEF25-75% in patients without without taking CFTR mutation into account. # p:0.038; * p:0.43; ¥ p:0.015. D. Bloxplot of FEF25-75% in patients with no mutations identified in CFTR gene. # p:0.933; * p:0.008; ¥ p:0.001. The data of the spirometry are in percentage of the predicted population value. The test used for the analyses was the T´student test.

The Gln27Glu polymorphism in ADRB2 gene showed no statistically significant association with the variables used as CF´s severity markers in this study.

The analysis of the polymorphisms in ADRB2 gene and their association with BD mediated bronchospasm response occurred for the Arg16Gly polymorphism (Table 2). The variables demonstrating modulations were: FEV1(%) (p = 0.01) and FEF25-75% (p = 0.02) (Figure 2). The Gly/Gly genotype was associated with a minor bronchodilator response. The variation values data for the spirometry test markers according to the haplotypes in the ADRB2 gene for the Arg16Gly and Gln27Glu polymorphisms are described in Table 3. In the haplotypes analysis the groups with the GG genotype were considered in at least one, both, or in none of the polymorphisms analyzed.

Table 2. Association of polymorphisms in ADRB2 gene with spirometry of Cystic Fibrosis patients1

thumbnailFigure 2. Bronchodilatador response in Cystic Fibrosis patients modulated by polymorphism in ADRB2 gene. Response to the inhaler bronchodilators by the alteration of spirometry markers values in the Cystic Fibrosis patients according to polymorphism Arg16Gly in ADRB2 gene. A. Bloxplot of the variation in the FEV1(%) before and after using bronchodilators in patients without without taking CFTR mutation into account. # p:0.361; * p:0.001; ¥ p:0.002. B. Bloxplot with the variation in the FEF25-75(%) before and after using bronchodilators in patients without without taking CFTR mutation into account. # p:0.031; * p:0.026; ¥ p:0.01. Analysis made group by group by the T´student test. The data from the pulmonary function test are in percentage of the predicted population value.

Table 3. Change in FVC, FEV1, and FEF25-75 FEF1/FVC post-bronchodilator by ADRB2 haplotype1

The statistical analysis performed by the MDR 2.0 program in comparison with the curve stipulated by the data held by the MDRPT 0.4.7 program, demonstrated the influence of the two polymorphisms analyzed with the variance of FEF25-75% before and after using the BD [Bal Acc. testing.: 0.772, p: 0.0034, ratio: 0.9934]. From the observed variation for the FEF25-75%, according to the test performed, the Arg16Gly polymorphism is responsible for 17.4% and the Gln27Glu for 6.8% of the variation.

Discussion

In the last decade, several studies have shown that the receptor for beta 2 agonist is intimately connected, physically and functionally, to the CFTR protein on the surface of the epithelial cells in the airways [20]. Interestingly, the function of this complex behaves differently if the stimulus is caused by long or short term beta 2 agonist substances [20-22]. The clinical response of the CF patients in relation to the long-term beta agonists in the different polymorphisms in ADRB2 gene has not been studied, while for the short term use, there are few studies in the literature [17-19]. With asthma, the Arg16Gly and Gln27Glu polymorphisms in ADRB2 gene cause different reactions to the Bronchodilation promoted by BD [12]; however, little is known about their impact on the severity and response to Bronchodilation caused by CF BD [17-19].

To the best of our knowledge it is known that the allele frequency for the Arg16Gly and Gln27Glu polymorphisms in ADRB2 gene is different in adults and children with CF [19]. Adult patients with CF have a higher frequency for the Gly16 and Glu27 alleles compared to people CF free. Children with CF have a lower frequency for Gly16 and similar with the Glu27. Young adults with CF in relation to the variant forms in ADRB2 gene did not differ from the population in general. In our population there was no difference in genotype distribution for the Arg16Gly (p:0.92) and Gln27Glu (p:0.88) polymorphisms in ADRB2 gene relative to the patients' age group.

Our study showed an association of the Arg16Gly polymorphism in ADRB2 gene with the severity of CF markers. The variation in the spirometry proof before and after the use of BD was associated with the Arg16Gly and Gln27Glu polymorphisms in ADRB2 gene. Twenty six of CF´s severity markers were used in the study; and the response to Bronchodilation was assessed by four spirometry markers.

Hart et al. (2005) [18] used the FEV1(%) and the FEF25-75% as severity markers, in addition to the following variables adjustment: age, gender, the F508del homozygous and Pseudomonas aeruginosa status. Buscher et al. (2002) [17] used the following markers: FEV1, FVC, flow at lower lung volumes (MEF50%VC), measurement of cAMP accumulation in intact mononuclear lymphocytes, age, gender, BMI, F508del homozygous and Pseudomonas aeruginosa status. Hart et al. (2005) [18] considered the presence of values 12% higher in the FEV1 after using the BD, (the examination of spirometry occurred 15 minutes after administration of BD), a positive response to Bronchodilation, while Buscher et al. (2002) [17] believed in the 10% variation for the same marker (the Spirometry test occurred 5 minutes after BD administration). Steagall et al. (2007) [19] used as markers: age, sex, F508del status, carbon monoxide diffusing capacity (DLCO), FEV1(%) and the FVC(%). The positive response to Bronchodilation was seen as a positive variation superior to 12% for the FEV1 and the FVC spirometry markers.

The presence of different genotypes in the analyzed mutations, (belonging to the classes I, II and/or III), of the CFTR gene, along with the polymorphisms in ADRB2 gene were associated to different markers related to CF´s severity.

An intriguing aspect of our study, not previously described, were the findings that CF´s patients with two mutations from classes I, II and/or III, Arg/Arg homozygous for the Arg16Gly polymorphism, have greater impairment of lung function than the Gly/Gly homozygous, provided by the Bhalla score. And the Gly/Gly homozygous showed higher pancreatic insufficiency than the Arg/Arg. The two clinical variables are associated with CF severity, and are modulated by the Gly/Gly genotype to Arg16Gly polymorphism in our population. The Gly allele is associated with fast protein degradation [13] that was identified as a severity factor.

The first isolation of the P. aeruginosa was confirmed later in patients with the Gly/Gly genotype and two mutations classes I, II and/or III in CFTR gene. The early colonization is associated with clinical deterioration and a greater degree of airway inflammation [31].

The response to this polymorphism and the clinical aspects of CF´s patients has not been studied in the literature referenced, except for Buscher et al., (2002) [17], whose analysis of some of the markers, (age, gender, BMI and P. aeruginosa status), showed no significant association, a fact that hampered data comparison. Another relevant fact is the Gln27Glu polymorphism lack of association with severity markers in the study. There were no references in the scientific literature indicating this polymorphism as a modulator of CF´s severity.

Our results show that CF´s patients with the Arg/Arg genotype from the Arg16Gly polymorphism have lower values of the FEV1 and FEF25-75%. The observation contrasts with the data from Buscher et al. (2002) [17] who reported higher values of the Arg/Arg genotype in 87 CF´s patients for the FEV1, FVC, and MEF50%VC markers, when compared with subjects with a genotype containing at least one Gly allele. The same was observed when the genotype for the delF508 mutation was used; 51 patients were analyzed, and higher values for the markers were found for the same genotype.

In our data the Gln27Glu polymorphism in ADRB2 gene was not associated with spirometry markers. Diversely, in the Buscher et al. (2002) [17] study, the Gln/Gln genotype for the Gln27Glu polymorphism, when compared with the others, showed a higher correlation for the FEV1, FVC, and MEF50%VC values. In the Steagall et al. (2007) [19] study there was no correlation between the DLCO, FEV1 and the FVC in patients with homozygous F508del stratified by the Arg16Gly and Gln27Glu polymorphisms genotype in ADRB2 gene.

The patients with no identified mutations in CFTR gene, in our study, showed higher values in the FEF25-75% for the Gly/Gly genotype. Thus, comparing the data discussed above, we denote the influence of the Arg16Gly polymorphism in ADRB2 gene that occurs in the spirometry, and that is also influenced by the genotype in the CFTR gene.

We found that the Arg27Gly polymorphism in ADRB2 gene was associated with the bronchospasm response mediated by beta 2 agonists. The FEV1(%) variation was lower in patients with the Gly/Gly genotype, when compared with the Arg/Arg and Arg/Gly genotypes. The FEF25-75% was lower in patients with the Gly/Gly genotype when compared to the Arg/Arg and Arg/Gly. Patients with the Arg/Arg genotype showed higher FEF25-75% when compared to the Arg/Gly genotype.

In the study by Hart et al. (2005) [18], one hundred and six patients with CF underwent spirometry before and after the BD administration, and the Arg16Gly and Gln27Glu polymorphisms genotype was determined. The positive response was observed in 15% (23/154) of the included patients and 17% (18/106) among the patients who had genotype for the gene ADBR2 determined. There was no significant relationship between the ADRB2 gene genotype for the Arg16Gly and Gln27Glu polymorphisms and the response to the BD [18]. However, after the FEV1 adjustment in percentage for the predicted and the status of infection by the P. aeruginosa, a significant difference occurred to the FEF25-75% percentage of change (4.9%, 18.0% and 22.4% for the genotypes AA, AG and GG; respectively). The FEF25-75% percentage of change showed no substantial difference for the codon 27, even after the adjustment for the infection by P. aeruginosa and by the predicted baseline of FEV1(%) [18]. After adjusting the FEV1 percentage predicted baseline, the codon 27 groups differed significantly from the percentage of change in the FEV1(%) (4.1%, 8.1% and 9.3% for the genotypes CC, CG and GG; respectively) [18]. The authors suggested that the effect of the two polymorphisms were complex and the haplotype analysis may be more informative than any genotype alone [18]. To that effect, a large number of patients would be needed, only possible in multi-centric studies. Then again, in multi-centric studies the environment and diverse management systems could provide significant bias in the clinical severity outcome.

In the study by Buscher et al. (2002) [17], no statistically significant difference was found for the FEV1 average value and in the absolute number of patients with positive response to BD among the Arg16Gly polymorphism genotypes in ADRB2 gene.

In the Steagall et al. (2007) [19] study homozygous patients with the delF508 mutation were analyzed for their reactions to Bronchodilation. Patients who showed no response to the Bronchodilation had, on average, higher values in the FVC and FEV1 for the Arg/Arg genotype in the Arg16Gly polymorphism of the ADRB2 gene when compared to other genotypes; however, in the analyzed group there were only two patients with the Arg/Arg and two with the delF508 mutations for the CFTR gene. For the Gln27Glu polymorphism, the Gln/Gln genotype was associated with higher FVC values. In the responders group only the Gln27Glu polymorphism was associated with higher values of the DLCO, FVC and FEV1 for the Gln/Glu genotype. In our study, the distribution of responders and non-responders to the pulmonary function test with the BD use, and the distribution by the polymorphisms in ADRB2 gene and mutations in classes I, II and/or III, was performed, but the sample power was less than 80%.

The long term decline in spirometry values was not evaluated in this study, even though it presents a promising field of study, verified by Buscher et al. (2002) [17] who demonstrated that, in 59 CF patients aged 6-20 years, the biggest FEV1 decline was in patients with at least one Gly allele, while no change in pulmonary function was seen in patients homozygous for Arg.

The genic interaction analysis performed by the MDR 2.0 program showed a combination of both polymorphisms with the variation for the FEF25-75% but not to other markers of severity. Thus, this corroborates that the polymorphisms in ADRB2 gene influence the Bronchodilation response.

In the haplotypes analysis the Ar/Arg + Gln/Gln presence was associated with the best response to Bronchodilation for the marker FEV1/FVC (N = 56; +4.61% ± 10.45), when compared to the other groups: 1 GG [Arg/Arg + Glu/Glu, Arg/Gly + Glu/Glu, Gly/Gly + Gln/Gln, Gly/Gly + Gln/Glu (N = 34; +0.53% ± 7.75)] and 2 GG [Gly/Gly + Glu/Glu (N = 4; -2.25% ± 9.605)]. In the study by Hart et al. (2005) [18], the haplotypes analysis for three different models demonstrated association with the FEV1 marker. And the values of 4.4 (± 5.8), 7.9 (± 8.7) and 9.0 (± 5.8); respectively to 0 GG (N = 27), 1GG (N = 64) and 2GG (N = 15), with p values equal to 0.033, 0.027 and 0.305; respectively for the models, additive, dominant and recessive.

In our results, the bronchodilator response was reduced with the presence of the variants with Gly or Glu allele, a fact contrary to that reported by Hart et al. (2005) [18].

Possible limitations of our study included: sample size, different age groups, and different severities of lung disease that could express differences in the BD response.

Our data can provide better understanding about the association between polymorphism associated with β2-AR protein and the clinical markers of CF´s severity, and others studies about the large macromolecular complex are necessary to improve knowledge about the interaction of the proteins on the bronchial epithelial surface.

Conclusion

The influence of polymorphisms in the CF´s severity and bronchospasm response is controversial in the scientific literature, and seldom studied. Our results support the idea that differences in the degree of airway responsiveness to the BD may be associated with the ADRB2 gene genotype in the CF. Arg16Gly and Gln27Glu polymorphisms are associated with the response to the Bronchodilation. For the spirometry and other clinical variables of severity; the Arg16Gly polymorphism showed statistically significant association; diversely, the Gln27Glu showed no association. The Arg/Arg genotype to Arg16Gly polymorphism was associated with a better spirometry to FEV1(%) and FEF25-75% clinical markers and minor risk to PI, in comparison with other genotypes. To bronchodilator response the haplotype data to the polymorphism show association with positive response to beta 2 agonists to absence of genotypes Gly16Gly and Glu27Glu to FEV1/FVC(%) marker.

We must pay attention to the need for more studies; with the suppressed polymorphisms and their association with the clinical severity variables using a larger number of CF´s patients with the same CFTR genotype for the mutation classes I, II and/or III; also patients with the same degree of change in the spirometry test to analyze the response to Bronchodilation.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

FALM: made substantial contributions to conception and design, or acquisition of data, or analysis and interpretation of data; involved in drafting the manuscript or revising it critically for important intellectual content. CSB: carried out the molecular genetic studies and drafted the manuscript. AFR: has been involved in drafting the manuscript or revising it critically for important intellectual content. JDR: has given final approval of the version to be published. All authors read and approved the final manuscript.

Acknowledgments

Luciana Cardoso Bonadia, Taís Daiene Russo Hortencio, Kátia Cristina Alberto Aguiar, Aline Gonçalves and Simoni Avansini – assistance in data collection and organization of ideas. Rodrigo Secolin and Bruna Favetta – English review. Maria Angela Ribeiro – spirometry analysis. We thank http://laboratoriomultiusuario.com.br/ to contribute with our work.

Financial support

Fapesp

References

  1. Vankeerberghen A, Cuppens H, Cassiman JJ: The cystic fibrosis transmembrane conductance regulator: an intriguing protein with pleiotropic functions.

    J Cyst Fibros 2002, 1:13-29. PubMed Abstract | Publisher Full Text OpenURL

  2. Cutting GR: Modifier genes in Mendelian disorders: the example of cystic fibrosis.

    Ann N Y Acad Sci 2010, 1214:57-69. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  3. Simmonds NJ, MacNeil SJ, Cullinan P, Hodson ME: Cystic fibrosis and survival to 40 years: a case–control study.

    Eur Respir J 2010, 36(6):1277-1283. PubMed Abstract | Publisher Full Text OpenURL

  4. Stanke F, Becker T, Kumar V, Hedtfeld S, Becker C, Cuppens H, Tamm S, Yarden J, Laabs U, Siebert B, Fernandez L, Macek M Jr, Radojkovic D, Ballmann M, Greipel J, Cassiman JJ, Wienker TF, Tümmler B: Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia.

    J Med Genet 2010, 48(1):24-31. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  5. Collaco JM, Blackman SM, McGready J, Naughton KM, Cutting GR: Quantification of the Relative Contribution of Environmental and Genetic Factors to Variation in Cystic Fibrosis Lung Function.

    J Pediatr 2010, 157(5):802-807. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  6. Matel JL, Milla CE: Nutrition in Cystic Fibrosis.

    Semin Respir Crit Care Med 2009, 30(5):579-586. PubMed Abstract | Publisher Full Text OpenURL

  7. Casier A, Goubert L, Theunis M, Huse D, De Baets F, Matthys D, Crombez G: Acceptance and Well-Being in Adolescents and Young Adults with Cystic Fibrosis: A Prospective Study.

    J Pediatr Psychol 2011, 36(4):476-487. PubMed Abstract | Publisher Full Text OpenURL

  8. Regamey N, Jeffery PK, Alton EWFW, Bush A, Davies JC: Airway remodelling and its relationship to inflammation in cystic fibrosis.

    Thorax 2011, 66(7):624-629. PubMed Abstract | Publisher Full Text OpenURL

  9. Heijerman H, Westerman E, Conway S, Touw D: Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: A European consensus.

    J Cyst Fibros 2009, 8(5):295-315. PubMed Abstract | Publisher Full Text OpenURL

  10. Patel M, Thomson NC: (R)-salbutamol in the treatment of asthma and chronic obstructive airways disease.

    Expert Opin Pharmacother 2011, 12(7):1133-1141. PubMed Abstract | Publisher Full Text OpenURL

  11. Barnes PJ: Beta-adrenergic Receptors and Their Regulation.

    Am J Respir Crit Care 1995, 152(3):838-860. OpenURL

  12. Hall IP, Blakey JD, Al Balushi KA, Wheatley A, Sayers I, Pembrey ME, Ring SM, McArdle WL, Strachan DP: β2-adrenoceptor polymorphisms and asthma from childhood to middle age in the British 1958 birth cohort: a genetic association study.

    Lancet 2006, 368(9537):771-779. PubMed Abstract | Publisher Full Text OpenURL

  13. Thakkinstian A, McEvoy M, Minelli C, Gibson P, Hancox B, Duffy D, Thompson J, Hall I, Kaufman J, Leung TF, Helms PJ, Hakonarson H, Halpi E, Navon R, Attia J: Systematic Review and Meta-Analysis of the Association between β2-Adrenoceptor Polymorphisms and Asthma: A HuGE Review.

    J Epidemiol 2005, 162(3):201-211. Publisher Full Text OpenURL

  14. Rasmussen SGF, Choi H, Rosenbaum DM, Kobilka TS, Thian FS, Edwards PC, Burghammer M, Ratnala VRP, Sanishvili R, Fischetti RF, Schertler GFX, Weis WI, Kobilka BK: Crystal structure of the human β2 adrenergic G-protein-coupled receptor.

    Nature 2007, 450:383-387. PubMed Abstract | Publisher Full Text OpenURL

  15. Dror RO, Arlow DH, Maragakis P, Mildorf TJ, Pan AC, Xu H, Borhani DW, Shaw DE: Activation mechanism of the β2-adrenergic receptor.

    PNAS 2011, 108(46):18684-18689. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  16. Drysdale CM, McGraw DW, Stack CB, Stephens JC, Judson RS, Nandabalan K, Arnold K, Ruano G, Liggett SB: Complex promoter and coding region beta-2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness.

    Proc Nat Acad Sci 2000, 97:10483-10488. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  17. Buscher R, Eilmes KJ, Graseman H, Torres B, Knauer N, Sroka K, Insel PA, Ratjen F: 2-adrenoreceptor gene polymorphisms in cystic fibrosis lung disease.

    Pharmacogenetics 2002, 12(5):347-353. PubMed Abstract | Publisher Full Text OpenURL

  18. Hart MA, Konstan MW, Darrah RJ, Schluchter MD, Storfer-Isser A, Xue L, Londono D, Goddard KA, Drumm ML: Beta 2 adrenergic receptor polymorphisms in cystic fibrosis.

    Pediatr Pulmonol 2005, 39(6):544-550. PubMed Abstract | Publisher Full Text OpenURL

  19. Steagall WK, Barrow BJ, Glasgow CG, Mendoza JW, Ehrmantraut M, Lin J, Insel PA, Moss J: Beta-2-adrenergic receptor polymorphisms in cystic fibrosis.

    Pharmacogenet Genomics 2007, 17(6):425-430. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  20. Collawn JF, Bebok Z, Matalon S: Search and rescue: finding ways to correct deltaF508 CFTR.

    Am J Respir Cell Mol Biol 2009, 40(4):385-387. PubMed Abstract | Publisher Full Text OpenURL

  21. Taouil K, Hinnrasky J, Hologne C, Corlieu P, Klossek J, Edith Puchelle E: Stimulation of β2 adrenergic receptor increases CFTR expression in human airway epithelial cells through a c-AMP/protein kinase A-independent pathway.

    J Biol Chem 2003, 278(19):17320-17327. PubMed Abstract | Publisher Full Text OpenURL

  22. Delavoie F, Molinari M, Milliot M, Zahm JM, Coraux C, Michel J, Balossier G: Salmeterol restores secretory functions in cystic fibrosis airway submucosal gland serous cells.

    Am J Respir Cell Mol Biol 2009, 40(4):388-397. PubMed Abstract | Publisher Full Text OpenURL

  23. American Thoracic Society (ATS)

    2011.

    http://www.thoracic.org/ webcite. Access in: 04.04.2012

  24. Santos CIS, Ribeiro JD, Ribeiro AF, Hessel G: Critical analysis of scoring systems used in the assessment of Cystic Fibrosis severity: state of the art.

    J Bras Pneumol 2004, 30(3):286-298. OpenURL

  25. WHOAntroPLUS [computer program]: WORLD HEALTH ORGANIZATION. Version 102 edition. Geneva WHO; 2007. OpenURL

  26. Littlejohn MD, Taylor DR, Miller AL, Kennedy MA: Determination of beta-2-adrenergic receptor (ADRB2) haplotypes by a multiplexed polymerase chain reaction assay.

    Hum Mutat 2002, 20(6):479-487. PubMed Abstract | Publisher Full Text OpenURL

  27. SPSS 17.0 for Windows (computer program):

    Statistical Package for Social Science (SPSS). Release Version 17.0.1. Chicago (IL): SPSS. Incorporation. 2011.

    Available from: http://www.spss.com webcite.

    OpenURL

  28. Dean AG, Dean JA, Coulombier D, Brendel KA, Smith DC, Burton AH, Dicker RC, Sullivan K, Fagan RF, Arner TG: EPI Info, Version 6.0: a word processing database and statistics program for epidemiology on microcomputer. [computer program]. Atlanta, Georgia: Center of Disease Control and Prevention; 1994. OpenURL

  29. Faul F, Erdfelder E, Lang AG, Buchner A: G*Power 3: A flexible sta-tistical power analysis program for the social, behavioral, and biomedical sciences.

    Behavior Res Methods 2007, 39:175-191. Publisher Full Text OpenURL

  30. Drăghici S: Data analysis tools for DNA microarrays. New York: Chapman & Hall/CRC; 2003. OpenURL

  31. Sagel SD, Gibson RL, Emerson J, McNamara S, Burns JL, Wagener JS, Ramsey BW: Impact of Pseudomonas and Staphylococcus infection on inflammation and clinical status in young children with cystic fibrosis.

    J Pediatr 2009, 154(2):183-188. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2466/12/50/prepub