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Association of ADAM33 gene polymorphisms with adult allergic asthma and rhinitis in a Chinese Han population

Contributed equally
BMC Medical Genetics20089:82

https://doi.org/10.1186/1471-2350-9-82

Received: 15 May 2008

Accepted: 09 September 2008

Published: 09 September 2008

Abstract

Background

Rhinitis and asthma are very common diseases involving genetic and environmental factors. Most patients with asthma also have rhinitis, which suggests the concept of 'one airway, one disease.' A disintegrin and metalloproteinase 33 (ADAM33) is the first asthma-susceptible gene to be discovered by positional cloning. To evaluate the potential influence of ADAM33 gene polymorphisms on allergic rhinitis (AR) and allergic asthma (AS), a case-control study was conducted on the Han population of northeast China.

Methods

Six polymorphic sites (V4, T+1, T2, T1, S1, and Q-1) were genotyped in 128 patients with AR, 181 patients with AS, and 151 healthy controls (CTR). Genotypes were determined by the polymerase chain restriction fragment length polymorphism (PCR-RFLP) method. Data were analyzed using the chi-square test with Haploview software.

Results

The single nucleotide polymorphisms (SNPs), V4 G/C, T+1 A/G, and T1 G/A, of the ADAM33 gene may be the causal variants in AR, whereas ADAM33 V4 G/C, T2 A/G, T1 G/A, and Q-1A/G may participate in the susceptibility of AS.

Conclusion

These results suggest that polymorphisms of the ADAM33 gene may modify individual susceptibility to AR and AS in a Chinese Han population.

Keywords

AsthmaRhinitisAllergic RhinitisAllergic RhinitisAllergic Asthma

Background

Rhinitis is defined as inflammation of the nasal mucosa and is characterised by nasal discharge, blockage, sneezing, and itching [1, 2]. Asthma is a chronic inflammatory disorder of the airway which causes recurrent episodes of wheezing, breathlessness, chest tightness, and coughing in susceptible individuals. These episodes are usually associated with widespread, but variable airflow obstruction that is often reversible, either spontaneously or with treatment. The inflammation also causes an associated increase in existing bronchial hyper-responsiveness (BHR) to a variety of stimuli [1, 2]. Epidemiologic studies have consistently shown that asthma and rhinitis often coexist in the same patients in every region of the world [35], suggesting the concept of 'one airway, one disease.' The basic premise is that rhinitis and asthma represent the manifestations of one syndrome in two parts of the respiratory tract [6]. In order to raise awareness of the theory of 'one airway, one disease,' the Allergic Rhinitis and Its Impact on Asthma (ARIA) Workshop Group publication proposes three considerations for patients with allergic respiratory disease [7].

ADAM33 is the first reported asthma-susceptible gene identified by positional cloning [8]. ADAM33 is a complex molecule, the expression of which is largely restricted to mesenchymal cells, including fibroblasts and smooth muscle cells, and codes for a protein important for cell fusion, cell adhesion, cell signalling, and proteolysis [9]. The ADAM33 gene is located on chromosome 20p13 and 37 single nucleotide polymorphisms (SNPs) have initially been identified [8]. Recently, several SNPs in the ADAM33 gene have been shown to be significantly associated with asthma, BHR, and atopy [10]. Taken together, these findings suggest an important role for ADAM33 in airway remodelling and asthma [8]. To date, most data available for ADAM33 and asthma have been obtained from Caucasians, but few data on ADAM33 SNPs associated with asthma and atopic disease are available for Asian populations [1114]. The aim of the present study was to determine whether ADAM33 SNPs are associated with allergic rhinitis (AR) and allergic asthma (AS) in a Chinese Han population.

Methods

Subjects

The study group consisted of 128 Chinese patients with AR, 181 patients with AS, and 151 healthy controls (CTR). They were recruited from The 2nd Clinical College of Harbin Medical University in China. The characteristics of the study population are shown in Table 1. The diagnosis of AR was made on the basis of the criteria of the Chinese Society of Allergology (2003). Patients had to satisfy the following AR criteria for inclusion: (1) nasal discharge, blockage, and sneezing, with the 3 symptoms occurring for more than 30 minutes on most days and for more than 6 months per year and (2) persistent symptoms for at least 1 year. AS was diagnosed according to the criteria of the Chinese Society of Allergology (2003). Patients had to satisfy the following AS criteria for inclusion: (1) continual episodes of wheezing and dyspnea which require therapy, (2) clinically-diagnosed wheezing, (3) reversible airway obstruction shown by >15% variation in daily values of volume in the 1st second of forced expiration (FEV1) and peak expiratory flow (PEF) after inhalation or administration of a bronchodilator, and (4) elevated levels of serum total IgE with at least one type of allergen-specific IgE. One hundred fifty-one unrelated healthy Chinese Han adults with no history of asthma and rhinitis were designated as CTR patients. Both patients and the healthy CTR were recruited from the Heilongjiang Province of China between August 2006 and June 2007. The present study was approved by the Ethics Committee of the Harbin Medical University and adhered to the tenets of the Helsinki Declaration. Additionally, the written informed consent was obtained from the patients.
Table 1

Description of study population

Characteristic

AR

AS

CTR

Number of patients

128

181

151

Age (years)

39.27 ± 13.53

36.69 ± 11.53

37.18 ± 10.60

Gender (Female)

44(34.38%)

67(37.02%)

54(35.76%)

FEV1 (%)

100.95 ± 5.36

73.38 ± 10.66

102.84 ± 3.11

DNA extraction and genotyping

Genomic DNA was extracted from 5 ml of frozen whole blood using a DNA Extraction Kit (Qiagen, Germany), according to the manufacturer's protocol and following the manufacturers' instructions. We selected 6 SNPs in the ADAM33 gene, which previously had been shown to have an allelic and/or haplotype association with AS, including V4(rs2787094), T+1(rs2280089), T2(rs2280090), T1(rs2280091), S1(rs3918396), and Q-1(rs612709). Using the unique rs accession numbers, SNP details and sequence data are available through NCBI databases http://www.ncbi.nlm.nih.gov. The polymorphic region was amplified by PCR with a TGradient Thermoblock PCR System (Iometra, Germany) in a 25 μl reaction solution containing 0.3 μg genomic DNA, 1× PCR buffer, 0.3 mM MgCl2, 0.2 mM dNTPs, 2 U TaqDNA polymerase (Takara, Japan), and 0.1 μmol of each primer (Invitrogen, USA). Genotyping primers and PCR programs are shown in Table 2. PCR products were digested overnight with restriction enzymes (NEB, UK), according to the manufacturer's protocol, and analyzed by 2% agarose gel electrophoresis. The restriction enzymes and the length of the digested fragments are shown in Table 3.
Table 2

Primers and PCR programs for ADAM33 PCR-RFLP genotyping

Reference SNP ID

Gene/SNP primer

Sequence

PCR program

rs2787094

ADAM33 V4C/G F

5'-ACACACAGAATGGGGGAGAG-3'

94°C 5 min; 35 cycles, 94°C 30 s,

 

ADAM33 V4C/G R

5'-CCAGAAGCAAAGGTCACACA-3'

53°C 30 s, 72°C 30 s; 72°C 5 min

rs2280089

ADAM33T+1A/G F

5'-CTGAGCCCAGAAACCTGATT-3'

94°C 5 min; 35 cycles, 94°C 30 s,

 

ADAM33T+1A/G R

5'-AGAAGGGAAGGGCTCATGC-3'

54°C 30 s, 72°C 30 s; 72°C 5 min

rs2280090

ADAM33 T2A/G F

5'-TTCTCAGGGTCTGGGAGAAA-3'

94°C 5 min; 35 cycles, 94°C 30 s,

 

ADAM33 T2A/G R

5'-GCCAACCTCCTGGACTCTTA-3'

52°C 30 s, 72°C 30 s; 72°C 5 min

rs2280091

ADAM33 T1A/G F

5'-ACTCAAGGTGACTGGGTGCT-3'

94°C 5 min; 35 cycles, 94°C 30 s,

 

ADAM33 T1A/G R

5'-GAGGGCATGAGGCTCACTTG-3'

54°C 30 s, 72°C 30 s; 72°C 5 min

rs3918396

ADAM33 S1A/G F

5'-TGTGCAGGCTGAAAGTATGC-3'

94°C 5 min; 35 cycles, 94°C 30 s,

 

ADAM33 S1A/G R

5'-AGAGCTCTGAGGAGGGGAAC-3'

50°C 30 s, 72°C 30 s; 72°C 5 min

rs612709

ADAM33 Q-1A/G F

5'-GGATTCAAACGGCAAGGAG-3'

94°C 5 min; 35 cycles, 94°C 30 s,

 

ADAM33 Q-1A/G R

5'-GTTCACCTAGATGGCCAGGA-3'

60°C 30 s, 72°C 30 s; 72°C 5 min

Table 3

Restriction enzymes and length of digested fragments

 

V4C/G

T+1A/G

T2A/G

T1A/G

S1A/G

Q-1A/G

Enzyme

PstI

HpyAV

HpyCH4III

NcoI

HinfI

BtsCI

Length of digested

G: 168+206

A: 284+28

A: 198+112

A: 140+260

G: 132+172

A: 20+138

fragments (bp)

C: 374

G: 312

G: 310

G: 400

A: 304

G: 158

Statistical analyses

We tested for the Hardy-Weinberg equilibrium (HWE) among cases and controls separately. The genotype and allele frequencies were obtained by direct counting. Statistical significance was defined as a P < 0.05. In order to obtain a measure of significance corrected for multiple testing bias, we ran 10,000 permutations to compute P-values using the Haploview program. Comparisons of the distributions of the allele and genotype frequencies were performed using the chi-square test. The relative risk associated with rare alleles was estimated as an odds ratio (OR) with a 95% confidence interval (CI).

Results

The genotype and allele frequencies of the ADAM33 gene polymorphisms in patients and healthy controls are shown in Tables 4, 5 and 6. All of the six SNPs genotyped were in HWE (P > 0.05) in the case and control cohorts. The ADAM33 V4 G, T+1 A, and T1 G allele carrier frequencies were significantly higher in AR patients than in the CTR patients (P < 0.0001, = 0.0037, and < 0.0001, respectively). Statistical analysis revealed no significant differences in the allele frequencies in T2 A/G, S1 G/A, and Q-1 A/G between AR and CTR patients. The differences at the V4, T2, T1, and Q-1 sites between the AS and CTR groups were significant (P < 0.0001). In contrast, no significant differences in the allele frequency distribution at the T+1 and S1 sites between the AS and CTR groups were observed. The ADAM33 V4 G, T2 A, T1 G, and Q-1 A allele frequencies were significantly higher in the AS patients than in the CTR patients (P < 0.0001). Correction for multiple tests was performed in this study.
Table 4

Genotype frequency distribution and association study in ADAM33 between AR and CTR

Genotype

Frequency, no.(%)

x2 P value

Odds ratio

  

AR(n = 128)

CTR(n = 151)

 

(95% CI)

rs2787094

CC

46(35.94)

113(74.84)

<0.0001

0.19(0.11–0.32)

 

CG

60(46.88)

32(21.19)

<0.0001

3.28(1.95–5.53)

 

GG

22(17.18)

6(3.97)

0.0003

5.02(1.97–12.80)

rs2290089

AA

4(3.13)

0

0.0432

 
 

AG

51(39.84)

41(27.15)

0.0246

1.78(1.07–2.94)

 

GG

73(57.03)

110(72.85)

0.0056

0.49(0.30–0.82)

rs2280090

AA

0

0

  
 

AG

24(18.75)

12(7.95)

0.0073

2.67(1.28–5.59)

 

GG

104(81.25)

139(92.05)

0.0073

0.37(0.18–0.78)

rs2280091

AA

56(43.75)

117(77.48)

<0.0001

0.23(0.13–0.38)

 

AG

55(42.97)

29(19.21)

<0.0001

3.17(1.86–5.41)

 

GG

17(13.28)

5(3.31)

0.0021

4.47(1.60–12.49)

rs3918396

AA

100(78.12)

110(72.85)

0.3086

 
 

AG

28(21.88)

41(27.15)

0.3086

 
 

GG

0

0

  

rs612709

AA

0

0

  
 

AG

16(12.5)

11(7.28)

0.142

 
 

GG

112(87.5)

140(92.72)

0.142

 
Table 5

Genotype frequency distribution and association study in ADAM33 between AS and CTR

Genotype

Frequency, no.(%)

x2 P value

Odds ratio

  

AS(n = 181)

CTR(n = 151)

 

(95% CI)

rs2787094

CC

49(27.07)

113(74.84)

<0.0001

0.12(0.08–0.20)

 

CG

78(43.09)

32(21.19)

<0.0001

2.82(1.73–4.59)

 

GG

54(29.84)

6(3.97)

<0.0001

10.28(4.28–24.69)

rs2290089

AA

0

0

  
 

AG

37(20.44)

41(27.15)

0.151

 
 

GG

144(79.56)

110(72.85)

0.151

 

rs2280090

AA

4(2.21)

0

0.1289

 
 

AG

49(27.07)

12(7.95)

<0.0001

4.30(2.19–8.44)

 

GG

128(70.72)

139(92.05)

<0.0001

0.21(0.11–0.41)

rs2280091

AA

63(34.81)

117(77.48)

<0.0001

0.16(0.10–0.25)

 

AG

78(43.09)

29(19.21)

<0.0001

3.19(1.93–5.26)

 

GG

40(22.10)

5(3.31)

<0.0001

8.28(3.18–21.59)

rs3918396

AA

140(77.35)

110(72.85)

0.3437

 
 

AG

41(22.65)

41(27.15)

0.3437

 
 

GG

0

0

  

rs612709

AA

0

0

  
 

AG

44(24.31)

11(7.28)

<0.0001

4.09(2.03–8.24)

 

GG

137(75.69)

140(92.72)

<0.0001

0.24(0.12–0.49)

Table 6

Allele frequency distribution and association study in ADAM33

Name

SNP

Minor allele frequency

P-value

Permutation p-value

Odds ratio (95% CI)

  

AR (n = 128)

AS (n = 181)

CTR (n = 151)

AR vs CTR

AS vs CTR

AR vs CTR

AS vs CTR

AR vs CTR

AS vs CTR

Rs2787094

G/C

0.406

0.514

0.146

<0.0001

<0.0001

<0.0001

<0.0001

0.25(0.17–0.37)

0.16(0.11–0.24)

rs2280089

A/G

0.231

0.102

0.136

0.0037

0.1812

0.0279

 

1.91(1.23–2.96)

 

rs2280090

A/G

0.094

0.158

0.04

0.0097

<0.0001

 

<0.0001

 

4.52(2.37–8.59)

rs2280091

G/A

0.348

0.437

0.129

<0.0001

<0.0001

<0.0001

<0.0001

0.28(0.18–0.42)

0.19(0.13–0.28)

rs3918396

G/A

0.109

0.113

0.136

0.3454

0.3802

    

rs612709

A/G

0.063

0.121

0.036

0.1526

<0.0001

 

0.0016

 

3.66(1.86–7.22)

Discussion

The work by van Eerdewegh et al. [8] that identified ADAM33 as an asthma-susceptible gene using positional cloning and an association study had a profound impact on researchers investigating the genetics of bronchial asthma. Polymorphisms of ADAM33 were originally shown to be associated with BHR. In previous studies, T1, T2, S2, and V-3 sites were reported in Japanese adult populations [13, 15], and these associations were also found in our samples. In contrast, no association was found between asthma and ADAM33 in Puerto Rican and Mexican populations [16], and a Korean population [12]. The study by van Eerdewegh [8] was the first to show that ADAM33 polymorphisms (Q-1, S1, ST+4, ST+7, V-1, and V4) and haplotypes were associated with asthma in Caucasian families. Recently, Raby et al. [17] performed a family-based association study for childhood asthma and ADAM33 SNPs in 652 nuclear families. They showed that no single SNP was associated with childhood asthma in Caucasians, but that a common haplotype of ADAM33 was associated with the disease. They also reported that T1 and T+1 were marginally associated with childhood asthma in Hispanics. In previous association studies of ADAM33 and asthma/asthma-associated phenotypes, no single ADAM33 SNP was consistently associated with asthma or intermediate phenotypes. This may be because of allelic heterogeneity, a single disorder caused by different mutations within a gene [14]. A number of studies have been conducted to replicate the original findings, some confirming and others refuting the association of ADAM33 with asthma [1719]. In the present study, adult asthma was associated with ADAM33 SNPs, V4, T2, T1, and Q-1, but not with the T+1 and S1, and the V4, T+1, and T1 sites were also found to have significant associations with AR after correction for multiple tests. Comparison of our results with those studies indicates that no single SNP was universally associated with the asthma phenotype. The genetic basis of asthma may differ between different ethnic groups; it is possible that a particular subset of SNPs may be a risk factor for asthma in Caucasians, and that a different subset may increase the risk in Asian populations [13].

Epidemiological studies have clearly shown that rhinitis and asthma are frequently concurrent [20, 21]. The majority of patients with AS also have AR, which presents in more than 75% of the patients with allergic asthma [22]. The relationship between AR and AS has become a focus of research. Recent advances have demonstrated that systemic inflammatory responses play a critical and integrating role in the pathophysiology of airway disease. Substantial evidence has also shown that AR and AS are closely linked, and the concept of 'one airway, one disease' has emerged [23]. Under this hypothesis, AS and AR are regarded as a combined entity of upper and lower airway disease influenced by the inflammatory process. An alteration of upper airway function could therefore affect the function of the lower airway. Improvement of AR symptoms is associated with resolution of AS symptoms. On the other hand, deterioration of AR symptoms may exacerbate AS symptoms. Consequently, appropriate management of AR could decrease the risk of AS developing or AS exacerbation [23]. The results of several epidemiologic surveys presented at the European Respiratory Society Annual Congress (ERS) in 2007 supported the concept of 'one airway, one disease' [24, 25]. In this context, we genotyped ADAM33 variants in AR cases and healthy individuals to evaluate the potential influences of ADAM33 gene polymorphisms on AR risk, and to determine whether ADAM33 is also the susceptible gene for AR. As expected, some significant associations were observed in AR patients. Although there are some differences between AR and AS in the statistical analysis results with respect to ADAM33 genetic susceptibility, polymorphisms of the ADAM33 gene may modify individual susceptibility to AR and AS in a Chinese Han population.

Conclusion

Our data suggest that the ADAM33 gene may be involved in the susceptibility to AR and AS in a Chinese Han population. The SNPs (V4 G/C, T+1 A/G, and T1 G/A) of the ADAM33 gene may play an important role in the susceptibility of AR disease, whereas ADAM33 V4 G/C, T2 A/G, T1 G/A, and Q-1A/G may participate in the susceptibility to AS. Considering that the limited sample size may produce relative risk estimates lacking adequate precision, extended analyses with a larger sample size should be carried out from different ethnic origins to further verify this association.

Notes

Declarations

Acknowledgements

This work was supported by the Project of Science Research Foundation of Heilongjiang (Grant No. 11531145) and a grant from the Innovative Fund of Harbin Medical University Graduate Student (HCXB2007004). We thank all patients and healthy blood donors for providing blood samples. We are grateful for the collaboration received from the participating hospitals and their staff.

Authors’ Affiliations

(1)
Department of Respiratory, The Second Affiliated Hospital of Harbin Medical University, Harbin, China
(2)
Department of Histology and Embryology, Harbin Medical University, Harbin, China
(3)
Department of Statistics, Harbin Medical University, Harbin, China

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  26. Pre-publication history

    1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2350/9/82/prepub

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© Su et al; licensee BioMed Central Ltd. 2008

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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