Associations of genetic variants in ADAM33 and TGF??1 genes with childhood asthma risk
- Authors:
- Published online on: May 19, 2014 https://doi.org/10.3892/br.2014.280
- Pages: 533-538
Abstract
Introduction
Asthma is the most frequent chronic respiratory disease during childhood and asthma exacerbation is a main cause of child morbidity and hospitalization (1). Epithelial damage, smooth muscle hyperplasia and increased matrix deposition are significant characteristics of the asthmatic airways that are considered to contribute to airway remodeling and responsiveness (2). Asthma is a complex disorder with variable clinical and physiological presentations, in which genetics and the environment interact to modify the susceptibility to and the severity of the disease (3–5). Accumulating evidence has shown that genetic factors are involved in the initiation and development of asthma, including a disintegrin and metalloproteinase domain 33 (ADAM33). ADAM33 was confirmed to be associated with bronchial hyperresponsiveness and asthma (6). Findings of previous studies have shown that several SNPs in the ADAM33 gene are significantly associated with the asthma risk in various populations, including the Han Chinese (7–9). Studies carried out in certain countries, including America, Germany and Japan, showed that genetic variants in ADAM33 were associated with a childhood asthma risk (10–12).
Transforming growth factor-β1 (TGF-β1) plays key roles in certain pathological and physiological processes, including asthma. TGF-β1 is located at chromosome 19q13.1–13.2 and has been cloned and sequenced (13,14). TGF-β1 is a multifunctional cytokine and functions by binding to its type I and II receptors to exert a number of biological effects, including anti-inflammatory activities (15,16). Genetic variants in the TGF-β1 gene have been confirmed and significant associations between specific SNPs and asthmatic phenotype have been reported by previously conducted studies (17–19).
ADAM33 and TGF-β1 have been previously shown to be involved in the initiation and development of asthma (20–23). However, the associations between the genetic variants in the genes involved in child asthma risk in a Chinese population remain to be verified, particularly as the interactions between ADAM33 and TGF-β1 with a multi-SNP combination on asthma risk are currently unclear. In the present study, the SNPs at ADAM33 V4, T2, S2 and T1, and TGF-β1 C509T and T869C were detected and their associations with child asthma risk were evaluated in a Chinese population.
Materials and methods
Study subjects
A total of 299 asthmatic children were recruited from the Department of Respiratory Medicine and Pediatric Inpatient and Outpatient at The First Affiliated Hospital of Xinxiang Medical University (Xinxiang, Henan, China) between March 2010 and October 2012. The participants included 166 males and 133 females aged 3.1–14.6 years who were in line with the global initiative for asthma (24). The asthmatic patients were further divided into the mild and severe groups, comprising 171 and 128 patients, respectively. In total, 311 patients with no personal or family history of asthma and allergies and did not suffer from non-respiratory diseases (including eczema, allergic rhinitis and atopic dermatitis) during the same period were enrolled into the control group. A structured questionnaire was adopted and information, including social-demographic characteristics and diagnosis of the disease, was collected. All the subjects were confirmed to be Chinese Han children from the North of Henan. Written informed consent was provided by each parent or legal guardian of the participant. Each participant provided a 2–3 ml venous blood sample following an interview, which was subsequently treated with EDTA Na2 and stored at −80°C.
Genomic DNA isolation and genotype detection
The study design was approved by the Ethics Committee of the Xinxiang Medical University. Genomic DNA in lymphocytes was isolated with the DNA Extraction kits (Sangon Biotech Co., Ltd., Songjiang, Shanghai, China) according to the manufacturer’s instructions. The DNA samples were diluted to 100 ng/μl and stored at −80°C.
Mutation rates of rs2787094, rs2280090, rs528557, rs2280091, rs1800469 and rs1982073 and the gene sequences covering the SNPs were obtained from an online database (http://www.ncbi.nlm.nih.gov/SNP/). The primers of six SNPs were designed with Primer Premier software (Premier Biosoft International, Palo Alto, CA, USA), and synthesized by Sangon Biotech Co., Ltd. The primer sequences for the genotype detection of each SNP, and the restriction enzymes used in the study are shown in Table I. PCR was performed in a 25 μl volume, containing 60 ng DNA, 2.5 μl 10X buffer, 1.8 μl MgCl2 (25 mmol/l), 2.5 μl dNTPs, 1 μl of each primer, 0.7 units Taq polymerase and double-distilled water. PCR was carried out under the following conditions: 95°C for 5 min, followed by 95°C for 30 sec, 56°C for 30 sec, 72°C for 40 sec for 35 cycles, and 72°C for 10 min. The PCR products were subsequently stored at 4°C. The enzyme digestion that followed utilized 10 μl of the PCR product and the reactions were performed in a final volume of 30 μl containing >3 units of each enzyme and incubated for >6 h at temperatures provided by the manufacturers. The digested PCR products were then separated in 2.0% agarose gels containing 1 μg/ml ethidium bromide and analyzed by the GelDoc-It 310 Imaging System (Ultra-Violet Products Ltd., Upland, CA, USA).
Statistical analysis
Data were presented as means ± SD. The means of multiple groups were compared with one-way analysis of variance, while those between two groups were compared with an independent t-test. The genotype-specific odds ratios (OR), 95% confidence intervals (95% CIs) and P-values were computed with unconditional logistic regression, and gender (as dichotomous variables) was included in the regression as a covariate. The statistical analyses were performed with SPSS version 13.0 (SPSS, Inc., Chicago, IL, USA). In addition, the associations of the ADAM33 and TGF-β1 haplotypes with the risk of asthma were assessed using R software version 2.15 (Developed by R Core Team, Vienna, Austria and improved by MathSoft company, Cambridge, MA, USA), and the ORs and 95% CIs were also estimated. P<0.05 was considered to indicate a statistically significant difference and all P-values are two-sided.
Results
Social-demographical characteristics
In the present study, 299 cases, including 171 patients suffering from mild asthma and 128 suffering from severe asthma, and 311 controls were recruited. As shown in Table II, no significant difference was detected in terms of gender and age between the control and case groups. The forced expiratory volume in one second (FEV1) of the mild asthma patients (88.4±12.1 l/sec) was higher than that of the severe patients (67.2±15.3 l/sec).
Associations of genetic variants with asthma risk
Associations between the genetic variants and asthma risk are shown in Tables III and IV. Table III shows that the SNPs at V4 (rs2787094) of ADAM33 and TGF-β1 C509T (rs1800469) were associated with an increased asthma risk. Compared with the V4 GG genotype carriers, increased susceptibilities to asthma for the GC and CC carriers were detected and the ORs were 2.92 (95% CI, 1.46–5.85) and 10.56 (95% CI, 2.17–51.67), respectively. Compared with the rs1800469CC genotype, an increased susceptibility for the CT/TT genotype carriers to asthma was observed and the OR was 2.26 (95% CI, 1.19–4.30). No significant association was detected between the remaining SNPs and asthma risk.
In Table IV, the SNP at V4 of ADAM33 (rs2787094) was found to be associated with mild and severe asthma risk. Compared with the GG genotype carriers, increased susceptibilities to mild and severe asthma for those carrying the GC/CC genotype was detected and the ORs were 3.19 (95% CI, 1.41–7.21) and 3.81 (95% CI, 1.67–8.71). The SNP at TGF-β1 C509T (CT/TT vs. CC) was associated with an increased mild asthma risk (OR, 2.34; 95% CI, 1.05–5.24) and a marginally significant association between the SNP and severe asthma risk was detected (OR, 2.19; 95% CI, 0.98–4.93).
Associations between haplotypes and asthma risk
Associations between the ADAM33 haplotypes and asthma risk are shown in Table V. The GGCA haplotype at V4, T2, S2 and T1 of ADAM33 was found to be most frequent and was regarded as a reference. Compared with the GGCA haplotype carriers, an increased risk for those with CGCA, CGCG, CGGA, GACA, GACG and GAGA haplotypes was detected and the ORs were 1.20 (95% CI, 0.41–3.48), 31.12 (95% CI, 4.79–202.31), 12.24 (95% CI, 3.58–41.92), 4.73 (95% CI, 1.35–16.50), 30.85 (95% CI, 4.92–193.55) and 4.83 (95% CI, 1.09–21.40), respectively. However, the associations of the GG, CG and GGGA haplotypes with asthma risk were not significant.
Associations of the TGF-β1 haplotype at T869C and T509C are shown in Table VI. The TT haplotype was the most frequent and compared with the haplotype, no significant association of the TC, CT or CC haplotype with asthma risk was detected.
Discussion
Asthma is a common chronic respiratory disease, with >155 million patients suffering from the disease worldwide (25). Bronchial asthma is a complex disease and finding the main factors that are involved in the pathogenesis of asthma is useful, in order to identify the genetic variants that are involved in asthma risk. The validated genetic variants are useful in identification of the individuals that have a high asthma risk and this could provide more information for disease prevention. Therefore, the associations of each single SNP, and the TGF-β1 and ADAM33 haplotypes with asthma risk were evaluated among Chinese children in the present study.
The ADAM33 gene is located on chromosome 20p13, and initially there were 37 SNPs identified (6). The first studies on the associations between ADAM33 polymorphisms and asthma risk were carried out among Caucasian populations in the United Kingdom and the USA. However, the conclusions of the majority of those studies were inconsistent (?). Previous studies reported that the genetic variants in ADAM33 were associated with an increased susceptibility to asthma in Thai (26), Colombia (8) and Indian populations (27). By contrast, no significant association was found between asthma and ADAM33 in Puerto Rican, Mexican (28) and Korean populations (29). The studies may have been affected by sample sizes, heterogeneity of populations and various environmental factors. Subsequent to the cases being divided into mild and severe asthma groups according to disease severity, associations of the SNPs and haplotypes of ADAM33 and TGF-β1 with asthma risk were analyzed in the present study. The SNPs of rs2787094 at ADAM33 V4 and rs1800469 at TGF-β1C-509T were found to be associated with an increased asthma risk and the ADAM33 haplotypes were useful in predicting the individuals with a high asthma risk.
TGF-β1 is a multifunctional cytokine that has the potential to inhibit T-cell activity by regulating cell proliferation, and as a result reduce the asthma onset (30,31). On the other hand, previous studies have indicated that epithelial fibrosis is one of the principle features in airway remodelling in asthma initiation and development, and could be enhanced in a number of patients (32). Numerous studies have revealed that TGF-β1 C-509T and T869C polymorphisms are associated with an increased TGF-β1 production. Burton et al (33) reported that the -509T allele was associated with increased transcriptional activity of TGF-β1 compared with the -509C allele. In addition, the polymorphism has been confirmed to be associated with asthma risk (34) and severity (35). The T869C polymorphism, which could result in a leucine to proline substitution, was found to be associated with increased TGF-β1 mRNA and production level in peripheral blood mononuclear cells (36). In their study, de Faria et al (5) also revealed that the T869C polymorphisms may be involved in the modulation of asthma. In the present study, the -509T allele frequency was observed to be significantly higher in the asthma group compared with the controls, and the CC genotype of C-509T carriers in the asthmatic groups were significantly different from the control group, indicating a possible association of this SNP with asthma. For the SNP T869C, the difference in genotype and allelic frequency was significant between the asthmatic group and controls. The conclusion was consistent with a previous study by Wiśniewski et al (37).
Asthma is a chronic respiratory disease that could be affected by a complex genetic background, and multiple genes have been involved in its development through modified gene expressions and functions. Accumulating evidence (38–41) has indicated that ADAM33 and TGF-β contribute to the biogenesis of asthma, and certain genetic variants in ADAM33 and TGF-β1 were found to be responsible for the modified childhood asthma risk in the present study. The ADAM33 haplotypes may be useful and effective biomarkers in predicting asthma risk. However, the sample size of the study is the main limitation and further studies with larger sample sizes are necessary to verify the conclusion of the study.
References
Huang JL: Asthma severity and genetics in Taiwan. J Microbiol Immunol Infect. 38:158–163. 2005.PubMed/NCBI | |
Holgate ST, Davies DE, Lackie PM, Wilson SJ, Puddicombe SM and Lordan JL: Epithelial-mesenchymal interactions in the pathogenesis of asthma. J Allergy Clin Immunol. 105:193–204. 2000. View Article : Google Scholar : PubMed/NCBI | |
Cookson W: The alliance of genes and environment in asthma and allergy. Nature. 402(6760 Suppl): B5–B11. 1999. View Article : Google Scholar : PubMed/NCBI | |
Ober C and Thompson EE: Rethinking genetic models of asthma: the role of environmental modifiers. Curr Opin Immunol. 17:670–678. 2005. View Article : Google Scholar : PubMed/NCBI | |
de Faria IC, de Faria EJ, Toro AA, Ribeiro JD and Bertuzzo CS: Association of TGF-beta1, CD14, IL-4, IL-4R and ADAM33 gene polymorphisms with asthma severity in children and adolescents. J Pediatr (Rio J). 84:203–210. 2008.PubMed/NCBI | |
Van Eerdewegh P, Little RD, Dupuis J, et al: Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness. Nature. 418:426–430. 2002.PubMed/NCBI | |
Zhang X, Su D, Zhang X, et al: Association of ADAM33 gene polymorphisms with adult concomitant allergic rhinitis and asthma in Chinese Han population. Mol Biol Rep. 36:1505–1509. 2009. View Article : Google Scholar : PubMed/NCBI | |
Vergara CI, Acevedo N, Jiménez S, et al: A Six-SNP haplotype of ADAM33 is associated with asthma in a population of Cartagena, Colombia. Int Arch Allergy Immunol. 152:32–40. 2010. View Article : Google Scholar : PubMed/NCBI | |
Awasthi S, Tripathi P, Ganesh S and Husain N: Association of ADAM33 gene polymorphisms with asthma in Indian children. J Hum Genet. 56:188–195. 2010. View Article : Google Scholar | |
Raby BA, Silverman EK, Kwiatkowski DJ, Lange C, Lazarus R and Weiss ST: ADAM33 polymorphisms and phenotype associations in childhood asthma. J Allergy Clin Immunol. 113:1071–1078. 2004. View Article : Google Scholar : PubMed/NCBI | |
Schedel M, Depner M, Schoen C, et al: The role of polymorphisms in ADAM33, a disintegrin and metalloprotease 33, in childhood asthma and lung function in two German populations. Respir Res. 7:912006. View Article : Google Scholar : PubMed/NCBI | |
Noguchi E, Ohtsuki Y, Tokunaga K, et al: ADAM33 polymorphisms are associated with asthma susceptibility in a Japanese population. Clin Exp Allergy. 36:602–608. 2006. View Article : Google Scholar : PubMed/NCBI | |
Fujii D, Brissenden JE, Derynck R and Francke U: Transforming growth factor beta gene maps to human chromosome 19 long arm and to mouse chromosome 7. Somat Cell Mol Genet. 12:281–288. 1986. View Article : Google Scholar : PubMed/NCBI | |
Kim SJ, Glick A, Sporn MB and Roberts AB: Characterization of the promoter region of the human transforming growth factor-beta 1 gene. J Biol Chem. 264:402–408. 1989.PubMed/NCBI | |
Nakao A: Is TGF-beta1 the key to suppression of human asthma? Trends Immunol. 22:115–118. 2001. View Article : Google Scholar : PubMed/NCBI | |
Lawrence DA: Transforming growth factor-beta: a general review. Eur Cytokine Netw. 7:363–374. 1996.PubMed/NCBI | |
Watanabe Y, Kinoshita A, Yamada T, et al: A catalog of 106 single-nucleotide polymorphisms (SNPs) and 11 other types of variations in genes for transforming growth factor-beta1 (TGF-beta1) and its signaling pathway. J Hum Genet. 47:478–483. 2002. View Article : Google Scholar : PubMed/NCBI | |
Nagpal K, Sharma S, B-Rao C, et al: TGFbeta1 haplotypes and asthma in Indian populations. J Allergy Clin Immunol. 115:527–533. 2005. View Article : Google Scholar : PubMed/NCBI | |
Pulleyn LJ, Newton R, Adcock IM and Barnes PJ: TGFbeta1 allele association with asthma severity. Hum Genet. 109:623–627. 2001. View Article : Google Scholar : PubMed/NCBI | |
Chiang CH, Lin MW, Chung MY and Yang UC: The association between the IL-4, ADRβ2 and ADAM 33 gene polymorphisms and asthma in the Taiwanese population. J Chin Med Assoc. 75:635–643. 2012.PubMed/NCBI | |
Tripathi P, Awasthi S, Prasad R and Ganesh S: Haplotypic association of ADAM33 (T+1, S+1 and V - 3) gene variants in genetic susceptibility to asthma in Indian population. Ann Hum Biol. 39:479–483. 2012.PubMed/NCBI | |
Majak P, Jurałowicz D, Jerzyńska J, Smejda K, Stelmach W and Stelmach I: Transforming growth factor-beta1 and IL-13 response to allergen predict steroid needs in asthmatic children. Pulm Pharmacol Ther. 26:290–295. 2013. View Article : Google Scholar : PubMed/NCBI | |
Ierodiakonou D, Postma DS, Koppelman GH, Gerritsen J, ten Hacken NH, Timens W, Boezen HM and Vonk JM: TGF-β1 polymorphisms and asthma severity, airway inflammation, and remodeling. J Allergy Clin Immunol. 131:582–585. 2013. | |
Bateman ED, Hurd SS, Barnes PJ, et al: Global strategy for asthma management and prevention: GINA executive summary. Eur Respir J. 31:143–178. 2008. View Article : Google Scholar : PubMed/NCBI | |
Hoffjan S and Ober C: Present status on the genetic studies of asthma. Curr Opin Immunol. 14:709–717. 2002. View Article : Google Scholar : PubMed/NCBI | |
Thongngarm T, Jameekornrak A, Limwongse C, et al: Association between ADAM33 polymorphisms and asthma in a Thai population. Asian Pac J Allergy Immunol. 26:205–211. 2008.PubMed/NCBI | |
Tripathi P, Awasthi S, Prasad R, Husain N and Ganesh S: Association of ADAM33 gene polymorphisms with adult-onset asthma and its severity in an Indian adult population. J Genet. 90:265–273. 2011. View Article : Google Scholar : PubMed/NCBI | |
Lind DL, Choudhry S, Ung N, et al: ADAM33 is not associated with asthma in Puerto Rican or Mexican populations. Am J Respir Crit Care Med. 168:1312–1316. 2003. View Article : Google Scholar : PubMed/NCBI | |
Lee JH, Park HS, Park SW, et al: ADAM33 polymorphism: association with bronchial hyper-responsiveness in Korean asthmatics. Clin Exp Allergy. 34:860–865. 2004. View Article : Google Scholar : PubMed/NCBI | |
Li MO, Sanjabi S and Flavell RA: Transforming growth factor-beta controls development, homeostasis, and tolerance of T cells by regulatory T cell-dependent and -independent mechanisms. Immunity. 25:455–471. 2006. View Article : Google Scholar : PubMed/NCBI | |
Wahl SM and Chen W: Transforming growth factor-beta-induced regulatory T cells referee inflammatory and autoimmune diseases. Arthritis Res Ther. 7:62–68. 2007. View Article : Google Scholar : PubMed/NCBI | |
Minshall EM, Leung DY, Martin RJ, et al: Eosinophil-associated TGF-beta1 mRNA expression and airways fibrosis in bronchial asthma. Am J Respir Cell Mol Biol. 17:326–333. 1997. View Article : Google Scholar : PubMed/NCBI | |
Burton T, Liang B, Dibrov A and Amara F: Transforming growth factor-beta-induced transcription of the Alzheimer beta-amyloid precursor protein gene involves interaction between the CTCF-complex and Smads. Biochem Biophys Res Commun. 295:713–723. 2002. View Article : Google Scholar : PubMed/NCBI | |
Silverman ES, Palmer LJ, Subramaniam V, et al: Transforming growth factor-beta1 promoter polymorphism C-509T is associated with asthma. Am J Respir Crit Care Med. 169:214–219. 2004. View Article : Google Scholar : PubMed/NCBI | |
Li H, Romieu I, Wu H, et al: Genetic polymorphisms in transforming growth factor beta-1 (TGFB1) and childhood asthma and atopy. Hum Genet. 121:529–538. 2007. View Article : Google Scholar : PubMed/NCBI | |
Dunning AM, Ellis PD, McBride S, et al: A transforming growth factorbeta1 signal peptide variant increases secretion in vitro and is associated with increased incidence of invasive breast cancer. Cancer Res. 63:2610–2615. 2003.PubMed/NCBI | |
Wiśniewski A, Obojski A, Pawlik A, et al: Polymorphism of the TGFB1 gene is not associated with bronchial allergic asthma in a Polish population. Hum Immunol. 70:134–138. 2009.PubMed/NCBI | |
Tripathi P, Awasthi S, Husain N, Prasad R and Mishra V: Increased expression of ADAM33 protein in asthmatic patients as compared to non-asthmatic controls. Indian J Med Res. 137:507–514. 2013.PubMed/NCBI | |
Al-khayyat Al, Al-Anazi M, Warsy A, Vazquez-Tello A, Alamri AM, Halwani R, Alangari A, Al-Frayh A, Hamid Q and Al-Muhsen S: T1 and T2 ADAM33 single nucleotide polymorphisms and the risk of childhood asthma in a Saudi Arabian population: a pilot study. Ann Saudi Med. 32:479–486. 2012.PubMed/NCBI | |
Eusebio M, Kraszula L, Kupczyk M, Kuna P and Pietruczuk M: The effects of interleukin-10 or TGF-beta on anti-CD3/CD28 induced activation of CD8+CD28−and CD8+CD28+T cells in allergic asthma. J Biol Regul Homeost Agents. 27:681–692. 2013.PubMed/NCBI | |
Jiang K, Chen HB, Wang Y, Lin JH, Hu Y and Fang YR: Changes in IL-17 and TGF-β1 levels in serum and bronchoalveolar lavage fluid and their clinical significance among children with asthma. Zhongguo Dang Dai Er Ke Za Zhi. 15:604–608. 2013.(In Chinese). |