Association of Single Nucleotide Polymorphisms in Toll-like Receptor Genes With Asthma Risk: a Systematic Review and Meta-analysis.
10.4168/aair.2015.7.2.130
- Author:
Kalthoum TIZAOUI
1
;
Wajih KAABACHI
;
Kamel HAMZAOUI
;
Agnes HAMZAOUI
Author Information
1. Division of Histology and Immunology, Department of Basic Sciences, Faculty of medicine Tunis, Tunis El Manar University, Tunis, Tunisia. kalttizaoui@gmail.com
- Publication Type:Meta-Analysis ; Original Article
- Keywords:
Asthma;
TLR genes;
SNPs;
association;
meta-analysis
- MeSH:
Alleles;
Asthma*;
Genetic Association Studies;
Humans;
Models, Genetic;
Polymorphism, Single Nucleotide*;
Toll-Like Receptors*
- From:Allergy, Asthma & Immunology Research
2015;7(2):130-140
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Asthma is a complex disease, with contributions from multiple genes, various genetic backgrounds, and environmental factors. Many human epidemiological studies have demonstrated that single nucleotide polymorphisms (SNPs) in Toll-like receptor (TLR) genes are inconsistently associated with asthma risk. Some have demonstrated differences concerning the study design and effect size, and conflicting results have been reported. A meta-analysis is necessary to determine the magnitude of this association. METHODS: Following the Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines, a systematic search and meta-analysis of the literature was conducted to estimate the association of SNPs in TLR genes with asthma risk. We screened the medical literature based on the following keyword searches in MEDLINE and EMBASE databases: 'TLR', 'polymorphism', 'asthma', and their combinations. RESULTS: Meta-analysis of eight studies on TLR4 Asp299Gly showed a marginal association of TLR4 with asthma risk (odds ratio [OR]=0.814 [95% confidence interval [CI], 0.652-1.016; P=0.069]) in the recessive model. TLR4 Thr399Ile was not associated with asthma risk under any genetic model. Meta-analysis of four studies on TLR2 Arg753Gln indicated that TLR2 might be significantly associated with asthma in the dominant and codominant models (P=0.029, P=0.030, and P=0.009, respectively). TLR9 -1237 was marginally associated with asthma risk (OR=0.408 [95% CI, 0.163-1.021; P=0.065]) in the codominant model. Analysis using the allele contrast model showed that the major TLR9 -1237 T allele tended to be a significant protective factor with OR=0.689 (95% CI, 0.471-1.007; P=0.055). CONCLUSIONS: The results showed that TLR4 Asp299Gly, TLR2 Arg753Gln, and TLR9-1237 might contribute significantly to asthma susceptibility. Future genetic association studies would consolidate these findings.
