Association between ADAM33 S2 and ST+4 polymorphisms and susceptibility to asthma: A meta-analysis |
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Authors: | Gwan Gyu Song Jae-Hoon KimYoung Ho Lee |
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Affiliation: | Division of Rheumatology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Republic of Korea |
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Abstract: | ObjectiveThe aim of this study was to determine whether ADAM33 (a disintegrin and metalloproteinase domain 33) polymorphisms confer susceptibility to asthma in different populations.MethodsWe performed a meta-analysis on the association between the ADAM33 S2, ST+4, F+1, S1, and V4 polymorphisms and asthma.ResultsThirteen studies in ten reports, which included 4942 patients and 7933 controls, were available for the meta-analysis. Meta-analysis stratified by ethnicity indicated an association between the ADAM33 S2 2 allele and asthma in Europeans (OR = 0.912, 95% CI = 0.851–0.977, p = 0.009). Meta-analysis revealed an association between asthma and the ADAM33 ST+4 2 allele (OR = 0.783, 95% CI = 0.762–0.999, p = 0.048). Stratification by ethnicity indicated an association between the ADAM33 ST+4 polymorphism and asthma in Asians. Stratification by age indicated an association between the ADAM33 ST+4 2 allele and asthma in adults (OR = 0.863, 95% CI = 0.782–0.964, p = 0.008). However, no association was found between asthma and the ADAM33 F+1, S1, and V4 polymorphisms.ConclusionsThis meta-analysis demonstrates that the ADAM33 S2 polymorphism confers susceptibility to asthma in Europeans and the ADAM33 ST+4 polymorphism is associated with asthma in Asians and adults. |
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Keywords: | ADAM33, a disintegrin and metalloproteinase domain 33 ORs, odds ratios CIs, confidence intervals H&ndash W, Hardy&ndash Weinberg F, fixed effects model R, random effects model |
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