Lack of association between the G+2044A polymorphism of interleukin-13 gene and chronic obstructive pulmonary disease: a meta-analysis

被引:2
|
作者
Duan, Lian [1 ]
Liang, Rui [2 ]
Wang, Zhendong [1 ]
Lei, Lei [1 ,3 ]
Jin, Lianhong [1 ,3 ]
Shen, Jingling [1 ,3 ]
Jin, Shoude [2 ]
机构
[1] Harbin Med Univ, Dept Histol & Embryol, Harbin, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 4, Div Resp Dis, Harbin, Heilongjiang, Peoples R China
[3] Harbin Med Univ, Embryo & Stem Cell Engn Lab, Harbin, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
IL-13; G+2044A; Polymorphism; Chronic obstructive pulmonary disease; Association; CHRONIC MUCUS HYPERSECRETION; AIRWAY HYPERRESPONSIVENESS; SERUM IGE; IL-13; ASTHMA; COPD; ATOPY; BURDEN; IL13; SMOKING;
D O I
10.1007/s11033-014-3512-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Numerous studies have investigated association of interleukin-13 (IL-13) G+2044A polymorphism with COPD susceptibility; however, the results were inconsistent and inconclusive. To evaluate the association between the IL-13 G+2044A polymorphism and susceptibility to COPD, a meta-analysis of published case-control studies was performed. Based on PubMed and Chinese database, this research selected studies that examined the association of the IL-13 G+2044A polymorphism with COPD. A genetic model-free approach was used to assess whether the combined data showed this association. Then a subgroup analysis was also performed, with stratifications for race, study design, and sample size. Six studies (total 1,213 COPD patients and 801 control subjects) for the IL-13 G+2044A polymorphism with COPD were included in the meta-analysis (G- vs A-allele: OR 1.12, 95 % CI 0.96-1.32, P = 0.15; genotypes GG+GA vs genotype AA: OR 0.99, 95 % CI 0.49-2.00, P = 0.98; genotype GG vs genotypes GA+AA: OR 1.18, 95 % CI 0.97-1.44, P = 0.09; genotype GA vs genotypes GG+AA: OR 0.85, 95 % CI 0.70-1.04, P = 0.11). This meta-analysis demonstrates that the IL-13 G+2044A polymorphism does not confer susceptibility to COPD. More detailed data about individual and environment, larger sample sizes with unbiased genotyping methods and matched controls in different populations are required.
引用
收藏
页码:6297 / 6303
页数:7
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