Relationship between the HLA-G 14bp insertion/deletion polymorphism and susceptibility to autoimmune disease: a meta-analysis

被引:11
作者
Kim, S. K. [1 ,2 ]
Jeong, K. H. [3 ]
Kang, I. J. [3 ]
Chung, J. H. [1 ,2 ]
Shin, M. K. [3 ]
Lee, M. H. [3 ]
机构
[1] Kyung Hee Univ, Kohwang Med Res Inst, Coll Med, Seoul, South Korea
[2] Kyung Hee Univ, Dept Pharmacol, Coll Med, Seoul, South Korea
[3] Kyung Hee Univ, Coll Med, Dept Dermatol, Seoul, South Korea
关键词
Autoimmune disease; Human leukocyte antigen-G; Indel polymorphism; Meta-analysis; Susceptibility; SYSTEMIC-LUPUS-ERYTHEMATOSUS; 14-BP DELETION POLYMORPHISM; G GENE; RHEUMATOID-ARTHRITIS; RISK-FACTOR; G GENOTYPE; CLASS-I; ASSOCIATION; POPULATION; EXPRESSION;
D O I
10.4238/2015.December.1.35
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 the potential relationship between the human leukocyte antigen (HLA)-G 14-bp insertion/deletion (INS/DEL) polymorphisms and autoimmune disease (AID). However, published results are inconclusive. Our aim was to determine whether the 14-bp INS/DEL polymorphism in the HLA-G gene contributes to the risk of AID. A systemic literature search of the PubMed and EMBASE databases was conducted to identify eligible studies investigating the association of the HLA-G 14-bp INS/DEL polymorphism with AID. Our analysis included 11 publications involving a total of 6462 individuals. Overall, no significant association between the HLA-G 14-bp INS/DEL polymorphism and AID was detected in any comparison model. Further subgroup analyses based on AID types and ethnicity also revealed no significant associations. Our results suggest that the HLA-G 14-bp INS/DEL polymorphism is unrelated to the development of AID. Further studies including larger sample sizes are warranted to confirm these results.
引用
收藏
页码:15839 / 15847
页数:9
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