TY - JOUR
T1 - Meta-Analysis of the Association between Vitiligo and Human Leukocyte Antigen-A
AU - Li, Zhangjun
AU - Ren, Jianwen
AU - Niu, Xinwu
AU - Xu, Qingqiang
AU - Wang, Xiaopeng
AU - Liu, Yale
AU - Xiao, Shengxiang
N1 - Publisher Copyright:
© 2016 Zhangjun Li et al.
PY - 2016
Y1 - 2016
N2 - Objective. The objective of this study was to systematically evaluate the association between vitiligo and human leukocyte antigen- (HLA-) A. Methods. PubMed, Embase, Web of Science, Chinese National Knowledge Infrastructure, and reference lists were searched for relevant original articles. Results. Nineteen case-control studies comprising 3042 patients and 5614 controls were included, in which 33 HLA-A alleles were reported. Overall, three alleles (HLA- A 02, A 33, and A w 31) were significantly associated with increased risk of vitiligo, two (HLA- A 09 and A w 19) were associated with decreased risk, and the remaining 28 were unassociated. Twelve alleles, seven alleles, and 19 alleles were common to three ethnicities, both types of vitiligo, and both typing methods, respectively. In the subgroup analysis by ethnicity and typing methods, the association of six alleles and five alleles was inconsistent in three populations and both typing methods, respectively. In the subgroup analysis by clinical type, the association of all seven alleles was consistent in both types of vitiligo. Conclusion. The meta-analysis suggests that HLA- A 02, A 33, and A w 31 are associated with increased risk of vitiligo, while HLA- A 09 and A w 19 are associated with decreased risk of vitiligo. The association of some alleles varies in terms of ethnicity and typing methods.
AB - Objective. The objective of this study was to systematically evaluate the association between vitiligo and human leukocyte antigen- (HLA-) A. Methods. PubMed, Embase, Web of Science, Chinese National Knowledge Infrastructure, and reference lists were searched for relevant original articles. Results. Nineteen case-control studies comprising 3042 patients and 5614 controls were included, in which 33 HLA-A alleles were reported. Overall, three alleles (HLA- A 02, A 33, and A w 31) were significantly associated with increased risk of vitiligo, two (HLA- A 09 and A w 19) were associated with decreased risk, and the remaining 28 were unassociated. Twelve alleles, seven alleles, and 19 alleles were common to three ethnicities, both types of vitiligo, and both typing methods, respectively. In the subgroup analysis by ethnicity and typing methods, the association of six alleles and five alleles was inconsistent in three populations and both typing methods, respectively. In the subgroup analysis by clinical type, the association of all seven alleles was consistent in both types of vitiligo. Conclusion. The meta-analysis suggests that HLA- A 02, A 33, and A w 31 are associated with increased risk of vitiligo, while HLA- A 09 and A w 19 are associated with decreased risk of vitiligo. The association of some alleles varies in terms of ethnicity and typing methods.
UR - https://www.scopus.com/pages/publications/84988975434
U2 - 10.1155/2016/5412806
DO - 10.1155/2016/5412806
M3 - 文献综述
AN - SCOPUS:84988975434
SN - 2314-6133
VL - 2016
JO - BioMed Research International
JF - BioMed Research International
M1 - 5412806
ER -