HLA associations and HLA sharing in recurrent miscarriage: A systematic review and meta-analysis

被引:51
|
作者
Meuleman, Tess [1 ]
Lashley, Lisa E. L. O. [1 ]
Dekkers, Olaf M. [2 ]
van Lith, Jan M. M. [1 ]
Claas, Frans H. J. [3 ]
Bloemenkamp, Kitty W. M. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Obstet, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Clin Epidemiol, NL-2300 RC Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Transfus, NL-2300 RC Leiden, Netherlands
关键词
HLA alleles; HLA sharing; Meta-analysis; Recurrent miscarriage; Systematic review; HUMAN-LEUKOCYTE ANTIGEN; IMMUNOGLOBULIN-LIKE RECEPTORS; NATURAL-KILLER-CELLS; CLASS-II ALLELES; G GENE; SPONTANEOUS-ABORTION; HISTOCOMPATIBILITY ANTIGENS; LUPUS-ERYTHEMATOSUS; BLOOD-TRANSFUSIONS; REVISED CRITERIA;
D O I
10.1016/j.humimm.2015.02.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Problem: The aim of this meta-analysis was to evaluate whether specific maternal HLA alleles and HLA sharing of couples are associated with the occurrence of recurrent miscarriage (RM). Method of study: A systematic literature search was performed for studies that evaluated the association between HLA alleles, HLA sharing and RM. RM was defined as three or more consecutive unexplained miscarriages and a control group was included of women with at least one live birth and no miscarriages in their history. Meta-analyses were performed and the pooled odds ratio (OR) was calculated. Results: We included 41 studies. Selection bias was present in 40 studies and information bias in all studies. Meta-analyses showed an increased risk of RM in mothers carrying a HLA-DRB1*4 (OR 1.41, 95% CI 1.05-1.90), HLA-DRB1*15 (OR 1.57, 95% CI 1.15-2.14), or a HLA-E*01:01 allele (OR 1.47, 95% CI 0.20-1.81), and a decreased risk with HLA-DRB1*13 (OR 0.63, 95% CI 0.45-0.89) or HLA-DRB1*14 (OR 0.54, 95% CI 0.31-0.94). Pooling results for HLA sharing showed that HLA-B sharing (OR 1.39, 95% CI 1.11-1.75) and HLA-DR sharing (OR 1.57, 95% CI 1.10-1.25) were both associated with the occurrence of RM. Conclusion: Although the present systematic review and meta-analysis demonstrates that specific HLA alleles and HLA sharing are associated with RM, a high degree of bias was present and therefore observed results should be interpreted carefully. (C) 2015 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
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页码:362 / 373
页数:12
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