{"title":"Association of HLA-G 14-bp Insertion/Deletion Polymorphism With Recurrent Spontaneous Abortion: A Meta-Analysis.","authors":"Yan Sun, Mingzhu Huo, Jihua Zhao, Wenbin Niu","doi":"10.1111/iji.70000","DOIUrl":null,"url":null,"abstract":"<p><p>We performed a meta-analysis to study the relationship between HLA-G 14-bp insertion/deletion polymorphism and recurrent spontaneous abortion (RSA). All literature was searched from PubMed, Web of Science, Embase and Wanfang databases. Statistical analyses were performed by the STATA software (Version 16.0). A total of 35 studies were analysed which included 3652 women with RSA and 3331 normal control subjects. The current meta-analysis revealed that 14-bp insertion/deletion polymorphism has a significant association with RSA (I vs. D: OR: 1.17; 95% CI (1.05-1.30); II + ID vs. DD: OR: 1.33; 95% CI (1.11-1.59); II vs. DD: OR: 1.34; 95% CI (1.07-1.66); ID vs. DD: OR: 1.30; 95% CI (1.08-1.58)). Subgroup analysis by the number of abortions indicated that there was no significant association between HLA-G 14-bp insertion/deletion polymorphism and RSA risk in women with two or more abortions. However, HLA-G 14-bp insertion/deletion polymorphism was associated with the risk of RSA in women with three or more abortions as well as the overall population (I vs. D: OR: 1.26; 95% CI (1.04-1.52); II + ID vs. DD: OR: 1.47; 95% CI (1.09-1.98); II vs. DD: OR: 1.52; 95% CI (1.08-2.13); ID vs. DD: OR: 1.45; 95% CI (1.06-1.99)). Subgroup analysis by ethnicity indicated that HLA-G 14-bp insertion/deletion polymorphism increased RSA risk in both Asian ancestry group (II + ID vs. DD: OR: 1.35; 95% CI (1.06-1.73); ID vs. DD: OR: 1.37; 95% CI (1.06-1.78)) and European ancestry group (I vs. D: OR: 1.25; 95% CI (1.08-1.45); II vs. ID + DD: OR: 1.48; 95% CI (1.14-1.91); II vs. DD: OR: 1.61; 95% CI (1.19-2.18)). A p<sub>OR</sub> value of < 0.05 was considered statistically significant for these analyses. Our current meta-analysis demonstrated that the HLA-G 14-bp insertion/deletion polymorphism increased the risk of RSA in Asian ancestry group and European ancestry group.</p>","PeriodicalId":14003,"journal":{"name":"International Journal of Immunogenetics","volume":" ","pages":"e70000"},"PeriodicalIF":2.3000,"publicationDate":"2025-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Immunogenetics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/iji.70000","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
We performed a meta-analysis to study the relationship between HLA-G 14-bp insertion/deletion polymorphism and recurrent spontaneous abortion (RSA). All literature was searched from PubMed, Web of Science, Embase and Wanfang databases. Statistical analyses were performed by the STATA software (Version 16.0). A total of 35 studies were analysed which included 3652 women with RSA and 3331 normal control subjects. The current meta-analysis revealed that 14-bp insertion/deletion polymorphism has a significant association with RSA (I vs. D: OR: 1.17; 95% CI (1.05-1.30); II + ID vs. DD: OR: 1.33; 95% CI (1.11-1.59); II vs. DD: OR: 1.34; 95% CI (1.07-1.66); ID vs. DD: OR: 1.30; 95% CI (1.08-1.58)). Subgroup analysis by the number of abortions indicated that there was no significant association between HLA-G 14-bp insertion/deletion polymorphism and RSA risk in women with two or more abortions. However, HLA-G 14-bp insertion/deletion polymorphism was associated with the risk of RSA in women with three or more abortions as well as the overall population (I vs. D: OR: 1.26; 95% CI (1.04-1.52); II + ID vs. DD: OR: 1.47; 95% CI (1.09-1.98); II vs. DD: OR: 1.52; 95% CI (1.08-2.13); ID vs. DD: OR: 1.45; 95% CI (1.06-1.99)). Subgroup analysis by ethnicity indicated that HLA-G 14-bp insertion/deletion polymorphism increased RSA risk in both Asian ancestry group (II + ID vs. DD: OR: 1.35; 95% CI (1.06-1.73); ID vs. DD: OR: 1.37; 95% CI (1.06-1.78)) and European ancestry group (I vs. D: OR: 1.25; 95% CI (1.08-1.45); II vs. ID + DD: OR: 1.48; 95% CI (1.14-1.91); II vs. DD: OR: 1.61; 95% CI (1.19-2.18)). A pOR value of < 0.05 was considered statistically significant for these analyses. Our current meta-analysis demonstrated that the HLA-G 14-bp insertion/deletion polymorphism increased the risk of RSA in Asian ancestry group and European ancestry group.
我们进行了一项荟萃分析,研究HLA-G 14bp插入/缺失多态性与复发性自然流产(RSA)的关系。所有文献检索自PubMed、Web of Science、Embase和万方数据库。采用STATA软件(Version 16.0)进行统计分析。共分析了35项研究,其中包括3652名RSA女性和3331名正常对照受试者。目前的荟萃分析显示,14bp插入/删除多态性与RSA显著相关(I vs. D: OR: 1.17;95% ci (1.05-1.30);II + ID vs. DD: OR: 1.33;95% ci (1.11-1.59);II vs. DD: OR: 1.34;95% ci (1.07-1.66);ID vs. DD: OR: 1.30;95% ci(1.08-1.58))。流产次数的亚组分析表明,在两次或两次以上流产的妇女中,HLA-G 14bp插入/缺失多态性与RSA风险之间没有显著关联。然而,HLA-G 14bp插入/缺失多态性与三次或三次以上流产妇女以及总体人群的RSA风险相关(I vs. D: or: 1.26;95% ci (1.04-1.52);II + ID vs. DD: OR: 1.47;95% ci (1.09-1.98);II vs. DD: OR: 1.52;95% ci (1.08-2.13);ID vs. DD: OR: 1.45;95% ci(1.06-1.99))。种族亚组分析表明,HLA-G 14bp插入/缺失多态性增加了亚洲血统组的RSA风险(II + ID vs. DD: OR: 1.35;95% ci (1.06-1.73);ID vs. DD: OR: 1.37;95% CI(1.06-1.78))和欧洲血统组(I vs. D: OR: 1.25;95% ci (1.08-1.45);II vs. ID + DD: OR: 1.48;95% ci (1.14-1.91);II vs. DD: OR: 1.61;95% ci(1.19-2.18))。pOR值< 0.05被认为在这些分析中具有统计学意义。我们目前的荟萃分析表明,HLA-G 14bp插入/删除多态性增加了亚洲血统组和欧洲血统组的RSA风险。
期刊介绍:
The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are:
-studies of blood groups and other surface antigens-
cell interactions and immune response-
receptors, antibodies, complement components and cytokines-
polymorphism-
evolution of the organisation, control and function of immune system components-
anthropology and disease associations-
the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies-
All papers are seen by at least two independent referees and only papers of the highest quality are accepted.