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患有特发性复发性自然流产的夫妇中VEGFA基因启动子区域的-2549插入/缺失多态性

The -2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion.

作者信息

Pereza Nina, Ostojić Saša, Smirčić Anamarija, Hodžić Alenka, Kapović Miljenko, Peterlin Borut

机构信息

Department of Biology and Medical Genetics, Faculty of Medicine, University of Rijeka, B. Branchetta 20, Rijeka, 51000, Croatia.

Department of Gynaecology and Obstetrics, Clinical Institute of Medical Genetics, UMC Ljubljana, Ljubljana, 1000, Slovenia.

出版信息

J Assist Reprod Genet. 2015 Dec;32(12):1789-94. doi: 10.1007/s10815-015-0593-0. Epub 2015 Oct 16.

Abstract

PURPOSE

The vascular endothelial growth factor A (VEGFA) is crucial for normal vasculogenesis and angiogenesis during pregnancy, and alterations in the VEGFA gene expression were detected in women with idiopathic recurrent spontaneous abortion (IRSA) and spontaneously aborted conceptuses. Our aim was to evaluate whether there is an association between the functional -2549 insertion/deletion (I/D) polymorphism in the promoter region of the VEGFA gene and IRSA in reproductive couples.

METHODS

We performed a case-control study involving 149 women and their 140 partners with three or more IRSA and 149 control women and men. Allele-specific polymerase chain reaction was used for genotyping.

RESULTS

We found no association of the -2549 I/D polymorphism with IRSA in women. However, men with the DD genotype have a 1.75-fold increased risk of IRSA compared with men carrying the ID and II genotypes (95 % confidence interval (CI) = 1.05-2.93, P = 0.032). In addition, the D allele in men contributes to a 1.42-fold increased risk of IRSA (95 % CI = 1.02-1.97, P = 0.036) compared to men carrying the I allele.

CONCLUSIONS

Our results indicate that the -2549 I/D polymorphism in the VEGFA gene in men might be associated with IRSA. Additional genetic association studies including both partners, as well as expression studies, are needed to elucidate the role of this polymorphism in IRSA.

摘要

目的

血管内皮生长因子A(VEGFA)在孕期正常血管生成和血管新生过程中至关重要,且在特发性复发性自然流产(IRSA)女性及自然流产的胚胎中检测到VEGFA基因表达改变。我们的目的是评估VEGFA基因启动子区域功能性-2549插入/缺失(I/D)多态性与生殖夫妇IRSA之间是否存在关联。

方法

我们进行了一项病例对照研究,纳入149名有三次或更多次IRSA的女性及其140名伴侣,以及149名对照女性和男性。采用等位基因特异性聚合酶链反应进行基因分型。

结果

我们发现-2549 I/D多态性与女性IRSA无关联。然而,与携带ID和II基因型的男性相比,携带DD基因型的男性患IRSA的风险增加1.75倍(95%置信区间(CI)=1.05 - 2.93,P = 0.032)。此外,与携带I等位基因的男性相比,男性中的D等位基因使患IRSA的风险增加1.42倍(95% CI = 1.02 - 1.97,P = 0.036)。

结论

我们的结果表明,男性VEGFA基因中的-2549 I/D多态性可能与IRSA有关。需要开展包括夫妇双方的更多遗传关联研究以及表达研究,以阐明该多态性在IRSA中的作用。

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