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人类白细胞抗原(HLA)-DQA1*0102/HLA-DQB1*0602多态性与子痫前期的关系。

Relationship between human leukocyte antigen (HLA)-DQA1*0102/HLA-DQB1*0602 polymorphism and preeclampsia.

作者信息

Mohammadi Mahmoud, Farazmandfar Touraj, Shahbazi Majid

机构信息

Medical Cellular and Molecular Research Center, Golestan University of Medical Sciences, Gorgan, Iran.

出版信息

Int J Reprod Biomed. 2017 Sep;15(9):569-574.

Abstract

BACKGROUND

Preeclampsia is a condition associated with systemic disorders in the mother and the fetus. However, the exact causes of preeclampsia are unknown, but several genetics and environmental factors play role in development of this disease. Major histocompatibility complex role is very important during pregnancy through which the fetus is not rejected by mother's immune system.

OBJECTIVE

In this study, we investigated the relationship of the human leukocyte antigen (HLA)-DQA10102/HLA-DQB10602 polymorphism with preeclampsia.

MATERIALS AND METHODS

Genomic DNA of 181 pregnant women with a history of preeclampsia as the case group and 228 pregnant women with no history of preeclampsia as the controls were extracted. The HLA-DQA10102/HLA-DQB10602 polymorphisms of all DNA samples were identified by the SSP-PCR method. Frequencies difference of variables between case and control groups were calculated by Chi-square test. The ethnic origin of the participants in this study was extracted from their medical records.

RESULTS

There was a significant association between preeclampsia and Sistani ethnic group (p=0.031). Moreover, there was a significant association between preeclampsia and frequencies of allele HLA-DQB10602 (p<0.001), and genotypes of heterozygote (+0102/-0602) (p<0.001) and negative homozygote (-0102/-0602) (p=0.005). There also was an association between allele HLA-DQB10602 and preeclampsia in Fars ethnic group (p=0.028).

CONCLUSION

It seems that immune incompatibility may have an important role in preeclampsia predisposition. According to our results, the lack of locus HLA-DQB1*0602 may be a risk factor for preeclampsia.

摘要

背景

子痫前期是一种与母亲和胎儿全身疾病相关的病症。然而,子痫前期的确切病因尚不清楚,但多种遗传和环境因素在该疾病的发展中起作用。主要组织相容性复合体在孕期起着非常重要的作用,通过它胎儿不会被母亲的免疫系统排斥。

目的

在本研究中,我们调查了人类白细胞抗原(HLA)-DQA10102/HLA-DQB10602多态性与子痫前期的关系。

材料与方法

提取181例有子痫前期病史的孕妇作为病例组的基因组DNA,以及228例无子痫前期病史的孕妇作为对照组的基因组DNA。采用序列特异性引物聚合酶链反应(SSP-PCR)方法鉴定所有DNA样本的HLA-DQA10102/HLA-DQB10602多态性。通过卡方检验计算病例组和对照组之间变量的频率差异。本研究参与者的种族来源从其病历中提取。

结果

子痫前期与锡斯坦尼族之间存在显著关联(p = 0.031)。此外,子痫前期与等位基因HLA-DQB10602的频率(p < 0.001)、杂合子(+0102/-0602)基因型(p < 0.001)和阴性纯合子(-0102/-0602)基因型(p = 0.005)之间存在显著关联。在法尔斯族中,等位基因HLA-DQB10602与子痫前期之间也存在关联(p = 0.028)。

结论

免疫不相容似乎在子痫前期易感性中起重要作用。根据我们的结果,缺乏HLA-DQB1*0602位点可能是子痫前期的一个危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d332/5893932/0e54c44df73d/ijrb-15-569-g001.jpg

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