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子痫前期中白细胞介素-10(G-1082A)启动子多态性的评估

Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia.

作者信息

Sowmya Sabnavis, Ramaiah Aruna, Sunitha Tella, Nallari Pratibha, Jyothy Akka, Venkateshwari Ananthapur

机构信息

Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Hyderabad, India.

出版信息

J Reprod Infertil. 2013 Apr;14(2):62-6.

Abstract

BACKGROUND

Preeclampsia is a pregnancy-specific syndrome that may be life-threatening, especially to the fetus. Several causes have been reported that may have a possible role in the development of the disorder. Interleukin-10 affect maternal intravascular inflammation, as well as endothelial dysfunction. The aim of this study was to investigate the association between IL-10 G-1082A polymorphism and preeclampsia.

METHODS

A total of eighty-eight pregnant women with preeclampsia and 100 women with normal pregnancy attending the Gynecological unit of Government Maternity Hospital, Petlaburz, Hyderabad, India, were considered for the study. A standard amplification refractory mutation system (ARMS) PCR was carried out for genotyping IL-10 G-1082A promoter polymorphism in all the participants. Genotypic distribution of the control and patient groups were compared with values predicted by Hardy-Weinberg equilibrium using χ(2) test. Odd ratios (OR) and their respective 95% confidence intervals were used to measure the strength of association between IL-10 gene polymorphism and preeclampsia.

RESULTS

The frequencies of IL-10 G-1082A genotypes, GG, GA and AA, were 17.8%, 41.09% and 41.09% in women with preeclampsia and 25%, 28% and 47% in the controls respectively. There was no significant difference in the distribution of genotypes and alleles of IL-10 G-1082A between the two groups (Test power=0.66).

CONCLUSION

The present study suggests that the IL-10 G-1082A gene promoter polymorphism is not a major genetic regulator in the etiology of preeclampsia.

摘要

背景

子痫前期是一种妊娠特异性综合征,可能危及生命,尤其是对胎儿。已有报道称多种原因可能在该疾病的发生发展中起作用。白细胞介素-10影响母体血管内炎症以及内皮功能障碍。本研究的目的是探讨白细胞介素-10基因G-1082A多态性与子痫前期之间的关联。

方法

本研究纳入了印度海得拉巴Petlaburz政府妇产医院妇科病房的88例子痫前期孕妇和100例正常孕妇。对所有参与者进行标准的扩增阻滞突变系统(ARMS)PCR,以对白细胞介素-10基因G-1082A启动子多态性进行基因分型。使用χ(2)检验将对照组和患者组的基因型分布与哈迪-温伯格平衡预测值进行比较。比值比(OR)及其各自的95%置信区间用于衡量白细胞介素-10基因多态性与子痫前期之间关联的强度。

结果

子痫前期患者中白细胞介素-10基因G-1082A基因型GG、GA和AA的频率分别为17.8%、41.09%和41.09%,对照组中分别为25%、28%和47%。两组之间白细胞介素-10基因G-1082A的基因型和等位基因分布无显著差异(检验效能=0.66)。

结论

本研究表明,白细胞介素-10基因G-1082A启动子多态性不是子痫前期病因中的主要遗传调节因素。

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