Sowmya Sabnavis, Ramaiah Aruna, Sunitha Tella, Nallari Pratibha, Jyothy Akka, Venkateshwari Ananthapur
Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Hyderabad, India.
J Reprod Infertil. 2013 Apr;14(2):62-6.
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.
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.
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).
The present study suggests that the IL-10 G-1082A gene promoter polymorphism is not a major genetic regulator in the etiology of preeclampsia.
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。
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。
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)。
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。