Department of Obstetrics and Gynecology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Am J Reprod Immunol. 2010 Apr 1;63(4):331-8. doi: 10.1111/j.1600-0897.2009.00801.x. Epub 2010 Jan 12.
As gene polymorphisms of cytokines receptors have been found to significantly influence cell responses to cytokines, the aim of this study was to test the hypothesis that IFN-gamma receptor 1 (IFNGR1) gene polymorphisms may contribute to the pathogenesis of pre-eclampsia.
One hundred and sixty-four pre-eclamptic patients (121 patients with mild pre-eclampsia and 43 patients with severe pre-eclampsia) and 171 controls were included. Polymorphisms of the IFNGR1 gene at positions -611, -270, +56 and +95 were genotyped with the matrix-assisted laser desorption/ionization time of flight mass spectrometry.
This study showed a positive association between -56C/C genotype (OR = 1.7; 95% CI = 1.1-2.7) and pre-eclampsia. Although the genotype frequencies (except for -56C/C) of the two polymorphisms were comparable between cases and controls, higher frequency of the -611A/-56C haplotype (OR = 1.450; 95% CI = 1.070-1.966) was noticed in patients versus controls. All patients and controls were homozygous for the -270T/T and +95T/T genotypes. Specifically, the frequency of the -56C allele (OR = 1.838; 95% CI = 1.127-2.995) was higher among patients with severe pre-eclampsia.
The IFNGR1 gene polymorphisms may contribute to the pathogenesis of pre-eclampsia in our population.
由于细胞因子受体的基因多态性已被发现显著影响细胞对细胞因子的反应,本研究旨在检验以下假设:IFN-γ 受体 1(IFNGR1)基因多态性可能导致先兆子痫的发病机制。
本研究纳入了 164 例先兆子痫患者(121 例轻度先兆子痫患者和 43 例重度先兆子痫患者)和 171 例对照。采用基质辅助激光解吸/电离飞行时间质谱法检测 IFNGR1 基因 -611、-270、+56 和 +95 位置的多态性。
本研究显示-56C/C 基因型(OR=1.7;95%CI=1.1-2.7)与先兆子痫呈正相关。虽然病例组和对照组两种多态性的基因型频率(-56C/C 除外)相似,但患者中-611A/-56C 单倍型的频率更高(OR=1.450;95%CI=1.070-1.966)。所有患者和对照均为 -270T/T 和 +95T/T 基因型纯合子。具体而言,重度先兆子痫患者中-56C 等位基因的频率(OR=1.838;95%CI=1.127-2.995)更高。
IFNGR1 基因多态性可能导致我们人群中先兆子痫的发病机制。