Lhotská P, Martínek P, Čedíková M, Lošan P, Králíčková M, Kališ V, Novotný Z
Ceska Gynekol. 2014 Jan;79(1):48-52.
The interleukin-11 (IL-11) is one of the most important signaling factors in the process of decidua-lization and embryo-maternal cross talk during the embryo implantation. We investigated the prevalence of the IL-11 gene point variants in the population of infertile women and fertile control subjects.
A cohort study.
Department of Obstetrics and Gynecology, Faculty of Medicine and University Hospital of Charles University, Pilsen.
The population to screen consisted of 354 infertile women. The control population was comprised of 195 healthy fertile subjects. For the mutational analysis, the temperature gradient gel electrophoresis (TGGE) and direct sequencing had been used. The groups of fertile controls and infertile patients were compared for statistically significant difference using the Fisher´s 2 by 2 Exact test.
Thirteen potentially functional IL-11 gene variants, the G to A transversions at the position 3651 (G3651A) leading to the arginin to histidin exchange on the position 113 (R113H) were detected in the group of infertile women. No mutations were identified in the control group, which means that the frequency of functionally relevant mutations of the IL-11 gene in infertile women is significantly enhanced in comparison with controls (p = 0.01, Fisher´s 2 by 2 Exact test).
The results prove the presence of the potentially functionally relevant IL-11 gene variants in the population of infertile women. The presence of variants does not have to lead directly to decrease fertility but may contribute to the dysbalance of cytokine milieu which is needed for the decidualization as well as subsequent embryo implantation. Even thought IL-11 gene variants occur infrequently, their impact on molecular events during early phases of pregnancy should be further elucidated.
白细胞介素-11(IL-11)是蜕膜化过程以及胚胎植入期间胚胎与母体相互作用过程中最重要的信号因子之一。我们调查了不育女性群体和可育对照人群中IL-11基因点变异的发生率。
一项队列研究。
皮尔森查理大学医学院及大学医院妇产科。
筛查人群包括354名不育女性。对照人群由195名健康可育对象组成。对于突变分析,使用了温度梯度凝胶电泳(TGGE)和直接测序法。采用Fisher 2×2精确检验对可育对照组和不育患者组进行统计学显著性差异比较。
在不育女性组中检测到13种潜在功能性IL-11基因变异,即第3651位的G到A颠换(G3651A),导致第113位的精氨酸变为组氨酸(R113H)。对照组未发现突变,这意味着与对照组相比,不育女性中IL-11基因功能相关突变的频率显著增加(p = 0.01,Fisher 2×2精确检验)。
结果证明不育女性群体中存在潜在功能相关的IL-11基因变异。这些变异的存在不一定直接导致生育力下降,但可能导致蜕膜化以及随后胚胎植入所需的细胞因子环境失衡。尽管IL-11基因变异很少见,但其对妊娠早期分子事件的影响仍需进一步阐明。