子宫内膜冲洗样品中油基子宫输卵管造影改善白血病抑制因子表达

N. Gungor, A. Yurci, Ş. Hatırnaz, K. Cil, Oğuz Güler
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摘要

目的:子宫输卵管造影(HSG)增强生育力的生物学机制尚不完全清楚。白血病抑制因子(Leukemia inhibitory factor, LIF)是参与着床的重要细胞因子。本研究旨在探讨HSG对子宫内膜冲洗标本中LIF mRNA表达的影响。方法:选取40例计划行输卵管输卵管移植的不孕症患者作为研究对象。输卵管造影前,在黄体中期进行子宫内膜冲洗,然后向腔内灌注造影剂。第二次冲洗在下一个周期的黄体中期进行。10例行诊断性宫腔镜检查的患者作为第二对照组。采用RT-PCR方法检测各组子宫内膜冲洗标本中LIF mRNA水平。结果:不育组hsg前LIF mRNA水平明显低于不育组。在不孕患者中,与基线水平相比,HSG后LIF mRNA表达增加了3.2倍。输卵管造影后,LIF值达到可生育水平。虽然宫腔镜组测量的LIF水平明显低于不育患者,但它们与不育患者的前hsg值相似。输卵管造影后不孕患者的LIF水平明显高于宫腔镜组。结论:在不孕症患者中,HSG通过增加LIF mRNA的合成来促进接受性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oil-Based Hysterosalpingography ?mproves Leukaemia ?nhibitory Factor Expression ?n Endometrial Flushing Samples
Objective: The biological mechanism of the fertility-enhancing effect of hysterosalpingography (HSG) is not fully known. Leukemia inhibitory factor (LIF) is an important cytokine involved in implantation. This study was planned to investigate the effect of HSG on LIF mRNA expression in endometrial flushing samples. Methods: Forty infertile patients scheduled for HSG were included in the study. Before HSG, endometrial flushing was performed in the mid-luteal phase, followed by contrast-medium infusion into the cavity. Second flushing was done in the mid-luteal phase of the next cycle. Ten patients who underwent diagnostic hysteroscopy were taken as the second control group. LIF mRNA levels were measured by RT-PCR in endometrial flushing samples collected from each group. Results: The pre-HSG LIF mRNA levels of the infertile group were significantly lower than those of the fertile group. In infertile patients, LIF mRNA expression increased 3.2 times after HSG compared to baseline levels. LIF values reached fertile levels after HSG. While the LIF levels measured in the hysteroscopy group were significantly lower than in fertile patients, they were similar to the pre-HSG values of infertile patients. LIF levels of infertile patients after HSG were found to be significantly higher than those of the hysteroscopy group. Conclusions: In infertile patients, HSG contributes to receptivity by increasing LIF mRNA synthesis.
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