Novotný Z, Krízan J, Síma R, Síma P, Uher P, Zech N, Hütelová R, Baborová P, Ulcová-Gallová Z, Subrt I, Ulmanová E, Houdek Z, Rokyta Z, Babuska V, Králícková M
Charles University in Prague, Faculty of Medicine in Pilsen and University Hospital, Department of Obstetrics and Gynecology, Pilsen, Czech Republic.
Folia Biol (Praha). 2009;55(3):92-7.
The frequency of functionally relevant mutations of the leukaemia inhibitory factor (LIF) gene in infertile women is significantly enhanced in comparison with fertile controls. The objective of this retrospective cohort study was to evaluate the impact of LIF gene mutations on the outcome of the treatment in women with various causes of infertility. Fifteen infertile women with the G to A transition at position 3400 leading to the valine to methionine exchange at codon 64 were analysed. Group A was made up of women with diagnoses that are frequently accompanied by changes in humoral as well as cell-mediated immunity - idiopathic infertility and endometriosis (N = 7). Group B consisted of patients with polycystic ovary syndrome (PCOS), andrological factor, tubal factor and hyperprolactinaemia (N = 8). The control group comprised 136 infertile women with no LIF gene mutation diagnosed with idiopathic infertility and endometriosis (N = 37) (group C) and patients with PCOS, tubal and andrological factor (N = 99) (group D). Seven of the mutation-positive patients were successfully treated by in vitro fertilization (IVF), but nobody in this group was diagnosed with idiopathic infertility and only one with endometriosis, which means that there is a statistically significant difference in the pregnancy rates between groups A and B (P = 0.01, Fisher's 2 by 2 exact test) but no statistically significant difference when comparing patients with the LIF gene mutation (group A+B) to no LIF gene mutation (group C+D). The results suggest that in mutation-positive women the idiopathic infertility and endometriosis have a negative impact on the outcome of IVF treatment.
与有生育能力的对照组相比,不育女性中白血病抑制因子(LIF)基因功能相关突变的频率显著增加。这项回顾性队列研究的目的是评估LIF基因突变对各种原因导致的不育女性治疗结果的影响。分析了15名不育女性,这些女性在3400位发生了从G到A的转变,导致密码子64处缬氨酸变为甲硫氨酸。A组由诊断常伴有体液免疫和细胞介导免疫变化的女性组成——特发性不育和子宫内膜异位症(N = 7)。B组由多囊卵巢综合征(PCOS)、男性因素、输卵管因素和高泌乳素血症患者组成(N = 8)。对照组包括136名未发生LIF基因突变的不育女性,她们被诊断为特发性不育和子宫内膜异位症(N = 37)(C组)以及PCOS、输卵管和男性因素患者(N = 99)(D组)。7名突变阳性患者通过体外受精(IVF)成功治疗,但该组中无人被诊断为特发性不育,只有1人患有子宫内膜异位症,这意味着A组和B组之间的妊娠率存在统计学显著差异(P = 0.01,Fisher 2×2精确检验),但将LIF基因突变患者(A组+B组)与无LIF基因突变患者(C组+D组)进行比较时,无统计学显著差异。结果表明,在突变阳性女性中,特发性不育和子宫内膜异位症对IVF治疗结果有负面影响。