sulf1基因多态性rs6990375与体外受精胎儿失败有显著相关性。

Eskandar Taghizadeh, Seyed Mehdi Kalantar, Reza Mahdian, Mohammad Hasan Sheikhha, Ehsan Farashahi-Yazd, Saeed Ghasemi, Zahra Shahbazi
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引用次数: 0

摘要

背景:磺化酶1 (SULF1)的功能是去除硫酸肝素中的6- o -硫酸盐基团。这一作用改变了细胞外生长因子的结合位点。据报道,SULF1的表达在血管生成中发生改变。我们假设SULF1的单核苷酸多态性(snp)会影响临床病理特征。目的:探讨体外受精(IVF)技术中SULF1基因多态性与胎儿失败的关系。材料与方法:采用聚合酶链反应和限制性片段长度多态性方法,对53例IVF技术胎儿失败的不孕妇女和53例至少有一个健康孩子的妇女进行了rs6990375共同(次要等位基因频率>0.05)调控SNP的研究。结果:我们发现rs6990375与体外受精早期失败显著相关,G等位基因在体外受精胎儿失败女性中出现频率高(p)。结论:这些发现提示suls1基因变异可能在体外受精胎儿失败中起作用。进一步的大样本量SULF1 snp研究可能有助于支持这一说法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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SULF 1 gene polymorphism, rs6990375 is in significant association with fetus failure in IVF technique.

Background: Sulfatase 1 (SULF1) function is to remove the 6-O-sulphate group from heparan sulfate. This action changes the binding sites of extracellular growth factors. SULF1 expression has been reported to be changed in angiogenesis. We hypothesized that single nucleotide polymorphisms (SNPs) of SULF1 would impact clinicopathologic characteristics.

Objective: Study of SULF1 gene polymorphism with fetus failure in in vitro fertilization (IVF) technique.

Materials and methods: We studied one common (minor allele frequency >0.05) regulatory SNP, rs6990375, with polymerase chain reaction and restriction fragment length polymorphism method, in 53 infertile women with fetus failure in IVF technique and 53 women with at least one healthy child as controls.

Results: We found that rs6990375 is significantly associated with an early failure in IVF and frequency of G allele is high in women with fetus failure in IVF technique (p<0.001).

Conclusion: These findings suggest that SULF1genetic variations may play a role in IVF technique fetus failure. Further studies with large sample sizes on SULF1 SNPs may be useful in support of this claim.

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6-12 weeks
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