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基质金属蛋白酶 1、2、3 和 9 的功能性单核苷酸多态性与特发性复发性自然流产的关系。

Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion.

机构信息

Department of Biology and Medical Genetics, Faculty of Medicine, University of Rijeka, B. Branchetta 20, 51000 Rijeka, Croatia.

出版信息

Reprod Biomed Online. 2012 May;24(5):567-75. doi: 10.1016/j.rbmo.2012.01.008. Epub 2012 Jan 24.

Abstract

Idiopathic recurrent spontaneous abortion (IRSA) has been associated with abnormalities in the remodelling of endometrial extracellular matrix, as well as aberrant matrix metalloproteinase (MMP) gene expression in endometrium of IRSA women and chorionic villi of IRSA concept. This study investigated the association of five functional MMP gene promoter polymorphisms (MMP1 -1607 1G/2G, MMP2 -735 C/T, MMP2 -1306 C/T, MMP3 -1612 5A/6A and MMP9 -1562 C/T) with IRSA. A total of 149 couples with at least three consecutive IRSA and 149 fertile couples were included in a case-control study. Genotype analysis was performed using PCR restriction fragment length polymorphism. Statistically significant differences were found in distributions of MMP2 -735 CT (chi-squared 10.21, P=0.006; OR 2.15, 95% CI 1.34-3.45, P=0.001), and MMP9 -1562 CC (chi-squared 9.06, P=0.010; OR 2.21, 95% CI 1.30-3.80, P=0.004) between IRSA women and controls. Combined analysis of MMP gene polymorphisms did not increase their predictive value. There were no statistically significant differences in genotype and allele frequencies of any polymorphism between IRSA men and controls. MMP2 -735 C/T and MMP9 -1562 C/T functional gene polymorphisms might be associated with an increased risk of IRSA in women. Considering the insufficient knowledge on genetic contribution to pregnancy loss, studies on genetic causes of idiopathic recurrent spontaneous abortion (IRSA) are of great importance. Development of a histologically and functionally normal endometrium is critical for subsequent endometrial decidualization, receptivity and implantation. The proper communication and interaction between maternal decidual cells and the embryo is essential for the establishment of a functional fetal-maternal interface. IRSA has been associated with abnormalities in the remodelling of endometrial extracellular matrix, as well as aberrant matrix metalloproteinase (MMP) gene expression in endometrium of IRSA women and chorionic villi of IRSA concepti. The aim of this study was to investigate the association of five functional MMP gene promoter polymorphisms with IRSA. A total of 149 couples with at least three consecutive IRSA and 149 fertile couples were included in a case-control study. Genotype analysis was performed using polymerase chain reaction and restriction fragment length polymorphism. Statistically significant differences were found in distribution of MMP2 -735 CT and MMP9 -1562 CC genotypes between IRSA and control women. Combined analysis of MMP gene polymorphisms did not increase their predictive value. There were no statistically significant differences in distribution of genotype and allele frequencies of any polymorphism between IRSA men and controls. Our results demonstrate that MMP2 -735 C/T and MMP9 -1562 C/T functional gene polymorphisms might be associated with an increased risk of IRSA in women.

摘要

特发性复发性流产(IRSA)与子宫内膜细胞外基质重塑异常以及 IRSA 女性子宫内膜和 IRSA 概念绒毛组织中基质金属蛋白酶(MMP)基因表达异常有关。本研究探讨了五个功能性 MMP 基因启动子多态性(MMP1-1607 1G/2G、MMP2-735C/T、MMP2-1306C/T、MMP3-16125A/6A 和 MMP9-1562C/T)与 IRSA 的关联。共有 149 对至少连续发生三次 IRSA 的夫妇和 149 对生育能力正常的夫妇纳入病例对照研究。采用 PCR 限制性片段长度多态性分析基因型。MMP2-735CT(卡方 10.21,P=0.006;OR2.15,95%CI1.34-3.45,P=0.001)和 MMP9-1562CC(卡方 9.06,P=0.010;OR2.21,95%CI1.30-3.80,P=0.004)在 IRSA 女性和对照组之间的分布存在统计学显著差异。MMP 基因多态性的联合分析并未增加其预测价值。IRSA 男性和对照组之间任何多态性的基因型和等位基因频率均无统计学显著差异。MMP2-735C/T 和 MMP9-1562C/T 功能性基因多态性可能与女性 IRSA 风险增加相关。考虑到遗传因素对妊娠丢失的认识不足,研究特发性复发性流产(IRSA)的遗传原因非常重要。发育出具有组织学和功能正常的子宫内膜对于随后的子宫内膜蜕膜化、容受性和着床至关重要。母体蜕膜细胞与胚胎之间的适当沟通和相互作用对于建立功能性胎儿-母体界面至关重要。IRSA 与子宫内膜细胞外基质重塑异常以及 IRSA 女性子宫内膜和 IRSA 概念绒毛组织中基质金属蛋白酶(MMP)基因表达异常有关。本研究旨在探讨五个功能性 MMP 基因启动子多态性与 IRSA 的关系。共有 149 对至少连续发生三次 IRSA 的夫妇和 149 对生育能力正常的夫妇纳入病例对照研究。采用聚合酶链反应和限制性片段长度多态性分析进行基因型分析。MMP2-735CT 和 MMP9-1562CC 基因型在 IRSA 女性和对照组之间的分布存在统计学显著差异。MMP 基因多态性的联合分析并未增加其预测价值。IRSA 男性和对照组之间任何多态性的基因型和等位基因频率分布均无统计学显著差异。我们的结果表明,MMP2-735C/T 和 MMP9-1562C/T 功能性基因多态性可能与女性 IRSA 风险增加有关。

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