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[基质金属蛋白酶-1和基质金属蛋白酶-3基因编码多态性与盆腔器官脱垂及压力性尿失禁发生风险]

[MMP-1 and MMP-3 gene encoding polymorphism and the risk of the development of pelvic organ prolapse and stress urinary incontinence].

作者信息

Skorupski Paweł, Miotła Paweł, Jankiewicz Katarzyna, Rechberger Tomasz

机构信息

II Klinika Ginekologii Operacyjnej UM w Lublinie.

出版信息

Ginekol Pol. 2010 Aug;81(8):594-9.

Abstract

OBJECTIVES

The estimation of the association between the polymorphism at position -1607/1608 of the gene promoter encoding matrix metalloproteinase type 1 (MMP- 1) and the polymorphism at position -1612/1617 of the gene promoter encoding stromelysin type 1 (MMP-3) and the risk of the occurrence of pelvic organ prolapse (POP) and stress urinary incontinence (SUI).

MATERIAL AND METHODS

347 women were included into the analysis. POP study: the study group consisted of patients with clinically significant POP (POP-Q scale: 2, 3, 4). Women with normal pelvic floor statics (POP-Q scale: 0, 1) and not reporting symptoms of urinary incontinence were included into the control group. SUI study: the study group--patients with symptoms of stress urinary incontinence, the control group--continent women with normal pelvic floor statics (POP-Q scale: 0, 1). Samples of DNA were isolated from whole blood. The type of polymorphism was detected by RFLP method.

RESULTS

Both, in the POP and the SUI study we have observed no statistically significant differences in the occurrences of MMP-1 and MMP-3 promoter polymorphisms between the study and the control groups. Also, the presence of the alleles G/GG (MMP-1) or 5A/6A (MMP-3) did not modify the risk of the POP and SUI development.

CONCLUSIONS

Polymorphism type G/GG of gene promoter encoding MMP-1 and polymorphism type 5A/6A of the gene promoter encoding MMP-3 are not associated with the risk of the development of POP and SUI.

摘要

目的

评估编码基质金属蛋白酶1(MMP-1)的基因启动子-1607/1608位点多态性与编码基质金属蛋白酶3(MMP-3)的基因启动子-1612/1617位点多态性之间的关联,以及盆腔器官脱垂(POP)和压力性尿失禁(SUI)的发生风险。

材料与方法

347名女性纳入分析。POP研究:研究组由具有临床显著意义的POP患者组成(POP-Q量表:2、3、4)。盆底静息状态正常(POP-Q量表:0、1)且未报告尿失禁症状的女性纳入对照组。SUI研究:研究组为有压力性尿失禁症状的患者,对照组为盆底静息状态正常的无尿失禁女性(POP-Q量表:0、1)。从全血中分离DNA样本。采用限制性片段长度多态性(RFLP)方法检测多态性类型。

结果

在POP和SUI研究中,我们均未观察到研究组与对照组之间MMP-1和MMP-3启动子多态性发生率存在统计学显著差异。此外,等位基因G/GG(MMP-1)或5A/6A(MMP-3)的存在并未改变POP和SUI发生的风险。

结论

编码MMP-1的基因启动子G/GG多态性类型和编码MMP-3的基因启动子5A/6A多态性类型与POP和SUI的发生风险无关。

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