Department of Obstetrics and Gynecology, Dong-A University School of Medicine, Pusan, South Korea.
Am J Reprod Immunol. 2013 Jan;69(1):73-84. doi: 10.1111/aji.12020. Epub 2012 Sep 17.
To characterize the genetic variation across the MMP-2 and TIMP-2 gene with the risk of advanced-stage endometriosis.
Ten single-nucleotide polymorphisms (SNPs) and haplotype associations between MMP-2 (9082A>G, 9152A>G, 105330C>T, 14931T>C, 15918T>C, 18796G>A, 19033G>A, 19218A>G, 25190A>G, and 28542C>T) and TMIP-2 gene (42138327C>T, 42141169G>A, 42144611A>G, 42152781C>T, 42155855G>A, 42175617C>T, 42181597G>A, 42183387T>C, 42196041G>C, and 42196430T>C) were examined in 201 patients and 183 controls.
In MMP-2, G/A haplotype of 9082A>G and 9152A>G in intron 2 was associated with a reduced risk of endometriosis (OR 0.7, 95% CI 0.5-1.0, P = 0.04). In TIMP-2, the CC genotype of 42196430T>C and C/C haplotype of 42196041G>C/42196430T>C in the promoter region showed an increased risk of endometriosis (OR 3.0, 95% CI 1.2-8.0, P = 0.02; OR 1.6, 95% CI 1.1-2.4, P = 0.02), and the CC genotype of 42183387T>C and the C/G/C haplotype of 42175617C>T/42181597G>A/42183387T>C in intron 1 were associated with a reduced risk (OR 0.5, 95% CI 0.3-0.97, P = 0.04; OR 0.6, 95% CI 0.4-0.95, P = 0.03).
The MMP-2 and TIMP-2 polymorphisms are associated with advanced-stage endometriosis. Especially, the risk of endometriosis was different according to the genetic position in the TIMP-2 gene.
描述基质金属蛋白酶-2(MMP-2)和基质金属蛋白酶抑制剂-2(TIMP-2)基因的遗传变异与晚期子宫内膜异位症的风险之间的关系。
研究分析了 MMP-2(9082A>G、9152A>G、105330C>T、14931T>C、15918T>C、18796G>A、19033G>A、19218A>G、25190A>G 和 28542C>T)和 TIMP-2 基因(42138327C>T、42141169G>A、42144611A>G、42152781C>T、42155855G>A、42175617C>T、42181597G>A、42183387T>C、42196041G>C 和 42196430T>C)中的 10 个单核苷酸多态性(SNP)和单倍型关联,共纳入了 201 名患者和 183 名对照。
在 MMP-2 中,2 号内含子的 9082A>G 和 9152A>G 的 G/A 单倍型与子宫内膜异位症风险降低相关(OR 0.7,95%CI 0.5-1.0,P=0.04)。在 TIMP-2 中,启动子区域的 42196430T>C 的 CC 基因型和 42196041G>C/42196430T>C 的 C/C 单倍型与子宫内膜异位症风险增加相关(OR 3.0,95%CI 1.2-8.0,P=0.02;OR 1.6,95%CI 1.1-2.4,P=0.02),1 号内含子的 42183387T>C 的 CC 基因型和 42175617C>T/42181597G>A/42183387T>C 的 C/G/C 单倍型与子宫内膜异位症风险降低相关(OR 0.5,95%CI 0.3-0.97,P=0.04;OR 0.6,95%CI 0.4-0.95,P=0.03)。
MMP-2 和 TIMP-2 多态性与晚期子宫内膜异位症相关。特别是,TIMP-2 基因中的遗传位置不同,子宫内膜异位症的风险也不同。