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与晚期子宫内膜异位症相关的基质金属蛋白酶-9基因单倍型分析

Haplotype analysis of the matrix metalloproteinase-9 gene associated with advanced-stage endometriosis.

作者信息

Han You Jung, Kim Han-Na, Yoon Jin-Kook, Yi Sun Young, Moon Hye-Sung, Ahn Jung Ja, Kim Hyung-Lae, Chung Hye Won

机构信息

Department of Obstetrics and Gynecology, School of Medicine, Ewha Womans University, Seoul, South Korea.

出版信息

Fertil Steril. 2009 Jun;91(6):2324-30. doi: 10.1016/j.fertnstert.2008.03.047. Epub 2008 Jun 12.

Abstract

OBJECTIVE

To investigate whether the -1562C>T, R279Q, P574R, and R668Q polymorphisms of the matrix metalloproteinase-9 (MMP-9) gene are related to endometriosis.

DESIGN

Case-control study.

SETTING

University-based hospital in Korea.

PATIENT(S): Patients with endometriosis stage III/IV (n = 225) who underwent pelvic surgery and controls (n = 198) with no endometriosis in a Korean population.

INTERVENTION(S): Peripheral blood samples were collected by venipuncture.

MAIN OUTCOME MEASURE(S): Frequencies of genotypes and haplotypes were compared with the risk of endometriosis including -1562C>T, R279Q, P574R, and R668Q polymorphisms of MMP-9.

RESULT(S): In the two-locus haplotype analyses using the four single nucleotide polymorphisms (SNPs), an increase in the distribution of the R279Q/P574R (2678G>A/4859C>G) (AC haplotype: odds ratio [OR] = 3.180, 95% confidence interval [CI] = 1.956-5.170; GG haplotype: OR = 4.374, 95% CI = 2.376-8.053) and -1562C>T/R668Q (-1562C>T/5546G>A) (CA haplotype: OR = 3.280, 95% CI = 1.406-7.653) haplotypes was significantly associated with endometriosis. By contrast, the risk of endometriosis was not associated with the individual SNPs studied.

CONCLUSION(S): These findings suggest that haplotype analysis was more informative than SNP analysis. The haplotypes in the MMP-9 gene may correlate with the progression of endometriosis, and further study of these variations might improve our understanding of the pathogenesis of endometriosis.

摘要

目的

研究基质金属蛋白酶-9(MMP-9)基因的-1562C>T、R279Q、P574R和R668Q多态性是否与子宫内膜异位症相关。

设计

病例对照研究。

地点

韩国一家大学附属医院。

患者

韩国人群中接受盆腔手术的III/IV期子宫内膜异位症患者(n = 225)和无子宫内膜异位症的对照组(n = 198)。

干预措施

通过静脉穿刺采集外周血样本。

主要观察指标

比较包括MMP-9基因的-1562C>T、R279Q、P574R和R668Q多态性在内的基因型和单倍型频率与子宫内膜异位症风险的关系。

结果

在使用四个单核苷酸多态性(SNP)进行的两位点单倍型分析中,R279Q/P574R(2678G>A/4859C>G)(AC单倍型:比值比[OR]=3.180,95%置信区间[CI]=1.956 - 5.170;GG单倍型:OR = 4.374,95% CI = 2.376 - 8.053)和-1562C>T/R668Q(-1562C>T/5546G>A)(CA单倍型:OR = 3.280,95% CI = 1.406 - 7.653)单倍型分布的增加与子宫内膜异位症显著相关。相比之下,子宫内膜异位症风险与所研究的单个SNP无关。

结论

这些发现表明单倍型分析比SNP分析提供的信息更多。MMP-9基因中的单倍型可能与子宫内膜异位症的进展相关,对这些变异的进一步研究可能会增进我们对子宫内膜异位症发病机制的理解。

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