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基质金属蛋白酶-9基因单核苷酸多态性与正常眼压性青光眼和原发性开角型青光眼的关联

The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma.

作者信息

Suh Wool, Won Hong-Hee, Kee Changwon

机构信息

a Department of Ophthalmology , Hallym University Dongtan Sacred Heart Hospital, Hallym University College of Medicine , Hwaseong , Gyeonggido , Korea.

b Samsung Advanced Institute for Health Sciences and Technology (SAIHST), Sungkyunkwan University, Samsung Medical Center , Seoul , Korea.

出版信息

Curr Eye Res. 2018 Apr;43(4):534-538. doi: 10.1080/02713683.2017.1410177. Epub 2017 Dec 4.

Abstract

PURPOSE

To evaluate the association of matrix metalloproteinases (MMP)-9 gene polymorphisms with normal tension glaucoma (NTG) and primary open-angle glaucoma (POAG) in the South Korean population.

MATERIALS AND METHODS

A total of 700 South Korean subjects were recruited: 146 patients with NTG, 174 patients with POAG, and 380 healthy adults. Five single-nucleotide polymorphisms (SNPs; rs3918429, rs2274755, rs3787268, rs3918261, and rs3918270) of MMP-9 were analyzed in all subjects. The association with each disease was tested using an allelic χ test and p values were corrected by permutation tests with 100 000 permutations.

RESULTS

Among the five SNPs, rs2274755 showed a significant association with NTG (p = 0.021). The T allele of rs2274755 had an allelic odds ratio of 1.67 (95% confidence interval, 1.12-2.50). The association remained significant after correction using permutation tests (p = 0.039). It was also significant in an association analysis for genotype frequency (p = 0.011). The SNP was predicted to be found within a splicing site and a conserved region. No SNPs analyzed were significantly associated with POAG (p > 0.05).

CONCLUSIONS

The rs2274755 SNP in the MMP-9 gene was significantly associated with NTG. This supports a possible role of the MMP-9 gene in NTG pathogenesis.

摘要

目的

评估基质金属蛋白酶(MMP)-9基因多态性与韩国人群正常眼压性青光眼(NTG)和原发性开角型青光眼(POAG)的相关性。

材料与方法

共招募700名韩国受试者:146例NTG患者、174例POAG患者和380名健康成年人。对所有受试者分析MMP-9的5个单核苷酸多态性(SNP;rs3918429、rs2274755、rs3787268、rs3918261和rs3918270)。使用等位基因χ检验检测与每种疾病的相关性,并通过100000次排列的排列检验校正p值。

结果

在这5个SNP中,rs2274755与NTG显示出显著相关性(p = 0.021)。rs2274755的T等位基因的等位基因优势比为1.67(95%置信区间,1.12 - 2.50)。使用排列检验校正后,该相关性仍然显著(p = 0.039)。在基因型频率的关联分析中也显著(p = 0.011)。该SNP预计位于剪接位点和保守区域内。分析的任何SNP与POAG均无显著相关性(p > 0.05)。

结论

MMP-9基因中的rs2274755 SNP与NTG显著相关。这支持了MMP-9基因在NTG发病机制中可能发挥的作用。

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