Suh Wool, Won Hong-Hee, Kee Changwon
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.
Curr Eye Res. 2018 Apr;43(4):534-538. doi: 10.1080/02713683.2017.1410177. Epub 2017 Dec 4.
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.
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.
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).
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.
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。
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。
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)。
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。