Department of Ophthalmology, Uijeongbu St. Mary's Hospital, College of Medicine, the Catholic University of Korea, Seoul, Republic of Korea.
J Glaucoma. 2022 Sep 1;31(9):763-766. doi: 10.1097/IJG.0000000000002060. Epub 2022 Jun 3.
We demonstrated that SIX1/SIX6 locus polymorphism (rs10483727 and rs33912345) was significantly associated with a genetic susceptibility to NTG in a Korean population. More studies are needed to investigate whether the SIX1/SIX6 locus is associated with NTG among various ethnic populations.
Several previous studies have reported that the relevance of the SIX1/SIX6 locus to open angle glaucoma (OAG) in various ethnic populations. However, definitions of OAG patients were different among those studies. The relevance of the SIX1/SIX6 locus to normal tension glaucoma (NTG) in a Korean population remains uncertain. Therefore, the purpose of this study was to investigate the relationship of the SIX1/SIX6 locus with NTG in a Korean cohort.
Patients with NTG and ethnically matched healthy controls were recruited from eye clinics in Korea (210 cases and 117 controls). Four polymorphisms (rs33912345, rs12436579, rs2179970, and rs10483727) of the SIX1/SIX6 locus were genotyped for 327 subjects using a TaqMan single nucleotide polymorphism genotyping assay.
The rs33912345 polymorphism was significantly correlated with NTG in the recessive model [odds ratio (OR): 0.265; 95% confidence interval (CI): 0.078-0.898, P =0.033], but not in the allelic and dominant models (both P >0.05). The SNP rs10483727 was significantly associated with NTG in the allelic model (OR: 0.674; 95% CI: 0.464-0.979, P =0.038) and the recessive model (OR: 0.187; 95% CI: 0.058-0.602, P =0.005). Genetic association analysis of SNP rs12436579 and rs2179970 revealed no significant difference in genotype distribution between NTG cases and controls in the allelic, dominant, or recessive models (all P >0.05).
The current study found that SIX1-SIX6 locus rs10483727 and rs33912345 polymorphisms were significantly associated with NTG risk in the Korean population.
我们证明了 SIX1/SIX6 基因座多态性(rs10483727 和 rs33912345)与韩国人群中 NTG 的遗传易感性显著相关。需要更多的研究来探讨 SIX1/SIX6 基因座是否与不同种族人群中的 NTG 相关。
几项先前的研究报告称,SIX1/SIX6 基因座与各种种族人群中的开角型青光眼(OAG)相关。然而,这些研究中 OAG 患者的定义不同。SIX1/SIX6 基因座与韩国人群中正常眼压性青光眼(NTG)的相关性仍不确定。因此,本研究的目的是在韩国队列中研究 SIX1/SIX6 基因座与 NTG 的关系。
从韩国的眼科诊所招募 NTG 患者和种族匹配的健康对照者(210 例病例和 117 例对照)。使用 TaqMan 单核苷酸多态性基因分型检测对 327 名受试者的 SIX1/SIX6 基因座的 4 个多态性(rs33912345、rs12436579、rs2179970 和 rs10483727)进行基因分型。
rs33912345 多态性在隐性模型中与 NTG 显著相关[比值比(OR):0.265;95%置信区间(CI):0.078-0.898,P=0.033],但在等位基因和显性模型中均无显著相关性(均 P>0.05)。SNP rs10483727 与 NTG 在等位基因模型(OR:0.674;95%CI:0.464-0.979,P=0.038)和隐性模型(OR:0.187;95%CI:0.058-0.602,P=0.005)中显著相关。SNP rs12436579 和 rs2179970 的遗传关联分析显示,NTG 病例和对照组在等位基因、显性或隐性模型中的基因型分布无显著差异(均 P>0.05)。
本研究发现 SIX1-SIX6 基因座 rs10483727 和 rs33912345 多态性与韩国人群中 NTG 风险显著相关。