NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology.
Department of Public Health & Primary Care, University of Cambridge.
J Glaucoma. 2018 Sep;27(9):743-749. doi: 10.1097/IJG.0000000000001026.
A common missense variant in the SIX6 gene (rs33912345) is strongly associated with primary open-angle glaucoma (POAG). We aimed to examine the association of rs33912345 with optic disc and retinal nerve fiber layer (RNFL) measures in a European population.
We examined participants of the population-based EPIC-Norfolk Eye Study. Participants underwent confocal laser scanning tomography (Heidelberg Retina Tomograph II, HRT) to estimate optic disc rim area and vertical cup-disc ratio (VCDR). Scanning laser polarimetry (GDxVCC) was used to estimate average RNFL thickness. The mean of right and left eye values was considered for each participant. Genotyping was performed using the Affymetrix UK Biobank Axiom Array. Multivariable linear regression with the optic nerve head parameter as outcome variable and dosage of rs33912345 genotype as primary explanatory variable was used, adjusted for age, sex, disc area, axial length, and intraocular pressure. We further repeated analyses stratified into age tertiles.
In total, 5433 participants with HRT data and 3699 participants with GDxVCC data were included. Each "C" allele of rs33912345 was associated with a smaller rim area (-0.030 mm [95% CI -0.040, -0.020]; P=5.4×10), a larger VCDR (0.025 [95% CI 0.017, 0.033]; P=3.3×10) and a thinner RNFL (-0.39 μm [95% CI -0.62, -0.15]; P=0.001). The RNFL association was strongest in the oldest age tertile, whereas rim area and VCDR associations were strongest in the youngest and oldest age tertiles.
The protein-coding SIX6 variant rs33912345, previously associated with POAG, has a functional effect on glaucoma-associated optic nerve head traits in Europeans.
SIX6 基因中的一个常见错义变异(rs33912345)与原发性开角型青光眼(POAG)强烈相关。我们旨在研究 rs33912345 与欧洲人群视盘和视网膜神经纤维层(RNFL)测量值的关联。
我们检查了基于人群的 EPIC-Norfolk 眼部研究的参与者。参与者接受了共焦激光扫描断层扫描(Heidelberg Retina Tomograph II,HRT)以估计视盘边缘区域和垂直杯盘比(VCDR)。扫描激光偏振仪(GDxVCC)用于估计平均 RNFL 厚度。每位参与者的右眼和左眼值的平均值被考虑在内。使用 Affymetrix UK Biobank Axiom 阵列进行基因分型。多变量线性回归,以视盘参数为因变量,以 rs33912345 基因型的剂量为主要解释变量,调整年龄、性别、视盘面积、眼轴长度和眼内压。我们进一步按年龄三分位重复分析。
总共包括 5433 名具有 HRT 数据的参与者和 3699 名具有 GDxVCC 数据的参与者。rs33912345 的每个“C”等位基因与较小的边缘区域(-0.030mm[95%CI-0.040,-0.020];P=5.4×10)、较大的 VCDR(0.025[95%CI0.017,0.033];P=3.3×10)和较薄的 RNFL(-0.39μm[95%CI-0.62,-0.15];P=0.001)相关。RNFL 关联在最年长的年龄三分位组中最强,而边缘区域和 VCDR 关联在最年轻和最年长的年龄三分位组中最强。
先前与 POAG 相关的蛋白质编码 SIX6 变异 rs33912345 对欧洲人青光眼相关视盘头部特征具有功能影响。