Cheng Ching-Yu, Allingham R Rand, Aung Tin, Tham Yih-Chung, Hauser Michael A, Vithana Eranga N, Khor Chiea Chuen, Wong Tien Yin
Singapore Eye Research Institute, Singapore National Eye Centre, Singapore.
Department of Ophthalmology, Duke University Medical Center, Durham, North Carolina, United States.
Invest Ophthalmol Vis Sci. 2014 Dec 23;56(1):478-83. doi: 10.1167/iovs.14-15863.
Recently the common SIX6 missense variant rs33912345 was found to be highly associated with glaucoma. The aim of this study was to investigate the association between this SIX6 variant and peripapillary retinal nerve fiber layer (RNFL) thickness measured by spectral-domain optical coherence tomography (SD-OCT) in a population setting.
Study subjects were enrolled from the Singapore Chinese Eye Study (SCES), a population-based survey of Singaporean Chinese aged 40 years or older. Subjects underwent a comprehensive ocular examination. Spectral-domain OCT was used to measure RNFL thicknesses. Genotyping of SIX6 rs33912345 (Asn141His) was performed using HumanExome BeadChip.
A total of 2129 eyes from 1243 SCES subjects (mean age: 55.0 ± 7.4 years) with rs33912345 genotype data and SD-OCT images were included for the analysis. Of these, 26 eyes of 21 subjects had glaucoma. The frequency of rs33912345 risk variant C (His141) was 80% in the study subjects. Each rs33912345 C allele was associated with a decrease of 1.44 μm in RNFL thickness after adjusting for age, sex, genetic principal components, and axial length (P = 0.001). These associations remained similar in 2096 nonglaucoma eyes in which each C allele was associated with a decrease of 1.39 μm in RNFL thickness (P = 0.001). The strongest association was observed in the superior RNFL sector (a decrease of 2.83 μm per risk allele, P < 0.001) followed by the inferior RNFL sector (a decrease of 2.24 μm per risk allele, P = 0.003), while the association did not reach significance in the nasal and temporal sectors.
Nonglaucomatous individuals with the SIX6 missense variant have reduced RNFL thickness in regions known to be particularly affected in those with glaucoma. This may be the primary mechanism for increased risk of POAG in individuals who carry the SIX6 His141 risk variant.
最近发现常见的SIX6错义变体rs33912345与青光眼高度相关。本研究的目的是在人群中研究该SIX6变体与通过光谱域光学相干断层扫描(SD-OCT)测量的视乳头周围视网膜神经纤维层(RNFL)厚度之间的关联。
研究对象来自新加坡华人眼研究(SCES),这是一项针对40岁及以上新加坡华人的基于人群的调查。受试者接受了全面的眼部检查。使用光谱域OCT测量RNFL厚度。使用人类外显子芯片对SIX6 rs33912345(Asn141His)进行基因分型。
共有来自1243名SCES受试者(平均年龄:55.0±7.4岁)的2129只眼睛具有rs33912345基因型数据和SD-OCT图像用于分析。其中,21名受试者的26只眼睛患有青光眼。研究对象中rs33912345风险变体C(His141)的频率为80%。在调整年龄、性别、遗传主成分和眼轴长度后,每个rs33912345 C等位基因与RNFL厚度减少1.44μm相关(P = 0.001)。在2096只非青光眼眼中,这些关联仍然相似,其中每个C等位基因与RNFL厚度减少1.39μm相关(P = 0.001)。在上半RNFL区域观察到最强的关联(每个风险等位基因减少2.83μm,P < 0.001),其次是下半RNFL区域(每个风险等位基因减少2.24μm,P = 0.003),而在鼻侧和颞侧区域的关联未达到显著水平。
携带SIX6错义变体的非青光眼个体在已知青光眼患者中特别受影响的区域RNFL厚度降低。这可能是携带SIX6 His141风险变体的个体患原发性开角型青光眼风险增加的主要机制。