Lack of Association Between Primary Angle-Closure Glaucoma Susceptibility Loci and the Ocular Biometric Parameters Anterior Chamber Depth and Axial Length

被引:19
作者
Nongpiur, Monisha E. [1 ]
Wei, Xin [1 ,2 ]
Xu, Liang [3 ]
Perera, Shamira A. [1 ]
Wu, Ren-Yi [1 ]
Zheng, Yingfeng [1 ]
Li, Yang [3 ]
Wang, Ya-Xing [3 ]
Cheng, Ching-Yu [1 ,4 ,5 ]
Jonas, Jost B. [6 ]
Wong, Tien-Yin [1 ,4 ,5 ]
Vithana, Eranga N. [1 ,4 ]
Aung, Tin [1 ,4 ]
Khor, Chiea-Chuen [1 ,4 ,5 ,7 ,8 ]
机构
[1] Singapore Eye Res Inst, Singapore, Singapore
[2] Natl Univ Singapore, Duke Univ, Grad Sch Med, Singapore 117548, Singapore
[3] Capital Univ Med Sci, Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing, Peoples R China
[4] Natl Univ Singapore, Natl Univ Hlth Syst, Yong Loo Lin Sch Med, Dept Ophthalmol, Singapore 117595, Singapore
[5] Natl Univ Singapore, Saw Swee Hock Sch Publ Hlth, Singapore 117548, Singapore
[6] Heidelberg Univ, Med Fac Mannheim, Dept Ophthalmol, Heidelberg, Germany
[7] Genome Inst Singapore, Singapore, Singapore
[8] Natl Univ Singapore, Yong Loo Lin Sch Med, Natl Univ Hlth Syst, Dept Paediat, Singapore 117595, Singapore
基金
英国医学研究理事会;
关键词
genetic; association; glaucoma; quantitative trait; anterior segment OCT; CENTRAL CORNEAL THICKNESS; GENOME-WIDE ASSOCIATION; EYE DISEASES; RISK-FACTOR; POPULATION; SINGAPORE; AREA; EPIDEMIOLOGY; DETERMINANTS; METHODOLOGY;
D O I
10.1167/iovs.13-11901
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. Three susceptibility loci for primary angle-closure glaucoma (PACG) were recently identified: PLEKHA7 rs11024102, COL11A1 rs3753841, and rs1015213 located in the intergenic region between PCMTD1 and ST18. The purpose of this study was to investigate the associations of these loci with the ocular biometric parameters anterior chamber depth (ACD) and axial length (AL). METHODS. Genotype and ocular biometric data were available for four population-based studies, including three from Singapore (Singapore Chinese Eye Study, Singapore Malay Eye Study, and Singapore Indian Eye Study) and one from China (Beijing Eye Study), exceeding 7000 participants. ACD and AL were measured using the IOLMaster for the Singapore cohorts and optical low-coherence reflectometry (Lenstar 900 Optical Biometer) for the Beijing cohort. Five readings were obtained for each participant and the average was computed. Analysis excluded any eye that was pseudophakic or aphakic. RESULTS. ACD measurements and genotype data of the three loci were available for 7245, 7243, and 7239 subjects, respectively. We noted nominal evidence of association between single nucleotide polymorphism (SNP) rs1015213 (PCMTD1-ST18) and a shallower ACD when all data were meta-analyzed (beta = -0.033, P = 0.021). When multiple testing was considered, the observation was nonsignificant. There was no association between ACD and rs11024102 (PLEKHA7) or rs3753841 (COL11A1). We did not observe significant associations between AL and any of the three SNPs. CONCLUSIONS. The lack of association between the PACG susceptibility loci with ACD or AL suggests that predilection to PACG may be mediated by factors other than shallow anterior chamber or short eyeball length.
引用
收藏
页码:5824 / 5828
页数:5
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