Please use this identifier to cite or link to this item: https://doi.org/10.1167/iovs.13-13552
Title: Genotype-phenotype correlation analysis for three primary angle closure glaucoma-associated genetic polymorphisms
Authors: Wei, X.
Nongpiur, M.E.
de Leon, M.S.
Baskaran, M.
Perera, S.A.
How, A.C.
Vithana, E.N.
Khor, C.-C. 
Aung, T.
Keywords: Angle closure glaucoma
Association
Genetics
Single nucleotide polymorphism
Issue Date: 28-Jan-2014
Source: Wei, X., Nongpiur, M.E., de Leon, M.S., Baskaran, M., Perera, S.A., How, A.C., Vithana, E.N., Khor, C.-C., Aung, T. (2014-01-28). Genotype-phenotype correlation analysis for three primary angle closure glaucoma-associated genetic polymorphisms. Investigative Ophthalmology and Visual Science 55 (2) : 1143-1148. ScholarBank@NUS Repository. https://doi.org/10.1167/iovs.13-13552
Abstract: Purpose. Recently, three genetic susceptibility loci for primary angle closure glaucoma (PACG) were identified: COL11A1 rs3753841, PCMTD1-ST18 rs1015213, and PLEKHA7 rs11024102. The purpose of this study was to investigate whether these single nucleotide polymorphisms (SNPs) affect the phenotype of PACG patients. Methods. A retrospective analysis was performed for 700 Singaporean Chinese PACG patients who had been genotyped. The associations between the three SNPs and clinical features related to severity of glaucoma were studied. For a subgroup of patients who had ≥5 years of follow-up and ≥5 reliable visual field (VF) tests, differences in glaucoma progression, as measured by the proportion of VF progression and blindness, were compared among groups with different genotypes. Results. The minor allele frequencies at COL11A1 rs3753841, PCMTD1-ST18 rs1015213, and PLEKHA7 rs11024102 were 36%, 2.1%, and 41.5%, respectively. There were no significant differences in sex, diagnosis (acute primary angle closure [APAC] versus non-APAC), age at diagnosis, laterality of glaucoma, or need for filtration surgery among patients with different genotypes (all P > 0.05). We also found no significant difference between genotypes and the IOP at presentation, and other clinical characteristics at DNA collection (vertical cup-to-disc ratio, best corrected visual acuity, baseline VF mean deviation, or pattern standard deviation). For the subgroup analysis, we did not observe significant associations between VF progression and the proportion of blindness with any of the PACG susceptibility loci. Conclusions. The three genetic susceptibility loci for PACG did not underlie any major phenotypic diversity in terms of disease severity or progression. © 2014 The Association for Research in Vision and Ophthalmology, Inc.
Source Title: Investigative Ophthalmology and Visual Science
URI: http://scholarbank.nus.edu.sg/handle/10635/108947
ISSN: 15525783
DOI: 10.1167/iovs.13-13552
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