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A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population

PURPOSE: Vertical cup-disc ratio (VCDR) is used as a clinical assessment measure to identify and monitor glaucomatous damage to the optic nerve. Previous genetic studies conducted in European and Asian populations have identified many loci associated with VCDR. The genetic factors in other ethnic po...

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Autores principales: Nannini, Drew R., Torres, Mina, Chen, Yii-Der I., Taylor, Kent D., Rotter, Jerome I., Varma, Rohit, Gao, Xiaoyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5231910/
https://www.ncbi.nlm.nih.gov/pubmed/28061514
http://dx.doi.org/10.1167/iovs.16-19891
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author Nannini, Drew R.
Torres, Mina
Chen, Yii-Der I.
Taylor, Kent D.
Rotter, Jerome I.
Varma, Rohit
Gao, Xiaoyi
author_facet Nannini, Drew R.
Torres, Mina
Chen, Yii-Der I.
Taylor, Kent D.
Rotter, Jerome I.
Varma, Rohit
Gao, Xiaoyi
author_sort Nannini, Drew R.
collection PubMed
description PURPOSE: Vertical cup-disc ratio (VCDR) is used as a clinical assessment measure to identify and monitor glaucomatous damage to the optic nerve. Previous genetic studies conducted in European and Asian populations have identified many loci associated with VCDR. The genetic factors in other ethnic populations, such as Latino, influencing VCDR remain to be determined. Here, we describe the first genome-wide association study (GWAS) on VCDR in Latino individuals. METHODS: We conducted this GWAS on VCDR using 4537 Latino individuals who were genotyped by using either the Illumina OmniExpress BeadChip (∼730K markers) or the Illumina Hispanic/SOL BeadChip (∼2.5 million markers). Study subjects were 40 years of age and older. Linear regression, adjusting for age, sex, and principal components of genetic ancestry, was conducted to assess the associations between single nucleotide polymorphisms (SNPs) and VCDR. We imputed SNPs from the 1000 Genomes Project to integrate additional SNPs not directly genotyped. RESULTS: We replicated two previously reported SNPs that reached GWAS significance, rs1900005 and rs7916697, in the ATOH7-PBLD region, as well as identified two suggestive associations in the CDC7-TGFBR3 region on chromosome 1p22.1 and in the ZNF770-DPH6 region on chromosome 15q14. We discovered a novel SNP, rs56238729 (P = 1.22 × 10(−13)), in the ATOH7-PBLD region that is significantly associated with VCDR in Latino individuals. We replicated eight previously reported regions, including COL8A1, CDKN2B-CDKN2BAS, BMP2, and CHEK2 (P < 2.17 × 10(−3)). CONCLUSIONS: Our results discovered a novel SNP that is significantly associated with VCDR in Latino individuals and confirmed previously reported loci, providing further insight into the genetic architecture of VCDR.
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spelling pubmed-52319102017-01-13 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population Nannini, Drew R. Torres, Mina Chen, Yii-Der I. Taylor, Kent D. Rotter, Jerome I. Varma, Rohit Gao, Xiaoyi Invest Ophthalmol Vis Sci Genetics PURPOSE: Vertical cup-disc ratio (VCDR) is used as a clinical assessment measure to identify and monitor glaucomatous damage to the optic nerve. Previous genetic studies conducted in European and Asian populations have identified many loci associated with VCDR. The genetic factors in other ethnic populations, such as Latino, influencing VCDR remain to be determined. Here, we describe the first genome-wide association study (GWAS) on VCDR in Latino individuals. METHODS: We conducted this GWAS on VCDR using 4537 Latino individuals who were genotyped by using either the Illumina OmniExpress BeadChip (∼730K markers) or the Illumina Hispanic/SOL BeadChip (∼2.5 million markers). Study subjects were 40 years of age and older. Linear regression, adjusting for age, sex, and principal components of genetic ancestry, was conducted to assess the associations between single nucleotide polymorphisms (SNPs) and VCDR. We imputed SNPs from the 1000 Genomes Project to integrate additional SNPs not directly genotyped. RESULTS: We replicated two previously reported SNPs that reached GWAS significance, rs1900005 and rs7916697, in the ATOH7-PBLD region, as well as identified two suggestive associations in the CDC7-TGFBR3 region on chromosome 1p22.1 and in the ZNF770-DPH6 region on chromosome 15q14. We discovered a novel SNP, rs56238729 (P = 1.22 × 10(−13)), in the ATOH7-PBLD region that is significantly associated with VCDR in Latino individuals. We replicated eight previously reported regions, including COL8A1, CDKN2B-CDKN2BAS, BMP2, and CHEK2 (P < 2.17 × 10(−3)). CONCLUSIONS: Our results discovered a novel SNP that is significantly associated with VCDR in Latino individuals and confirmed previously reported loci, providing further insight into the genetic architecture of VCDR. The Association for Research in Vision and Ophthalmology 2017-01 /pmc/articles/PMC5231910/ /pubmed/28061514 http://dx.doi.org/10.1167/iovs.16-19891 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Genetics
Nannini, Drew R.
Torres, Mina
Chen, Yii-Der I.
Taylor, Kent D.
Rotter, Jerome I.
Varma, Rohit
Gao, Xiaoyi
A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
title A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
title_full A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
title_fullStr A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
title_full_unstemmed A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
title_short A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
title_sort genome-wide association study of vertical cup-disc ratio in a latino population
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5231910/
https://www.ncbi.nlm.nih.gov/pubmed/28061514
http://dx.doi.org/10.1167/iovs.16-19891
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