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Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.
Document Type
article
Author
Genetics of Glaucoma in People of African Descent (GGLAD) ConsortiumHauser, Michael AAllingham, R RandAung, TinVan Der Heide, Carly JTaylor, Kent DRotter, Jerome IWang, Shih-Hsiu JBonnemaijer, Pieter WMWilliams, Susan EAbdullahi, Sadiq MAbu-Amero, Khaled KAnderson, Michael GAkafo, StephenAlhassan, Mahmoud BAsimadu, IfeomaAyyagari, RadhaBakayoko, SaydouNyamsi, Prisca BiangoupBowden, Donald WBromley, William CBudenz, Donald LCarmichael, Trevor RChalla, PratapChen, Yii-Der IdaChuka-Okosa, Chimdi MCooke Bailey, Jessica NCosta, Vital PaulinoCruz, Dianne ADuBiner, HarveyErvin, John FFeldman, Robert MFlamme-Wiese, MilesGaasterland, Douglas EGarnai, Sarah JGirkin, Christopher AGuirou, NouhoumGuo, XiuqingHaines, Jonathan LHammond, Christopher JHerndon, LeonHoffmann, Thomas JHulette, Christine MHydara, AbbaIgo, Robert PJorgenson, EricKabwe, JoyceKilangalanga, Ngoy JanvierKizor-Akaraiwe, NkiruKuchtey, Rachel WLamari, HasnaaLi, ZhengLiebmann, Jeffrey MLiu, YutaoLoos, Ruth JFMelo, Monica BMoroi, Sayoko EMsosa, Joseph MMullins, Robert FNadkarni, GirishNapo, AbdoulayeNg, Maggie CYNunes, Hugo FreireObeng-Nyarkoh, EbenezerOkeke, AnthonyOkeke, SuhanyaOlaniyi, OlusegunOlawoye, OlusolaOliveira, Mariana BorgesPasquale, Louise RPerez-Grossmann, Rodolfo APericak-Vance, Margaret AQin, XueRamsay, MicheleResnikoff, SergeRichards, Julia ESchimiti, Rui BarrosoSim, Kar SengSponsel, William ESvidnicki, Paulo ViniciusThiadens, Alberta AHJUche, Nkechinyere Jvan Duijn, Cornelia Mde Vasconcellos, José Paulo CabralWiggs, Janey LZangwill, Linda MRisch, NeilMilea, DanAshaye, AdeyinkaKlaver, Caroline CWWeinreb, Robert NAshley Koch, Allison EFingert, John HKhor, Chiea Chuen
Source
JAMA. 322(17)
Subject
Genetics of Glaucoma in People of African Descent (GGLAD) Consortium
Humans
Glaucoma
Open-Angle
Genetic Predisposition to Disease
Adaptor Proteins
Signal Transducing
Immunohistochemistry
Risk Factors
Case-Control Studies
Genotype
Polymorphism
Single Nucleotide
Aged
Middle Aged
African Continental Ancestry Group
Female
Male
Meta-Analysis as Topic
Genome-Wide Association Study
Amyloid beta-Peptides
Eye Disease and Disorders of Vision
Clinical Research
Human Genome
Aging
Neurodegenerative
Genetics
Neurosciences
2.1 Biological and endogenous factors
General & Internal Medicine
Medical and Health Sciences
Language
Abstract
Importance:Primary open-angle glaucoma presents with increased prevalence and a higher degree of clinical severity in populations of African ancestry compared with European or Asian ancestry. Despite this, individuals of African ancestry remain understudied in genomic research for blinding disorders. Objectives:To perform a genome-wide association study (GWAS) of African ancestry populations and evaluate potential mechanisms of pathogenesis for loci associated with primary open-angle glaucoma. Design, Settings, and Participants:A 2-stage GWAS with a discovery data set of 2320 individuals with primary open-angle glaucoma and 2121 control individuals without primary open-angle glaucoma. The validation stage included an additional 6937 affected individuals and 14 917 unaffected individuals using multicenter clinic- and population-based participant recruitment approaches. Study participants were recruited from Ghana, Nigeria, South Africa, the United States, Tanzania, Britain, Cameroon, Saudi Arabia, Brazil, the Democratic Republic of the Congo, Morocco, Peru, and Mali from 2003 to 2018. Individuals with primary open-angle glaucoma had open iridocorneal angles and displayed glaucomatous optic neuropathy with visual field defects. Elevated intraocular pressure was not included in the case definition. Control individuals had no elevated intraocular pressure and no signs of glaucoma. Exposures:Genetic variants associated with primary open-angle glaucoma. Main Outcomes and Measures:Presence of primary open-angle glaucoma. Genome-wide significance was defined as P C) with primary open-angle glaucoma (odds ratio [OR], 1.32 [95% CI, 1.20-1.46]; P = 2 × 10-8). The association was validated in an analysis of an additional 6937 affected individuals and 14 917 unaffected individuals (OR, 1.15 [95% CI, 1.09-1.21]; P