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Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry

Authors :
Hauser, M.A.
Allingham, R.R.
Aung, T.
Heide, C.J. Van Der
Taylor, K.D.
Rotter, J.I.
Wang, S.J.
Bonnemaijer, P.W.M.
Williams, S.E.
Abdullahi, S.M.
Abu-Amero, K.K.
Anderson, M.G.
Akafo, S.
Alhassan, M.B.
Asimadu, I.
Ayyagari, R.
Bakayoko, S.
Nyamsi, P.B.
Bowden, D.W.
Bromley, W.C.
Budenz, D.L.
Carmichael, T.R.
Challa, P.
Chen, Yi
Chuka-Okosa, C.M.
Bailey, J.N.
Costa, V.P.
Cruz, Dario
DuBiner, H.
Ervin, J.F.
Feldman, R.M.
Flamme-Wiese, M.
Gaasterland, D.E.
Garnai, S.J.
Girkin, C.A.
Guirou, N.
Guo, X.
Haines, J.L.
Hammond, C.J.
Herndon, L.
Hoffmann, T.J.
Hulette, C.M.
Hydara, A.
Igo, R.P., Jr.
Jorgenson, E.
Kabwe, J.
Kilangalanga, N.J.
Kizor-Akaraiwe, N.
Kuchtey, R.W.
Lamari, H.
Li, Z
Liebmann, J.M.
Liu, Y
Loos, R.J.
Melo, M.B.
Moroi, S.E.
Msosa, J.M.
Mullins, R.F.
Nadkarni, G.
Napo, A.
Ng, M.C.
Nunes, H.F.
Obeng-Nyarkoh, E.
Okeke, A.
Okeke, S.
Olaniyi, O.
Olawoye, O.
Oliveira, M.B.
Pasquale, L.R.
Perez-Grossmann, R.A.
Pericak-Vance, M.A.
Qin, X.
Ramsay, M.
Resnikoff, S.
Richards, J.E.
Schimiti, R.B.
Sim, K.S.
Sponsel, W.E.
Svidnicki, P.V.
Thiadens, A.
Uche, N.J.
Duijn, C.M. van
Vasconcellos, J.P.C. de
Wiggs, J.L.
Zangwill, L.M.
Risch, N.
Milea, D.
Ashaye, A.
Klaver, C.C.W.
Weinreb, R.N.
Koch, A.E.
Fingert, J.H.
Khor, C.C.
Hauser, M.A.
Allingham, R.R.
Aung, T.
Heide, C.J. Van Der
Taylor, K.D.
Rotter, J.I.
Wang, S.J.
Bonnemaijer, P.W.M.
Williams, S.E.
Abdullahi, S.M.
Abu-Amero, K.K.
Anderson, M.G.
Akafo, S.
Alhassan, M.B.
Asimadu, I.
Ayyagari, R.
Bakayoko, S.
Nyamsi, P.B.
Bowden, D.W.
Bromley, W.C.
Budenz, D.L.
Carmichael, T.R.
Challa, P.
Chen, Yi
Chuka-Okosa, C.M.
Bailey, J.N.
Costa, V.P.
Cruz, Dario
DuBiner, H.
Ervin, J.F.
Feldman, R.M.
Flamme-Wiese, M.
Gaasterland, D.E.
Garnai, S.J.
Girkin, C.A.
Guirou, N.
Guo, X.
Haines, J.L.
Hammond, C.J.
Herndon, L.
Hoffmann, T.J.
Hulette, C.M.
Hydara, A.
Igo, R.P., Jr.
Jorgenson, E.
Kabwe, J.
Kilangalanga, N.J.
Kizor-Akaraiwe, N.
Kuchtey, R.W.
Lamari, H.
Li, Z
Liebmann, J.M.
Liu, Y
Loos, R.J.
Melo, M.B.
Moroi, S.E.
Msosa, J.M.
Mullins, R.F.
Nadkarni, G.
Napo, A.
Ng, M.C.
Nunes, H.F.
Obeng-Nyarkoh, E.
Okeke, A.
Okeke, S.
Olaniyi, O.
Olawoye, O.
Oliveira, M.B.
Pasquale, L.R.
Perez-Grossmann, R.A.
Pericak-Vance, M.A.
Qin, X.
Ramsay, M.
Resnikoff, S.
Richards, J.E.
Schimiti, R.B.
Sim, K.S.
Sponsel, W.E.
Svidnicki, P.V.
Thiadens, A.
Uche, N.J.
Duijn, C.M. van
Vasconcellos, J.P.C. de
Wiggs, J.L.
Zangwill, L.M.
Risch, N.
Milea, D.
Ashaye, A.
Klaver, C.C.W.
Weinreb, R.N.
Koch, A.E.
Fingert, J.H.
Khor, C.C.
Source :
Jama : Journal of the American Medical Association; 1682; 1691; 0098-7484; 17; 322; ~Jama : Journal of the American Medical Association~1682~1691~~~0098-7484~17~322~~
Publication Year :
2019

Abstract

Item does not contain fulltext<br />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 14917 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 < 5 x 10-8 in the discovery stage and in the meta-analysis of combined discovery and validation data. Results: A total of 2320 individuals with primary open-angle glaucoma (mean [interquartile range] age, 64.6 [56-74] years; 1055 [45.5%] women) and 2121 individuals without primary open-angle glaucoma (mean [interquartile range] age, 63.4 [55-71] years; 1025 [48.3%] women) were included in the discovery GWAS. Th

Details

Database :
OAIster
Journal :
Jama : Journal of the American Medical Association; 1682; 1691; 0098-7484; 17; 322; ~Jama : Journal of the American Medical Association~1682~1691~~~0098-7484~17~322~~
Publication Type :
Electronic Resource
Accession number :
edsoai.on1284077789
Document Type :
Electronic Resource