A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.

Citation data:

Nature communications, ISSN: 2041-1723, Vol: 9, Issue: 1, Page: 2278

Publication Year:
2018
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Repository URL:
https://mouseion.jax.org/stfb2018/141; http://kpresearchpublications.kp.org/handle/kp/20093
PMID:
29891935
DOI:
10.1038/s41467-018-04555-4
Author(s):
Choquet, Hélène; Paylakhi, Seyyedhassan; Kneeland, Stephen C; Thai, Khanh K; Hoffmann, Thomas J; Yin, Jie; Kvale, Mark N; Banda, Yambazi; Tolman, Nicholas G; Williams, Pete A; Schaefer, Catherine; Melles, Ronald B; Risch, Neil; John, Simon W M; Nair, K Saidas; Jorgenson, Eric Show More Hide
Publisher(s):
Springer Nature
Tags:
Chemistry; Biochemistry, Genetics and Molecular Biology; Physics and Astronomy; Life Sciences; Medicine and Health Sciences
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article description
Primary open-angle glaucoma (POAG) is a leading cause of irreversible vision loss, yet much of the genetic risk remains unaccounted for, especially in African-Americans who have a higher risk for developing POAG. We conduct a multiethnic genome-wide association study (GWAS) of POAG in the GERA cohort, with replication in the UK Biobank (UKB), and vice versa, GWAS in UKB with replication in GERA. We identify 24 loci (P < 5.0 × 10), including 14 novel, of which 9 replicate (near FMNL2, PDE7B, TMTC2, IKZF2, CADM2, DGKG, ANKH, EXOC2, and LMX1B). Functional studies support intraocular pressure-related influences of FMNL2 and LMX1B, with certain Lmx1b mutations causing high IOP and glaucoma resembling POAG in mice. The newly identified loci increase the proportion of variance explained in each GERA race/ethnicity group, with the largest gain in African-Americans (0.5-3.1%). A meta-analysis combining GERA and UKB identifies 24 additional loci. Our study provides important insights into glaucoma pathogenesis.