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1.
PLoS Genet ; 10(3): e1004089, 2014 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-24603532

RESUMEN

Anterior chamber depth (ACD) is a key anatomical risk factor for primary angle closure glaucoma (PACG). We conducted a genome-wide association study (GWAS) on ACD to discover novel genes for PACG on a total of 5,308 population-based individuals of Asian descent. Genome-wide significant association was observed at a sequence variant within ABCC5 (rs1401999; per-allele effect size =  -0.045 mm, P = 8.17 × 10(-9)). This locus was associated with an increase in risk of PACG in a separate case-control study of 4,276 PACG cases and 18,801 controls (per-allele OR = 1.13 [95% CI: 1.06-1.22], P = 0.00046). The association was strengthened when a sub-group of controls with open angles were included in the analysis (per-allele OR = 1.30, P = 7.45 × 10(-9); 3,458 cases vs. 3,831 controls). Our findings suggest that the increase in PACG risk could in part be mediated by genetic sequence variants influencing anterior chamber dimensions.


Asunto(s)
Cámara Anterior/patología , Estudio de Asociación del Genoma Completo , Glaucoma de Ángulo Cerrado/genética , Proteínas Asociadas a Resistencia a Múltiples Medicamentos/genética , Cámara Anterior/metabolismo , Pueblo Asiatico , Glaucoma de Ángulo Cerrado/patología , Humanos , Polimorfismo de Nucleótido Simple , Factores de Riesgo
2.
Nat Genet ; 44(10): 1142-1146, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22922875

RESUMEN

Primary angle closure glaucoma (PACG) is a major cause of blindness worldwide. We conducted a genome-wide association study including 1,854 PACG cases and 9,608 controls across 5 sample collections in Asia. Replication experiments were conducted in 1,917 PACG cases and 8,943 controls collected from a further 6 sample collections. We report significant associations at three new loci: rs11024102 in PLEKHA7 (per-allele odds ratio (OR)=1.22; P=5.33×10(-12)), rs3753841 in COL11A1 (per-allele OR=1.20; P=9.22×10(-10)) and rs1015213 located between PCMTD1 and ST18 on chromosome 8q (per-allele OR=1.50; P=3.29×10(-9)). Our findings, accumulated across these independent worldwide collections, suggest possible mechanisms explaining the pathogenesis of PACG.


Asunto(s)
Proteínas Portadoras/genética , Colágeno Tipo XI/genética , Predisposición Genética a la Enfermedad , Estudio de Asociación del Genoma Completo , Glaucoma de Ángulo Cerrado/genética , Proteína D-Aspartato-L-Isoaspartato Metiltransferasa/genética , Estudios de Casos y Controles , Sitios Genéticos , Humanos , Modelos Logísticos , Polimorfismo de Nucleótido Simple , Análisis de Componente Principal , Proteínas Represoras/genética
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