Abstract

CFH and HTRA1 genes are traditional markers of increased risk of age-related macular degeneration (AMD) across populations. Recent findings suggest that additional genes—for instance, in the dystrophin-associated protein complex—might be promising markers for AMD. Here, we performed a case-control study to assess the effect of SGCD single nucleotide polymorphisms (SNPs), a member of this protein family, on AMD diagnosis and phenotype. We performed a case-control study of an under-studied population from Hispanics in Mexico City, with 134 cases with 134 unpaired controls. Cases were 60 years or older (Clinical Age-Related Maculopathy Staging (CARMS) grade 4–5, as assessed by experienced ophthalmologists following the American Association of Ophthalmology (AAO) guidelines), without other retinal disease or history of vitreous-retinal surgery. Controls were outpatients aged 60 years or older, with no drusen or retinal pigment epithelium (RPE) changes on a fundus exam and a negative family history of AMD. We examined SNPs in the SGCD gene (rs931798, rs140617, rs140616, and rs970476) by sequencing and real-time PCR. Genotyping quality checks and univariate analyses were performed with PLINK v1.90b3.42. Furthermore, logistic regression models were done in SAS v.9.4 and haplotype configurations in R v.3.3.1. After adjusting for clinical covariates, the G/A genotype of the SGCD gene (rs931798) significantly increases the odds of being diagnosed with AMD in 81% of cases (1.81; 95% CI 1.06–3.14; p = 0.031), especially the geographic atrophy phenotype (1.82; 95% CI 1.03–3.21; p = 0.038) compared to the G/G homozygous genotype. Moreover, the GATT haplotype in this gene (rs931798, rs140617, rs140616, and rs970476) is associated with lower odds of AMD (adjusted odds ratio (OR) 0.13; 95% CI 0.02–0.91; p = 0.041). SGCD is a promising gene for AMD research. Further corroboration in other populations is warranted, especially among other Hispanic ethnicities.

Highlights

  • Age-related macular degeneration (AMD) is the leading cause of blindness in individuals over 60 years old in developed countries [1], and the third leading cause worldwide [2]

  • We studied 268 individuals; half of these were cases diagnosed with age-related macular degeneration (AMD)

  • For North America, in 2015, around 15.9% of regional blindness was directly attributable to AMD in those aged 50 years or older [3]

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Summary

Introduction

Age-related macular degeneration (AMD) is the leading cause of blindness in individuals over 60 years old in developed countries [1], and the third leading cause worldwide [2]. (1) choroidal neovascularization (CNV, exudative, or wet AMD) or (2) geographic atrophy (GA) of the retinal pigment epithelium (nonexudative or dry AMD) [7] Such progression is not homogeneous across race/ethnicities, clearly indicating an effect modification in the development and progression of the AMD, primarily due to a genetic component. It is clear that these advanced forms have a complex genetic background currently not thoroughly characterized, arguing for the need of study of new genetic markers in non-traditional loci

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