A quantitative trait GWAS on lens thickness identifies novel risk loci on in the narrow angle individuals susceptible to PACG.

PURPOSE

PACG is one of the leading causes of blindness where lens thickness is a major risk factor for narrow-angle individuals. To our knowledge, no literature has been reported on candidate gene for lens thickness as a quantitative trait (QT). Here, we performed a genome-wide association analysis on lens thickness in the narrow-angle individuals.

MATERIALS AND METHODS

We conducted a genome-wide association study (GWAS) in the narrow angle individuals to investigate comprehensive genetic insights on lens thickness.

RESULTS

In QT-GWAS, we identified 145 genome-wide suggestive significant loci in the discovery cohort. Subsequently, we observed 13 SNPs that showed statistical significance around the region of PTRRM. Regional association analysis for top significant genotyped variants identified PTPRM as the most likely candidate for increased LT. Integrative bioinformatic analyses confirmed that the associated genomic region has potential regulatory roles for modulating transcription as enhancers. In the replication cohort, the sentinel genotype SNP was further associated significantly (P-value =0.000448) with high LT individuals. In both cohorts, the T allele of rs1941137 in the gene indicates as a risk allele for the increased LT.

CONCLUSION

In this study, we discovered evidence of a genomic association between chromosomal areas around the and increased lens thickness, resulting in a narrow angle. The regulatory components corresponding to variations might have a role in the thicker lens. We report that the genomic region near , a gene of potential interest, is associated with increased lens thickness.