SIRT1: Genetic Variants and Serum Levels in Age-Related Macular Degeneration

• Published in: Life (Basel, Switzerland) Switzerland), 2022-05, Vol.12 (5), p.753
• Main Authors: Kaikaryte, Kriste, Gedvilaite, Greta, Vilkeviciute, Alvita, Kriauciuniene, Loresa, Mockute, Ruta, Cebatoriene, Dzastina, Zemaitiene, Reda, Balciuniene, Vilma Jurate, Liutkeviciene, Rasa
• Format: Article
• Language: English
• Subjects: Age; Age related diseases; age-related macular degeneration (AMD); Alleles; Angiogenesis; Atrophy; Blood; Disease; Exudation; Eye diseases; Gene polymorphism; Genetic diversity; Genetic variance; Genotypes; Genotyping; Haplotypes; Health sciences; Inflammation; Macular degeneration; Nucleotides; Ophthalmology; Pathology; Polymorphism; Retina; rs3758391; rs3818292; rs7895833; Serum levels; Single-nucleotide polymorphism; SIRT1; SIRT1 levels; SIRT1 protein; Statistical analysis
• ISSN: 2075-1729; 2075-1729
• DOI: 10.3390/life12050753

The aim of this paper was to determine the frequency of rs3818292, rs3758391, rs7895833 single nucleotide polymorphism genotypes and SIRT1 serum levels associated with age-related macular degeneration (AMD) in the Lithuanian population. Genotyping of rs3818292, rs3758391 and rs7895833 was performed using RT-PCR. SIRT1 serum level was determined using the ELISA method. We found that rs3818292 and rs7895833 were associated with an increased risk of developing exudative AMD. Additional sex-differentiated analysis revealed only rs7895833 was associated with an increased risk of developing exudative AMD in women after strict Bonferroni correction. The analysis also revealed that individuals carrying rs3818292, rs3758391 and rs7895833 haplotype G-T-G are associated with increased odds of exudative AMD. Still, the rare haplotypes were associated with the decreased odds of exudative AMD. After performing an analysis of serum SIRT1 levels and genetic variant, we found that carriers of the rs3818292 minor allele G had higher serum SIRT1 levels than the AA genotype. In addition, individuals carrying at least one rs3758391 T allele also had elevated serum SIRT1 levels compared with individuals with the wild-type CC genotype. Our study showed that the polymorphisms rs3818292 and rs7895833 and rs3818292-rs3758391-rs7895833 haplotype G-T-G could be associated with the development of exudative AMD. Also, two SNPs (rs3818292 and rs3758391) are associated with elevated SIRT1 levels.