Autophagy Genes for Wet Age-Related Macular Degeneration in a Finnish Case-Control Study

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Paterno , J J , Koskela , A , Hyttinen , J M T , Vattulainen , E , Synowiec , E , Tuuminen , R , Watala , C , Blasiak , J & Kaarniranta , K 2020 , ' Autophagy Genes for Wet Age-Related Macular Degeneration in a Finnish Case-Control Study ' , Genes , vol. 11 , no. 11 , 1318 . https://doi.org/10.3390/genes11111318

Title: Autophagy Genes for Wet Age-Related Macular Degeneration in a Finnish Case-Control Study
Author: Paterno, Jussi J.; Koskela, Ali; Hyttinen, Juha M. T.; Vattulainen, Elina; Synowiec, Ewelina; Tuuminen, Raimo; Watala, Cezary; Blasiak, Janusz; Kaarniranta, Kai
Contributor organization: Medicum
HUS Head and Neck Center
Department of Ophthalmology and Otorhinolaryngology
Date: 2020-11
Language: eng
Number of pages: 13
Belongs to series: Genes
ISSN: 2073-4425
DOI: https://doi.org/10.3390/genes11111318
URI: http://hdl.handle.net/10138/326796
Abstract: Age-related macular degeneration is an eye disease that is the main cause of legal blindness in the elderly in developed countries. Despite this, its pathogenesis is not completely known, and many genetic, epigenetic, environmental and lifestyle factors may be involved. Vision loss in age-related macular degeneration (AMD) is usually consequence of the occurrence of its wet (neovascular) form that is targeted in the clinic by anti-VEGF (vascular endothelial growth factor) treatment. The wet form of AMD is associated with the accumulation of cellular waste in the retinal pigment epithelium, which is removed by autophagy and the proteosomal degradation system. In the present work, we searched for the association between genotypes and alleles of single nucleotide polymorphisms (SNPs) of autophagy-related genes and wet AMD occurrence in a cohort of Finnish patients undergoing anti-VEGF therapy and controls. Additionally, the correlation between treatment efficacy and genotypes was investigated. Overall, 225 wet AMD patients and 161 controls were enrolled in this study. Ten SNPs (rs2295080, rs11121704, rs1057079, rs1064261, rs573775, rs11246867, rs3088051, rs10902469, rs73105013, rs10277) in the mTOR (Mechanistic Target of Rapamycin), ATG5 (Autophagy Related 5), ULK1 (Unc-51-Like Autophagy Activating Kinase 1), MAP1LC3A (Microtubule Associated Protein 1 Light Chain 3 alpha), SQSTM1 (Sequestosome 1) were analyzed with RT-PCR-based genotyping. The genotype/alleles rs2295080-G, rs11121704-C, rs1057079-C and rs73105013-T associated with an increased, whereas rs2295080-TT, rs2295080-T, rs11121704-TT, rs1057079-TT, rs1057079-T, rs573775-AA and rs73105013-C with a decreased occurrence of wet AMD. In addition, the rs2295080-GG, rs2295080-GT, rs1057079-TT, rs11246867-AG, rs3088051-CC and rs10277-CC genotypes were a positively correlated cumulative number of anti-VEGF injections in 2 years. Therefore, variability in autophagy genes may have an impact on the risk of wet AMD occurrence and the efficacy of anti-VEGF treatment.
Subject: aging
autophagy
degeneration
macula
neovascularization
RETINAL-PIGMENT EPITHELIUM
RANIBIZUMAB TREATMENT
ASSOCIATION
ARMS2
DELETION
RPE
CFH
3125 Otorhinolaryngology, ophthalmology
Peer reviewed: Yes
Rights: cc_by
Usage restriction: openAccess
Self-archived version: publishedVersion


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