Nature communications · 2025
Loss of CFHR5 function reduces the risk for age-related macular degeneration.
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Reeve Mary Pat, Loomis Stephanie, Nissilä Eija, Soare Thomas W, Rausch Tobias, Zheng Zhili, Della Briotta Parolo Pietro, Ben-Isvy Daniel, Aho Elias, Cesetti Emilia, Okunuki Yoko, McLaughlin Helen, Mäkelä Johanna, FinnGen, Kurki Mitja, Talkowski Michael E, Korbel Jan O, Connor Kip, Meri Seppo, Daly Mark J, Runz Heiko
Аннотация
Age-related macular degeneration (AMD) is a prevalent cause of vision loss in the elderly with limited therapeutic options. A single chromosomal region around the complement factor H gene (CFH) is reported to explain nearly 25% of genetic AMD risk. Here, we used association testing, statistical finemapping and conditional analyses in 12,495 AMD cases and 461,686 controls to deconvolute four major CFH haplotypes that convey protection from AMD. We show that beyond CFH, two of these are explained by Finn-enriched frameshift and missense variants in the CFH modulator CFHR5. We demonstrate through a FinnGen sample recall study that CFHR5 variant carriers exhibit dose-dependent reductions in serum levels of the CFHR5 gene product FHR-5 and two functionally related proteins at the locus. Genetic reduction in FHR-5 correlates with higher complement activation capacity and a thicker retinal photoreceptor layer. Our results propose therapeutic downregulation of FHR-5 as promising to prevent or treat AMD.
Предметные рубрики MeSH
HumansMacular DegenerationAgedMaleFemaleComplement Factor HGenetic Predisposition to DiseaseHaplotypesAged, 80 and overComplement ActivationMiddle AgedPolymorphism, Single NucleotideComplement C3b Inactivator ProteinsFrameshift MutationCase-Control StudiesRetinaMutation, MissenseComplement System Proteins