Linking the microbiome to the complement system in geographic atrophy.

Age-related macular degeneration (AMD) is the leading cause of vision loss in the aged population with the late stage geographic atrophy (GA). Risk factors for AMD include age, genetic variants in the complement system, nutritional factors, and alterations in the gut microbiome (GM). To identify taxonomic and functional differences in the microbiome associated to disease pathophysiology and genetic risk factors, this study investigated the GM and the ocular surface microbiome (OSM) of GA patients compared to healthy controls by whole-metagenome shotgun sequencing. 16 AMD-associated SNPs were genotyped from blood samples using TaqMan assays and Sanger sequencing. While GA patients showed differences in the GM, and altered metabolic pathways including inosine 5'-phosphate degradation, NAD salvage, and ketogenesis, no alterations in the OSM were found. Genetic analysis associated SNP rs1061170 in the complement factor H gene with GA. These findings suggest that microbial alterations may contribute to GA through inflammation and oxidative stress.Registry: ClinicalTrials.gov, NCT02438111, Registration date: 28 April 2015, and NCT04658238, Registration date: 01 December 2020.

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Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2026-02-02
DOI
https://doi.org/10.48620/94411
Primary Topic
Retinal Diseases and Treatments
Type
article
Field-Weighted Citation Impact
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article

Linking the microbiome to the complement system in geographic atrophy.

Martin Sebastian Zinkernagel, Denise C. Zysset‐Burri, Justyna M. Studer, Daniel Schärer et al.
Open Access CRIS of the University of Bern
Retinal Diseases and Treatments
article

Linking the microbiome to the complement system in geographic atrophy.

Martin Sebastian Zinkernagel, Denise C. Zysset‐Burri, Justyna M. Studer, Daniel Schärer, Marco Kreuzer, Damian Jaggi, Jérémy Rotzetter, Livia Spörri, Carlo R. Largiadèr
article en

Abstract

Age-related macular degeneration (AMD) is the leading cause of vision loss in the aged population with the late stage geographic atrophy (GA). Risk factors for AMD include age, genetic variants in the complement system, nutritional factors, and alterations in the gut microbiome (GM). To identify taxonomic and functional differences in the microbiome associated to disease pathophysiology and genetic risk factors, this study investigated the GM and the ocular surface microbiome (OSM) of GA patients compared to healthy controls by whole-metagenome shotgun sequencing. 16 AMD-associated SNPs were genotyped from blood samples using TaqMan assays and Sanger sequencing. While GA patients showed differences in the GM, and altered metabolic pathways including inosine 5'-phosphate degradation, NAD salvage, and ketogenesis, no alterations in the OSM were found. Genetic analysis associated SNP rs1061170 in the complement factor H gene with GA. These findings suggest that microbial alterations may contribute to GA through inflammation and oxidative stress.Registry: ClinicalTrials.gov, NCT02438111, Registration date: 28 April 2015, and NCT04658238, Registration date: 01 December 2020.

Open Access CRIS of the University of Bern
GP Forschungsgruppe (DE), Universitätsklinik für Augenheilkunde (CH), Ophthalmology Clinic (DE)
Zero hunger
Openalex Percentile: Top 65%
Retinal Diseases and Treatments
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