Oxidative Stress, Persistent Inflammation and Blood Coagulation Alterations in Serum Proteome of Patients with Neovascular Age-Related Macular Degeneration

Author:

Winiarczyk Mateusz1ORCID,Thiede Bernd2ORCID,Utheim Tor Paaske34,Kaarniranta Kai567ORCID,Winiarczyk Dagmara8ORCID,Michalak Katarzyna9,Mackiewicz Jerzy1

Affiliation:

1. Department of Vitreoretinal Surgery, Medical University of Lublin, 20-079 Lublin, Poland

2. Department of Biosciences, University of Oslo, 0371 Oslo, Norway

3. Department of Medical Biochemistry, Oslo University Hospital, 0372 Oslo, Norway

4. Department of Ophthalmology, Oslo University Hospital, 0450 Oslo, Norway

5. Department of Ophthalmology, University of Eastern Finland, 70211 Kuopio, Finland

6. Department of Ophthalmology, Kuopio University Hospital, 70200 Kuopio, Finland

7. Department of Molecular Genetics, University of Lodz, 90-136 Lodz, Poland

8. Department and Clinic of Animal Internal Diseases, Faculty of Veterinary Medicine, University of Life Sciences, 20-612 Lublin, Poland

9. Department of Epizootiology and Clinic of Infectious Diseases, University of Life Sciences, 20-612 Lublin, Poland

Abstract

Neovascular age-related macular degeneration (AMD) is a major cause of irreversible blindness in elderly populations in developed countries. AMD’s etiopathology is multifactorial, with strong environmental and genetic components, but the exact molecular pathomechanisms underlying the disease are still unknown. In this study, we analyzed blood serum collected from 74 neovascular AMD patients and 58 healthy controls to identify proteins that may serve as potential biomarkers and expand our knowledge about the etiopathogenesis of the disease. The study revealed 17 differentially expressed proteins—11 up-regulated and 6 down-regulated—in neovascular AMD, which are involved in the biological processes previously linked with the disease—oxidative stress and persistent inflammation, impaired cellular transport, lipid metabolism and blood coagulation. In conclusion, the differences in the expressions of the proteins identified in this study may contribute to our understanding of the mechanisms underlying AMD and possibly serve in future as promising biomarkers.

Funder

Research Council of Norway INFRASTRUKTUR-program

Publisher

MDPI AG

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