Results from the Population-Based Gutenberg Health Study Revealing Four Altered Autoantibodies in Retinal Vein Occlusion Patients

Author:

Bell Katharina1ORCID,Beutgen Vanessa M.1ORCID,Nickels Stefan1,Lorenz Katrin1,Scheller Yvonne1,Elbaz Hisham12,Peto Tunde3,Ponto Katharina A.14,Schulz Andreas1,Wild Philipp S.456,Münzel Thomas7ORCID,Lackner Karl J.8,Schmidtmann Irene9,Beutel Manfred10,Pfeiffer Norbert1,Grus Franz H.1,Schuster Alexander K.1ORCID

Affiliation:

1. Department of Ophthalmology, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany

2. Department of Ophthalmology, Otto-Von-Guericke University, Magdeburg, Germany

3. Centre for Public Health, Queen’s University Belfast, Belfast, UK

4. Center for Thrombosis and Hemostasis (CTH), University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany

5. Preventive Cardiology and Preventive Medicine/Center for Cardiology, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany

6. German Center of Cardiovascular Research (DZHK), Partner Site Rhine-Main, Mainz, Germany

7. Center for Cardiology I, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany

8. Department for Clinical Chemistry and Laboratory Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany

9. Institute of Medical Biostatistics,Epidemiology and Informatics, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany

10. Department of Psychosomatic Medicine and Psychotherapy, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany

Abstract

Purpose. Retinal vein occlusion (RVO) is the second most common retinal vascular disease and a major cause of visual impairment. In this study, we aimed to observe whether RVO cases have different antibody profiles as a new potential risk factor and whether a conversion of retinal vein occlusion (RVO) to neovascular glaucoma (NVG), one of the major complications, is occurring within a 5-year timeframe. Methods. We performed a nested case-control study (1 : 4) within the Gutenberg Health Study (GHS), a population-based, prospective cohort study in the Rhine-Main Region of Germany including 15,010 participants. RVO subjects (n = 59) were identified by grading of fundus photographs. Optic nerves of RVO subjects and age- and sex-matched controls (n = 229) at baseline and their follow-up examination after 5 years were analyzed for glaucomatous alterations. Of all RVO subjects and controls, serum autoantibody profiles were measured using in-house manufactured antigen-antibody microarrays. Results. Of the 59 RVO patients, 3 patients (5%) showed glaucomatous optic disc alterations at baseline, whereas no new glaucoma case was detected at 5-year follow-up. Four of the autoantibodies measured (against dermcidin, neurotrophin-3, superoxide dismutase 1, and signal recognition particle 14 kDa protein) were significantly increased in the serum of RVO patients p<0.001. Multivariable conditional logistic regression analysis showed that 3 of these 4 antibodies were independent of cardiovascular risk factors. Conclusions. We found several autoantibodies associated with RVO, targeting proteins and structures possibly involved in RVO pathogenesis.

Funder

Stiftung Rheinland-Pfalz für Innovation

Publisher

Hindawi Limited

Subject

Ophthalmology

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