Association of autoantibody levels with different stages of age-related macular degeneration (AMD) : results from the population-based Gutenberg Health Study (GHS)

dc.contributor.authorKorb, Christina A.
dc.contributor.authorLackner, Karl J.
dc.contributor.authorWolters, Dominik
dc.contributor.authorSchuster, Alexander K.
dc.contributor.authorNickels, Stefan
dc.contributor.authorBeutgen, Vanessa M.
dc.contributor.authorMünzel, Thomas
dc.contributor.authorWild, Philipp S.
dc.contributor.authorBeutel, Manfred E.
dc.contributor.authorSchmidtmann, Irene
dc.contributor.authorPfeiffer, Norbert
dc.contributor.authorGrus, Franz H.
dc.date.accessioned2023-08-28T10:04:53Z
dc.date.available2023-08-28T10:04:53Z
dc.date.issued2023
dc.description.abstractPurpose Anti-retinal autoantibodies are assumed to be associated with age-related macular degeneration (AMD). To our knowledge, this is the first evaluation of autoantibodies in human sera of participants with different stages of AMD in a large population-based, observational cohort study in Germany. Methods The Gutenberg Health Study (GHS) is a population-based, observational cohort study in Germany, including 15,010 participants aged between 35 and 74. Amongst others, non-mydriatic fundus photography (Visucam PRO NM™, Carl Zeiss Meditec AG, Jena, Germany) was performed. Fundus images of the first 5000 participants were graded based on the Rotterdam Eye Study classification. Sera of participants with AMD (n=541) and sera of age-matched participants without AMD (n=490) were analyzed by antigen-microarrays. Besides descriptive statistics, autoantibody-levels were compared by Mann-Whitney-U test and the associations of level of autoantibodies with AMD were calculated by logistic regression analysis. Likewise, possible associations of the autoantibodies and both clinical and laboratory parameters on AMD subjects were analyzed. Results Autoantibodies against transferrin (p<0.001) were significantly downregulated in participants with early AMD and soft, distinct drusen (≥63 μm) or pigmentary abnormalities only compared to Controls. Mitogen-activated protein kinase 3 (p=0.041), glutathione peroxidase 4 (p=0.048), clusterin (p=0.045), lysozyme (p=0.19), protein kinase C substrate 80K-H (p=0.02), heat shock 70 kDa protein 1A (p=0.04) and insulin (p=0.018) show a trend between Control and participants with early AMD and soft, distinct drusen (≥63 μm) or pigmentary abnormalities only. Conclusions This study contributes to a growing knowledge of autoantibodies in association with different AMD stages compared to controls in the context of a large population-based study in Germany. Especially autoantibodies against inflammatory proteins were downregulated in participants with early AMD and soft, distinct drusen (≥63 μm) or pigmentary abnormalities only.en_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-9463
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/9481
dc.language.isoeng
dc.rightsCC-BY-4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleAssociation of autoantibody levels with different stages of age-related macular degeneration (AMD) : results from the population-based Gutenberg Health Study (GHS)en_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.pricePAR-Fee
jgu.apc.transformationcontractSpringer (DEAL)
jgu.journal.titleGraefe's archive for clinical and experimental ophthalmology
jgu.journal.volumeVersion of Record (VoR)
jgu.organisation.departmentFB 04 Medizinde_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.publisher.doi10.1007/s00417-023-06085-2
jgu.publisher.issn1435-702X
jgu.publisher.nameSpringer
jgu.publisher.placeBerlin u.a.
jgu.publisher.year2023
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode610
jgu.subject.dfgLebenswissenschaftende_DE
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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