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  3. Genetic susceptibility to schizophrenia through neuroinflammatory pathways associated with retinal thinness.
 

Genetic susceptibility to schizophrenia through neuroinflammatory pathways associated with retinal thinness.

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BORIS DOI
10.48620/88977
Date of Publication
2025
Publication Type
Article
Division/Institute

Clinic of Ophthalmolo...

Author
Rabe, Finn
Smigielski, Lukasz
Georgiadis, Foivos
Kallen, Nils
Omlor, Wolfgang
Edkins, Victoria
Kirschner, Matthias
Cathomas, Flurin
Grünblatt, Edna
Silverstein, Steven
Blose, Brittany
Barthelmes, Daniel
Schaal, Karen
Clinic of Ophthalmology
Rubio, Jose
Lencz, Todd
Homan, Philipp
Subject(s)

600 - Technology::610...

Series
nature mental health
ISSN or ISBN (if monograph)
2731-6076
Publisher
Nature Research
Language
English
Publisher DOI
10.1038/s44220-025-00414-6
PubMed ID
40365461
Uncontrolled Keywords

Diagnostic markers

Genetics research

Schizophrenia

Description
Schizophrenia is associated with structural and functional changes in the central nervous system, including the most distal part of it, the retina. However, the question of whether retinal atrophy is present before individuals develop schizophrenia or is a secondary consequence of the disorder remains unanswered. Here we address this question by examining the association between polygenic risk scores for schizophrenia and retinal morphologies in individuals without a schizophrenia diagnosis. We used population data for 34,939 white British and Irish individuals from the UK Biobank. Our robust regression results show that higher polygenic risk scores for schizophrenia were associated with thinner overall maculae, while controlling for confounding factors (b = -0.17, P = 0.018). Similarly, we found that greater polygenic risk scores for schizophrenia specific to neuroinflammation gene sets were associated with thinner ganglion cell inner plexiform layers (b = -0.10, self-contained P = 0.014, competitive P = 0.02). These results provide new evidence for genetic factors that could predispose individuals to heightened neuroinflammatory responses. Over time, these responses could contribute to neurodegenerative processes such as retinal thinning.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/211190
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