Retinal thickness changes in different subfields reflect the volume change of cerebral white matter hyperintensity

Lv, Xiaohan; Teng, Zhenjie; Jia, Zhiyang; Dong, Yanhong; Xu, Jing; Lv, Peiyuan

doi:10.3389/fneur.2022.1014359

Cited by 1 publication

(1 citation statement)

References 63 publications

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“…We focused on the macula, the area with the highest density of neurons in the retina (Figure 1). Different subfields of the macula may have different functions and may be affected differently by various diseases or conditions 15,16 and may therefore be more informative when investigating polygenic associations. Furthermore, we explored gene set-specific polygenic risk scores for schizophrenia: biological pathways that are related to neurotransmitter regulation, inflammation and microvasculature, all of which may be altered in individuals with schizophrenia.…”

Section: Introductionmentioning

confidence: 99%

Genetic susceptibility to schizophrenia through neuroinflammatory pathways is associated with retinal thinning: Findings from the UK-Biobank

Rabe,

Smigielski,

Georgiadis

et al. 2024

Preprint

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The human retina is part of the central nervous system and can be easily and non- invasively imaged through optical coherence tomography. Imaging the retina may provide insights on central nervous system related disorders such as schizophrenia. Here, our objective was to investigate if variations in retinal phenotypes could be at- tributed to common genetic variations conveying a risk of schizophrenia as measured by polygenic risk scores. We used population data from the UK Biobank, including White British and Irish individuals without diagnosed schizoprenia, and estimated a polygenic risk score for schizophrenia based on the newest genome-wide association study (PGC release 2022). We hypothesized that greater genetic susceptibility to schizophrenia is associated with retinal thinning, especially within the macula. To gain additional mechanistic insights, we conducted pathway-specific polygenic risk score associations analyses, focusing on gene pathways that are related to schizophrenia. Of 65484 individuals recruited, 48208 participants with available matching imaging- genetic data were included in the analysis of whom 22427 (53.48%) were female and 25781 (46.52%) were male. 5148 individuals were excluded on the basis of incomplete optical coherence tomog- raphy data (for all phenotypes), 198 individuals based on the use of antipsychotics and 197 individuals with schizophrenia, schizotypal- and delusional disorders. Our robust principal component regression results showed that polygenic risk scores for schizophrenia were associated with retinal thinning while controlling for confounding factors (b = -0.03, p = 0.007). Similarly, we found that polygenic risk for schizophrenia specific to neuroinflammation gene sets revealed significant associations with retinal thinning (b = -0.03, self-contained p = 0.041 (reflecting the level of association), com- petitive p = 0.05 (reflecting the level of enrichment)). These results go beyond previ- ous studies suggesting a relationship between manifested schizophrenia and retinal phenotypes. They indicate that the retina is a mirror reflecting the genetic complex- ities of schizophrenia. These associations also suggest the potential involvement of the neuroinflammatory pathway, with indications of genetic overlap in certain retinal phenotypes. The findings further indicate that this gene pathway in individuals with a high polygenic risk for schizophrenia could contribute through acute-phase proteins to structural changes in the retina.

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Section: Introductionmentioning

confidence: 99%