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通过与视网膜变薄相关的神经炎症途径对精神分裂症的遗传易感性。

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

作者信息

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, Rubio Jose, Lencz Todd, Homan Philipp

机构信息

Department of Adult Psychiatry and Psychotherapy, University of Zurich, Zurich, Switzerland.

Department of Child and Adolescent Psychiatry and Psychotherapy, University Hospital of Psychiatry Zurich, University of Zurich, Zurich, Switzerland.

出版信息

Nat Ment Health. 2025;3(5):538-547. doi: 10.1038/s44220-025-00414-6. Epub 2025 Apr 21.

Abstract

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 ( = -0.17,  = 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 ( = -0.10, self-contained  = 0.014, competitive  = 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.

摘要

精神分裂症与中枢神经系统的结构和功能变化有关,包括其最远端部分——视网膜。然而,视网膜萎缩是在个体患精神分裂症之前就已存在,还是该疾病的继发后果,这个问题仍未得到解答。在此,我们通过研究无精神分裂症诊断个体的精神分裂症多基因风险评分与视网膜形态之间的关联来解决这个问题。我们使用了来自英国生物银行的34939名英国白人和爱尔兰人的人群数据。我们的稳健回归结果表明,在控制混杂因素的情况下,精神分裂症较高的多基因风险评分与整体黄斑变薄有关(β = -0.17,P = 0.018)。同样,我们发现特定于神经炎症基因集的精神分裂症多基因风险评分越高,与神经节细胞内网状层越薄有关(β = -0.10,自含检验P = 0.014,竞争检验P = 0.02)。这些结果为可能使个体易发生神经炎症反应增强的遗传因素提供了新证据。随着时间的推移,这些反应可能导致诸如视网膜变薄等神经退行性过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca3/12066354/4d30998a2ff8/44220_2025_414_Fig1_HTML.jpg

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