精神病发作前后的认知:变化、异质性和预后的自然研究

IF 3 Q2 PSYCHIATRY
Maria Lee , Alexis E. Cullen , Granville J. Matheson , Zheng-An Lu , Sarah E. Bergen , Carl M. Sellgren , Sophie Erhardt , Helena Fatouros-Bergman , Simon Cervenka
{"title":"精神病发作前后的认知:变化、异质性和预后的自然研究","authors":"Maria Lee ,&nbsp;Alexis E. Cullen ,&nbsp;Granville J. Matheson ,&nbsp;Zheng-An Lu ,&nbsp;Sarah E. Bergen ,&nbsp;Carl M. Sellgren ,&nbsp;Sophie Erhardt ,&nbsp;Helena Fatouros-Bergman ,&nbsp;Simon Cervenka","doi":"10.1016/j.scog.2025.100387","DOIUrl":null,"url":null,"abstract":"<div><h3>Aims</h3><div>Cognitive dysfunction is a core feature of psychotic disorders. The degree of impairment varies greatly between individuals, which may reflect different levels of decline from pre-morbid functioning. Diverse trajectories of cognitive change prior to or during development of psychosis have been hypothesized to reflect distinct underlying pathological processes. Our primary aim was to model cognitive change over time in a sample of individuals with first-episode psychosis (FEP) and controls. The secondary aim was to explore associations between cognitive change, clinical outcomes and select biological markers.</div></div><div><h3>Methods</h3><div>Our sample consisted of 72 individuals with FEP and 53 controls. School grades from nationwide population registers were used as a proxy for pre-morbid cognitive ability. All participants underwent formal cognitive testing at psychosis onset, with a subset returning for testing at 1,5 year follow up. Cognitive change was modelled using linear mixed-effects models, and resulting change scores were correlated to polygenic risk scores, cerebrospinal fluid levels of complement protein C4A and clinical outcomes.</div></div><div><h3>Results</h3><div>Groups did not differ in school performance prior to psychosis. Psychosis onset was associated with marked cognitive decline in FEP individuals, who subsequently performed significantly worse than controls. However, cognitive change over time varied widely between FEP individuals. Degree of cognitive change was not associated with the selected biological variables but did predict worse clinical outcomes.</div></div><div><h3>Conclusions</h3><div>Individual cognitive trajectories may be a clinically relevant topic for further study, and larger studies are needed to further explore their potential role in stratified models of care.</div></div>","PeriodicalId":38119,"journal":{"name":"Schizophrenia Research-Cognition","volume":"42 ","pages":"Article 100387"},"PeriodicalIF":3.0000,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cognition before and after psychosis onset: A naturalistic study of change, heterogeneity, and prognosis\",\"authors\":\"Maria Lee ,&nbsp;Alexis E. Cullen ,&nbsp;Granville J. Matheson ,&nbsp;Zheng-An Lu ,&nbsp;Sarah E. Bergen ,&nbsp;Carl M. Sellgren ,&nbsp;Sophie Erhardt ,&nbsp;Helena Fatouros-Bergman ,&nbsp;Simon Cervenka\",\"doi\":\"10.1016/j.scog.2025.100387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Aims</h3><div>Cognitive dysfunction is a core feature of psychotic disorders. The degree of impairment varies greatly between individuals, which may reflect different levels of decline from pre-morbid functioning. Diverse trajectories of cognitive change prior to or during development of psychosis have been hypothesized to reflect distinct underlying pathological processes. Our primary aim was to model cognitive change over time in a sample of individuals with first-episode psychosis (FEP) and controls. The secondary aim was to explore associations between cognitive change, clinical outcomes and select biological markers.</div></div><div><h3>Methods</h3><div>Our sample consisted of 72 individuals with FEP and 53 controls. School grades from nationwide population registers were used as a proxy for pre-morbid cognitive ability. All participants underwent formal cognitive testing at psychosis onset, with a subset returning for testing at 1,5 year follow up. Cognitive change was modelled using linear mixed-effects models, and resulting change scores were correlated to polygenic risk scores, cerebrospinal fluid levels of complement protein C4A and clinical outcomes.</div></div><div><h3>Results</h3><div>Groups did not differ in school performance prior to psychosis. Psychosis onset was associated with marked cognitive decline in FEP individuals, who subsequently performed significantly worse than controls. However, cognitive change over time varied widely between FEP individuals. Degree of cognitive change was not associated with the selected biological variables but did predict worse clinical outcomes.</div></div><div><h3>Conclusions</h3><div>Individual cognitive trajectories may be a clinically relevant topic for further study, and larger studies are needed to further explore their potential role in stratified models of care.</div></div>\",\"PeriodicalId\":38119,\"journal\":{\"name\":\"Schizophrenia Research-Cognition\",\"volume\":\"42 \",\"pages\":\"Article 100387\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-08-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Schizophrenia Research-Cognition\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2215001325000459\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PSYCHIATRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Schizophrenia Research-Cognition","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2215001325000459","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0

摘要

目的认知功能障碍是精神障碍的核心特征。个体之间的损伤程度差异很大,这可能反映了发病前功能下降的不同程度。在精神病发展之前或发展过程中,认知变化的不同轨迹已经被假设为反映不同的潜在病理过程。我们的主要目的是在首发精神病(FEP)和对照组的个体样本中模拟认知变化随时间的变化。第二个目的是探索认知变化、临床结果和选择的生物学标志物之间的联系。方法样本包括72例FEP患者和53例对照组。来自全国人口登记的学校成绩被用作病前认知能力的代表。所有参与者在精神病发作时都接受了正式的认知测试,其中一部分在随访1年半后再次接受测试。使用线性混合效应模型对认知变化进行建模,结果变化评分与多基因风险评分、脑脊液补体蛋白C4A水平和临床结果相关。结果各组在精神病前的学业表现无显著差异。精神疾病的发作与FEP个体明显的认知能力下降有关,他们随后的表现明显比对照组差。然而,随着时间的推移,FEP个体之间的认知变化差异很大。认知改变的程度与选定的生物学变量无关,但确实预示着较差的临床结果。结论个体认知轨迹可能是一个值得进一步研究的临床相关课题,需要更大规模的研究来进一步探索其在分层护理模式中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cognition before and after psychosis onset: A naturalistic study of change, heterogeneity, and prognosis

Aims

Cognitive dysfunction is a core feature of psychotic disorders. The degree of impairment varies greatly between individuals, which may reflect different levels of decline from pre-morbid functioning. Diverse trajectories of cognitive change prior to or during development of psychosis have been hypothesized to reflect distinct underlying pathological processes. Our primary aim was to model cognitive change over time in a sample of individuals with first-episode psychosis (FEP) and controls. The secondary aim was to explore associations between cognitive change, clinical outcomes and select biological markers.

Methods

Our sample consisted of 72 individuals with FEP and 53 controls. School grades from nationwide population registers were used as a proxy for pre-morbid cognitive ability. All participants underwent formal cognitive testing at psychosis onset, with a subset returning for testing at 1,5 year follow up. Cognitive change was modelled using linear mixed-effects models, and resulting change scores were correlated to polygenic risk scores, cerebrospinal fluid levels of complement protein C4A and clinical outcomes.

Results

Groups did not differ in school performance prior to psychosis. Psychosis onset was associated with marked cognitive decline in FEP individuals, who subsequently performed significantly worse than controls. However, cognitive change over time varied widely between FEP individuals. Degree of cognitive change was not associated with the selected biological variables but did predict worse clinical outcomes.

Conclusions

Individual cognitive trajectories may be a clinically relevant topic for further study, and larger studies are needed to further explore their potential role in stratified models of care.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.60
自引率
10.70%
发文量
54
审稿时长
67 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信