早发性精神分裂症患者工作记忆的功能性神经发育:一项纵向FMRI研究

IF 2.3 Q2 PSYCHIATRY
Vasileios Ioakeimidis , Corinna Haenschel , Anne-Kathrin Fett , Marinos Kyriakopoulos , Danai Dima
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引用次数: 1

摘要

精神分裂症是一种使人衰弱的疾病,典型的临床症状表现在成年早期,其特征是执行过程中的认知障碍,如工作记忆(WM)。然而,有一个罕见的病例,早发性精神分裂症(EOS)的个体开始在他们的18岁生日之前,而WM及其神经基质仍处于成熟阶段。使用功能磁共振成像的WM n-back任务,我们评估了EOS青少年和年龄和性别匹配的典型发育对照中WM的功能神经发育。参与者在17岁和21岁时分别在同一台扫描仪上接受了两次神经成像(平均扫描间隔= 4.3年)。采用一般线性模型分析来探讨组内和组间WM神经发育的变化。在多重回归中输入精神病理评分,以检测由基线症状预测其纵向功能变化的脑区。WM神经发育的特点是在患者和对照组的额颞叶和扣带脑区广泛的功能减少。各组间WM变化轨迹无明显差异。基线症状评分预测额叶、扣带、顶叶、枕叶和小脑区域的功能性神经发育变化。青少年大脑经历了突触修剪等发育过程,这可能是网络细化WM的基础。前额叶和顶枕活动减少受临床症状的影响。在罕见的EOS患者诊断样本中使用纵向神经成像方法可能有助于推进神经发育生物标志物作为治疗WM损伤的药理学靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study

Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study

Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study

Schizophrenia, a debilitating disorder with typical manifestation of clinical symptoms in early adulthood, is characterized by cognitive impairments in executive processes such as in working memory (WM). However, there is a rare case of individuals with early-onset schizophrenia (EOS) starting before their 18th birthday, while WM and its neural substrates are still undergoing maturation. Using the WM n-back task with functional magnetic resonance imaging, we assessed the functional neurodevelopment of WM in adolescents with EOS and age- and gender-matched typically developing controls. Participants underwent neuroimaging in the same scanner twice, once at age 17 and at 21 (mean interscan interval = 4.3 years). General linear model analysis was performed to explore WM neurodevelopmental changes within and between groups. Psychopathological scores were entered in multiple regressions to detect brain regions whose longitudinal functional change was predicted by baseline symptoms in EOS. WM neurodevelopment was characterized by widespread functional reductions in frontotemporal and cingulate brain areas in patients and controls. No between-group differences were found in the trajectory of WM change. Baseline symptom scores predicted functional neurodevelopmental changes in frontal, cingulate, parietal, occipital, and cerebellar areas. The adolescent brain undergoes developmental processes such as synaptic pruning, which may underlie the refinement WM of network. Prefrontal and parietooccipital activity reduction is affected by clinical presentation of symptoms. Using longitudinal neuroimaging methods in a rare diagnostic sample of patients with EOS may help the advancement of neurodevelopmental biomarkers intended as pharmacological targets to tackle WM impairment.

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来源期刊
CiteScore
5.60
自引率
10.70%
发文量
54
审稿时长
67 days
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