Linking Psychotic-Like Experiences and Brain White Matter Microstructure in Young Women

IF 2.7 3区 心理学 Q2 BEHAVIORAL SCIENCES
Rikka Kjelkenes, Sara Fernandez-Cabello, Irene Voldsbekk, Madelene Christin Holm Bukhari, Andreas Dahl, Ingvild Sandø Lofthus, Henning Stople Rise, Christian K. Tamnes, Ivan I. Maximov, Lars T. Westlye
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引用次数: 0

Abstract

Background

Psychotic-like experiences (PLE) represent a risk factor for later psychotic disorders and a marker for general mental distress. The connectivity and microstructure of key brain white matter pathways, including fronto–temporal trajectories, have been implicated in psychosis and psychosis-risk. Although sex differences in PLE prevalence and characteristics have been reported, most neuroimaging studies of PLE have primarily included mixed-sex, samples and little research has been carried out in females only. This study examines the associations between PLE and white matter characteristics in young to middle-aged females.

Methods

We analyzed cross-sectional diffusion magnetic resonance imaging (dMRI) and self-reported data from 661 females aged 9–44 years using the 15-item version of The Community Assessment of Psychic Experiences (CAPE) questionnaire. Associations between CAPE subscales and other psychopathology measures were tested. Using linked independent component analysis (LICA), we decomposed the voxel-wise data from 24 dMRI metrics across five different diffusion models into 10 spatially independent components. We then examined the association between the LICA subject weights and age. Next, we tested for associations between the LICA subject weights and both CAPE total and subscales scores using Bayesian statistics.

Results

PLE were broadly associated with various domains of psychopathology and psychosocial factors. Moderate evidence emerged for an association between PLE and an LICA component reflecting a broad and complex pattern of diffusivity in major pathways, including the inferior fronto– occipital fasciculus, anterior thalamic radiation, and forceps minor. The persecutory ideations subscale showed the strongest evidence of an effect.

Conclusion

PLE in young females are associated with a distinct multimodal white matter pattern reflecting microstructural characteristics in key commissural, association, and thalamocortical pathways in young females. The findings support that LICA is a valuable tool for fusing and decomposing advanced dMRI metrics to delineate white matter patterns that show sensitivity to PLE and mental distress.

Abstract Image

年轻女性精神病样经历与脑白质微观结构的联系
精神样经历(PLE)是后期精神障碍的危险因素,也是一般精神痛苦的标志。包括额颞叶轨迹在内的关键脑白质通路的连通性和微观结构与精神病和精神病风险有关。虽然已经报道了PLE患病率和特征的性别差异,但大多数关于PLE的神经影像学研究主要包括混合性别样本,仅针对女性进行的研究很少。本研究探讨了年轻至中年女性PLE与白质特征之间的关系。方法对661名9 ~ 44岁女性的横断扩散磁共振成像(dMRI)和自我报告数据进行分析,并采用15项版本的社区心理体验评估(CAPE)问卷。CAPE亚量表与其他精神病理学测量之间的关联进行了测试。使用链接独立分量分析(LICA),我们将来自5种不同扩散模型的24个dMRI指标的体素数据分解为10个空间独立分量。然后,我们检查了LICA受试者体重与年龄之间的关系。接下来,我们使用贝叶斯统计检验了LICA受试者权重与CAPE总分和子量表得分之间的关联。结果PLE与精神病理和社会心理因素广泛相关。中度证据表明,PLE和LICA成分之间存在关联,反映了主要通路中广泛而复杂的扩散模式,包括额枕下束、丘脑前辐射和小钳。迫害意念分量表显示出影响的最有力证据。结论年轻女性的PLE与一种不同的多模态白质模式相关,反映了年轻女性主要的交联、关联和丘脑皮质通路的微观结构特征。研究结果支持LICA是一种有价值的工具,用于融合和分解高级dMRI指标,以描绘对PLE和精神痛苦敏感的白质模式。
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来源期刊
Brain and Behavior
Brain and Behavior BEHAVIORAL SCIENCES-NEUROSCIENCES
CiteScore
5.30
自引率
0.00%
发文量
352
审稿时长
14 weeks
期刊介绍: Brain and Behavior is supported by other journals published by Wiley, including a number of society-owned journals. The journals listed below support Brain and Behavior and participate in the Manuscript Transfer Program by referring articles of suitable quality and offering authors the option to have their paper, with any peer review reports, automatically transferred to Brain and Behavior. * [Acta Psychiatrica Scandinavica](https://publons.com/journal/1366/acta-psychiatrica-scandinavica) * [Addiction Biology](https://publons.com/journal/1523/addiction-biology) * [Aggressive Behavior](https://publons.com/journal/3611/aggressive-behavior) * [Brain Pathology](https://publons.com/journal/1787/brain-pathology) * [Child: Care, Health and Development](https://publons.com/journal/6111/child-care-health-and-development) * [Criminal Behaviour and Mental Health](https://publons.com/journal/3839/criminal-behaviour-and-mental-health) * [Depression and Anxiety](https://publons.com/journal/1528/depression-and-anxiety) * Developmental Neurobiology * [Developmental Science](https://publons.com/journal/1069/developmental-science) * [European Journal of Neuroscience](https://publons.com/journal/1441/european-journal-of-neuroscience) * [Genes, Brain and Behavior](https://publons.com/journal/1635/genes-brain-and-behavior) * [GLIA](https://publons.com/journal/1287/glia) * [Hippocampus](https://publons.com/journal/1056/hippocampus) * [Human Brain Mapping](https://publons.com/journal/500/human-brain-mapping) * [Journal for the Theory of Social Behaviour](https://publons.com/journal/7330/journal-for-the-theory-of-social-behaviour) * [Journal of Comparative Neurology](https://publons.com/journal/1306/journal-of-comparative-neurology) * [Journal of Neuroimaging](https://publons.com/journal/6379/journal-of-neuroimaging) * [Journal of Neuroscience Research](https://publons.com/journal/2778/journal-of-neuroscience-research) * [Journal of Organizational Behavior](https://publons.com/journal/1123/journal-of-organizational-behavior) * [Journal of the Peripheral Nervous System](https://publons.com/journal/3929/journal-of-the-peripheral-nervous-system) * [Muscle & Nerve](https://publons.com/journal/4448/muscle-and-nerve) * [Neural Pathology and Applied Neurobiology](https://publons.com/journal/2401/neuropathology-and-applied-neurobiology)
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