Multimodal fusion of brain signals for robust prediction of psychosis transition.

IF 3 Q2 PSYCHIATRY Schizophrenia (Heidelberg, Germany) Pub Date : 2024-05-21 DOI:10.1038/s41537-024-00464-2
Jenna M Reinen, Pablo Polosecki, Eduardo Castro, Cheryl M Corcoran, Guillermo A Cecchi, Tiziano Colibazzi
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Abstract

The prospective study of youths at clinical high risk (CHR) for psychosis, including neuroimaging, can identify neural signatures predictive of psychosis outcomes using algorithms that integrate complex information. Here, to identify risk and psychosis conversion, we implemented multiple kernel learning (MKL), a multimodal machine learning approach allowing patterns from each modality to inform each other. Baseline multimodal scans (n = 74, 11 converters) included structural, resting-state functional imaging, and diffusion-weighted data. Multimodal MKL outperformed unimodal models (AUC = 0.73 vs. 0.66 in predicting conversion). Moreover, patterns learned by MKL were robust to training set variations, suggesting it can identify cross-modality redundancies and synergies to stabilize the predictive pattern. We identified many predictors consistent with the literature, including frontal cortices, cingulate, thalamus, and striatum. This highlights the advantage of methods that leverage the complex pathophysiology of psychosis.

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多模态融合大脑信号,稳健预测精神病转变。
对处于精神病临床高风险(CHR)的青少年进行前瞻性研究,包括神经影像学研究,可以利用整合复杂信息的算法识别预测精神病结果的神经特征。在这里,为了识别风险和精神病转换,我们采用了多核学习(MKL),这是一种多模态机器学习方法,可以让每种模态的模式相互借鉴。基线多模态扫描(n = 74,11 名转换者)包括结构、静息态功能成像和弥散加权数据。多模态 MKL 的表现优于单模态模型(预测转换的 AUC = 0.73 对 0.66)。此外,MKL 学习到的模式对训练集的变化具有鲁棒性,这表明它可以识别跨模态冗余和协同作用,从而稳定预测模式。我们发现了许多与文献一致的预测因子,包括额叶皮层、扣带回、丘脑和纹状体。这凸显了利用精神病复杂病理生理学的方法的优势。
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Publisher Correction: Structural and functional connectivity in relation to executive functions in antipsychotic-naïve patients with first episode schizophrenia. Gene expression changes in Brodmann's Area 46 differentiate epidermal growth factor and immune system interactions in schizophrenia and mood disorders. Gut microbiome and schizophrenia: insights from two-sample Mendelian randomization. Publisher Correction: Longitudinal study on hippocampal subfields and glucose metabolism in early psychosis. Updated rationale for the initial antipsychotic selection for patients with schizophrenia.
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