Transcriptomic and Neuroimaging Data Integration Enhances Machine Learning Classification of Schizophrenia

Mengya Wang, Shu Zhao, Di Wu, Ya-Hong Zhang, Yan-Kun Han, Kun Zhao, Ting Qi, Yong Liu, Long-Biao Cui, Yongbin Wei
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Abstract

Schizophrenia is a polygenetic disorder associated with changes in brain structure and function. Integrating macroscale brain features and microscale genetic data may provide a more complete overview of the disease etiology and may serve as potential diagnostic markers for schizophrenia. We aim to systematically evaluate the impact of multi-scale neuroimaging and transcriptomic data fusion in schizophrenia classification models. we collected brain imaging data and blood RNA-seq data from 43 schizophrenia patients and 60 age-, gender-matched healthy controls, and we extracted multi-omics features of macroscale brain morphology, brain structural connectivity and functional connectivity, and gene transcription of schizophrenia risk genes. Multi-scale data fusion was performed using a machine learning integration framework, together with several conventional machine learning methods and neural networks for patient classification. We found that multi-omics data fusion in conventional machine learning models achieved the highest accuracy in contrast to the single-modality models, with AUC improvements of 8.88% to 22.64%. Similar findings were observed for the neural network, showing an increase of 16.57% for the multimodal classification accuracy compared to the single-modal average. In addition, we identified several brain regions in the left posterior cingulate and right frontal pole that contribute to disease classification. We provide empirical evidence for the increased accuracy achieved by imaging genetic data integration in schizophrenia classification. Multi-scale data fusion holds promise for enhancing diagnostic precision, facilitating early detection and personalizing treatment regimens in schizophrenia.
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转录组和神经影像学数据整合增强了精神分裂症的机器学习分类能力
精神分裂症是一种与大脑结构和功能变化相关的多基因疾病。整合宏观尺度的大脑特征和微观尺度的遗传数据可以更全面地了解疾病的病因,并可作为精神分裂症的潜在诊断标志物。 我们收集了 43 名精神分裂症患者和 60 名年龄、性别匹配的健康对照者的脑成像数据和血液 RNA-seq 数据,提取了宏观脑形态学、脑结构连通性和功能连通性以及精神分裂症风险基因转录的多组学特征。多尺度数据融合采用了机器学习集成框架,并结合几种传统的机器学习方法和神经网络对患者进行分类。 我们发现,在传统的机器学习模型中,多组学数据融合的准确率与单模态模型相比最高,AUC提高了8.88%至22.64%。神经网络也有类似发现,多模态分类准确率比单模态平均准确率提高了 16.57%。此外,我们还发现了左侧扣带回后部和右侧额极的几个脑区有助于疾病分类。 我们为在精神分裂症分类中通过成像基因数据整合提高准确性提供了经验证据。多尺度数据融合有望提高精神分裂症的诊断精确度、促进早期检测和个性化治疗方案。
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