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Combining neuroanatomical and clinical data to improve individualized early diagnosis of schizophrenia in subjects at high familial risk

机译:结合神经解剖学和临床数据来改善家族性高危受试者的精神分裂症的个体化早期诊断

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To date, there are no reliable markers for making an early diagnosis of schizophrenia before clinical diagnostic criteria are fully met. Neuroimaging and pattern classification techniques are promising tools towards predicting transition to schizophrenia. Here, we investigated the diagnostic performance of a combination of neuroanatomical and clinical data in predicting transition to schizophrenia in subjects at high familial risk (HR) for the disorder. Baseline structural magnetic resonance imaging (MRI) and clinical data from 17 HR subjects, who subsequently developed schizophrenia and an age and sex-matched group of 17 HR subjects who did not make a transition to the disease, yet had psychotic symptoms, were included in the analysis. We employed Support Vector Machine, along with a recursive feature selection technique to classify subjects at an individual level. Combination of both structural MRI and clinical data achieved an accuracy of 94% in predicting at baseline disease conversion in subjects at genetic HR. Overall, this paper presents a promising step in combining neuroanatomical and clinical information to improve early prediction of schizophrenia.
机译:迄今为止,尚没有可靠的标记物可以在完全符合临床诊断标准之前对精神分裂症进行早期诊断。神经影像和模式分类技术是预测向精神分裂症过渡的有前途的工具。在这里,我们调查了神经解剖学和临床数据的组合在预测患有高家族风险(HR)的受试者中向精神分裂症过渡的诊断性能。基线结构磁共振成像(MRI)和来自17名HR受试者的临床数据,这些受试者随后发展为精神分裂症,并进行了年龄和性别匹配的17例HR受试者的组,这些受试者未转变为疾病,但有精神病症状。分析。我们使用了支持向量机,以及递归特征选择技术来对个体进行分类。结构MRI和临床数据的组合在预测遗传HR患者的基线疾病转化率方面达到了94%的准确性。总体而言,本文提出了将神经解剖学和临床信息相结合以改善精神分裂症的早期预测的有希望的步骤。

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