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Precision psychiatry with immunological and cognitive biomarkers: a multi-domain prediction for the diagnosis of bipolar disorder or schizophrenia using machine learning

机译:具有免疫和认知生物标志物的精神精神病学:使用机器学习诊断双相障碍或精神分裂症的多域预测

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Precision psychiatry is attracting increasing attention lately as a recognized priority. One of the goals of precision psychiatry is to develop tools capable of aiding a clinically informed psychiatric diagnosis objectively. Cognitive, inflammatory and immunological factors are altered in both bipolar disorder (BD) and schizophrenia (SZ), however, most of these alterations do not respect diagnostic boundaries from a phenomenological perspective and possess great variability in different individuals with the same phenotypic diagnosis and, consequently, none so far has proven to have the ability of reliably aiding in the differential diagnosis of BD and SZ. We developed a probabilistic multi-domain data integration model consisting of immune and inflammatory biomarkers in peripheral blood and cognitive biomarkers using machine learning to predict diagnosis of BD and SZ. A total of 416 participants, being 323, 372, and 279 subjects for blood, cognition and combined biomarkers analysis, respectively. Our multi-domain model performances for the BD vs. control (sensitivity 80% and specificity 71%) and for the SZ vs. control (sensitivity 84% and specificity 81%) pairs were high in general, however, our multi-domain model had only moderate performance for the differential diagnosis of BD and SZ (sensitivity 71% and specificity 73%). In conclusion, our results show that the diagnosis of BD and of SZ, and that the differential diagnosis of BD and SZ can be predicted with possible clinical utility by a computational machine learning algorithm employing blood and cognitive biomarkers, and that their integration in a multi-domain outperforms algorithms based in only one domain. Independent studies are needed to validate these findings.
机译:精密精神病学最近作为公认的优先事项吸引了不断的关注。精密精神病学的目标之一是开发能够客观地帮助临床知识的精神病诊断的工具。在双相障碍(BD)和精神分裂症(SZ)中,认知,炎症和免疫因子被改变,然而,大多数这些改变不尊重从现象学的角度来尊重诊断界限,并且在具有相同表型诊断的不同个体中具有很大的变化性,因此,到目前为止已被证明具有可靠地帮助在BD和SZ的差异诊断中的能力。我们开发了一种概率的多领域数据集成模型,包括使用机器学习的外周血和认知生物标志物中的免疫和炎症生物标志物,以预测BD和SZ的诊断。共有416名参与者,323,372和279名血液,认知和合并生物标志物分析。我们的BD与控制(灵敏度80%和特异性71%)的多域模型性能和SZ与控制(灵敏度84%和特异性81%)对均高,但是我们的多域模型只有适度的BD和SZ差异诊断(敏感性71%和特异性73%)。总之,我们的结果表明,BD和SZ的诊断,以及BD和SZ的差异诊断可以通过采用血液和认知生物标志物的计算机器学习算法来预测可能的临床效用,以及它们在多个中的集成-Domain优于仅基于一个域的算法。需要独立的研究来验证这些发现。

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