Nevada institute of personalized medicine, University of Nevada Las Vegas, Las Vegas, NV, 89154-4009, USA.
Department of Psychology, University of Nevada Las Vegas, 4505 S. Maryland Parkway, Las Vegas, NV, 89154-4009, USA.
J Neuroimmune Pharmacol. 2018 Dec;13(4):532-540. doi: 10.1007/s11481-018-9811-8. Epub 2018 Oct 1.
Schizophrenia is genetically heterogeneous and comorbid with many conditions. In this study, we explored polygenic scores (PGSs) from genetically related conditions and traits to predict schizophrenia diagnosis using both logistic regression and deep neural network (DNN) models. We used the combined Molecular Genetics of Schizophrenia and Swedish Schizophrenia Case Control Study (MGS + SSCCS) data for training and testing the models, and used the Clinical Antipsychotic Trials for Intervention Effectiveness (CATIE) data as independent validation. We screened 28 conditions and traits comorbid with schizophrenia to identify traits as potential predictors and used LASSO regression to select predictors for model construction. We investigated how PGS calculation influenced model performance. We found that the inclusion of comorbid traits improved model performance and PGSs calculated from two traits were more generalizable in independent validation. With a DNN model using 19 PGS predictors, we accomplished a prediction accuracy of 0.813 and an AUC of 0.905 in the MGS + SSCCS data. When this model was validated with the CATIE data, it achieved an accuracy of 0.721 and AUC of 0.747. Our results indicate that PGSs alone may not be sufficient to predict schizophrenia accurately and the inclusion of behavioral and clinical data may be necessary for more accurate prediction model.
精神分裂症在遗传上具有异质性,并且与许多疾病共病。在这项研究中,我们使用逻辑回归和深度神经网络(DNN)模型,探索了与遗传相关的疾病和特征的多基因评分(PGS),以预测精神分裂症的诊断。我们使用合并的精神分裂症分子遗传学和瑞典精神分裂症病例对照研究(MGS + SSCCS)数据进行训练和测试模型,并使用临床抗精神病药物干预有效性试验(CATIE)数据进行独立验证。我们筛选了 28 种与精神分裂症共病的疾病和特征,以确定特征作为潜在预测因子,并使用 LASSO 回归选择模型构建的预测因子。我们研究了 PGS 计算如何影响模型性能。我们发现,共病特征的纳入可以提高模型性能,并且从两个特征计算的 PGS 在独立验证中更具有普遍性。使用具有 19 个 PGS 预测因子的 DNN 模型,我们在 MGS + SSCCS 数据中实现了 0.813 的预测准确率和 0.905 的 AUC。当该模型使用 CATIE 数据进行验证时,它的准确率为 0.721,AUC 为 0.747。我们的结果表明,PGS 本身可能不足以准确预测精神分裂症,并且可能需要包含行为和临床数据,以便构建更准确的预测模型。