한빛사논문
Dong Yun Lee a,b#, Narae Kim a,c#, ChulHyoung Park a,b, Sujin Gan c, Sang Joon Son d, Rae Woong Park a,c ‡, Bumhee Park a,e ‡
aDepartment of Biomedical Informatics, Ajou University School of Medicine, Suwon, South Korea
bDepartment of Medical Sciences, Graduate School of Ajou University, Suwon, Republic of Korea
cDepartment of Biomedical Sciences, Graduate School of Ajou University, Suwon, Republic of Korea
dDepartment of Psychiatry, Ajou University School of Medicine, Suwon, South Korea
eOffice of Biostatistics, Medical Research Collaborating Center, Ajou Research Institute for innovative medicine, Ajou University Medical Center, Suwon, Republic of Korea
#Those authors contributed equally as co-first author.
‡Those authors contributed equally as co-corresponding author.
Abstract
Although 20% of patients with depression receiving treatment do not achieve remission, predicting treatment-resistant depression (TRD) remains challenging. In this study, we aimed to develop an explainable multimodal prediction model for TRD using structured electronic medical record data, brain morphometry, and natural language processing. In total, 247 patients with a new depressive episode were included. TRD-predictive models were developed based on the combination of following parameters: selected tabular dataset features, independent components-map weightings from brain T1-weighted magnetic resonance imaging (MRI), and topic probabilities from clinical notes. All models applied the extreme gradient boosting (XGBoost) algorithm via five-fold cross-validation. The model using all data sources showed the highest area under the receiver operating characteristic of 0.794, followed by models that used combined brain MRI and structured data, brain MRI and clinical notes, clinical notes and structured data, brain MRI only, structured data only, and clinical notes only (0.770, 0.762, 0.728, 0.703, 0.684, and 0.569, respectively). Classifications of TRD were driven by several predictors, such as previous exposure to antidepressants and antihypertensive medications, sensorimotor network, default mode network, and somatic symptoms. Our findings suggest that a combination of clinical data with neuroimaging and natural language processing variables improves the prediction of TRD.
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