Interpretable machine learning model for characterizing magnetic susceptibility-based biomarkers in first episode psychosis

IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS
Pamela Franco , Cristian Montalba , Raúl Caulier-Cisterna , Carlos Milovic , Alfonso González , Juan Pablo Ramirez-Mahaluf , Juan Undurraga , Rodrigo Salas , Nicolás Crossley , Cristian Tejos , Sergio Uribe
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引用次数: 0

Abstract

Background and Purpose

Several studies have shown changes in neurochemicals within the deep-brain nuclei of patients with psychosis. These alterations indicate a dysfunction in dopamine within subcortical regions affected by fluctuations in iron concentrations. Quantitative Susceptibility Mapping (QSM) is a method employed to measure iron concentration, offering a potential means to identify dopamine dysfunction in these subcortical areas. This study employed a random forest algorithm to predict susceptibility features of the First-Episode Psychosis (FEP) and the response to antipsychotics using Shapley Additionality Explanation (SHAP) values.

Methods

3D multi-echo Gradient Echo (GRE) and T1-weighted GRE were obtained in 61 healthy-volunteers (HV) and 76 FEP patients (32 % Treatment-Resistant Schizophrenia (TRS) and 68 % treatment-Responsive Schizophrenia (RS)) using a 3T Philips Ingenia MRI scanner. QSM and R2* were reconstructed and averaged in twenty-two segmented regions of interest. We used a Sequential Forward Selection as a feature selection algorithm and a Random Forest as a model to predict FEP patients and their response to antipsychotics. We further applied the SHAP framework to identify informative features and their interpretations. Finally, multiple correlation patterns from magnetic susceptibility parameters were extracted using hierarchical clustering.

Results

Our approach accurately classifies HV and FEP patients with 76.48 ± 10.73 % accuracy (using four features) and TRS vs RS patients with 76.43 ± 12.57 % accuracy (using four features), using 10-fold stratified cross-validation. The SHAP analyses indicated the top four nonlinear relationships between the selected features. Hierarchical clustering revealed two groups of correlated features for each study.

Conclusions

Early prediction of treatment response enables tailored strategies for FEP patients with treatment resistance, ensuring timely and effective interventions.

Abstract Image

表征首发精神病中基于磁化率的生物标志物的可解释机器学习模型
背景与目的几项研究表明,精神病患者脑深部核内的神经化学物质发生了变化。这些改变表明受铁浓度波动影响的皮质下区域多巴胺功能障碍。定量敏感性制图(QSM)是一种测量铁浓度的方法,为识别这些皮质下区域的多巴胺功能障碍提供了一种潜在的手段。本研究采用随机森林算法预测首发精神病(FEP)的易感性特征,并使用Shapley附加性解释(SHAP)值预测抗精神病药物的反应。方法采用Philips Ingenia 3T MRI扫描,对61例健康志愿者(HV)和76例FEP患者(治疗难治性精神分裂症(TRS)占32%,治疗反应性精神分裂症(RS)占68%)进行三维多回波梯度回波(GRE)和t1加权GRE采集。在22个感兴趣的分割区域中重构QSM和R2*并取平均值。我们使用顺序前向选择作为特征选择算法和随机森林作为模型来预测FEP患者及其对抗精神病药物的反应。我们进一步应用SHAP框架来识别信息特征及其解释。最后,利用分层聚类方法提取磁化率参数的多重相关模式。结果该方法对HV和FEP患者的分类准确率为76.48±10.73%(使用4个特征),对TRS和RS患者的分类准确率为76.43±12.57%(使用4个特征),采用10倍分层交叉验证。SHAP分析表明了所选特征之间的前四种非线性关系。分层聚类揭示了每项研究的两组相关特征。结论早期预测治疗反应可以为FEP耐药患者提供针对性的治疗策略,确保及时有效的干预。
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来源期刊
Computer methods and programs in biomedicine
Computer methods and programs in biomedicine 工程技术-工程:生物医学
CiteScore
12.30
自引率
6.60%
发文量
601
审稿时长
135 days
期刊介绍: To encourage the development of formal computing methods, and their application in biomedical research and medical practice, by illustration of fundamental principles in biomedical informatics research; to stimulate basic research into application software design; to report the state of research of biomedical information processing projects; to report new computer methodologies applied in biomedical areas; the eventual distribution of demonstrable software to avoid duplication of effort; to provide a forum for discussion and improvement of existing software; to optimize contact between national organizations and regional user groups by promoting an international exchange of information on formal methods, standards and software in biomedicine. Computer Methods and Programs in Biomedicine covers computing methodology and software systems derived from computing science for implementation in all aspects of biomedical research and medical practice. It is designed to serve: biochemists; biologists; geneticists; immunologists; neuroscientists; pharmacologists; toxicologists; clinicians; epidemiologists; psychiatrists; psychologists; cardiologists; chemists; (radio)physicists; computer scientists; programmers and systems analysts; biomedical, clinical, electrical and other engineers; teachers of medical informatics and users of educational software.
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