Predicting antipsychotic responsiveness using a machine learning classifier trained on plasma levels of inflammatory markers in schizophrenia.

IF 6.2 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2025-02-14 DOI:10.1038/s41398-025-03264-z
Jie Yin Yee, Ser-Xian Phua, Yuen Mei See, Anand Kumar Andiappan, Wilson Wen Bin Goh, Jimmy Lee
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Abstract

We apply machine learning techniques to navigate the multifaceted landscape of schizophrenia. Our method entails the development of predictive models, emphasizing peripheral inflammatory biomarkers, which are classified into treatment response subgroups: antipsychotic-responsive, clozapine-responsive, and clozapine-resistant. The cohort comprises 146 schizophrenia patients (49 antipsychotics-responsive, 68 clozapine-responsive, 29 clozapine-resistant) and 49 healthy controls. Protein levels of immune biomarkers were quantified using the Olink Target 96 Inflammation Panel (Olink®, Uppsala, Sweden). To predict labels, a support vector machine (SVM) classifier is trained on the Olink®data matrix and evaluated via leave-one-out cross-validation. Associated protein biomarkers are identified via recursive feature elimination. We constructed three separate predictive models for binary classification: one to discern healthy controls from individuals with schizophrenia (AUC = 0.74), another to differentiate individuals who were responsive to antipsychotics (AUC = 0.88), and a third to distinguish treatment-resistant individuals (AUC = 0.78). Employing machine learning techniques, we identified features capable of distinguishing between treatment response subgroups. In this study, SVM demonstrates the power of machine learning to uncover subtle signals often overlooked by traditional statistics. Unlike t-tests, it handles multiple features simultaneously, capturing complex data relationships. Chosen for simplicity, robustness, and reliance on strong feature sets, its integration with explainable AI techniques like SHapely Additive exPlanations enhances model interpretability, especially for biomarker screening. This study highlights the potential of integrating machine learning techniques in clinical practice. Not only does it deepen our understanding of schizophrenia's heterogeneity, but it also holds promise for enhancing predictive accuracy, thereby facilitating more targeted and effective interventions in the treatment of this complex mental health disorder.

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使用根据精神分裂症患者血浆炎症标志物水平训练的机器学习分类器预测抗精神病药的反应性。
我们应用机器学习技术来导航精神分裂症的多面景观。我们的方法需要开发预测模型,强调外周炎症生物标志物,将其分为治疗反应亚组:抗精神病反应,氯氮平反应和氯氮平耐药。该队列包括146名精神分裂症患者(49名抗精神病药应答,68名氯氮平应答,29名氯氮平耐药)和49名健康对照。免疫生物标志物的蛋白水平使用Olink Target 96 Inflammation Panel (Olink®,Uppsala, Sweden)进行量化。为了预测标签,支持向量机(SVM)分类器在Olink®数据矩阵上进行训练,并通过留一交叉验证进行评估。通过递归特征消除识别相关蛋白质生物标志物。我们构建了三个独立的二元分类预测模型:一个用于区分精神分裂症患者和健康对照者(AUC = 0.74),另一个用于区分抗精神病药物应答者(AUC = 0.88),第三个用于区分治疗抵抗者(AUC = 0.78)。利用机器学习技术,我们确定了能够区分治疗反应亚组的特征。在这项研究中,支持向量机展示了机器学习的力量,可以发现传统统计经常忽略的微妙信号。与t测试不同,它同时处理多个特征,捕获复杂的数据关系。选择简单、健壮和依赖强大的功能集,它与可解释的人工智能技术(如shape Additive exPlanations)的集成增强了模型的可解释性,特别是在生物标志物筛选方面。这项研究强调了在临床实践中整合机器学习技术的潜力。它不仅加深了我们对精神分裂症异质性的理解,而且还有望提高预测的准确性,从而促进更有针对性和更有效的干预措施,治疗这种复杂的精神健康障碍。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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