Department of Psychiatry (DB, KP, GT), McGill University, Montreal, Canada; Department of Psychiatry (DB), Stanford University, Stanford, CA; Aifred Health (DB, CA, JM, RF, KP, SI, CP, GG, SQ, AA, MTS), Montreal, Canada.
Bar-Ilan University (AK, AR), Ramat Gan, Israel.
Am J Geriatr Psychiatry. 2024 Mar;32(3):280-292. doi: 10.1016/j.jagp.2023.09.009. Epub 2023 Sep 22.
Major depressive disorder (MDD) is a heterogeneous condition; multiple underlying neurobiological and behavioral substrates are associated with treatment response variability. Understanding the sources of this variability and predicting outcomes has been elusive. Machine learning (ML) shows promise in predicting treatment response in MDD, but its application is limited by challenges to the clinical interpretability of ML models, and clinicians often lack confidence in model results. In order to improve the interpretability of ML models in clinical practice, our goal was to demonstrate the derivation of treatment-relevant patient profiles comprised of clinical and demographic information using a novel ML approach.
We analyzed data from six clinical trials of pharmacological treatment for depression (total n = 5438) using the Differential Prototypes Neural Network (DPNN), a ML model that derives patient prototypes which can be used to derive treatment-relevant patient clusters while learning to generate probabilities for differential treatment response. A model classifying remission and outputting individual remission probabilities for five first-line monotherapies and three combination treatments was trained using clinical and demographic data. Prototypes were evaluated for interpretability by assessing differences in feature distributions (e.g. age, sex, symptom severity) and treatment-specific outcomes.
A 3-prototype model achieved an area under the receiver operating curve of 0.66 and an expected absolute improvement in remission rate for those receiving the best predicted treatment of 6.5% (relative improvement of 15.6%) compared to the population remission rate. We identified three treatment-relevant patient clusters. Cluster A patients tended to be younger, to have increased levels of fatigue, and more severe symptoms. Cluster B patients tended to be older, female, have less severe symptoms, and the highest remission rates. Cluster C patients had more severe symptoms, lower remission rates, more psychomotor agitation, more intense suicidal ideation, and more somatic genital symptoms.
It is possible to produce novel treatment-relevant patient profiles using ML models; doing so may improve interpretability of ML models and the quality of precision medicine treatments for MDD.
重度抑郁症(MDD)是一种异质性疾病;与治疗反应变异性相关的有多个潜在的神经生物学和行为学基础。理解这种变异性的来源并预测结果一直难以捉摸。机器学习(ML)在预测 MDD 的治疗反应方面显示出了前景,但由于 ML 模型的临床可解释性挑战以及临床医生对模型结果缺乏信心,其应用受到限制。为了提高 ML 模型在临床实践中的可解释性,我们的目标是展示如何使用一种新的 ML 方法,从临床和人口统计学信息中得出与治疗相关的患者特征。
我们使用差异原型神经网络(DPNN)分析了六项抗抑郁药物治疗临床试验的数据(总 n = 5438),这是一种 ML 模型,它可以从数据中提取患者原型,用于从学习生成差异治疗反应的概率中得出与治疗相关的患者聚类。使用临床和人口统计学数据训练了一个分类缓解并为五种一线单药治疗和三种联合治疗输出个体缓解概率的模型。通过评估特征分布(例如年龄、性别、症状严重程度)和特定于治疗的结果之间的差异来评估原型的可解释性。
一个 3 原型模型的接收器操作特征曲线下面积为 0.66,对于接受最佳预测治疗的患者,缓解率的预期绝对提高为 6.5%(相对提高 15.6%),而人群缓解率为 0.66。我们确定了三个与治疗相关的患者聚类。聚类 A 的患者往往更年轻,疲劳程度更高,症状更严重。聚类 B 的患者年龄较大,女性,症状较轻,缓解率最高。聚类 C 的患者症状更严重,缓解率较低,精神运动性激越、自杀意念更强烈,以及更多的躯体生殖器症状。
使用 ML 模型可以生成新的与治疗相关的患者特征;这样做可能会提高 ML 模型的可解释性和 MDD 的精准医学治疗质量。