Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, USA.
Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, USA.
J Child Psychol Psychiatry. 2022 Nov;63(11):1347-1358. doi: 10.1111/jcpp.13580. Epub 2022 Mar 15.
The treatment of depression in children and adolescents is a substantial public health challenge. This study examined artificial intelligence tools for the prediction of early outcomes in depressed children and adolescents treated with fluoxetine, duloxetine, or placebo.
The study samples included training datasets (N = 271) from patients with major depressive disorder (MDD) treated with fluoxetine and testing datasets from patients with MDD treated with duloxetine (N = 255) or placebo (N = 265). Treatment trajectories were generated using probabilistic graphical models (PGMs). Unsupervised machine learning identified specific depressive symptom profiles and related thresholds of improvement during acute treatment.
Variation in six depressive symptoms (difficulty having fun, social withdrawal, excessive fatigue, irritability, low self-esteem, and depressed feelings) assessed with the Children's Depression Rating Scale-Revised at 4-6 weeks predicted treatment outcomes with fluoxetine at 10-12 weeks with an average accuracy of 73% in the training dataset. The same six symptoms predicted 10-12 week outcomes at 4-6 weeks in (a) duloxetine testing datasets with an average accuracy of 76% and (b) placebo-treated patients with accuracies of 67%. In placebo-treated patients, the accuracies of predicting response and remission were similar to antidepressants. Accuracies for predicting nonresponse to placebo treatment were significantly lower than antidepressants.
PGMs provided clinically meaningful predictions in samples of depressed children and adolescents treated with fluoxetine or duloxetine. Future work should augment PGMs with biological data for refined predictions to guide the selection of pharmacological and psychotherapeutic treatment in children and adolescents with depression.
儿童和青少年抑郁症的治疗是一个重大的公共卫生挑战。本研究考察了人工智能工具在预测接受氟西汀、度洛西汀或安慰剂治疗的抑郁儿童和青少年早期结局方面的应用。
研究样本包括接受氟西汀治疗的重度抑郁症(MDD)患者的训练数据集(N=271)和接受度洛西汀(N=255)或安慰剂(N=265)治疗的 MDD 患者的测试数据集。使用概率图模型(PGM)生成治疗轨迹。无监督机器学习确定了特定的抑郁症状特征和急性治疗期间相关的改善阈值。
在 4-6 周时使用儿童抑郁评定量表修订版评估的 6 种抑郁症状(乐趣减少、社交退缩、过度疲劳、易怒、自尊心下降和抑郁情绪)的变化,预测了 10-12 周时接受氟西汀治疗的结局,在训练数据集中的平均准确率为 73%。同样的 6 种症状在 4-6 周时预测了(a)度洛西汀测试数据集中 10-12 周的结局,平均准确率为 76%,(b)接受安慰剂治疗的患者的准确率为 67%。在接受安慰剂治疗的患者中,预测反应和缓解的准确率与抗抑郁药相似。预测对安慰剂治疗无反应的准确率明显低于抗抑郁药。
PGM 为接受氟西汀或度洛西汀治疗的抑郁儿童和青少年样本提供了有临床意义的预测。未来的工作应将 PGM 与生物学数据相结合,以进行更精细的预测,从而为儿童和青少年抑郁症的药物和心理治疗选择提供指导。