Nguyen Kevin P, Fatt Cherise Chin, Treacher Alex, Mellema Cooper, Trivedi Madhukar H, Montillo Albert
University of Texas Southwestern Medical Center.
Predict Intell Med. 2019 Oct;11843:53-62. doi: 10.1007/978-3-030-32281-6_6. Epub 2019 Oct 10.
Major depressive disorder is a primary cause of disability in adults with a lifetime prevalence of 6-21% worldwide. While medical treatment may provide symptomatic relief, response to any given antidepressant is unpredictable and patient-specific. The standard of care requires a patient to sequentially test different antidepressants for 3 months each until an optimal treatment has been identified. For 30-40% of patients, no effective treatment is found after more than one year of this trial-and-error process, during which a patient may suffer loss of employment or marriage, undertreated symptoms, and suicidal ideation. This work develops a predictive model that may be used to expedite the treatment selection process by identifying for individual patients whether the patient will respond favorably to bupropion, a widely prescribed antidepressant, using only pretreatment imaging data. This is the first model to do so for individuals for bupropion. Specifically, a deep learning predictor is trained to estimate the 8-week change in Hamilton Rating Scale for Depression (HAMD) score from pretreatment task-based functional magnetic resonance imaging (fMRI) obtained in a randomized controlled antidepressant trial. An unbiased neural architecture search is conducted over 800 distinct model architecture and brain parcellation combinations, and patterns of model hyperparameters yielding the highest prediction accuracy are revealed. The winning model identifies bupropion-treated subjects who will experience remission with the number of subjects needed-to-treat (NNT) to lower morbidity of only 3.2 subjects. It attains a substantially high neuroimaging study effect size explaining 26% of the variance ( = 0.26) and the model predicts post-treatment change in the 52-point HAMD score with an RMSE of 4.71. These results support the continued development of fMRI and deep learning-based predictors of response for additional depression treatments.
重度抑郁症是成年人残疾的主要原因,在全球范围内终生患病率为6%-21%。虽然药物治疗可能会缓解症状,但对任何一种特定抗抑郁药的反应都是不可预测的,且因人而异。护理标准要求患者依次对不同的抗抑郁药进行为期3个月的试验,直到确定最佳治疗方案。在这种反复试验的过程中,超过一年后,30%-40%的患者仍未找到有效的治疗方法,在此期间,患者可能会面临失业或婚姻破裂、症状未得到充分治疗以及有自杀念头等问题。这项研究开发了一种预测模型,该模型可通过仅使用治疗前的影像数据来确定个体患者是否会对广泛使用的抗抑郁药安非他酮产生良好反应,从而加快治疗选择过程。这是首个针对个体使用安非他酮的此类模型。具体而言,在一项随机对照抗抑郁试验中,通过基于任务的治疗前功能磁共振成像(fMRI)训练一个深度学习预测器,以估计汉密尔顿抑郁量表(HAMD)评分在8周内的变化。对800种不同的模型架构和脑部分割组合进行了无偏神经架构搜索,并揭示了产生最高预测准确率的模型超参数模式。获胜模型识别出使用安非他酮治疗后将实现缓解的受试者,所需治疗的受试者数量(NNT)低至仅3.2名受试者。它获得了相当高的神经影像研究效应大小,解释了26%的方差( = 0.26),并且该模型预测治疗后52分HAMD评分的变化,均方根误差(RMSE)为4.71。这些结果支持了基于fMRI和深度学习的反应预测器在其他抑郁症治疗中的持续开发。