Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati 45219, OH, USA.
Huaxi MR Research Center (HMRRC), Department of Radiology, West China Hospital of Sichuan University, Chengdu 610041, PR China.
Psychol Med. 2023 Jul;53(9):4083-4093. doi: 10.1017/S0033291722000757. Epub 2022 Apr 8.
Identification of treatment-specific predictors of drug therapies for bipolar disorder (BD) is important because only about half of individuals respond to any specific medication. However, medication response in pediatric BD is variable and not well predicted by clinical characteristics.
A total of 121 youth with early course BD (acute manic/mixed episode) were prospectively recruited and randomized to 6 weeks of double-blind treatment with quetiapine ( = 71) or lithium ( = 50). Participants completed structural magnetic resonance imaging (MRI) at baseline before treatment and 1 week after treatment initiation, and brain morphometric features were extracted for each individual based on MRI scans. Positive antimanic treatment response at week 6 was defined as an over 50% reduction of Young Mania Rating Scale scores from baseline. Two-stage deep learning prediction model was established to distinguish responders and non-responders based on different feature sets.
Pre-treatment morphometry and morphometric changes occurring during the first week can both independently predict treatment outcome of quetiapine and lithium with balanced accuracy over 75% (all < 0.05). Combining brain morphometry at baseline and week 1 allows prediction with the highest balanced accuracy (quetiapine: 83.2% and lithium: 83.5%). Predictions in the quetiapine and lithium group were found to be driven by different morphometric patterns.
These findings demonstrate that pre-treatment morphometric measures and acute brain morphometric changes can serve as medication response predictors in pediatric BD. Brain morphometric features may provide promising biomarkers for developing biologically-informed treatment outcome prediction and patient stratification tools for BD treatment development.
确定双相情感障碍(BD)药物治疗的特定治疗预测因素非常重要,因为只有大约一半的个体对任何特定药物有反应。然而,儿科 BD 的药物反应是可变的,并且不能很好地通过临床特征来预测。
总共前瞻性招募了 121 名早期 BD 青少年(急性躁狂/混合发作),并随机分为 6 周的喹硫平(n = 71)或锂(n = 50)双盲治疗。参与者在治疗前和治疗开始后 1 周完成了结构磁共振成像(MRI),并根据 MRI 扫描为每位个体提取了脑形态计量学特征。第 6 周的阳性抗躁狂治疗反应定义为杨氏躁狂评定量表(YMRS)评分从基线下降超过 50%。基于不同的特征集,建立了两阶段深度学习预测模型,以区分反应者和非反应者。
治疗前的形态计量学和治疗开始后第一周发生的形态计量学变化均可独立预测喹硫平和锂的治疗结果,平衡准确率均超过 75%(均<0.05)。结合基线和第 1 周的脑形态计量学可实现预测,平衡准确率最高(喹硫平:83.2%,锂:83.5%)。在喹硫平和锂组中,预测结果是由不同的形态计量学模式驱动的。
这些发现表明,治疗前的形态计量学测量和急性脑形态计量学变化可以作为儿科 BD 的药物反应预测指标。脑形态计量学特征可能为开发基于生物学的治疗结果预测和 BD 治疗开发中的患者分层工具提供有前途的生物标志物。