Wolfson Centre for Young People's Mental Health, Section of Child and Adolescent Psychiatry, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
J Child Psychol Psychiatry. 2023 Mar;64(3):367-375. doi: 10.1111/jcpp.13704. Epub 2022 Sep 12.
Parental depression is common and is a major risk factor for depression in adolescents. Early identification of adolescents at elevated risk of developing major depressive disorder (MDD) in this group could improve early access to preventive interventions.
Using longitudinal data from 337 adolescents at high familial risk of depression, we developed a risk prediction model for adolescent MDD. The model was externally validated in an independent cohort of 1,384 adolescents at high familial risk. We assessed predictors at baseline and MDD at follow-up (a median of 2-3 years later). We compared the risk prediction model to a simple comparison model based on screening for depressive symptoms. Decision curve analysis was used to identify which model-predicted risk score thresholds were associated with the greatest clinical benefit.
The MDD risk prediction model discriminated between those adolescents who did and did not develop MDD in the development (C-statistic = .783, IQR (interquartile range) = .779, .778) and the validation samples (C-statistic = .722, IQR = -.694, .741). Calibration in the validation sample was good to excellent (calibration intercept = .011, C-slope = .851). The MDD risk prediction model was superior to the simple comparison model where discrimination was no better than chance (C-statistic = .544, IQR = .536, .572). Decision curve analysis found that the highest clinical utility was at the lowest risk score thresholds (0.01-0.05).
The developed risk prediction model successfully discriminated adolescents who developed MDD from those who did not. In practice, this model could be further developed with user involvement into a tool to target individuals for low-intensity, selective preventive intervention.
父母抑郁在青少年中很常见,是青少年抑郁的主要危险因素。在该群体中,早期识别有发生重度抑郁障碍(MDD)风险的青少年,可改善他们早期获得预防干预的机会。
我们利用来自 337 名有抑郁家族高风险的青少年的纵向数据,为青少年 MDD 建立了风险预测模型。该模型在一个有抑郁家族高风险的 1384 名青少年的独立队列中进行了外部验证。我们在基线评估预测指标,并在随访时(中位随访时间为 2-3 年后)评估 MDD。我们比较了风险预测模型与基于抑郁症状筛查的简单比较模型。决策曲线分析用于确定与最大临床获益相关的模型预测风险评分阈值。
MDD 风险预测模型在发展队列(区分度 C 统计量=0.783,IQR(四分位间距)=0.779,0.778)和验证样本(区分度 C 统计量=0.722,IQR=0.694,0.741)中均能区分出那些患有和未患有 MDD 的青少年。验证样本中的校准良好至优秀(校准截距=0.011,C-斜率=0.851)。MDD 风险预测模型优于简单比较模型,后者的区分度不如随机(区分度 C 统计量=0.544,IQR=0.536,0.572)。决策曲线分析发现,最高的临床实用性在最低风险评分阈值(0.01-0.05)。
所开发的风险预测模型成功地区分出患有 MDD 的青少年和未患有 MDD 的青少年。在实践中,该模型可以通过用户参与进一步开发成一种针对个体的低强度、选择性预防干预工具。