Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, USA.
Department of Neurology and Neurosurgery, Icahn School of Medicine at Mount Sinai, New York, USA.
Neuropsychopharmacology. 2023 Dec;48(13):1901-1909. doi: 10.1038/s41386-023-01653-w. Epub 2023 Jul 25.
Recurrent episodes in major depressive disorder (MDD) are common but the neuroimaging features predictive of recurrence are not established. Participants in the Predictors of Remission in Depression to Individual and Combined Treatments (PReDICT) study who achieved remission after 12 weeks of treatment withcognitive behavior therapy, duloxetine, or escitalopram were prospectively monitored for up to 21 months for recurrence. Neuroimaging markers predictive of recurrence were identified from week 12 functional magnetic resonance imaging scans by analyzing whole-brain resting state functional connectivity (RSFC) using seeds for four brain networks that are altered in MDD. Neuroimaging correlates of established clinical predictors of recurrence, including the magnitude of depressive (Hamilton Depression Rating Scale), anxiety (Hamilton Anxiety Rating Scale) symptom severity at time of remission, and a comorbid anxiety disorder were examined for their similarity to the neuroimaging predictors of recurrence. Of the 344 patients randomized in PReDICT, 61 achieved remission and had usable scans for analysis, 9 of whom experienced recurrence during follow-up. Recurrence was predicted by: 1) increased RSFC between subcallosal cingulate cortex (SCC) and right anterior insula, 2) decreased RSFC between SCC and bilateral primary visual cortex, and 3) decreased RSFC between insula and bilateral caudate. Week 12 depression and anxiety scores were negatively correlated with RSFC strength between executive control and default mode networks, but they were not correlated with the three RSFC patterns predicting recurrence. We conclude that altered RSFC in SCC and anterior insula networks are prospective risk factors associated with MDD recurrence, reflecting additional sources of risk beyond clinical measures.
复发性重度抑郁症(MDD)较为常见,但可预测复发的神经影像学特征尚不确定。在Predictors of Remission in Depression to Individual and Combined Treatments(PReDICT)研究中,接受认知行为疗法、度洛西汀或依他普仑治疗 12 周后达到缓解的参与者,前瞻性监测长达 21 个月的复发情况。通过分析 MDD 改变的四个大脑网络的种子,从第 12 周的功能磁共振成像扫描中确定了可预测复发的神经影像学标志物。研究了与复发相关的既定临床预测因子(包括缓解时抑郁(汉密尔顿抑郁评定量表)、焦虑(汉密尔顿焦虑评定量表)症状严重程度的幅度,以及共病焦虑障碍)与预测复发的神经影像学标志物的相似性。在 PReDICT 中随机分配的 344 名患者中,有 61 名患者达到缓解并进行了可用于分析的扫描,其中 9 名在随访期间复发。复发可由以下因素预测:1)扣带回下皮质(SCC)和右侧前岛叶之间的 rsfc 增加;2)SCC 与双侧初级视觉皮层之间的 rsfc 减少;3)岛叶与双侧尾状核之间的 rsfc 减少。第 12 周的抑郁和焦虑评分与执行控制和默认模式网络之间的 rsfc 强度呈负相关,但与预测复发的三个 rsfc 模式无关。我们的结论是,SCC 和前岛叶网络中改变的 rsfc 是与 MDD 复发相关的前瞻性风险因素,反映了临床测量之外的额外风险源。