Department of Magnetic Resonance Imaging, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Key Laboratory for Functional Magnetic Resonance Imaging and Molecular Imaging of Henan Province, Zhengzhou, China.
Hum Brain Mapp. 2021 Aug 1;42(11):3656-3666. doi: 10.1002/hbm.25460. Epub 2021 May 1.
Depression associated with structural brain abnormalities is hypothesized to be related with accelerated brain aging. However, there is far from a unified conclusion because of clinical variations such as medication status, cumulative illness burden. To explore whether brain age is accelerated in never-treated first-episode patients with depression and its association with clinical characteristics, we constructed a prediction model where gray matter volumes measured by voxel-based morphometry derived from T1-weighted MRI scans were treated as features. The prediction model was first validated using healthy controls (HCs) in two Chinese Han datasets (Dataset 1, N = 130 for HCs and N = 195 for patients with depression; Dataset 2, N = 270 for HCs) separately or jointly, then the trained prediction model using HCs (N = 400) was applied to never-treated first-episode patients with depression (N = 195). The brain-predicted age difference (brain-PAD) scores defined as the difference between predicted brain age and chronological age, were calculated for all participants and compared between patients with age-, gender-, educational level-matched HCs in Dataset 1. Overall, patients presented higher brain-PAD scores suggesting patients with depression having an "older" brain than expected. More specially, this difference occurred at illness onset (illness duration <3 months) and following 2 years then disappeared as the illness further advanced (>2 years) in patients. This phenomenon was verified by another data-driven method and significant correlation between brain-PAD scores and illness duration in patients. Our results reveal that accelerated brain aging occurs at illness onset and suggest it is a stage-dependent phenomenon in depression.
抑郁症与结构性脑异常相关,据推测与大脑老化加速有关。然而,由于药物状态、累积疾病负担等临床差异,目前远未得出统一的结论。为了探讨未经治疗的首发抑郁症患者的大脑年龄是否加速以及与临床特征的关系,我们构建了一个预测模型,其中基于体素的形态测量学测量的灰质体积作为特征。该预测模型首先使用来自 T1 加权 MRI 扫描的体素形态测量学测量的灰质体积作为特征,在两个中国汉族数据集(数据集 1,健康对照组(HCs)N=130,抑郁症患者 N=195;数据集 2,HCs N=270)中分别或联合进行了验证,然后使用 HCs(N=400)对该预测模型进行了训练,将其应用于未经治疗的首发抑郁症患者(N=195)。将预测的大脑年龄与实际年龄之间的差异定义为大脑预测年龄差异(brain-PAD)评分,对所有参与者进行计算,并在数据集 1 中比较了与年龄、性别、教育水平匹配的患者 HCs 的差异。总体而言,患者的 brain-PAD 评分较高,这表明抑郁症患者的大脑比预期的要“老”。更特别的是,这种差异出现在疾病发作时(病程<3 个月),并在 2 年后进一步出现,然后随着疾病的进一步发展(>2 年)而消失。这一现象通过另一种数据驱动的方法得到了验证,并且在患者中,brain-PAD 评分与病程之间存在显著相关性。我们的结果表明,大脑老化加速发生在疾病发作时,并提示这是抑郁症中一种与疾病阶段相关的现象。