Orygen, The National Centre of Excellence in Youth Mental Health, 35 Poplar Road, Parkville, Victoria 3052, Australia; Centre for Youth Mental Health, The University of Melbourne, 35 Poplar Road, Parkville, Victoria 3052, Australia.
Orygen, The National Centre of Excellence in Youth Mental Health, 35 Poplar Road, Parkville, Victoria 3052, Australia.
Dev Cogn Neurosci. 2019 Oct;39:100700. doi: 10.1016/j.dcn.2019.100700. Epub 2019 Aug 8.
Major depressive disorder (MDD) often emerges during adolescence with detrimental effects on development as well as lifetime consequences. Identifying neurobiological markers that are associated with the onset or course of this disorder in childhood and adolescence is important for early recognition and intervention and, potentially, for the prevention of illness onset. In this systematic review, 68 longitudinal neuroimaging studies, from 34 unique samples, that examined the association of neuroimaging markers with onset or changes in paediatric depression published up to 1 February 2019 were examined. These studies employed different imaging modalities at baseline; structural magnetic resonance imaging (MRI), diffusion tensor imaging (DTI), functional MRI (fMRI) or electroencephalography (EEG). Most consistent evidence across studies was found for blunted reward-related (striatal) activity (fMRI and EEG) as a potential biological marker for both MDD onset and course. With regard to structural brain measures, the results were highly inconsistent, likely caused by insufficient power to detect complex mediating effects of genetic and environmental factors in small sample sizes. Overall, there were a limited number of samples, and confounding factors such as sex and pubertal development were often not considered, whereas these factors are likely to be relevant especially in this age range.
重度抑郁症(MDD)常于青少年期发病,对发育和终生都会产生不良影响。识别与儿童和青少年时期该障碍发病或病程相关的神经生物学标志物,对于早期识别和干预,以及潜在的疾病预防至关重要。在这项系统综述中,我们共纳入了 34 个独特样本的 68 项纵向神经影像学研究,这些研究探讨了神经影像学标志物与儿科抑郁症发病或变化之间的关系,相关研究均于 2019 年 2 月 1 日前发表。这些研究在基线时使用了不同的成像方式,包括结构磁共振成像(MRI)、弥散张量成像(DTI)、功能磁共振成像(fMRI)或脑电图(EEG)。大多数研究发现,与奖赏相关的(纹状体)活动减弱(fMRI 和 EEG)是 MDD 发病和病程的潜在生物学标志物。至于结构脑测量,结果高度不一致,这可能是由于在小样本量中检测遗传和环境因素的复杂中介效应的能力不足所致。总体而言,样本数量有限,而且经常没有考虑混杂因素,如性别和青春期发育,而这些因素在这个年龄段可能特别相关。