Reproducibility of functional brain alterations in major depressive disorder: Evidence from a multisite resting-state functional MRI study with 1,434 individuals

重性抑郁障碍 静息状态功能磁共振成像 再现性 心理学 神经影像学 眶额皮质 神经科学 样本量测定 功能连接 临床心理学 听力学 医学 心情 认知 统计 数学 前额叶皮质
作者
Mingrui Xia,Tianmei Si,Xiaoyi Sun,Qing Ma,Bangshan Liu,Li Wang,Jie Meng,Miao Chang,Xiaoqi Huang,Ziqi Chen,Yanqing Tang,Ke Xu,Qiyong Gong,Fei Wang,Jiang Qiu,Peng Xie,Lingjiang Li,Yong He
出处
期刊:NeuroImage [Elsevier BV]
卷期号:189: 700-714 被引量:87
标识
DOI:10.1016/j.neuroimage.2019.01.074
摘要

Resting-state functional MRI (R-fMRI) studies have demonstrated widespread alterations in brain function in patients with major depressive disorder (MDD). However, a clear and consistent conclusion regarding a repeatable pattern of MDD-relevant alterations is still limited due to the scarcity of large-sample, multisite datasets. Here, we address this issue by including a large R-fMRI dataset with 1434 participants (709 patients with MDD and 725 healthy controls) from five centers in China. Individual functional activity maps that represent very local to long-range connections are computed using the amplitude of low-frequency fluctuations, regional homogeneity and distance-related functional connectivity strength. The reproducibility analyses involve different statistical strategies, global signal regression, across-center consistency, clinical variables, and sample size. We observed significant hypoactivity in the orbitofrontal, sensorimotor, and visual cortices and hyperactivity in the frontoparietal cortices in MDD patients compared to the controls. These alterations are not affected by different statistical analysis strategies, global signal regression and medication status and are generally reproducible across centers. However, these between-group differences are partially influenced by the episode status and the age of disease onset in patients, and the brain-clinical variable relationship exhibits poor cross-center reproducibility. Bootstrap analyses reveal that at least 400 subjects in each group are required to replicate significant alterations (an extent threshold of P < .05 and a height threshold of P < .001) at 50% reproducibility. Together, these results highlight reproducible patterns of functional alterations in MDD and relevant influencing factors, which provides crucial guidance for future neuroimaging studies of this disorder.
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