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Xia, M.

Publications and source records attributed to Xia, M..

2 recordsLinked to original sources

Transcriptional Signatures of the Hierarchical Chronnectome Organization in the Human Brain

The chronnectome of the human brain represents the dynamics of functional organization in interacting regions, but its organizational principle and the underlying molecular mechanisms remain unclear. Using task-free fMRI and postmortem gene expression data, we conduct a transcriptome-chronnectome association study to investigate the spatial configurations of dynamic brain networks and their associations with transcriptional signatures. We reveal a spatial layout of network dynamics in the human brain chronnectome that reflects the cortical hierarchy and myelin content spanning from primary to transmodal areas. We further identify the transcriptional signature of this layout, with the top-related genes enriched for the ion channel and mitochondria terms. Moreover, the expression of these genes significantly predicts brain dynamics-behavior coupling. These findings highlight the hierarchical organizing principle and underlying molecular basis of the spatial configurations of dynamic brain networks, thereby contributing to our understanding of the associations among gene expression, network dynamics, and behaviors.

neuroscience

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

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 1,434 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.

neuroscience