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Aberrant resting-state co-activation network dynamics in major depressive disorder
Abstract
Major depressive disorder (MDD) is a globally prevalent and highly disabling disease characterized by dysfunction of large-scale brain networks. Previous studies have found that static functional connectivity is not sufficient to reflect the complicated and time-varying properties of the brain. The underlying dynamic interactions between brain functional networks of MDD remain largely unknown, and it is also unclear whether neuroimaging-based dynamic properties are sufficiently robust to discriminate individuals with MDD from healthy controls since the diagnosis of MDD mainly depends on symptom-based criteria evaluated by clinical observation. Resting-state functional magnetic resonance imaging (fMRI) data of 221 MDD patients and 215 healthy controls were shared by REST-meta-MDD consortium. We investigated the spatial-temporal dynamics of MDD using co-activation pattern analysis and made individual diagnoses using support vector machine (SVM). We found that MDD patients exhibited aberrant dynamic properties (such as dwell time, occurrence rate, transition probability, and entropy of Markov trajectories) in some transient networks including subcortical network (SCN), activated default mode network (DMN), de-activated SCN-cerebellum network, a joint network, activated attention network (ATN), and de-activated DMN-ATN, where some dynamic properties were indicative of depressive symptoms. The trajectories of other networks to deactivated DMN-ATN were more accessible in MDD patients. Subgroup analyses also showed subtle dynamic changes in first-episode drug-naïve (FEDN) MDD patients. Finally, SVM achieved preferable accuracies of 84.69%, 76.77%, and 88.10% in discriminating patients with MDD, FEDN MDD, and recurrent MDD from healthy controls with their dynamic metrics. Our findings reveal that MDD is characterized by aberrant dynamic fluctuations of brain network and the feasibility of discriminating MDD patients using dynamic properties, which provide novel insights into the neural mechanism of MDD.
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“A positive association between family income and superior cingulum bundle mean diffusivity was evident in the lower-to-higher income group”
From Prenatal Social Determinants of Health: Narrative review of maternal environments and neonatal brain development (2024) · cites this paper as [46]
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“while a negative association was observed in the axial diffusivity of the inferior cingulum and fornix in the extremely low income group.46”
From Prenatal Social Determinants of Health: Narrative review of maternal environments and neonatal brain development (2024) · cites this paper as [46]
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“Similar moderating effects of income have been found in the relationship between inflammatory markers (e.g., cytokine tumor necrosis factor alpha; TNF-α) and white matter diffusivity.”
From Prenatal Social Determinants of Health: Narrative review of maternal environments and neonatal brain development (2024) · cites this paper as [46]
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“Similarly, increased maternal inflammation in response to environmental stressors also affect brain development, as evidenced by the associations between cytokine levels and structural connectivity.”
From Prenatal Social Determinants of Health: Narrative review of maternal environments and neonatal brain development (2024) · cites this paper as [46]
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Methods to detect, characterize, and remove motion artifact in resting state fMRI
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Tracking whole-brain connectivity dynamics in the resting state
Allen, E. A., Damaraju, E., Plis, S. M., Erhardt, E. B., Eichele, T., & Calhoun, V. D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs352 · Cited by 2,992
Resting-state connectivity biomarkers define neurophysiological subtypes of depression
Drysdale, A. T., Grosenick, L., Downar, J., Dunlop, K., Mansouri, F., Meng, Y., Fetcho, R. N., Zebley, B., Oathes, D. J., Etkin, A., et al. (2017) · Nature Medicine · doi:10.1038/nm.4246 · Cited by 2,170
Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems
Fox, M. D., Corbetta, M., Snyder, A. Z., Vincent, J. L., & Raichle, M. E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604187103 · Cited by 2,101
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for the ENIGMA-Major Depressive Disorder Working Group, Schmaal, L., Veltman, D. J., van Erp, T. G. M., Sämann, P. G., Frodl, T., Jahanshad, N., Loehrer, E., Tiemeier, H., Hofman, A., et al. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.69 · Cited by 1,172
Cerebellar contributions to major depression
Depping, M. S., Schmitgen, M. M., Kubera, K. M., & Wolf, R. C. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00634 · Cited by 156
Bhaumik, R., Jenkins, L. M., Gowins, J. R., Jacobs, R. H., Barba, A., Bhaumik, D. K., & Langenecker, S. A. (2017) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.02.018 · Cited by 72
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Cited by
Herzberg, M. P., & Smyser, C. D. (2024) · Pediatric Research · doi:10.1038/s41390-024-03345-7 · Cited by 22
Metadata
- Authors
- An, Z., Tang, K., Xie, Y., Tong, C., Liu, J., Tao, Q., DIRECT Consortium, Yan, C.-G., Chen, X., Cao, L.-P., Chen, W., Cheng, Y.-Q., Fang, Y.-R., Gong, Q.-Y., Guo, W.-B., Kuang, L., Li, B.-J., Li, T., Liu, Y.-S., Liu, Z.-N., Lu, J.-P., Luo, Q.-H., Meng, H.-Q., Peng, D.-H., Qiu, J., Shen, Y.-D., Si, T.-M., Tang, Y.-Q., Wang, C.-Y., Wang, F., Wang, H.-N., Wang, K., Wang, X., Wang, Y., Wu, X.-P., Xie, C.-M., Xie, G.-R., Xie, P., Xu, X.-F., Yang, H., Yang, J., Yao, S.-Q., Yu, Y.-Q., Yuan, Y.-G., Zhang, K.-R., Zhang, W., Zhang, Z.-J., Zhu, J.-J., Zuo, X.-N., Zhao, J.-P., Zang, Y.-F., & Feng, Y.
- Venue
- Translational Psychiatry
- Published
- 2024-01-03
- Volume
- 14
- Issue
- 1
- ISSN
- 2158-3188
- Cited by
- 66
- References
- 8
- Language
- en
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