4.7 Article

Dissociable Disruptions in Thalamic and Hippocampal Resting-State Functional Connectivity in Youth with 22q11.2 Deletions

期刊

JOURNAL OF NEUROSCIENCE
卷 39, 期 7, 页码 1301-1319

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.3470-17.2018

关键词

22q11; connectivity; fMRI; hippocampus; networks; thalamus

资金

  1. National Institutes of Health [DP5-OD012109, R01-MH108590, R01-MH112189, R01-MH085953, U54-EB020403, T32MH073526]
  2. Brain and Behavior Foundation (National Alliance for Research on Schizophrenia and Depression) Independent Investigator Grant
  3. Joanne and George Miller Family Endowed Term Chair
  4. Human Connectome Project, WU-Minn Consortium [1U54MH091657]
  5. McDonnell Center for Systems Neuroscience at Washington University

向作者/读者索取更多资源

The 22q11.2 deletion syndrome (22q11DS) is a recurrent copy number variant with high penetrance for developmental neuropsychiatric disorders. Study of individuals with 22q11DS therefore may offer key insights into neural mechanisms underlying such complex illnesses. Resting-state functional connectivity MRI studies in idiopathic schizophrenia have consistently revealed disruption of thalamic and hippocampal circuitry. Here, we sought to test whether this circuitry is similarly disrupted in the context of this genetic high-risk condition. To this end, resting-state functional connectivity patterns were assessed in a sample of human youth with 22q11DS (n = 42; 59.5% female) and demographically matched healthy controls (n = 39; 53.8% female). Neuroimaging data were acquired via single-band protocols and analyzed in line with methods provided by the Human Connectome Project. We computed functional relationships between individual-specific anatomically defined thalamic and hippocampal seeds and all gray matter voxels in the brain. Whole-brain Type I error protection was achieved through nonparametric permutation-based methods. The 22q11DS patients displayed dissociable disruptions in thalamic and hippocampal functional connectivity relative to control subjects. Thalamocortical coupling was increased in somatomotor regions and reduced across associative networks. The opposite effect was observed for the hippocampus in regards to somatomotor and associative network connectivity. The thalamic and hippocampal dysconnectivity observed in 22q11DS suggests that high genetic risk for psychiatric illness is linked with disruptions in large-scale corticosubcortical networks underlying higher-order cognitive functions. These effects highlight the translational importance of large-effect copy number variants for informing mechanisms underlying neural disruptions observed in idiopathic developmental neuropsychiatric disorders.

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