Literature DB >> 27214526

Early life stress predicts thalamic hyperconnectivity: A transdiagnostic study of global connectivity.

Noah S Philip1, Audrey R Tyrka2, Sarah E Albright3, Lawrence H Sweet4, Jorge Almeida2, Lawrence H Price2, Linda L Carpenter2.   

Abstract

Early life stress (ELS) is an established risk factor for psychiatric illness and is associated with altered functional connectivity within- and between intrinsic neural networks. The widespread nature of these disruptions suggests that broad imaging measures of neural connectivity, such as global based connectivity (GBC), may be particularly appropriate for studies of this population. GBC is designed to identify brain regions having maximal functional connectedness with the rest of the brain, and alterations in GBC may reflect a restriction or broadening of network synchronization. We evaluated whether ELS severity predicted GBC in a sample (N = 46) with a spectrum of ELS exposure. Participants included healthy controls without ELS, those with at least moderate ELS but without psychiatric disorders, and a group of patients with ELS- related psychiatric disorders. The spatial distribution of GBC peaked in regions of the salience and default mode networks, and ELS severity predicted increased GBC of the left thalamus (corrected p < 0.005, r = 0.498). Thalamic connectivity was subsequently evaluated and revealed reduced connectivity with the salience network, particularly the dorsal anterior cingulate cortex (corrected p < 0.005), only in the patient group. These findings support a model of disrupted thalamic connectivity in ELS and trauma-related negative affect states, and underscore the importance of a transdiagnostic, dimensional neuroimaging approach to understanding the sequelae of trauma exposure. Published by Elsevier Ltd.

Entities:  

Keywords:  Default mode network; Dorsal anterior cingulate cortex; Early life stress; Functional connectivity; Salience network; Thalamus

Mesh:

Year:  2016        PMID: 27214526      PMCID: PMC4894492          DOI: 10.1016/j.jpsychires.2016.05.003

Source DB:  PubMed          Journal:  J Psychiatr Res        ISSN: 0022-3956            Impact factor:   4.791


  71 in total

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