Strengthened and posterior-shifted structural rich-club organization in people who use cocaine.
Journal Article (Journal Article)
BACKGROUND: People with cocaine use disorder (CUD) often have abnormal cognitive function and brain structure. Cognition is supported by brain networks that typically have characteristics like rich-club organization, which is a group of regions that are highly connected across the brain and to each other, and small worldness, which is a balance between local and long-distance connections. However, it is unknown whether there are abnormalities in structural brain network connectivity of CUD. METHODS: Using diffusion-weighted imaging, we measured structural connectivity in 37 people with CUD and 38 age-matched controls. We identified differences in rich-club organization and whether such differences related to small worldness and behavior. We also tested whether rich-club reorganization was associated with caudate and putamen structural connectivity due to the relevance of the dopamine system to cocaine use. RESULTS: People with CUD had a higher normalized rich-club coefficient than controls, more edges connecting rich-club nodes to each other and to non-rich-club nodes, and fewer edges connecting non-rich-club nodes. Rich-club nodes were shifted posterior and lateral. Rich-club reorganization was related to lower clustered connectivity around individual nodes found in CUD, to increased impulsivity, and to a decrease in caudate connectivity. CONCLUSIONS: These findings are consistent with previous work showing increased rich-club connectivity in conditions associated with a hypofunctional dopamine system. The posterior shift in rich-club nodes in CUD suggests that the structural connectivity of posterior regions may be more impacted than previously recognized in models based on brain function and morphology.
Full Text
Duke Authors
Cited Authors
- Hall, SA; Bell, RP; Gadde, S; Towe, SL; Nadeem, MT; McCann, PS; Song, AW; Meade, CS
Published Date
- June 1, 2022
Published In
Volume / Issue
- 235 /
Start / End Page
- 109436 -
PubMed ID
- 35413558
Electronic International Standard Serial Number (EISSN)
- 1879-0046
Digital Object Identifier (DOI)
- 10.1016/j.drugalcdep.2022.109436
Language
- eng
Conference Location
- Ireland