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Abnormal fronto-striatal intrinsic connectivity reflects executive dysfunction in alcohol use disorders
Caterina Galandra1, Gianpaolo Basso2, Marina Manera3
1Scuola universitaria superiore IUSS, Pavia, Italy; Cognitive Neuroscience Laboratory, ICS Maugeri, Pavia, Italy; LabNIT, ICS Maugeri, Pavia, Italy.
Alcohol use disorders (AUDs) impair executive functions like attention and working memory. This cognitive decline in AUD patients is linked to abnormal brain connectivity within key control networks.
Area of Science:
- Neuroscience
- Cognitive Psychology
- Neuroimaging
Background:
- Alcohol use disorders (AUDs) are associated with cognitive impairments, but the underlying neural mechanisms remain debated.
- Explanations range from specific frontal lobe damage to global brain dysfunction.
- Resting-state brain activity offers insights into intrinsic functional connectivity relevant to cognitive performance.
Purpose of the Study:
- To investigate the neural bases of cognitive impairments in AUD patients.
- To explore the relationship between resting-state brain activity, functional connectivity, and executive functions in AUD.
- To compare brain activity and connectivity in AUD patients versus healthy controls.
Main Methods:
- Coupled resting-state functional magnetic resonance imaging (fMRI) with comprehensive neuropsychological assessments.
- Analyzed intrinsic brain activity intensity and functional network connectivity.
- Compared 22 AUD patients with 18 healthy controls.
Main Results:
- AUD patients exhibited executive dysfunction, particularly in attentional and working-memory tasks.
- Cognitive impairment in AUD correlated with altered intrinsic activity in the executive control network (dorsolateral prefrontal cortex, striatum).
- Functional connectivity between these executive control network nodes was reduced in AUD patients compared to controls.
Conclusions:
- Executive impairment in AUD stems from dysfunctional connectivity within the cortical-subcortical networks governing cognitive control.
- These findings highlight abnormal neural architecture in AUD and provide a baseline for treatment outcome studies.
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