Associations between drinking and cortical thickness in younger adult drinkers: Findings from the Human Connectome Project

VL Morris, MM Owens, SK Syan…�- Alcoholism: Clinical�…, 2019 - Wiley Online Library
Alcoholism: Clinical and Experimental Research, 2019Wiley Online Library
Background Previous neuroimaging studies examining relations between alcohol misuse
and cortical thickness have revealed that increased drinking quantity and alcohol‐related
problems are associated with thinner cortex. Although conflicting regional effects are often
observed, associations are generally localized to frontal regions (eg, dorsolateral prefrontal
cortex [DLPFC], inferior frontal gyrus [IFG], and anterior cingulate cortex). Inconsistent
findings may be attributed to methodological differences, modest sample sizes, and limited�…
Background
Previous neuroimaging studies examining relations between alcohol misuse and cortical thickness have revealed that increased drinking quantity and alcohol‐related problems are associated with thinner cortex. Although conflicting regional effects are often observed, associations are generally localized to frontal regions (e.g., dorsolateral prefrontal cortex [DLPFC], inferior frontal gyrus [IFG], and anterior cingulate cortex). Inconsistent findings may be attributed to methodological differences, modest sample sizes, and limited consideration of sex differences.
Methods
This study examined neuroanatomical correlates of drinking quantity and heavy episodic drinking in a large sample of younger adults (N�=706; Mage�=�28.8; 51% female) using magnetic resonance imaging data from the Human Connectome Project. Exploratory analyses examined neuroanatomical correlates of executive function (flanker task) and working memory (list sorting).
Results
Hierarchical linear regression models (controlling for age, sex, education, income, smoking, drug use, twin status, and intracranial volume) revealed significant inverse associations between drinks in past week and frequency of heavy drinking and cortical thickness in a majority of regions examined. The largest effect sizes were found for frontal regions (DLPFC, IFG, and the precentral gyrus). Follow‐up regression models revealed that the left DLPFC was uniquely associated with both drinking variables. Sex differences were also observed, with significant effects largely specific to men.
Conclusions
This study adds to the understanding of brain correlates of alcohol use in a large, gender‐balanced sample of younger adults. Although the cross‐sectional methodology precludes causal inferences, these findings provide a foundation for rigorous hypothesis testing in future longitudinal investigations.
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