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DOI 10.1080/17470919.2024.2377666

Медицинская библиотека · Social neuroscience · 2024

Alcohol attention bias modulates neural engagement during moral processing.

Fede Samantha J, Kisner Mallory A, Dean Sarah F, Buckler Emma, Chholak Robin, Momenan Reza

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАResearch Support, N.I.H., IntramuralПеревод в очереди

Аннотация

The neurobiology of typical moral cognition involves the interaction of frontal, limbic, and temporoparietal networks. There is still much to be understood mechanistically about how moral processing is disrupted; such understanding is key to combating antisociality. Neuroscientific models suggest a key role for attention mechanisms in atypical moral processing. We hypothesized that attention-bias toward alcohol cues in alcohol use disorder (AUD) leads to a failure to properly engage with morally relevant stimuli, reducing moral processing. We recruited patients with AUD (n = 30) and controls (n = 30). During functional magnetic resonance imaging, participants viewed pairs of images consisting of a moral or neutral cue and an alcohol or neutral distractor. When viewing moral cues paired with alcohol distractors, individuals with AUD had lower medial prefrontal cortex engagement; this pattern was also seen for left amygdala in younger iAUDs. Across groups, individuals had less engagement of middle/superior temporal gyri. These findings provide initial support for AUD-related attention bias interference in sociomoral processing. If supported in future longitudinal and causal study designs, this finding carries potential societal and clinical benefits by suggesting a novel, leverageable mechanism and in providing a cognitive explanation that may help combat persistent stigma.

Для цитирования: Fede Samantha J, Kisner Mallory A, Dean Sarah F, Buckler Emma, Chholak Robin, Momenan Reza. Alcohol attention bias modulates neural engagement during moral processing.. Social neuroscience. 2024. DOI: 10.1080/17470919.2024.2377666.

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