4.7 Article

Individual Differences in Attentional Bias Associated with Cocaine Dependence Are Related to Varying Engagement of Neural Processing Networks

期刊

NEUROPSYCHOPHARMACOLOGY
卷 39, 期 5, 页码 1135-1147

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/npp.2013.314

关键词

cocaine; attentional bias; functional magnetic resonance imaging; individual differences; neural networks; independent component analysis

资金

  1. [1T32 DA 022981]
  2. [5 R01 DA019999]
  3. [5 R21 DA025243]
  4. [UL1 TR000039]
  5. [R01 DA01999]
  6. [R21 NS065937]
  7. [1R21 MH097784]
  8. [2 U19 MH069056-06A1]
  9. [KL2 TR000063]
  10. [1F31 DA025491]

向作者/读者索取更多资源

Cocaine and other drug dependencies are associated with significant attentional bias for drug use stimuli that represents a candidate cognitive marker of drug dependence and treatment outcomes. We explored, using fMRI, the role of discrete neural processing networks in the representation of individual differences in the drug attentional bias effect associated with cocaine dependence (AB-coc) using a word counting Stroop task with personalized cocaine use stimuli (cocStroop). The cocStroop behavioral and neural responses were further compared with those associated with a negative emotional word Stroop task (eStroop) and a neutral word counting Stroop task (cStroop). Brain behavior correlations were explored using both network-level correlation analysis following independent component analysis (ICA) and voxel-level, brain-wide univariate con-elation analysis. Variation in the attentional bias effect for cocaine use stimuli among cocaine-dependent men and women was related to the recruitment of two separate neural processing networks related to stimulus attention and salience attribution (inferior frontal parietal ventral insula), and the processing of the negative affective properties of cocaine stimuli (frontal temporal cingulate). Recruitment of a sensory motor dorsal insula network was negatively correlated with AB-coc and suggested a regulatory role related to the sensorimotor processing of cocaine stimuli. The attentional bias effect for cocaine stimuli and for negative affective word stimuli were significantly correlated across individuals, and both were correlated with the activity of the frontal temporal cingulate network. Functional connectivity for a single prefrontal striatal occipital network correlated with variation in general cognitive control (cStroop) that was unrelated to behavioral or neural network correlates of cocStroop- or eStroop-related attentional bias. A brain-wide mass univariate analysis demonstrated the significant correlation of individual attentional bias effect for cocaine stimuli with distributed activations in the frontal, occipitotemporal, parietal, cingulate, and premotor cortex. These findings support the involvement of multiple processes and brain networks in mediating individual differences in risk for relapse associated with drug dependence.

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