AI Article Synopsis

  • Behavioral addiction (BA) is characterized by compulsive behaviors despite negative outcomes, but its neurogenetic causes are not well understood.
  • A study found that individuals with BA had thinner cortical thickness (CTh) in specific brain areas linked to cognitive control, such as the precuneus and dorsolateral prefrontal cortex.
  • Additionally, the study identified a correlation between CTh and the expression of 12 genes related to dopamine metabolism and behavioral responses, suggesting that genetic factors may influence the neural mechanisms underlying BA.

Article Abstract

Behavioral addiction (BA) is a conceptually new addictive phenotype characterized by compulsive reward-seeking behaviors despite adverse consequences. Currently, its underlying neurogenetic mechanism remains unclear. Here, this study aimed to investigate the association between cortical thickness (CTh) and genetic phenotypes in BA. We conducted a systematic search in five databases and extracted gene expression data from the Allen Human Brain Atlas. Meta-analysis of 10 studies (343 addicted individuals and 355 controls) revealed that the BA group showed thinner CTh in the precuneus, postcentral gyrus, orbital-frontal cortex, and dorsolateral prefrontal cortex (P < 0.005). Meta-regression showed that the CTh in the precuneus and postcentral gyrus were negatively associated with the addiction severity (P < 0.0005). More importantly, the CTh phenotype of BA was spatially correlated with the expression of 12 genes (false discovery rate [FDR] < 0.05), and the dopamine D2 receptor had the highest correlation (rho = 0.55). Gene enrichment analysis further revealed that the 12 genes were involved in the biological processes of behavior regulation and response to stimulus (FDR < 0.05). In conclusion, our findings demonstrated the thinner CTh in cognitive control-related brain areas in BA, which could be associated with the expression of genes involving dopamine metabolism and behavior regulation.

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Source
http://dx.doi.org/10.1093/cercor/bhae298DOI Listing

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