Univ. Bordeaux, INCIA CNRS-UMR 5287, Bordeaux, France.
EPHE, PSL Research University, Paris, France.
Transl Psychiatry. 2024 Jun 19;14(1):260. doi: 10.1038/s41398-024-02949-1.
Functional inhibition is known to improve treatment outcomes in substance use disorder (SUD), potentially through craving management enabled by underlying cerebral integrity. Whereas treatment is challenged by a multitude of substances that patients often use, no study has yet unraveled if inhibition and related cerebral integrity could prevent relapse from multiples substances, that is, one's primary drug of choice and secondary ones. Individuals with primary alcohol, cannabis, or tobacco use disorders completed intensive Ecological Momentary Assessment (EMA) coupled with resting-state functional MRI (rs-fMRI) to characterize the extent to which inhibition and cerebral substrates interact with craving and use of primary and any substances. Participants were 64 patients with SUD and 35 healthy controls who completed one week EMA using Smartphones to report 5 times daily their craving intensity and substance use and to complete Stroop inhibition testing twice daily. Subsamples of 40 patients with SUD and 34 control individuals underwent rs-fMRI. Mixed Model Analysis revealed that reported use of any substance by SUD individuals predicted later use of any and primary substance, whereas use of the primary substance only predicted higher use of that same substances. Craving and inhibition level independently predicted later use but did not significantly interact. Preserved inhibition performance additionally influenced use indirectly by mediating the link between subsequent uses and by being linked to rs-fMRI connectivity strength in fronto-frontal and cerebello-occipital connections. As hypothesized, preserved inhibition performance, reinforced by the integrity of inhibitory neurofunctional substrates, may partake in breaking an unhealthy substance use pattern for a primary substance but may not generalize to non-target substances or to craving management.
功能抑制已被证实可以改善物质使用障碍(SUD)的治疗效果,其潜在机制可能是通过大脑完整性来实现对成瘾渴求的管理。虽然治疗受到患者经常使用的多种物质的挑战,但目前还没有研究表明抑制和相关的大脑完整性是否可以防止多种物质的复发,即一个人的主要药物和次要药物。患有原发性酒精、大麻或烟草使用障碍的个体完成了密集的生态瞬时评估(EMA)和静息态功能磁共振成像(rs-fMRI),以描述抑制和大脑基质与成瘾和主要及任何物质使用之间的相互作用程度。参与者包括 64 名 SUD 患者和 35 名健康对照组,他们使用智能手机完成了一周的 EMA,每天报告 5 次他们的成瘾强度和物质使用情况,并每天完成两次 Stroop 抑制测试。SUD 患者和 34 名对照组的亚样本接受了 rs-fMRI 检查。混合模型分析显示,SUD 个体报告的任何物质使用预测了随后任何物质和主要物质的使用,而主要物质的使用仅预测了同一物质的更高使用。成瘾和抑制水平独立预测了随后的使用,但没有显著相互作用。抑制表现的保留还通过中介随后使用与额-额和小脑-枕叶连接的 rs-fMRI 连通性强度之间的联系来间接地影响使用,并且与抑制神经功能基质的完整性有关。正如假设的那样,抑制表现的保留,通过抑制神经功能基质的完整性得到加强,可能有助于打破对主要物质的不健康物质使用模式,但可能不会推广到非目标物质或成瘾渴求管理。