Department of Psychiatry and Addiction Center, University of Michigan, 4250 Plymouth Rd, Ann Arbor, MI 48109, USA.
Department of Psychiatry and Addiction Center, University of Michigan, 4250 Plymouth Rd, Ann Arbor, MI 48109, USA.
Drug Alcohol Depend. 2024 Oct 1;263:112421. doi: 10.1016/j.drugalcdep.2024.112421. Epub 2024 Aug 22.
Detecting and responding to errors is central to goal-directed behavior and cognitive control and is thought to be supported by a network of structures that includes the anterior cingulate cortex and anterior insula. Sex differences in the maturational timing of cognitive control systems create differential periods of vulnerability for psychiatric conditions, such as substance use disorders.
We examined sex differences in error-related activation across an array of distributed brain regions during a Go/No-Go task in young adults with problem alcohol use (N=69; 34 females; M=19.4 years). Regions of interest previously linked to error-related activation, including anterior cingulate cortex, insula, and frontoparietal structures, were selected in a term-based meta-analysis. Individual differences in their responses to false alarm (FA) inhibitory errors relative to "go" trials (FA>GO) and correct rejections (FA>CR) were indexed using multivariate summary measures derived from principal components analysis.
FA>GO and FA>CR activation both revealed a first component that explained the majority of the variance across error-associated regions and displayed the strongest loadings on salience network structures. Compared to females, males exhibited significantly higher levels of the FA>GO component but not the FA>CR component.
Males exhibit greater salience network activation in response to inhibitory errors, which could be attributed to sex differences in error-monitoring processes or to other functions (e.g., novelty detection). The findings are relevant for the further characterization of sex differences in cognitive control and may have implications for understanding individual differences in those at risk for substance use or other cognitive control disorders.
错误检测和响应是目标导向行为和认知控制的核心,被认为是由包括前扣带皮层和前岛叶在内的一系列结构支持的网络。认知控制系统的成熟时间存在性别差异,这为精神疾病(如物质使用障碍)创造了不同的脆弱期。
我们在一项有问题饮酒的年轻成年人(N=69;34 名女性;M=19.4 岁)的 Go/No-Go 任务中,检查了性别差异在一系列分布式大脑区域中与错误相关的激活情况。以前与错误相关的激活相关的感兴趣区域,包括前扣带皮层、岛叶和额顶叶结构,在基于术语的元分析中进行了选择。使用主成分分析得出的多元摘要指标,对他们相对于“go”试验(FA>GO)和正确拒绝(FA>CR)对错误的抑制错误(FA>GO)和正确拒绝(FA>CR)的反应的个体差异进行了指数化。
FA>GO 和 FA>CR 激活都揭示了第一个组件,该组件解释了与错误相关区域的大部分方差,并在突显网络结构上显示出最强的负荷。与女性相比,男性在 FA>GO 成分上表现出显著更高的水平,但在 FA>CR 成分上则没有。
男性在对抑制性错误的反应中表现出更大的突显网络激活,这可能归因于错误监测过程中的性别差异,或归因于其他功能(例如,新奇检测)。这些发现与认知控制中性别差异的进一步特征化有关,并可能对理解那些有物质使用或其他认知控制障碍风险的个体差异具有意义。