University College London Great Ormond Street Institute of Child Health, London, UK.
Department of Psychological Sciences, Birkbeck, University of London, London, UK.
Dev Cogn Neurosci. 2023 Apr;60:101230. doi: 10.1016/j.dcn.2023.101230. Epub 2023 Mar 21.
Pubertal development is a potential trigger for increases in risk-taking behaviours during adolescence. Here, we sought to investigate the relationship between puberty and neural activation during risky decision-making in males using functional magnetic resonance imaging (fMRI). Forty-seven males aged 12.5-14.5 years completed an fMRI risk-taking task (BART) and reported their tendencies for risky decision-making using a self-report questionnaire. Puberty was assessed through self-reported pubertal status and salivary testosterone levels. Testosterone concentration, but not physical pubertal status, was positively correlated with self-reported risk-taking behaviour, while neither was correlated with BART performance. Across the whole sample, participants had greater activation of the bilateral nucleus accumbens and right caudate on trials when they made a successful risky decision compared to trials when they made a safe choice or when their risky decision was unsuccessful. There was a negative correlation between pubertal stage and brain activation during unsuccessful risky decision-making trials compared within unsuccessful control trials. Males at a lower stage of pubertal development showed increased activation in the left insula, right cingulate cortex, dorsomedial prefrontal cortex (dmPFC), right putamen and right orbitofrontal cortex (OFC) relative to more pubertally mature males during trials when they chose to take a risk and the balloon popped compared to when they watched the computer make an unsuccessful risky decision. Less pubertally mature males also showed greater activation in brain regions including the dmPFC, right temporal and frontal cortices, right OFC, right hippocampus and occipital cortex in unsuccessful risky trials compared to successful risky trials. These results suggest a puberty-related shift in neural activation within key brain regions when processing outcomes of risky decisions, which may reduce their sensitivity to negative feedback, and in turn contribute to increases in adolescent risk-taking behaviours.
青春期是冒险行为增加的潜在触发因素。在这里,我们试图使用功能磁共振成像 (fMRI) 研究男性青春期和冒险决策时的神经激活之间的关系。47 名年龄在 12.5-14.5 岁的男性完成了 fMRI 风险决策任务 (BART),并使用自我报告问卷报告了他们的冒险决策倾向。青春期通过自我报告的青春期状态和唾液睾酮水平来评估。睾酮浓度,而不是身体青春期状态,与自我报告的冒险行为呈正相关,而与 BART 表现均不相关。在整个样本中,与做出安全选择或冒险决策不成功相比,参与者在成功做出冒险决策时双侧伏隔核和右侧尾状核的激活更大。与不成功的控制试验相比,青春期阶段与不成功的冒险决策试验中的大脑激活呈负相关。与青春期成熟男性相比,处于较低青春期发育阶段的男性在选择冒险且气球爆炸时,大脑左岛叶、右扣带回皮质、背内侧前额叶皮质 (dmPFC)、右壳核和右眶额皮质 (OFC) 的激活增加,而在观看计算机做出不成功的冒险决策时则减少。与成功的冒险试验相比,青春期发育不成熟的男性在不成功的冒险试验中大脑区域的激活也更大,包括 dmPFC、右颞叶和额叶皮质、右 OFC、右海马体和枕叶皮质。这些结果表明,在处理冒险决策的结果时,关键大脑区域的神经激活与青春期有关,这可能会降低他们对负面反馈的敏感性,并进而导致青少年冒险行为的增加。