Kodali Vikas N, Jacobson Joseph L, Lindinger Nadine M, Dodge Neil C, Molteno Christopher D, Meintjes Ernesta M, Jacobson Sandra W
Department of Psychiatry and Behavioral Neurosciences , Wayne State University School of Medicine, Detroit, Michigan.
Department of Human Biology , University of Cape Town Faculty of Health Sciences, Cape Town, South Africa.
Alcohol Clin Exp Res. 2017 Feb;41(2):334-344. doi: 10.1111/acer.13307. Epub 2017 Jan 11.
Response inhibition is a distinct aspect of executive function that is frequently impaired in children with fetal alcohol spectrum disorders (FASD). We used a Go/NoGo (GNG) task in a functional MRI protocol to investigate differential activation of brain regions in the response inhibition network in children diagnosed with full or partial fetal alcohol syndrome (FAS/PFAS), compared with healthy controls.
A rapid, event-related task with 120 Go and 60 NoGo trials was used to study children aged 8 to 12 years-8 with FAS/PFAS, 17 controls. Letters were projected sequentially, with Go and NoGo trials randomly interspersed across the task. BOLD signal in the whole brain was contrasted for the correct NoGo minus correct Go trials between the FAS/PFAS and control groups.
Compared to the FAS/PFAS group, controls showed greater activation of the inferior frontal and anterior cingulate network linked to response inhibition in typically developing children. By contrast, the FAS/PFAS group showed greater BOLD response in dorsolateral prefrontal cortex and other middle prefrontal regions, suggesting compensation for inefficient function of pathways that normally mediate inhibitory processing. All group differences were significant after control for potential confounding variables. None of the effects of prenatal alcohol exposure on activation of the regions associated with response inhibition were attributable to the effects of this exposure on IQ.
This is the first FASD GNG study in which all participants in the exposed group met criteria for a diagnosis of full FAS or PFAS. Although FASD is frequently comorbid with attention deficit hyperactivity disorder, the pattern of brain activation seen in these disorders differs, suggesting that different neural pathways mediate response inhibition in FASD and that different interventions for FASD are, therefore, warranted.
反应抑制是执行功能的一个独特方面,在胎儿酒精谱系障碍(FASD)儿童中经常受损。我们在功能性磁共振成像(fMRI)方案中使用了一个“走/停”(Go/NoGo,GNG)任务,以研究与健康对照组相比,被诊断为完全或部分胎儿酒精综合征(FAS/PFAS)的儿童在反应抑制网络中脑区的差异激活情况。
采用一项快速的、事件相关任务,包含120次“走”和60次“停”试验,对8至12岁的儿童进行研究——8名患有FAS/PFAS的儿童和17名对照组儿童。字母依次呈现,“走”和“停”试验在整个任务中随机穿插。将FAS/PFAS组和对照组在正确的“停”试验减去正确的“走”试验之间的全脑血氧水平依赖(BOLD)信号进行对比。
与FAS/PFAS组相比,对照组在与典型发育儿童反应抑制相关的额下回和前扣带回网络中表现出更强的激活。相比之下,FAS/PFAS组在背外侧前额叶皮层和其他中前额叶区域表现出更强的BOLD反应,这表明对通常介导抑制性加工的通路功能低效进行了代偿。在控制了潜在的混杂变量后,所有组间差异均具有统计学意义。产前酒精暴露对与反应抑制相关脑区激活的影响均不能归因于该暴露对智商的影响。
这是第一项针对FASD的GNG研究,其中暴露组的所有参与者均符合完全FAS或PFAS诊断标准。尽管FASD常与注意力缺陷多动障碍共病,但这些疾病中观察到的脑激活模式不同,这表明不同的神经通路介导FASD中的反应抑制,因此需要针对FASD采取不同的干预措施。