BEHAVIORAL & MRI EVALUATION OF PRENATAL ALCOHOL EXPOSURE

本子项目是利用由NIH/NCRR资助的中心赠款提供的资源的众多研究子项目之一。子项目和研究者（PI）可能已经从另一个NIH来源获得了主要资金，因此可以在其他CRISP条目中表示。列出的机构是中心的，不一定是研究者的机构。胎儿酒精综合症（FAS）包括范围广泛的残疾，涉及结构和功能变化。其中最具破坏性的影响是由中枢神经系统（CMS）的改变引起的。在大多数FAS研究中，这些CMS变化导致认知和行为缺陷。此外，人们认识到，在缺乏FAS诊断所需的面部特征的情况下，大脑和行为也会发生变化。在我们的研究中，产前大量接触酒精（PEA）的儿童，虽然没有FAS的明显身体特征，但在大脑和行为上都表现出与FAS相似的变化。胎儿酒精谱系障碍（FASD）一词现在被用来描述产前酒精暴露造成的一系列影响，并反映出这些影响可能发生在畸形和非畸形个体身上。我们的结构磁共振成像（MRI）研究表明，大脑中的白质可能对产前酒精暴露的影响特别敏感。与此同时，我们注意到产前酒精暴露对行为的影响与白质损伤造成的影响之间存在相似之处。拟议的项目本质上是多学科的，包括神经心理学评估和脑成像研究。我们计划继续我们的结构MRI研究，此外，我们提出了两种新的成像技术：扩散张量成像（DTI）来评估白质损伤和功能MRI （fMRI）来评估在执行已知对产前酒精暴露敏感的任务时脑功能的变化。这项建议是我们过去十年来一直在进行的工作的延续。我们的行为评估将强调假设对白质变化敏感的任务，我们的成像研究将补充这些行为调查，并使我们能够将大脑的变化与我们的行为发现联系起来。此外，我们将在患有FASD的畸形和非畸形个体中进行这些调查。我们相信，到目前为止，我们的方法是成功的，这个多学科项目将扩大我们对产前酒精暴露的破坏性影响的理解，希望能充分告知我们，我们可能会开始提出合理的干预策略

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Fetal alcohol syndrome (FAS) encompasses a broad range of disabilities involving both structural and functional changes. Among the most devastating effects are those caused by alterations in the central nervous system (CMS). These CMS changes result in the cognitive and behavioral deficits reported in most studies of FAS. In addition, it is recognized that brain and behavioral changes can occur in the absence of the facial features required for an FAS diagnosis. In our studies, children with heavy prenatal exposure to alcohol (PEA), who do not have the obvious physical features of FAS, show changes in both brain and behavior similar to those seen in FAS. The term fetal alcohol spectrum disorders (FASD) is now being used to describe the range of effects resulting from prenatal alcohol exposure and to reflect that these effects can occur in both dysmorphic and nondysmorphic individuals. Our structural magnetic resonance imaging (MRI) studies have indicated that white matter in the brain may be particularly sensitive to the effects of prenatal alcohol exposure. At the same time we have noticed a similarity between the behavioral effects of prenatal alcohol exposure and those resulting from white matter damage. The proposed project is multidisciplinary in nature, including neuropsychological assessment and brain imaging studies. We plan to continue our structural MRI studies, and in addition, we are proposing two new imaging techniques: diffusion tensor imaging (DTI) to assess white matter damage and functional MRI (fMRI) to assess changes in brain function while performing a task known to be sensitive to prenatal alcohol exposure. This proposal represents a continuation of work that we have been conducting over the last 10 years. Our behavioral assessments will stress tasks hypothesized to be sensitive to white matter changes and our imaging studies will complement these behavioral investigations and allow us to correlate changes in brain with our behavioral findings. Furthermore, we will conduct these investigations in both dysmorphic and nondysmorphic individuals with FASD. We believe that our approach has been successful thus far, and that this multidisciplinary project will expand our understanding of the devastating effects of prenatal alcohol exposure, hopefully informing us sufficiently that we might begin to propose reasonable intervention strategies