Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, Graduate Institute of Brain and Mind Sciences, National Taiwan University College of Medicine, Taipei 100, Taiwan, Department of Radiology, Johns Hopkins Hospital, Baltimore, Maryland 21287, and Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21224.
J Neurosci. 2013 Nov 13;33(46):18008-14. doi: 10.1523/JNEUROSCI.1402-13.2013.
To develop targeted intervention strategies for the treatment of Alzheimer's disease, we first need to identify early markers of brain changes that occur before the onset of cognitive impairment. Here, we examine changes in resting-state brain function in humans from the Baltimore Longitudinal Study of Aging. We compared longitudinal changes in regional cerebral blood flow (rCBF), assessed by (15)O-water PET, over a mean 7 year period between participants who eventually developed cognitive impairment (n = 22) and those who remained cognitively normal (n = 99). Annual PET assessments began an average of 11 years before the onset of cognitive impairment in the subsequently impaired group, so all participants were cognitively normal during the scanning interval. A voxel-based mixed model analysis was used to compare groups with and without subsequent impairment. Participants with subsequent impairment showed significantly greater longitudinal rCBF increases in orbitofrontal, medial frontal, and anterior cingulate regions, and greater longitudinal decreases in parietal, temporal, and thalamic regions compared with those who maintained cognitive health. These changes were linear in nature and were not influenced by longitudinal changes in regional tissue volume. Although all participants were cognitively normal during the scanning interval, most of the accelerated rCBF changes seen in the subsequently impaired group occurred within regions thought to be critical for the maintenance of cognitive function. These changes also occurred within regions that show early accumulation of pathology in Alzheimer's disease, suggesting that there may be a connection between early pathologic change and early changes in brain function.
为了制定针对阿尔茨海默病治疗的靶向干预策略,我们首先需要确定认知障碍发生前大脑变化的早期标志物。在这里,我们研究了巴尔的摩老龄化纵向研究中人类静息态大脑功能的变化。我们比较了最终出现认知障碍的参与者(n=22)和认知正常的参与者(n=99)在 7 年的平均时间内区域脑血流(rCBF)的纵向变化,通过(15)O-水 PET 进行评估。认知障碍组的年度 PET 评估在随后出现认知障碍的参与者中平均提前 11 年开始,因此在扫描间隔期间,所有参与者的认知均正常。采用基于体素的混合模型分析比较了有和无后续认知障碍的组。与认知健康组相比,随后出现认知障碍的参与者在前额回、额内侧回和前扣带回区域的 rCBF 纵向增加更为明显,而在顶叶、颞叶和丘脑区域的 rCBF 纵向减少更为明显。这些变化具有线性特征,不受区域组织体积的纵向变化影响。尽管在扫描间隔期间所有参与者的认知均正常,但在随后出现认知障碍的组中观察到的大多数加速 rCBF 变化发生在被认为对维持认知功能至关重要的区域内。这些变化也发生在阿尔茨海默病中病理早期积累的区域,这表明早期病理变化和早期大脑功能变化之间可能存在联系。