Department of Radiology and Imaging Sciences, Indiana University School of Medicine, 355 W 16th St. IU Neuroscience Center, GH 4101, 46202, Indianapolis, IN, USA.
Indiana Alzheimer's Disease Research Center, Indiana University School of Medicine, Indianapolis, IN, USA.
Brain Imaging Behav. 2023 Apr;17(2):223-256. doi: 10.1007/s11682-022-00750-6. Epub 2022 Dec 9.
The prevalence of Alzheimer's disease is projected to reach 13 million in the U.S. by 2050. Although major efforts have been made to avoid this outcome, so far there are no treatments that can stop or reverse the progressive cognitive decline that defines Alzheimer's disease. The utilization of preventative treatment before significant cognitive decline has occurred may ultimately be the solution, necessitating a reliable biomarker of preclinical/prodromal disease stages to determine which older adults are most at risk. Quantitative cerebral blood flow is a promising potential early biomarker for Alzheimer's disease, but the spatiotemporal patterns of altered cerebral blood flow in Alzheimer's disease are not fully understood. The current systematic review compiles the findings of 81 original studies that compared resting gray matter cerebral blood flow in older adults with mild cognitive impairment or Alzheimer's disease and that of cognitively normal older adults and/or assessed the relationship between cerebral blood flow and objective cognitive function. Individuals with Alzheimer's disease had relatively decreased cerebral blood flow in all brain regions investigated, especially the temporoparietal and posterior cingulate, while individuals with mild cognitive impairment had consistent results of decreased cerebral blood flow in the posterior cingulate but more mixed results in other regions, especially the frontal lobe. Most papers reported a positive correlation between regional cerebral blood flow and cognitive function. This review highlights the need for more studies assessing cerebral blood flow changes both spatially and temporally over the course of Alzheimer's disease, as well as the importance of including potential confounding factors in these analyses.
到 2050 年,预计美国的阿尔茨海默病患病率将达到 1300 万。尽管已经做出了巨大努力来避免这种结果,但到目前为止,还没有可以阻止或逆转定义阿尔茨海默病的进行性认知衰退的治疗方法。在出现明显认知衰退之前使用预防治疗最终可能是解决问题的方法,这需要一种可靠的临床前/前驱疾病阶段的生物标志物来确定哪些老年人的风险最高。定量脑血流是阿尔茨海默病的一种很有前途的潜在早期生物标志物,但阿尔茨海默病患者脑血流改变的时空模式尚未完全清楚。本系统综述汇总了 81 项原始研究的结果,这些研究比较了轻度认知障碍或阿尔茨海默病老年患者与认知正常老年患者的静息灰质脑血流,并评估了脑血流与客观认知功能之间的关系。阿尔茨海默病患者所有研究区域的脑血流相对减少,尤其是颞顶叶和后扣带回,而轻度认知障碍患者的后扣带回脑血流持续减少,但其他区域(尤其是额叶)的结果则更加混杂。大多数论文报告了区域脑血流与认知功能之间存在正相关。本综述强调了需要更多研究来评估阿尔茨海默病病程中脑血流的空间和时间变化,以及在这些分析中纳入潜在混杂因素的重要性。