Hedges Dawson, Janis Rebecca, Mickelson Stephen, Keith Cierra, Bennett David, Brown Bruce L
Department of Psychology, Brigham Young University, Provo, UT, USA The Neuroscience Center, Brigham Young University, Provo, UT, USA
Department of Psychology, Brigham Young University, Provo, UT, USA.
Clin EEG Neurosci. 2016 Jan;47(1):48-55. doi: 10.1177/1550059414550567. Epub 2014 Sep 23.
Alzheimer's disease accounts for 60% of all dementia. Numerous biomarkers have been developed that can help in making an early diagnosis. The P300 is an event-related potential that may be abnormal in Alzheimer's disease. Given the possible association between P300 amplitude and Alzheimer's disease and the need for biomarkers in early Alzheimer's disease, the main purpose of this meta-analysis and meta-regression was to characterize P300 amplitude in probable Alzheimer's disease compared to healthy controls. Using online search engines, we identified peer-reviewed articles containing amplitude measures for the P300 in response to a visual or auditory oddball stimulus in subjects with Alzheimer's disease and in a healthy control group and pooled effect sizes for differences in P300 amplitude between Alzheimer's disease and control groups to obtain summary effect sizes. We also used meta-regression to determine whether age, sex, educational attainment, or dementia severity affected the association between P300 amplitude and Alzheimer's disease. Twenty articles containing a total of 646 subjects met inclusion and exclusion criteria. The overall effect size from all electrode locations was 1.079 (95% confidence interval=0.745-1.412, P<.001). The pooled effect sizes for the Cz, Fz, and Pz locations were 1.226 (P<.001), 0.724 (P=.0007), and 1.430 (P<.001), respectively. Meta-regression showed an association between amplitude and educational attainment, but no association between amplitude and age, sex, and dementia severity. In conclusion, P300 amplitude is smaller in subjects with Alzheimer's disease than in healthy controls.
阿尔茨海默病占所有痴呆症病例的60%。目前已开发出多种生物标志物,有助于早期诊断。P300是一种事件相关电位,在阿尔茨海默病中可能出现异常。鉴于P300波幅与阿尔茨海默病之间可能存在关联,且早期阿尔茨海默病需要生物标志物,本荟萃分析和荟萃回归的主要目的是比较可能患有阿尔茨海默病的患者与健康对照者的P300波幅特征。通过在线搜索引擎,我们检索了同行评审的文章,这些文章包含了阿尔茨海默病患者和健康对照组在视觉或听觉oddball刺激下P300波幅的测量数据,并汇总了阿尔茨海默病组和对照组之间P300波幅差异的效应量,以获得综合效应量。我们还使用荟萃回归来确定年龄、性别、教育程度或痴呆严重程度是否会影响P300波幅与阿尔茨海默病之间的关联。20篇文章共纳入646名受试者,符合纳入和排除标准。所有电极位置的总体效应量为1.079(95%置信区间=0.745-1.412,P<0.001)。Cz、Fz和Pz位置的合并效应量分别为1.226(P<0.001)、0.724(P=0.0007)和1.430(P<0.001)。荟萃回归显示波幅与教育程度之间存在关联,但与年龄、性别和痴呆严重程度之间无关联。总之,阿尔茨海默病患者的P300波幅低于健康对照者。