P300(潜伏期)事件相关电位:记忆损伤的准确预测因子。

Eric R Braverman, Kenneth Blum
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引用次数: 55

摘要

为了确定P300潜伏期变化是否先于记忆和精神状态并与之相关,研究人员对1997年至2002年接受医学和精神病学诊断的患者(N=1506,年龄20-100岁)进行了P300 (N=1496)、WMS-III (N=694)和MMSE (N=456)的评估。患者和对照组包括:a)所有4个分量表WMS-III正常(N=36), b) WMS-III和MMSE正常(N=189),主观记忆/精神状态主诉,c) WMS-III正常且无记忆主诉的医学患者(N=205), d)无医学、精神或记忆问题的P300对照组(ROC)。记忆受损/边缘性记忆患者P300潜伏期延长(p24)。在WMS-III评分受损<或= 69,或边界<或= 79 (P至少=0.004)的患者中,P300潜伏期比正常值(>或= 300 + 30 + Age)更长,而MMSE > 24则失败。通过ROC曲线,我们证实P300潜伏期可以准确识别边缘/受损记忆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P300 (latency) event-related potential: an accurate predictor of memory impairment.

To determine if P300 latency changes precede and correlate with memory and mental status, patients (N=1506 aged 20-100 years) who received medical and psychiatric diagnoses (from 1997 to 2002), were assessed for P300 (N=1496), WMS-III (N=694), and MMSE (N=456). Patient and control groups included, a) normal WMS-III on all 4 subscales (N=36), b) normal WMS-III and MMSE (N=189) with subjective memory/mental status complaints, and c) medical patients with normal WMS-III and no memory complaints (N=205), and d) P300 control group without medical, psychiatric or memory problems for ROC. Patients with impaired/borderline memory had a prolonged P300 latency (P<0.02) compared to age matched non-impaired controls; in patients with normal WMS-III/MMSE, with subjective mild memory/mental status impairment, P300 latency was prolonged compared to controls (P=0.0004). The P300 latency increased by 0.72ms per year (P=7.9x10(-65)) and voltage decreased by 0.03dV per year (P=6.7x10(-10)), and both parameters were linearly correlated with the age of the subjects. Male subjects had an average voltage of 6.1dV and female 6.8dV (P=0.00009). Statistically, prolonged latency began at age range 41-50 (P=0.0002); reduced P300 voltage began at age range 51-60 (P=0.003). WMS-III memory decline for all measures began in females at age range 61-70 (P value at least=0.02) and for males at age range 61-80 (P=0.02). Prolonged P300 latency (P<0.0001) and memory impairment (at least <0.02) were greater for females than males. MMSE memory decline, male and female, began at age range 81-90 (P value of at least 0.00007). In our logistic regression model P300 latency was more predictive of WMS-III impairment than MMSE > 24. In patients whose WMS-III score is impaired < or = 69, or borderline < or = 79 (P at least=0.004), a P300 latency more prolonged than the norm (> or = 300 + 30 + Age) identifies these patients, whereas a MMSE > 24 failed. With the ROC curve, we confirmed that P300 latency could accurately identify borderline/impaired memory.

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