Laboratory of Cognitive Neurorehabilitation, Division of Neurorehabilitation, Department of Clinical Neurosciences, University Hospital of Geneva and University of Geneva, Av. de Beau-Séjour 26, 1211, Geneva, Switzerland.
Laboratory of Neuroimaging of Aging (LANVIE), University of Geneva, Geneva, Switzerland.
Brain Topogr. 2022 Nov;35(5-6):667-679. doi: 10.1007/s10548-022-00908-x. Epub 2022 Aug 20.
Patients with early Alzheimer's disease (AD) have difficulty in learning new information and in detecting novel stimuli. The underlying physiological mechanisms are not well known. We investigated the electrophysiological correlates of the early (< 400 ms), automatic phase of novelty detection and encoding in AD. We used high-density EEG Queryin patients with early AD and healthy age-matched controls who performed a continuous recognition task (CRT) involving new stimuli (New), thought to provoke novelty detection and encoding, which were then repeated up to 4 consecutive times to produce over-familiarity with the stimuli. Stimuli then reappeared after 9-15 intervening items (N-back) to be re-encoded. AD patients had substantial difficulty in detecting novel stimuli and recognizing repeated ones. Main evoked potential differences between repeated and new stimuli emerged at 180-260 ms: neural source estimations in controls revealed more extended MTL activation for N-back stimuli and anterior temporal lobe activations for New stimuli compared to highly familiar repetitions. In contrast, AD patients exhibited no activation differences between the three stimulus types. In direct comparison, healthy subjects had significantly stronger MTL activation in response to New and N-back stimuli than AD patients. These results point to abnormally weak early MTL activity as a correlate of deficient novelty detection and encoding in early AD.
早期阿尔茨海默病(AD)患者在学习新信息和检测新刺激方面存在困难。其潜在的生理机制尚不清楚。我们研究了 AD 患者和健康年龄匹配的对照组在执行连续识别任务(CRT)时,早期(<400ms)、自动新奇检测和编码的电生理相关性,该任务涉及新刺激(New),被认为会引发新奇检测和编码,然后重复最多 4 次以产生对刺激的过度熟悉。然后在 9-15 个介入项目(N-back)后重新出现刺激以重新编码。AD 患者在检测新刺激和识别重复刺激方面存在很大困难。在重复和新刺激之间出现的主要诱发电位差异出现在 180-260ms:在对照组中进行的神经源估计显示,与高度熟悉的重复刺激相比,N-back 刺激引起了更广泛的 MTL 激活,而新刺激引起了前颞叶激活。相比之下,AD 患者在三种刺激类型之间没有表现出激活差异。直接比较显示,与 AD 患者相比,健康受试者对新刺激和 N-back 刺激的 MTL 激活明显更强。这些结果表明,早期 MTL 活动异常微弱是早期 AD 中新奇检测和编码缺陷的相关因素。