Hirni Daniela I, Kivisaari Sasa L, Krumm Sabine, Monsch Andreas U, Berres Manfred, Oeksuez Fatma, Reinhardt Julia, Ulmer Stephan, Kressig Reto W, Stippich Christoph, Taylor Kirsten I
Memory Clinic, University Center for Medicine of Aging Basel, Felix-Platter Hospital, Basel, Switzerland.
University of Basel, Basel, Switzerland.
J Alzheimers Dis. 2016 Mar 26;52(2):573-80. doi: 10.3233/JAD-150158.
Neurofibrillary pathology in Alzheimer's dementia (AD) is associated with cognitive impairments and cortical thinning, and begins in medial perirhinal cortex (mPRC) before entering entorhinal cortex (ERC). Thus, mPRC dysfunction (e.g., semantic object memory impairments) may predate or accompany ERC (i.e., episodic memory) dysfunction in the preclinical course of typical AD. We developed formulae estimating mPRC and ERC integrity (i.e., cortical thickness) using common neuropsychological tests in 31 healthy individuals and 58 early AD patients. These formulae estimated the longitudinal courses of mPRC and ERC functioning in independent groups of 28 optimally healthy individuals who developed AD (NC-AD) over 2.8-13.4 years and 28 pairwise-matched, stable, healthy individuals (NC-NC). Mixed models demonstrated significantly worse NC-AD than NC-NC estimated mPRC and ERC functioning at the earliest observation, 12 years preceding diagnosis, and a significant decline 4 years preceding the AD diagnosis. These findings demonstrate that specific neuropsychological impairments occur early in the course of preclinical AD and that tasks measuring mPRC functioning may serve as additional, powerful markers of preclinical AD.
阿尔茨海默病性痴呆(AD)中的神经纤维病理改变与认知障碍及皮质变薄相关,且在进入内嗅皮质(ERC)之前始于内侧鼻周皮质(mPRC)。因此,在典型AD的临床前期过程中,mPRC功能障碍(如语义物体记忆障碍)可能先于或伴随ERC(即情景记忆)功能障碍出现。我们利用常见的神经心理学测试,为31名健康个体和58名早期AD患者制定了估算mPRC和ERC完整性(即皮质厚度)的公式。这些公式估算了28名在2.8至13.4年期间发展为AD的最佳健康个体(NC-AD)独立组以及28名配对匹配的稳定健康个体(NC-NC)中mPRC和ERC功能的纵向变化过程。混合模型显示,在最早观察时,即诊断前12年,NC-AD组估算的mPRC和ERC功能明显比NC-NC组差,且在AD诊断前4年出现显著下降。这些发现表明,特定的神经心理学损害在临床前期AD病程早期就已出现,且测量mPRC功能的任务可能成为临床前期AD的额外有力标志物。