Neuropsychological Markers of Medial Perirhinal and Entorhinal Cortex Functioning are Impaired Twelve Years Preceding Diagnosis of Alzheimer's Dementia

被引:21
作者
Hirni, Daniela I. [1 ,2 ]
Kivisaari, Sasa L. [3 ]
Krumm, Sabine [1 ,2 ]
Monsch, Andreas U. [1 ,2 ]
Berres, Manfred [4 ]
Oeksuez, Fatma [1 ]
Reinhardt, Julia [5 ]
Ulmer, Stephan [6 ,7 ]
Kressig, Reto W. [1 ,2 ]
Stippich, Christoph [2 ,5 ]
Taylor, Kirsten I. [1 ,2 ,8 ,9 ]
机构
[1] Felix Platter Hosp, Univ Ctr Med Aging Basel, Memory Clin, Basel, Switzerland
[2] Univ Basel, Basel, Switzerland
[3] Aalto Univ, Sch Sci, Dept Neurosci & Biomed Engn, Aalto, Finland
[4] RheinAhrCampus, Dept Math & Technol, Remagen, Germany
[5] Univ Basel Hosp, Dept Radiol, Div Diagnost & Intervent Neuroradiol, CH-4031 Basel, Switzerland
[6] Univ Hosp Schleswig Holstein, Inst Neuroradiol, Kiel, Germany
[7] Mission Res Inc, Zurich, Switzerland
[8] Univ Cambridge, Dept Expt Psychol, Ctr Speech Language & Brain, Downing St, Cambridge CB2 3EB, England
[9] F Hoffmann La Roche Ltd, Biomarkers & Clin Imaging, Roche Pharma Res & Early Dev, NORD,Roche Innovat Ctr Basel, Grenzacherstr 124, CH-4070 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
Episodic memory; longitudinal; neurofibrillary pathology; preclinical cognitive marker; rhinal cortex; semantic memory; MILD COGNITIVE IMPAIRMENT; MINI-MENTAL-STATE; SEMANTIC MEMORY; OBJECT FEATURES; DISEASE; CONSORTIUM; ESTABLISH; SYMPTOMS; REGISTRY; DECLINE;
D O I
10.3233/JAD-150158
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:573 / 580
页数:8
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