Research criteria for the diagnosis of Alzheimer"s disease: revising the NINCDS-ADRDA criteria

被引:3197
作者
Dubois, Bruno [1 ]
Feldman, Howard H.
Jacova, Claudia
Dekosky, Steven T.
Barberger-Gateau, Pascale
Cummings, Jeffrey
Delocourte, Andre
Galasko, Douglas
Gauthier, Serge
Jicha, Gregory
Meguro, Kenichi
O'Brien, John
Pasquier, Florence
Robert, Philippe
Rossor, Martin
Solloway, Steven
Stern, Yaakov
Visser, Pieter J.
Scheltens, Philip
机构
[1] Univ Paris 06, Hop La Pitie Salpetriere, INSERM, U610, Paris, France
[2] Univ British Columbia, Div Neurol, Vancouver Coastal Hlth, Vancouver, BC V5Z 1M9, Canada
[3] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
[4] Univ Victor Segalen, INSERM, U593, Bordeaux, France
[5] Univ Calif Los Angeles, Alzheimers Dis Ctr, Los Angeles, CA USA
[6] CHU Lille, Ctr INSERM JPA, Lille, France
[7] Univ Calif San Diego, Dept Neurosci, San Diego, CA 92103 USA
[8] Douglas Hosp, McGill Ctr Studies Aging, Montreal, PQ, Canada
[9] Univ Kentucky, Med Ctr, Sanders Brown Ctr Aging, Dept Neurol, Lexington, KY USA
[10] Tohoku Univ, Grad Sch Med, Dept Neurol & Behav Cognit Neurosci, Aoba Ku, Sendai, Miyagi, Japan
[11] Newcastle Gen Hosp, Wolfson Res Ctr, Inst Ageing & Hlth, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[12] Lille Univ Hosp, Dept Neurol, Mem Clin, Lille, France
[13] Hop Louis Pasteur, Ctr Mem Resources & Rech, Nice, France
关键词
D O I
10.1016/S1474-4422(07)70178-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The NINCDS-ADRDA and the DSM-IV-TR criteria for Alzheimer's disease (AD) are the prevailing diagnostic standards in research; however, they have now fallen behind the unprecedented growth of scientific knowledge. Distinctive and reliable biomarkers of AD are now available through structural MRI, molecular neuroimaging with PET, and cerebrospinal fluid analyses. This progress provides the impetus for our proposal of revised diagnostic criteria for AD. Our framework was developed to capture both the earliest stages, before full-blown dementia, as well as the full spectrum of the illness. These new criteria are centred on a clinical core of early and significant episodic memory impairment. They stipulate that there must also be at least one or more abnormal biomarkers among structural neuroimaging with MRI, molecular neuroimaging with PET, and cerebrospinal fluid analysis of amyloid 0 or tau proteins. The timeliness of these criteria is highlighted by the many drugs in development that are directed at changing pathogenesis, particularly at the production and clearance of amyloid 0 as well as at the hyperphosphorylation state of tau. Validation studies in existing and prospective cohorts are needed to advance these criteria and optimise their sensitivity, specificity, and accuracy.
引用
收藏
页码:734 / 746
页数:13
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