Mixed Brain Pathologies in Dementia: The BrainNet Europe Consortium Experience

被引:149
作者
Kovacs, Gabor G. [1 ,2 ]
Alafuzoff, Irina [4 ,5 ]
Al-Sarraj, Safa [6 ]
Arzberger, Thomas [7 ]
Bogdanovic, Nenad [8 ,9 ]
Capellari, Sabina [10 ]
Ferrer, Isidro [11 ]
Gelpi, Ellen [1 ]
Kovari, Viktor [2 ]
Kretzschmar, Hans [7 ]
Nagy, Zoltan [2 ]
Parchi, Piero
Seilhean, Danielle [12 ]
Soininen, Hilkka [3 ]
Troakes, Claire [6 ]
Budka, Herbert [1 ]
机构
[1] Med Univ Vienna, Inst Neurol, AT-1097 Vienna, Austria
[2] Former Natl Inst Psychiat & Neurol, Budapest, Hungary
[3] Kuopio Univ Hosp, Dept Neurol, SF-70210 Kuopio, Finland
[4] Kuopio Univ Hosp, Dept Pathol, SF-70210 Kuopio, Finland
[5] Univ Kuopio, Neurol Unit, Dept Clin Med, FIN-70211 Kuopio, Finland
[6] Kings Coll London, Inst Psychiat, MRC Neurodegenerat Brain Bank, London WC2R 2LS, England
[7] Univ Munich, Inst Neuropathol & Prionforsch, Munich, Germany
[8] Karolinska Inst, Dept NEUROTEC, Div Geriatr Med, Stockholm, Sweden
[9] Karolinska Inst, Huddinge Brain Bank KFC, Stockholm, Sweden
[10] Univ Bologna, Dipartimento Sci Neurol, Bologna, Italy
[11] IDIBELL Hosp Univ Bellvitge, Inst Neuropathol, Barcelona, Spain
[12] Univ Paris 06, AP HP, Dept Neuropathol, Paris, France
基金
英国医学研究理事会;
关键词
Alzheimer disease; Synucleinopathy; Vascular pathology; Argyrophilic grain dementia;
D O I
10.1159/000161560
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
Background: Dementia results from heterogeneous diseases of the brain. Mixed disease forms are increasingly recognized. Methods: We performed a survey within brain banks of BrainNet Europe to estimate the proportion of mixed disease forms underlying dementia and age- and gender-specific influences. Results: Data collected in 9 centres from 3,303 individuals were analysed. The proportion of patients with mixed diagnoses among all cases with Alzheimer disease (AD), vascular pathology (VP), argyrophilic grain dementia (AGD), and synucleinopathies, such as Lewy body dementia (LBD), Parkinson disease (PD) and synuclein pathology only in the amygdala, was 53.3%. Mixed pathology was more frequently reported with LBD, PD, AGD, and VP than with AD. The percentage of mixed diagnoses for AGD and VP significantly differed between centres. In patients younger than 75 years, synucleinopathies, and pure forms of AD, VP, and AGD were more frequent in men. Above 75 years of age, more women had pure AD and pure AGD. Conclusions: The most obvious neuropathological alteration should not terminate the diagnostic procedure since copathology is likely to be found. Neuropathological interpretation of AGD and VP has not been sufficiently established in a consensus. Pure forms of synucleinopathies are unlikely sole substrates for dementia. Copyright (C) 2008 S. Karger AG, Basel
引用
收藏
页码:343 / 350
页数:8
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