Circle of Willis atherosclerosis is a risk factor for sporadic Alzheimer's disease

被引:237
作者
Roher, AE
Esh, C
Kokjohn, TA
Kalback, W
Luehrs, DC
Seward, JD
Sue, LI
Beach, TG
机构
[1] Sun Hlth Res Inst, Longtine Ctr Mol Biol & Genet, Sun City, AZ 85351 USA
[2] Midwestern Univ, Sch Osteopath Med, Dept Microbiol, Glendale, AZ USA
[3] Sun Hlth Res Inst, Dept Epidemiol & Biostat, Sun City, AZ USA
[4] Sun Hlth Res Inst, WH Civin Lab Neuropathol, Sun City, AZ USA
关键词
atherosclerosis; circle of Willis; Alzheimer's disease; brain hypoperfusion;
D O I
10.1161/01.ATV.0000095973.42032.44
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives - We conducted a quantitative investigation of brain arterial atherosclerotic damage and its relationship to sporadic Alzheimer's disease ( AD). Methods and Results - Fifty- four consecutive autopsy cases, 32 AD and 22 nondemented control subjects, were examined to establish the degree of arterial stenosis. Vessel external and lumenal area measurements were taken from 3- mm arterial cross- sections to calculate a stenosis index. AD patient circle of Willis arteries possessed a significant degree of stenosis as a consequence of multiple and severe atherosclerotic lesions. These lesions were significantly more severe in AD cases than in age- matched controls ( P < 0.0001), and the number of stenoses and the index of occlusion ( R = 0.67; P < 0.00001) were positively correlated. In addition, the index of stenosis significantly correlated with the following measures of AD neuropathological lesions: total plaque score, neuritic plaque score, neurofibrillary tangle score, Braak stage score, and white matter rarefaction score. Conclusions - Our study reveals an association between severe circle of Willis atherosclerosis and sporadic AD that should be considered a risk factor for this dementia. These observations strongly suggest that atherosclerosis- induced brain hypoperfusion contributes to the clinical and pathological manifestations of AD.
引用
收藏
页码:2055 / 2062
页数:8
相关论文
共 75 条
[1]   Annual deaths attributable to obesity in the United States [J].
Allison, DB ;
Fontaine, KR ;
Manson, JE ;
Stevens, J ;
VanItallie, TB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (16) :1530-1538
[2]  
Alsop DC, 2000, ANN NEUROL, V47, P93, DOI 10.1002/1531-8249(200001)47:1<93::AID-ANA15>3.0.CO
[3]  
2-8
[4]   WOMEN, MYOCARDIAL-INFARCTION, AND DEMENTIA IN THE VERY OLD [J].
ARONSON, MK ;
OOI, WL ;
MORGENSTERN, H ;
HAFNER, A ;
MASUR, D ;
CRYSTAL, H ;
FRISHMAN, WH ;
FISHER, D ;
KATZMAN, R .
NEUROLOGY, 1990, 40 (07) :1102-1106
[5]   Consensus recommendations for the postmortem diagnosis of Alzheimer's disease [J].
Ball, M ;
Braak, H ;
Coleman, P ;
Dickson, D ;
Duyckaerts, C ;
Gambetti, P ;
Hansen, L ;
Hyman, B ;
Jellinger, K ;
Markesbery, W ;
Perl, D ;
Powers, J ;
Price, J ;
Trojanowski, JQ ;
Wisniewski, H ;
Phelps, C ;
Khachaturian, Z .
NEUROBIOLOGY OF AGING, 1997, 18 (04) :S1-S2
[6]   THE HISTORY OF ALZHEIMERS-DISEASE - 3 DEBATES [J].
BEACH, TG .
JOURNAL OF THE HISTORY OF MEDICINE AND ALLIED SCIENCES, 1987, 42 (03) :327-349
[7]  
Bodovitz S, 1996, J BIOL CHEM, V271, P4436
[8]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[9]   Vascular risk factors for Alzheimer's disease: An epidemiologic perspective [J].
Breteler, MMB .
NEUROBIOLOGY OF AGING, 2000, 21 (02) :153-160
[10]   Vascular involvement in cognitive decline and dementia - Epidemiologic evidence from the Rotterdam Study and the Rotterdam Scan Study [J].
Breteler, MMB .
VASCULAR FACTORS IN ALZHEIMER'S DISEASE, 2000, 903 :457-465