Cerebral amyloid angiopathy associated with hemorrhage: Immunohistochemical study of 41 biopsy cases

被引:12
作者
Izumihara, A
Ishihara, T
Hoshii, Y
Ito, H
机构
[1] Yaeyama Prefectural Hosp, Dept Neurosurg, Okinawa 9070022, Japan
[2] Yamaguchi Univ, Sch Med, Dept Pathol 1, Yamaguchi, Japan
[3] Yamaguchi Rosai Hosp, Dept Neurosurg, Yamaguchi, Japan
来源
NEUROLOGIA MEDICO-CHIRURGICA | 2001年 / 41卷 / 10期
关键词
cerebral amyloid angiopathy; biopsy; immunohistochemistry; lobar hemorrhage;
D O I
10.2176/nmc.41.471
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The relationship between cerebral amyloid angiopathy and hemorrhage was investigated by an immunohistochemical study of biopsy cases to characterize the involvement of amyloid beta -protein, apolipoprotein E, and cystatin C in cerebral amyloid angiopathy associated with hemorrhage. The amyloid-laden vessels were examined in biopsy specimens from 41 surgical cases of sporadic cerebral amyloid angiopathy (36 cases with hemorrhage and 5 cases without hemorrhage), using immunohistochemical staining with antibodies against amyloid beta -protein, apolipoprotein E, cystatin C, and alpha -mooth muscle actin. The relationship between the occurrence, recurrence, and enlargement of the hemorrhage, and the semiquantitative estimation of the cerebrovascular amyloid-related protein deposition was analyzed using Fisher's exact test. Severe amyloid beta -protein (p < 0.013) and apolipoprotein E (p < 0.013) immunoreactivity were risk factors for the occurrence of the hemorrhage. Severe cystatin C immunoreactivity was a risk factor for the occurrence (p < 0.002) and enlargement (p < 0.014) of the hemorrhage, and tended to induce recurrent hemorrhage (p < 0.103). In addition, loss of the vascular smooth muscle was observed in the intensely amyloid-laden vascular walls that showed cystatin C-immunoreactivity. The present study indicates that intense amyloid <beta>-protein deposition with cystatin C deposition weakens the cerebrovascular walls, and that cystatin C deposition is a strong predictor of hemorrhage in cerebral amyloid angiopathy.
引用
收藏
页码:471 / 477
页数:7
相关论文
共 37 条
[1]   IMMUNOCHEMICAL IDENTIFICATION OF THE SERINE PROTEASE INHIBITOR ALPHA-1-ANTICHYMOTRYPSIN IN THE BRAIN AMYLOID DEPOSITS OF ALZHEIMERS-DISEASE [J].
ABRAHAM, CR ;
SELKOE, DJ ;
POTTER, H .
CELL, 1988, 52 (04) :487-501
[2]   CEREBROVASCULAR AMYLOID IN SCRAPIE-AFFECTED SHEEP REACTS WITH ANTIBODIES TO PRION PROTEIN [J].
ALLSOP, D ;
IKEDA, S ;
BRUCE, M ;
GLENNER, GG .
NEUROSCIENCE LETTERS, 1988, 92 (02) :234-239
[3]   THE PLACE OF HUMAN GAMMA-TRACE (CYSTATIN-C) AMONGST THE CYSTEINE PROTEINASE-INHIBITORS [J].
BARRETT, AJ ;
DAVIES, ME ;
GRUBB, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 120 (02) :631-636
[4]   C-terminal fragments of alpha- and beta-tubulin form amyloid fibrils in vitro and associate with amyloid deposits of familiar cerebral amyloid angiopathy, British type [J].
Baumann, MH ;
Wisniewski, T ;
Levy, E ;
Plant, GT ;
Ghiso, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 219 (01) :238-242
[5]  
CASTANO EM, 1988, LAB INVEST, V58, P122
[6]  
Fujihara S, 1989, Prog Clin Biol Res, V317, P939
[7]   AMYLOID FIBRILS IN HEREDITARY CEREBRAL-HEMORRHAGE WITH AMYLOIDOSIS OF ICELANDIC TYPE IS A VARIANT OF GAMMA-TRACE BASIC-PROTEIN (CYSTATIN-C) [J].
GHISO, J ;
JENSSON, O ;
FRANGIONE, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (09) :2974-2978
[8]   ALZHEIMERS-DISEASE - INITIAL REPORT OF THE PURIFICATION AND CHARACTERIZATION OF A NOVEL CEREBROVASCULAR AMYLOID PROTEIN [J].
GLENNER, GG ;
WONG, CW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 120 (03) :885-890
[9]   ALZHEIMERS-DISEASE AND DOWNS-SYNDROME - SHARING OF A UNIQUE CEREBROVASCULAR AMYLOID FIBRIL PROTEIN [J].
GLENNER, GG ;
WONG, CW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 122 (03) :1131-1135
[10]  
GLENNER GG, 1981, ANN PATHOL, V1, P120