REDUCED TRANSFERRIN-BINDING IN DOWN-SYNDROME - A ROUTE OF SENILE PLAQUE-FORMATION AND DEMENTIA

被引:19
作者
HODGKINS, PS
PRASHER, V
FARRAR, G
ARMSTRONG, R
STURMAN, S
CORBETT, J
BLAIR, JA
机构
[1] UNIV ASTON,BIRMINGHAM B4 7ET,W MIDLANDS,ENGLAND
[2] MRC,RADIOBIOL UNIT,DIDCOT,OXON,ENGLAND
[3] UNIV BIRMINGHAM,QUEEN ELIZABETH PSYCHIAT HOSP,DEPT PSYCHIAT,BIRMINGHAM,W MIDLANDS,ENGLAND
[4] ROCHE PROD LTD,WELWYN GARDEN CIT,HERTS,ENGLAND
[5] UNIV BIRMINGHAM,QUEEN ELIZABETH HOSP,DEPT NEUROL,BIRMINGHAM,W MIDLANDS,ENGLAND
关键词
DEMENTIA; DOWN SYNDROME; ALZHEIMERS DISEASE; TRANSFERRIN; SENILE PLAQUE; IMMUNE RESPONSE;
D O I
10.1097/00001756-199310000-00005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
PLASMA transferrin binding in Down syndrome and Alzheimer's disease is significantly reduced compared with age matched controls and it was thought this may help elucidate a pathological time sequence for the onset of dementia in Down syndrome. In Down syndrome, there was a reduction in gallium and aluminium transferrin binding both with age and the onset of dementia. Nontransferrin bound gallium species were identified as nontransportable phosphate or silicate. Thus, the route of entry of metals into the brain must be via a transferrin mediated complex only. A clear sequence of pathological events has been demonstrated in Down syndrome which shows the pathway to development of plaques and dementia and this is believed to have an immunological origin.
引用
收藏
页码:21 / 24
页数:4
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