The beta APP717 Alzheimer mutation increases the percentage of plasma amyloid-beta protein ending at A beta 42(43)

被引:95
作者
Kosaka, T
Imagawa, M
Seki, K
Arai, H
Sasaki, H
Tsuji, S
AsamiOdaka, A
Fukushima, T
Imai, K
Iwatsubo, T
机构
[1] UNIV TOKYO, FAC PHARMACEUT SCI, DEPT NEUROPATHOL & NEUROSCI, BUNKYO KU, TOKYO 113, JAPAN
[2] UNIV TOKYO, FAC PHARMACEUT SCI, DEPT ANALYT CHEM, TOKYO 113, JAPAN
[3] TAKEDA CHEM IND LTD, OSAKA 532, JAPAN
[4] TAKEDA CHEM IND LTD, TSUKUBA, IBARAKI, JAPAN
[5] HYOGO KENRITSU AMAGASAKI HOSP, AMAGASAKI, HYOGO, JAPAN
[6] MISHIMA HOSP, NIIGATA, JAPAN
[7] TOHOKU UNIV, SCH MED, DEPT GERIATR MED, SENDAI, MIYAGI 980, JAPAN
[8] NIIGATA UNIV, DEPT NEUROL, NIIGATA, JAPAN
关键词
D O I
10.1212/WNL.48.3.741
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We measured plasma levels of amyloid beta protein (A beta) ending at positions 40 (A beta 40) and 42(43) [A beta 42(43)] in six carriers of beta APP717 (Val to lie) mutation linked to familial Alzheimer's disease (FAD) as well as in patients with sporadic AD (sAD) and controls. The percentage and the level of A beta 42(43) were significantly higher in carriers of beta APP717 mutation relative to sAD, whereas A beta 40 levels were decreased. In contrast, A beta levels and ratios were at similar levels in sAD, regardless of the stage of the disease, compared with non-AD neurologic disease controls and nondemented control individuals, These results suggest that the reported increase in the percentage of A beta 42(43) secretion in transfected cells with beta APP717 mutant genes actually takes place in the bodies of carriers of beta APP717 mutation, and that plasma A beta could be used as an indicator of the alterations of beta APP/A beta metabolism in subtypes of AD.
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收藏
页码:741 / 745
页数:5
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