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- W1963669299 abstract "All mutations known to cause familial Alzheimer's disease (AD) act by increasing the levels of soluble β-amyloid peptide (Aβ), especially the longer form, Aβ42. However, in vivo elevation of soluble Aβ in sporadic AD has so far not been shown. In the present study, we used enzyme-linked immunosorbent assays specific for Aβ42 and Aβ40 to investigate cerebrospinal fluid from sporadic AD at different stages of disease severity, to clarify the roles of Aβ42 and Aβ40 during disease progression. We also evaluated three other groups—one group of patients with mild cognitive impairment who were at risk of developing dementia, a cognitively intact, nondemented reference group diagnosed with depression, and a perfectly healthy control group. We found that Aβ42 is strongly elevated in early and mid stages of AD, and thereafter it declines with disease progression. On the contrary, Aβ40 levels were decreased in early and mid stages of AD. The group of cognitively impaired patients and the depression reference group had significantly higher levels of Aβ42 than the healthy control group, implying that Aβ42 is increased not only in AD, but in other central nervous system conditions as well. Our data also point out the importance of having thoroughly examined control material. The initial increase and subsequent decrease of Aβ42 adds a new biochemical tool to follow the progression of AD and might be important in the monitoring of therapeutics. Ann Neurol 1999;45:504–511" @default.
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- W1963669299 date "1999-04-01" @default.
- W1963669299 modified "2023-10-18" @default.
- W1963669299 title "Cerebrospinal fluid A?42 is increased early in sporadic Alzheimer's disease and declines with disease progression" @default.
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- W1963669299 doi "https://doi.org/10.1002/1531-8249(199904)45:4<504::aid-ana12>3.0.co;2-9" @default.
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