Amyloid β protein 42(43) in cerebrospinal fluid of patients with Alzheimer's disease

Akira Tamaoka*, Naoya Sawamura, Tetsuo Fukushima, Shin'ichi Shoji, Etsuro Matsubara, Mikio Shoji, Shunsaku Hirai, Yoshiko Furiya, Riuko Endoh, Hiroshi Mori

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

126 Citations (Scopus)


To investigate the pathomechanism of amyloid β protein (Aβ) deposition in brains with Alzheimer's disease (AD), cerebrospinal fluid (CSF) levels of Aβ species (CSF-Aβ) with different carboxy termini, i.e. AβX-40 and AβX-42(43) as well as Aβ1-40 and Aβ1-42(43), were measured in patients with AD and age-matched controls without dementia (CTR) using sandwich enzyme-linked immunosorbent assays (ELISAs). The present study revealed that both CSF-AβX-42(43) and Aβ1-42(43) levels were significantly lower in the AD patients (P<0.005) than in the CTR group, whereas neither CSF-AβX-40 nor CSF-Aβ1-40 levels showed any differences between the two groups. In addition, although there was no difference between the ratios of AβX-40 to Aβ1-40 in the AD and CTR groups, the ratios of AβX-42(43)to Aβ1-42(43) were increased in the AD group compared with those in the CTR group (P<0.05). Therefore, it can be assumed that the ratios of amino terminal truncations and/or modifications of CSF-Aβ42(43) with carboxy termini ending at residue 42(43) were more increased in the AD group than in the CTR group. Increased adsorption of Aβ42(43) to Aβ deposition in AD brains, decreased secretion of Aβ42(43) to CSF and/or increased clearance of Aβ42(43) from CSF might explain the diminished levels of Aβ42(43) in the CSF of AD patients. In addition, CSF-Aβ42(43) could reflect increased amino terminal truncations and/or modifications of Aβ42(43) in AD brains.

Original languageEnglish
Pages (from-to)41-45
Number of pages5
JournalJournal of the Neurological Sciences
Issue number1
Publication statusPublished - 1997 May 1
Externally publishedYes


  • Alzheimer's disease
  • amyloid β protein
  • cerebrospinal fluid
  • enzyme-linked immunosorbent assay

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology


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