1. Academic Validation
  2. Detection and quantification of Aβ-3-40 (APP669-711) in cerebrospinal fluid

Detection and quantification of Aβ-3-40 (APP669-711) in cerebrospinal fluid

  • J Neurochem. 2022 Mar;160(5):578-589. doi: 10.1111/jnc.15571.
Hans-Wolfgang Klafki 1 Oliver Wirths 1 Brit Mollenhauer 2 3 Thomas Liepold 4 Petra Rieper 1 Hermann Esselmann 1 Jonathan Vogelgsang 1 Jens Wiltfang 1 5 6 Olaf Jahn 1 4
Affiliations

Affiliations

  • 1 Department of Psychiatry and Psychotherapy, University Medical Center Goettingen (UMG), Georg-August-University, Goettingen, Germany.
  • 2 Department of Neurology, University Medical Center Goettingen (UMG), Georg-August-University, Goettingen, Germany.
  • 3 Paracelsus-Elena-Klinik, Kassel, Germany.
  • 4 Max Planck Institute of Experimental Medicine, Proteomics Group, Goettingen, Germany.
  • 5 German Center for Neurodegenerative Diseases (DZNE), Goettingen, Germany.
  • 6 Neurosciences and Signaling Group, Department of Medical Sciences, Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal.
Abstract

Neurochemical biomarkers can support the diagnosis of Alzheimer's disease and may facilitate clinical trials. In blood plasma, the ratio of the Amyloid-β (Aβ) Peptides Aβ-3-40/Aβ1-42 can predict cerebral Amyloid-β pathology with high accuracy (Nakamura et al., 2018). Whether or not Aβ-3-40 (aka. amyloid precursor protein (APP) 669-711) is also present in cerebrospinal fluid (CSF) is not clear. Here, we investigated whether Aβ-3-40 can be detected in CSF and to what extent the CSF Aβ-3-40/Aβ42 ratio is able to differentiate between individuals with or without Amyloid-β positron emission tomography (PET) evidence of brain amyloid. The occurrence of Aβ-3-40 in human CSF was assessed by immunoprecipitation followed by mass spectrometry. For quantifying the CSF concentrations of Aβ-3-40 in 23 amyloid PET-negative and 17 amyloid PET-positive subjects, we applied a sandwich-type immunoassay. Our findings provide clear evidence of the presence of Aβ-3-40 and Aβ-3-38 in human CSF. While there was no statistically significant difference in the CSF concentration of Aβ-3-40 between the two diagnostic groups, the CSF Aβ-3-40/Aβ42 ratio was increased in the amyloid PET-positive individuals. We conclude that Aβ-3-40 appears to be a regular constituent of CSF and may potentially serve to accentuate the selective decrease in CSF Aβ42 in Alzheimer's disease.

Keywords

Alzheimer's disease; biomarker; cerebrospinal fluid; immunoassay; immunoprecipitation; mass spectrometry.

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