Affiliations: Department of Neurosciences, Biomedicine and Movement, University of Verona, Verona, Italy
Correspondence:
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Correspondence to: Michele Fiorini, PhD, Department of Neurosciences, Biomedicine and Movement Sciences, Policlinico G.B. Rossi, Piazzale L.A. Scuro, 10, 37134 Verona, Italy. Tel.: +39 045 8124461; E-mail: michele.fiorini@univr.it.
Abstract: Cerebrospinal fluid (CSF) biomarkers are currently included in the diagnostic criteria for Alzheimer’s disease (AD), in particular, decreased concentrations of amyloid-β peptide 1–42 (Aβ42) in the CSF, coupled with increased levels of tau and phosphorylated tau proteins, are supportive of AD diagnosis. To date, the quantification of Aβ42 levels with antibody-dependent immunoassay shows a marked variability among different laboratories and is also affected by different pre-analytical factors, suggesting that part of Aβ42 peptides might be aggregated and thus undetected by antibodies. To bypass an antibody-dependent measurement, we determined the Aβ40 and Aβ42 levels by immunoblot. We analyzed CSF samples from 35 patients with clinical diagnosis of probable AD and from 15 age-matched normal controls; CSF Aβ levels were determined by two different ELISA kits and by immunoblot analysis. Aβ40 levels measured by ELISA were comparable to those obtained by immunoblot, whereas CSF concentrations of Aβ42 measured by ELISA were significantly lower compared to values obtained by immunoblot quantification. Biochemical analysis, following 1D- and 2D-PAGE analysis, showed that the qualitative composition of Aβ peptides in the CSF is similar in AD and controls but different from that of AD brain tissues. Moreover, sedimentation velocity in sucrose gradient of CSF and brain homogenate from AD demonstrated that Aβ42 in CSF is different from Aβ42 in brain in terms of solubility and aggregation state.
