The objective of this study was to assess cerebrospinal fluid (CSF) ?-site amyloid precursor protein (APP)-cleaving enzyme 1 (BACE1) activity in relation to Alzheimer's disease (AD) and to correlate the enzyme activity with protein markers of APP metabolism and axonal degeneration.BACE1 activity and protein concentrations were measured and analyzed in 342 participants of the Alzheimer's Disease Neuroimaging Initiative, including 99 normal control, 75 stable mild cognitive impairment (MCI), 87 progressive MCI, and 79 AD dementia cases. All statistical analyses were Bonferroni corrected for multiple comparisons.No significant differences between controls and any of the three patient groups were detected for BACE1 activity and soluble APP? (sAPP?) concentrations in CSF. Significant correlations with BACE1 activity were found for CSF APP? and total tau in all four groups and for CSF phosphorylated tau181 in all groups but the progressive MCI group. There were no correlations for CSF amyloid ? (A?)1-42 or for plasma A?1-42 and A?1-40.The consistent correlation between BACE1 activity and sAPP? supports their role as biomarkers of target engagement in clinical trials on BACE1 inhibition.
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The objective of this study was to assess cerebrospinal fluid (CSF) ?-site amyloid precursor protein (APP)-cleaving enzyme 1 (BACE1) activity in relation to Alzheimer's disease (AD) and to correlate the enzyme activity with protein markers of APP metabolism and axonal degeneration.BACE1 activity and protein concentrations were measured and analyzed in 342 participants of the Alzheimer's Disease Neuroimaging Initiative, including 99 normal control, 75 stable mild cognitive impairment (MCI), 87 pr...
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