Associations between fluid biomarkers and PET imaging (UCB-J) of synaptic pathology in Alzheimer's disease
Johanna NilssoniD, Adam P. MeccaiD, Nicholas James AshtoniD, Elaheh Salardini, Ryan S. O’DelliD, Richard E. CarsoniD, Andréa Lessa BenedetiD, Kaj BlennowiD, Henrik ZetterbergiD, Christopher H. van DyckiD, Ann BrinkmalmiD
Abstract
INTRODUCTIONPositron Emission Tomography (PET) imaging with ligands for synaptic vesicle glycoprotein 2A (SV2A) has emerged as a promising methodology for measuring synaptic density in Alzheimers disease (AD). We investigate the relationship between SV2A PET and CSF synaptic protein changes of AD patients. METHODTwenty-one participants with early AD and 7 cognitively normal (CN) individuals underwent [11C]UCB-J PET. We used mass spectrometry to measure a panel of synaptic proteins in CSF. RESULTSIn the AD group, higher levels of syntaxin-7 and PEBP-1 were associated with lower global synaptic density. In the total sample, lower global synaptic density was associated with higher levels of AP2B1, neurogranin, {gamma}-synuclein, GDI-1, PEBP-1, syntaxin-1B, and syntaxin-7 but not with the levels of the neuronal pentraxins or 14-3-3 zeta/delta. CONCLUSIONReductions of synaptic density found in AD compared to CN participants using [11C]UCB-J PET were observed to be associated with CSF biomarker levels of synaptic proteins.
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