Abstract
The role of microglia in tau accumulation is currently unclear but could provide an important insight into the mechanisms underlying Alzheimer's disease (AD)(1). Here, we measured the microglial marker soluble TREM2 and the disease-associated microglial activation stage 2 markers AXL, MERTK, GAS6, LPL, CST7, SPP1 and CSF1 in nondemented individuals from the Swedish BioFINDER-2 cohort who underwent longitudinal tau-positron emission tomography (PET), amyloid-PET and global cognitive assessment. To assess whether baseline microglial markers had an effect on AD-related changes, we studied three sub-groups of individuals: 121 with evidence of amyloid-PET pathology (A(+)), 64 with additional evidence of tau-PET pathology (A(+)T(+)) and 159 without amyloid- or tau-PET pathology (A(-)T(-)). Our results showed that increased levels of TREM2 were associated with slower amyloid accumulation in A(+) individuals in addition to slower tau deposition and cognitive decline in A(+)T(+) subjects. Similarly, higher levels of AXL, MERTK, GAS6, LPL, CST7 and CSF1 predicted slower tau accumulation and/or cognitive decline in the A(+)T(+) group. These findings have important implications for future therapeutic strategies aiming to boost microglial protective functions in AD.