Four of the five proteins that were increased in both MCI and AD respect to control form part of the LKB1 pathway known to promote tau phosphorylation via activation of MARK2 and PAR-1 [40, 92] (Supplementary Fig. 6; Supplementary dataset 8, online resource), while the rest of the proteins were reduced and involved in synaptic vesicle pathways and the metabolism of synaptic RNA, which has an important role controlling the composition of the local proteome. This evidence concerns the gene MARK2 and Alzheimer disease.