This work identified seven proteins (complement C3, γ-fibrinogen, serum albumin, complement factor-I, clusterin, α-1-microglobulin, and serum amyloid-P) that were able to explain 34% of the variance in hippocampal volume in MCI and AD, and five proteins (complement component C4a, complement C8, clusterin, ApoA1, and transthyretin) that were able to discriminate fast from slow progressing AD groups. This evidence concerns the gene CFI and Alzheimer disease.