Fasting blood samples were collected according to the international guidelines for AD biomarker studies.37 (link) Our previously validated proteomic profile was assayed using electrochemiluminescence (ECL) per our published methods on the following biomarkers: fatty acid binding protein 3 (FABP3); beta 2 microglobulin (B2M); C-reactive protein (CRP); thrombopoietin (TPO); alpha 2 macroglobulin (A2M) eotaxin 3; tumor necrosis factor alpha (TNFa); tenascin C (TNC); interleukin (IL)-5, IL-6, IL-7, IL-10, IL-18; I-309; factor VII (factor 7); soluble intercellular adhesion molecule 1 (sICAM1); circulating vascular cell adhesion molecule 1 (sVCAM1); pancreatic polypeptide (PPY); thymus activation regulated chemokine (TARC); and serum amyloid A (SAA).27 (link),28 (link),30 (link) Glucagon-like peptide 1 (GLP-1), insulin, glucagon, and peptide YY (PYY) were also assayed weekly via ECL multiplex kit. The ITR Biomarker Core has conducted > 20,000 assays using these specifications and the platform performs excellently (coefficient of variation [CV] < = 10%). The Quanterix Simoa HD-1 platform was used for assay of plasma amyloid beta (Aβ)40, Aβ42, total tau (3-plex plate), and neurofilament light (NfL). The ITR Biomarker Core has conducted n > 5000 assays with CVs < = 5%.