“…They may reflect differences in plasma concentrations; filtration (autonomic control of renal glomerular blood flow); renal tubule peptidases, reabsorption or secretion; or even bladder epithelial origins. If CFS represents a systemic illness with proteomic changes in multiple cell types (e.g., platelets and muscle [39][40][41][42][43][44]) then the tissues immediately responsible for the analytes present in the urine or their chemical modification may offer novel clues into disease pathophysiology.…”