Storace Daniela, Cammarata Sergio, Borghi Roberta, Sanguineti Roberta, Giliberto Luca, Piccini Alessandra, Pollero Valeria, Novello Cristina, Caltagirone Carlo, Smith Mark A, Bossù Paola, Perry George, Odetti Patrizio, Tabaton Massimo
Department of Internal Medicine and Medical Specialties, University of Genoa, Italy.
Arch Neurol. 2010 Jul;67(7):867-72. doi: 10.1001/archneurol.2010.137.
To develop a blood-based test for screening populations at risk for Alzheimer disease.
Case-control study. Subjects A total of 180 patients with mild cognitive impairment (MCI) and 105 age-matched, cognitively normal controls.
The titer of beta-amyloid 1-42 autoantibodies in the plasma was obtained at the time of diagnosis and evaluated by enzyme-linked immunosorbent assay before and after dissociation of the antigen-antibody complexes. A total of 107 patients with MCI were followed up for 36 months; 70 of the 107 cases progressed to Alzheimer disease.
The average level of beta-amyloid 1-42 plasma autoantibodies in patients with MCI that progressed to Alzheimer disease, but not that of the stable cases, was significantly higher than in cognitively normal controls (P < .001).
The results suggest that the plasma beta-amyloid 1-42 autoantibodies parallel beta-amyloid 42 deposition in the brain, which is known to precede by several years the clinical onset of Alzheimer disease. The evaluation of beta-amyloid 1-42 autoantibodies after dissociation of the complexes is a simple and inexpensive method that can be used to predict the occurrence of Alzheimer disease.