Author/Authors :
Jerzy Wimagegiel، نويسنده , , Henryk M. Wisniewski، نويسنده , , Janusz Moryimage، نويسنده , , Michal Tarnawski، نويسنده , , Izabela Kuchna، نويسنده , , Jerzy Dziewiatkowski، نويسنده , , Tuula Pirttil?، نويسنده , , Tarmo Krivim?ki، نويسنده , , Terho Lehtim?ki، نويسنده , , Boleslaw Lach، نويسنده ,
Abstract :
The decrease in the number of neurons free of neurofibrillary changes, neurons with neurofibrillary degeneration, and the total volume of β-amyloid (Aβ) deposits in the amygdala of people with Down syndrome and in late stages of Alzheimer disease were estimated by using morphometry and regression analysis. This model predicts that the duration of neurofibrillary changes from the pretangle stage to ghost tangles is approximately 4.7 years. The correlation between the decrease in the number of neurons and the decrease in the amount of Aβ indicates that amyloid deposition is associated with neurons and that loss of neurons causes decrease in Aβ deposition. The presence of neurons only with neurofibrillary tangles, and the absence of the amyloid deposits predicted by regression analysis suggest that neurons with tangles are not engaged in amyloid deposition. The disappearance of amyloid by approximately 2.2 years after loss of neurons free of neurofibrillary changes indicates that Aβ deposits are degradable and removable and that even in severely atrophic amygdala, there are mechanisms of amyloid resolution. This study shows that in normal aging in the amygdala, extracellular Aβ appears later than neurofibrillary changes.
Keywords :
Amyloidosis beta , Morphometry , Amygdala , Neurofibrillary degeneration , Alzheimer disease , Down syndrome