Abstract

Fourteen AD patients and 14 healthy control subjects, matched for gender and age, were investigated with functional magnetic resonance imaging (WRI) during a visuospatial discrimination task. The task consisted of serially presented analogue clocks with the clock hands forming different angle sizes. All subjects were advised to press a button every time a specified angle occurred. The examination was carried out using a 1 .S Tesla MRI scanner. Fifteen slices covering the whole cortex were obtained every 4 seconds using a single-shot echo-planar (EPI) functional imaging sequence. We additionally examined a subsample of 5 patients and 5 controls which underwent three training sessions practicing the same task and who were re-examined one week after the initial fMRI measurement. ReSUlt.9 The task performance of AD patients and controls did not differ significantly. A specific fMRI activation pattern could be established for the control group, with a greater activation in the right superior parietal lobule (rSPL) compared to right primary visual cortex (rPVC). The AD group showed an inverse pattern with lower activation in the right superior parietal lobule (rSPL) than in rPVC. The subsample of trained controls revealed a significant reduction of BOLD signal change in right and left SPL after training. Only 3 of 5 trained patients showed a reduction of SPL activation after training, which was significantly smaller extent than in controls. Discussion These results correspond to neuropathological findings of differential damage to cortical areas of the visual system in AD. This study indicates that assessing local task related alterations of brain activity by fMR1 can help to elucidate the neurobiological and neuropathological mechanisms of AD. The results of the training study suggest a redundant activation in SPL in healthy subjects, which is lowered -perhaps owing to a more efficient use of cortical tissue - after training. A (albeit smaller) effect of practice could also be observed in some AD patients, which indicates that mechanisms of neuronal plasticity are preserved to some extent in AD.

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