bioRxivNeurosciencePreprint
Diagnostic images for mild cognitive impairment reveal biomarker status and abnormal scene processing
Yuetong BaiiD, Oliver PetersiD, Silka Dawn FreieslebeniD, Friederike FenskiiD, Josef PrilleriD, Eike Jakob SpruthiD, Anja SchneideriD, Klaus FließbachiD, Jens WiltfangiD, Claudia BartelsiD, Ayda RostamzadehiD, Wenzel GlanziD, Stefan Johannes TeipeliD, Ingo KilimanniD, Christoph LaskeiD, Matthias H. J. MunkiD, Annika E. SpottkeiD, Nina Roy‐KluthiD, Frederic BrosseroniD, Michael WagneriD, Ingo FrommanniD, Falk LüsebrinkiD, Alfredo Ramı́reziD, Peter DechentiD, Stefan HetzeriD, , Wilma Alice BainbridgeiD
Abstract
Research on the impairment of episodic memory in Alzheimers disease often focuses on the processes of memory rather than the content of the specific images being remembered. We recently showed that patients with mild cognitive impairment (MCI), Stage 3 of Alzheimers disease, can memorize certain images quite well, suggesting that episodic memory is not uniformly impaired. Certain images, on the other hand, could not be memorized by MCI patients and were instead diagnostic for distinguishing MCI from healthy older adults. In this study, we investigate whether poor memory for diagnostic images is related to impaired neural processing in specific brain regions due to Alzheimers biomarker pathology. 64 healthy controls and 48 MCI participants in the DELCODE dataset performed a visual scene memory task during fMRI, with CSF Alzheimers disease biomarker data collected (i.e., amyloid and tau biomarkers). We found that diagnostic images have larger behavior-biomarker correlations for total tau, phospho-tau, A{beta}42/A{beta}40, A{beta}42/phospho-tau compared to non-diagnostic images, suggesting that memory for these specific images are more affected by Alzheimers disease pathology. The fMRI data revealed an interaction effect between group membership (healthy control / MCI) and image diagnosticity (diagnostic / non-diagnostic scene images), with MCI participants having higher activation in scene processing regions (parahippocampal place area, retrosplenial cortex and occipital place area) for diagnostic images than non-diagnostic images. In contrast, healthy controls showed no differences in processing between diagnostic and non-diagnostic images. These results suggest that MCI individuals may engage in inefficiently heightened encoding activation for these diagnostic images. Our results show that special "diagnostic" images exist that can reveal amyloid and tau pathology and differences in neural activity in scene regions.
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