Alzheimer’s disease (AD) manifests with progressive memory loss and spatial disorientation. Neuropathological studies suggest early AD pathology in the entorhinal cortex (EC) of young adults at genetic risk for AD (APOE4-carriers). Because the EC harbors grid cells, a likely neural substrate of path integration (PI), we examined PI performance in APOE4-carriers during a virtual navigation task. We report a selective impairment in APOE4-carriers specifically when recruitment of compensatory navigational strategies via supportive spatial cues was disabled. A separate fMRI study revealed that PI performance was associated with the strength of entorhinal grid-like representations when no compensatory strategies were available, suggesting grid cell dysfunction as a mechanistic explanation for PI deficits in APOE4-carriers. Furthermore, posterior cingulate/retrosplenial cortex was involved in the recruitment of compensatory navigational strategies via supportive spatial cues. Our results provide evidence for selective PI deficits in AD risk carriers, decades before potential disease onset.
Unmasking selective path integration deficits inAlzheimer’s disease risk carriers / Lukaskunz, Annebierbrauer; Gomes, Carlos A.; Luhmann, Maike; Deuker, Lorena; Getzmann, Stephan; Wascher, Edmund; Gajewski, Patrick D.; Hengstler, Jan G.; Fernandez-Alvarez, Marina; Atienza, Mercedes; Cammisuli, Davide M.; Bonatti, Francesco; Pruneti, Carlo; Percesepe, Antonio; Bellaali, Youssef; Hanseeuw, Bernard; Strange, Bryan A.; Cantero, Jose L.; Axmacher, Nikolai. - In: SCIENCE ADVANCES. - ISSN 2375-2548. - 6:(2020), pp. 1-21.
Unmasking selective path integration deficits inAlzheimer’s disease risk carriers
Francesco BonattiMembro del Collaboration Group
;Carlo PrunetiMembro del Collaboration Group
;Antonio PercesepeMembro del Collaboration Group
;
2020-01-01
Abstract
Alzheimer’s disease (AD) manifests with progressive memory loss and spatial disorientation. Neuropathological studies suggest early AD pathology in the entorhinal cortex (EC) of young adults at genetic risk for AD (APOE4-carriers). Because the EC harbors grid cells, a likely neural substrate of path integration (PI), we examined PI performance in APOE4-carriers during a virtual navigation task. We report a selective impairment in APOE4-carriers specifically when recruitment of compensatory navigational strategies via supportive spatial cues was disabled. A separate fMRI study revealed that PI performance was associated with the strength of entorhinal grid-like representations when no compensatory strategies were available, suggesting grid cell dysfunction as a mechanistic explanation for PI deficits in APOE4-carriers. Furthermore, posterior cingulate/retrosplenial cortex was involved in the recruitment of compensatory navigational strategies via supportive spatial cues. Our results provide evidence for selective PI deficits in AD risk carriers, decades before potential disease onset.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.