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 (APOE4-carriers). Because the EC harbors grid cells, a likely neural substrate of path integration (PI), we examined PI performance in APOE4-carriers during a virtual navigation task. We report a selective impairment in APOE4-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 APOE4-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 Bonatti
Membro del Collaboration Group
;
Carlo Pruneti
Membro del Collaboration Group
;
Antonio Percesepe
Membro del Collaboration Group
;
2020

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 (APOE4-carriers). Because the EC harbors grid cells, a likely neural substrate of path integration (PI), we examined PI performance in APOE4-carriers during a virtual navigation task. We report a selective impairment in APOE4-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 APOE4-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.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11381/2880098
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