F046 Monitoring visuospatial memory decline in Huntington’s disease using the object-location task

<h3>Background</h3> Visuospatial memory tasks have shown promise in capturing deficits in the early manifest stages of Huntington’s Disease (HD), but their presence during premanifest stages remains unclear<sup>1</sup>. <h3>Aim</h3> We assessed the validity and sensitivity of the modified Object-Location task<sup>2</sup> (OLT) in capturing early HD deficits and their evolution over time. <h3>Methods</h3> Participants included 70 manifest HD, 22 premanifest, and 38 controls. 48 manifest HD and 36 controls were followed for one year (Repair-HD multicentre study, NCT03119246). We measured visuospatial memory performance under conditions of varying cognitive load (figure 1). Striatal and hippocampal volumes were calculated in 49 HD gene carriers at baseline and in 30 manifest HD participants longitudinally (FreeSurfer). <h3>Results</h3> Premanifest HD participants exhibited deficits in object-location memory, while manifest HD individuals showed impairments in object-identity memory, object-location memory and in binding object identity and localization (swap errors) (figure 2A). Localization errors were correlated with putamen volumes at baseline (figure 2B). Manifest HD participants reported more localization errors and more localization around distractors over one year in high-load memory conditions (figure 3). Decline in object identity was associated with increased caudate atrophy (R=0.45, p=0.02), while decline in object localization with increased putamen atrophy (R=-0.37, p=0.05). <h3>Conclusions</h3> These results highlight the significance of visuospatial memory deficits to the cognitive phenotype of HD1. Visuospatial memory tests like the OLT bridge the gap between animal models and human trials, offering a consistent and culturally unbiased framework, and enabling the evaluation of early clinical intervention from the premanifest stage. <h3>References</h3> Glikmann-Johnston Y, Fink KD, Deng P, Torrest A, Stout JC. Spatial memory in Huntington’s disease: A comparative review of human and animal data. <i>Neurosci Biobehav Rev</i>. 2019;<b>98</b>:194–207. doi:10.1016/j.neubiorev.2019.01.015. Pertzov Y, Dong MY, Peich MC, Husain M. Forgetting What Was Where: The Fragility of Object-Location Binding. <i>PLOS ONE</i>. 2012;<b>7</b>(10):e48214. doi:10.1371/journal.pone.0048214

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Published
2024-09-01
DOI
https://doi.org/10.1136/jnnp-2024-ehdn.164
Primary Topic
CCD and CMOS Imaging Sensors
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article

F046 Monitoring visuospatial memory decline in Huntington’s disease using the object-location task

Nicolas Fraisse, Anne Rosser, Marine Lunven, Anne‐Catherine Bachoud‐Lévi et al.
CCD and CMOS Imaging Sensors
article

F046 Monitoring visuospatial memory decline in Huntington’s disease using the object-location task

Nicolas Fraisse, Anne Rosser, Marine Lunven, Anne‐Catherine Bachoud‐Lévi, Katia Youssov, Monica Busse, Graça Morgado, Blanche Bapst, David Craufurd, Andrès Gil Salcedo, Pamela van den Enden
article en

Abstract

<h3>Background</h3> Visuospatial memory tasks have shown promise in capturing deficits in the early manifest stages of Huntington’s Disease (HD), but their presence during premanifest stages remains unclear<sup>1</sup>. <h3>Aim</h3> We assessed the validity and sensitivity of the modified Object-Location task<sup>2</sup> (OLT) in capturing early HD deficits and their evolution over time. <h3>Methods</h3> Participants included 70 manifest HD, 22 premanifest, and 38 controls. 48 manifest HD and 36 controls were followed for one year (Repair-HD multicentre study, NCT03119246). We measured visuospatial memory performance under conditions of varying cognitive load (figure 1). Striatal and hippocampal volumes were calculated in 49 HD gene carriers at baseline and in 30 manifest HD participants longitudinally (FreeSurfer). <h3>Results</h3> Premanifest HD participants exhibited deficits in object-location memory, while manifest HD individuals showed impairments in object-identity memory, object-location memory and in binding object identity and localization (swap errors) (figure 2A). Localization errors were correlated with putamen volumes at baseline (figure 2B). Manifest HD participants reported more localization errors and more localization around distractors over one year in high-load memory conditions (figure 3). Decline in object identity was associated with increased caudate atrophy (R=0.45, p=0.02), while decline in object localization with increased putamen atrophy (R=-0.37, p=0.05). <h3>Conclusions</h3> These results highlight the significance of visuospatial memory deficits to the cognitive phenotype of HD1. Visuospatial memory tests like the OLT bridge the gap between animal models and human trials, offering a consistent and culturally unbiased framework, and enabling the evaluation of early clinical intervention from the premanifest stage. <h3>References</h3> Glikmann-Johnston Y, Fink KD, Deng P, Torrest A, Stout JC. Spatial memory in Huntington’s disease: A comparative review of human and animal data. <i>Neurosci Biobehav Rev</i>. 2019;<b>98</b>:194–207. doi:10.1016/j.neubiorev.2019.01.015. Pertzov Y, Dong MY, Peich MC, Husain M. Forgetting What Was Where: The Fragility of Object-Location Binding. <i>PLOS ONE</i>. 2012;<b>7</b>(10):e48214. doi:10.1371/journal.pone.0048214

Inserm (FR), Université Paris-Est Créteil (FR), Université Paris Sciences et Lettres (FR), Manchester Academic Health Science Centre (GB), University of Manchester (GB), École Normale Supérieure - PSL (FR), Manchester University NHS Foundation Trust (GB), Assistance Publique – Hôpitaux de Paris (FR), St Mary's Hospital (GB), Hôpitaux Universitaires Henri-Mondor (FR), Hôpital Albert-Chenevier (FR), Institut Mondor de Recherche Biomédicale (FR), Centre d’Investigation Clinique 1436 (FR), Cardiff University (GB)
Openalex Percentile: Top 87%
CCD and CMOS Imaging Sensors
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