F045 Explorating memory function in Huntington disease

<h3>Introduction</h3> Cognitive alteration in Huntington disease starts in the pre-symptomatic stages and progressively worsens over time. <h3>Aims</h3> To investigate the alteration and relevance of memory impairment in Huntington disease. <h3>Methods</h3> We included a cohort of 21 symptomatic HD patients, stage 3 (Tabrizi 2022) and TFC &gt;= 9 and 9 pre-symptomatic HD subjects (Migliore 2024). The cognitive domains were analysed using the ENROLL protocol: Verbal Fluency Test (Category, Letters (VFTc, VFTl)), Stroop Color Reading Test (SCR), Stroop Word Reading Test (SWR) and The Symbol Digit Modality Test (SDMT). To explore memory function we administered the Rey Auditory Verbal Learning Test (RAVLT- Rey’s 15 Words Test). Motor function was described by UHDRS Total Motor Score and subitems (Reilman 2017). In symptomatic patients we then analysed the correlation between cognitive tests and motor performances. <h3>Results</h3> We found a significant inverse correlation between memory score at immediate and delayed recall of Rey’s 15 Words Test, and the Total Motor Score (-0,65, -0,57) and some of its specific subitems (naimly chorea-0,51, dystonia-0,74 – -0,69, eye -0,51, oropharyngeal-0,51, -0,53). Symbol digit, SWR and SCR were negatively correlated as well. Moreover, all the mentioned tests resulted positively related to TFC. Among the motor domains the ‘gait and balance’ correlated with the VFTl. Interestingly, while the 9 premanifest individuals presented normal performance at SDMT, SCR and SWR, two of them resulted impaired at RAVLT scores. <h3>Conclusion</h3> Memory impairment is associated with the severity of motor dysfunctions and Rey’s 15 Words Test could be used to monitor the rate of disease progression and to detect early alterations in pre-symptomatic subjects.

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Published
2024-09-01
DOI
https://doi.org/10.1136/jnnp-2024-ehdn.163
Primary Topic
Genetic Neurodegenerative Diseases
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article
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article

F045 Explorating memory function in Huntington disease

Sandro Sorbi, Francesco Rotella, Camilla Ferrari, Alessandra Govoni et al.
Genetic Neurodegenerative Diseases
article

F045 Explorating memory function in Huntington disease

Sandro Sorbi, Francesco Rotella, Camilla Ferrari, Alessandra Govoni, Silvia Bagnoli, Elena Capacci, Elena Giachi, Edoardo Paolelli, Benedetta Nacmias
article en

Abstract

<h3>Introduction</h3> Cognitive alteration in Huntington disease starts in the pre-symptomatic stages and progressively worsens over time. <h3>Aims</h3> To investigate the alteration and relevance of memory impairment in Huntington disease. <h3>Methods</h3> We included a cohort of 21 symptomatic HD patients, stage 3 (Tabrizi 2022) and TFC &gt;= 9 and 9 pre-symptomatic HD subjects (Migliore 2024). The cognitive domains were analysed using the ENROLL protocol: Verbal Fluency Test (Category, Letters (VFTc, VFTl)), Stroop Color Reading Test (SCR), Stroop Word Reading Test (SWR) and The Symbol Digit Modality Test (SDMT). To explore memory function we administered the Rey Auditory Verbal Learning Test (RAVLT- Rey’s 15 Words Test). Motor function was described by UHDRS Total Motor Score and subitems (Reilman 2017). In symptomatic patients we then analysed the correlation between cognitive tests and motor performances. <h3>Results</h3> We found a significant inverse correlation between memory score at immediate and delayed recall of Rey’s 15 Words Test, and the Total Motor Score (-0,65, -0,57) and some of its specific subitems (naimly chorea-0,51, dystonia-0,74 – -0,69, eye -0,51, oropharyngeal-0,51, -0,53). Symbol digit, SWR and SCR were negatively correlated as well. Moreover, all the mentioned tests resulted positively related to TFC. Among the motor domains the ‘gait and balance’ correlated with the VFTl. Interestingly, while the 9 premanifest individuals presented normal performance at SDMT, SCR and SWR, two of them resulted impaired at RAVLT scores. <h3>Conclusion</h3> Memory impairment is associated with the severity of motor dysfunctions and Rey’s 15 Words Test could be used to monitor the rate of disease progression and to detect early alterations in pre-symptomatic subjects.

Azienda Ospedaliero-Universitaria Careggi (IT), University of Florence (IT)
Openalex Percentile: Top 85%
Genetic Neurodegenerative Diseases
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