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LASSI-L detects early cognitive changes in pre-motor manifest Huntington’s disease: a replication and validation study

BACKGROUND AND OBJECTIVES: Cognitive decline is an important early sign in pre-motor manifest Huntington’s disease (preHD) and is characterized by deficits across multiple domains including executive function, psychomotor processing speed, and memory retrieval. Prior work suggested that the Loewenst...

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Autores principales: Sierra, Luis A., Hughes, Shelby B., Ullman, Clementina J., Hall, Andrew, Pandeya, Sarbesh R., Schubert, Robin, Frank, Samuel A., Halko, Mark A., Corey-Bloom, Jody, Laganiere, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393264/
https://www.ncbi.nlm.nih.gov/pubmed/37533473
http://dx.doi.org/10.3389/fneur.2023.1191718
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author Sierra, Luis A.
Hughes, Shelby B.
Ullman, Clementina J.
Hall, Andrew
Pandeya, Sarbesh R.
Schubert, Robin
Frank, Samuel A.
Halko, Mark A.
Corey-Bloom, Jody
Laganiere, Simon
author_facet Sierra, Luis A.
Hughes, Shelby B.
Ullman, Clementina J.
Hall, Andrew
Pandeya, Sarbesh R.
Schubert, Robin
Frank, Samuel A.
Halko, Mark A.
Corey-Bloom, Jody
Laganiere, Simon
author_sort Sierra, Luis A.
collection PubMed
description BACKGROUND AND OBJECTIVES: Cognitive decline is an important early sign in pre-motor manifest Huntington’s disease (preHD) and is characterized by deficits across multiple domains including executive function, psychomotor processing speed, and memory retrieval. Prior work suggested that the Loewenstein-Acevedo Scale for Semantic Interference and Learning (LASSI-L)–a verbal learning task that simultaneously targets these domains - could capture early cognitive changes in preHD. The current study aimed to replicate, validate and further analyze the LASSI-L in preHD using larger datasets. METHODS: LASSI-L was administered to 50 participants (25 preHD and 25 Healthy Controls) matched for age, education, and sex in a longitudinal study of disease progression and compared to performance on MMSE, Trail A & B, SCWT, SDMT, Semantic Fluency (Animals), and CVLT-II. Performance was then compared to a separate age-education matched-cohort of 25 preHD participants. Receiver operating curve (ROC) and practice effects (12 month interval) were investigated. Group comparisons were repeated using a preHD subgroup restricted to participants predicted to be far from diagnosis (Far subgroup), based on CAG-Age-Product scaled (CAPs) score. Construct validity was assessed through correlations with previously established measures of subcortical atrophy. RESULTS: PreHD performance on all sections of the LASSI-L was significantly different from controls. The proactive semantic interference section (PSI) was sensitive (p = 0.0001, d = 1.548), similar across preHD datasets (p = 1.0), reliable on test–retest over 12 months (spearman rho = 0.88; p = <0.00001) and associated with an excellent area under ROC (AUROC) of 0.855. In the preHD Far subgroup comparison, PSI was the only cognitive assessment to survive FDR < 0.05 (p = 0.03). The number of intrusions on PSI was negatively correlated with caudate volume. DISCUSSION: The LASSI-L is a sensitive, reliable, efficient tool for detecting cognitive decline in preHD. By using a unique verbal learning test paradigm that simultaneously targets executive function, processing speed and memory retrieval, the LASSI-L outperforms many other established tests and captures early signs of cognitive impairment. With further longitudinal validation, the LASSI-L could prove to be a useful biomarker for clinical research in preHD.
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spelling pubmed-103932642023-08-02 LASSI-L detects early cognitive changes in pre-motor manifest Huntington’s disease: a replication and validation study Sierra, Luis A. Hughes, Shelby B. Ullman, Clementina J. Hall, Andrew Pandeya, Sarbesh R. Schubert, Robin Frank, Samuel A. Halko, Mark A. Corey-Bloom, Jody Laganiere, Simon Front Neurol Neurology BACKGROUND AND OBJECTIVES: Cognitive decline is an important early sign in pre-motor manifest Huntington’s disease (preHD) and is characterized by deficits across multiple domains including executive function, psychomotor processing speed, and memory retrieval. Prior work suggested that the Loewenstein-Acevedo Scale for Semantic Interference and Learning (LASSI-L)–a verbal learning task that simultaneously targets these domains - could capture early cognitive changes in preHD. The current study aimed to replicate, validate and further analyze the LASSI-L in preHD using larger datasets. METHODS: LASSI-L was administered to 50 participants (25 preHD and 25 Healthy Controls) matched for age, education, and sex in a longitudinal study of disease progression and compared to performance on MMSE, Trail A & B, SCWT, SDMT, Semantic Fluency (Animals), and CVLT-II. Performance was then compared to a separate age-education matched-cohort of 25 preHD participants. Receiver operating curve (ROC) and practice effects (12 month interval) were investigated. Group comparisons were repeated using a preHD subgroup restricted to participants predicted to be far from diagnosis (Far subgroup), based on CAG-Age-Product scaled (CAPs) score. Construct validity was assessed through correlations with previously established measures of subcortical atrophy. RESULTS: PreHD performance on all sections of the LASSI-L was significantly different from controls. The proactive semantic interference section (PSI) was sensitive (p = 0.0001, d = 1.548), similar across preHD datasets (p = 1.0), reliable on test–retest over 12 months (spearman rho = 0.88; p = <0.00001) and associated with an excellent area under ROC (AUROC) of 0.855. In the preHD Far subgroup comparison, PSI was the only cognitive assessment to survive FDR < 0.05 (p = 0.03). The number of intrusions on PSI was negatively correlated with caudate volume. DISCUSSION: The LASSI-L is a sensitive, reliable, efficient tool for detecting cognitive decline in preHD. By using a unique verbal learning test paradigm that simultaneously targets executive function, processing speed and memory retrieval, the LASSI-L outperforms many other established tests and captures early signs of cognitive impairment. With further longitudinal validation, the LASSI-L could prove to be a useful biomarker for clinical research in preHD. Frontiers Media S.A. 2023-07-18 /pmc/articles/PMC10393264/ /pubmed/37533473 http://dx.doi.org/10.3389/fneur.2023.1191718 Text en Copyright © 2023 Sierra, Hughes, Ullman, Hall, Pandeya, Schubert, Frank, Halko, Corey-Bloom and Laganiere. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Sierra, Luis A.
Hughes, Shelby B.
Ullman, Clementina J.
Hall, Andrew
Pandeya, Sarbesh R.
Schubert, Robin
Frank, Samuel A.
Halko, Mark A.
Corey-Bloom, Jody
Laganiere, Simon
LASSI-L detects early cognitive changes in pre-motor manifest Huntington’s disease: a replication and validation study
title LASSI-L detects early cognitive changes in pre-motor manifest Huntington’s disease: a replication and validation study
title_full LASSI-L detects early cognitive changes in pre-motor manifest Huntington’s disease: a replication and validation study
title_fullStr LASSI-L detects early cognitive changes in pre-motor manifest Huntington’s disease: a replication and validation study
title_full_unstemmed LASSI-L detects early cognitive changes in pre-motor manifest Huntington’s disease: a replication and validation study
title_short LASSI-L detects early cognitive changes in pre-motor manifest Huntington’s disease: a replication and validation study
title_sort lassi-l detects early cognitive changes in pre-motor manifest huntington’s disease: a replication and validation study
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393264/
https://www.ncbi.nlm.nih.gov/pubmed/37533473
http://dx.doi.org/10.3389/fneur.2023.1191718
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