Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional study
Abstract Introduction Behavioral and cognitive changes can be observed across all Huntington disease (HD) stages. Our multicenter and retrospective study investigated the association between cognitive and behavioral scale scores in manifest HD, at three different yearly timepoints. Methods We analyz...
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doaj-7edc97dd09c94566a718a1ac02bd3ea52021-07-30T08:47:51ZengWileyBrain and Behavior2162-32792021-07-01117n/an/a10.1002/brb3.2151Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional studySimone Migliore0Giulia D’Aurizio1Sabrina Maffi2Consuelo Ceccarelli3Giovanni Ristori4Silvia Romano5Anna Castaldo6Caterina Mariotti7Giuseppe Curcio8Ferdinando Squitieri9Huntington and Rare Diseases Unit Fondazione IRCCS Casa Sollievo della Sofferenza Hospital San Giovanni Rotondo ItalyDepartment of Biotechnological and Applied Clinical Sciences University of L'Aquila L'Aquila ItalyHuntington and Rare Diseases Unit Fondazione IRCCS Casa Sollievo della Sofferenza Hospital San Giovanni Rotondo ItalyItalian League for Research on Huntington and Related Diseases (LIRH) Foundation Rome ItalyDepartment of Neuroscience, Mental Health and Sensory Organs Faculty of Medicine and Psychology Centre for Experimental Neurological Therapies S. Andrea Hospital Sapienza University Rome ItalyDepartment of Neuroscience, Mental Health and Sensory Organs Faculty of Medicine and Psychology Centre for Experimental Neurological Therapies S. Andrea Hospital Sapienza University Rome ItalyDepartment of Medical Genetics and Neurogenetics Fondazione IRCCS Istituto Neurologico Carlo Besta Milan ItalyDepartment of Medical Genetics and Neurogenetics Fondazione IRCCS Istituto Neurologico Carlo Besta Milan ItalyDepartment of Biotechnological and Applied Clinical Sciences University of L'Aquila L'Aquila ItalyHuntington and Rare Diseases Unit Fondazione IRCCS Casa Sollievo della Sofferenza Hospital San Giovanni Rotondo ItalyAbstract Introduction Behavioral and cognitive changes can be observed across all Huntington disease (HD) stages. Our multicenter and retrospective study investigated the association between cognitive and behavioral scale scores in manifest HD, at three different yearly timepoints. Methods We analyzed cognitive and behavioral domains by the Unified Huntington's Disease Rating Scale (UHDRS) and by the Problem Behaviors Assessment Short Form (PBA‐s), at three different yearly times of life (t0 or baseline, t1 after one year, t2 after two years), in 97 patients with manifest HD (mean age 48.62 ± 13.1), from three ENROLL‐HD Centers. In order to test the disease progression, we also examined patients’ motor and functional changes by the UHDRS, overtime. Results The severity of apathy and of perseveration/obsession was associated with the severity of the cognitive decline (p < .0001), regardless of the yearly timepoint. The score of irritability significantly and positively correlated with perseveration errors in the verbal fluency test at t0 (r = .34; p = .001), while the psychosis significantly and negatively correlated with the information processing speed at t0 (r = −.21; p = .038) and significantly and positively correlated with perseveration errors in the verbal fluency test at t1 (r = .35; p < .0001). The disease progression was confirmed by the significant worsening of the UHDRS‐Total Motor Score (TMS) and of the UHDRS‐Total Functional Capacity (TFC) scale score after two‐year follow‐up (p < .0001). Conclusion Although the progression of abnormal behavioral manifestations cannot be predicted in HD, the severity of apathy and perseveration/obsessions are significantly associated with the severity of the cognitive function impairment, thus contributing, together, to the disease development and to patients’ loss of independence, in addition to the neurological manifestations. This cognitive‐behavior pattern determines a common underlying deficit depending on a dysexecutive syndrome.https://doi.org/10.1002/brb3.2151behavioral symptomscognitive deficitdysexecutive syndromeHD progressionHuntington disease |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Simone Migliore Giulia D’Aurizio Sabrina Maffi Consuelo Ceccarelli Giovanni Ristori Silvia Romano Anna Castaldo Caterina Mariotti Giuseppe Curcio Ferdinando Squitieri |
spellingShingle |
Simone Migliore Giulia D’Aurizio Sabrina Maffi Consuelo Ceccarelli Giovanni Ristori Silvia Romano Anna Castaldo Caterina Mariotti Giuseppe Curcio Ferdinando Squitieri Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional study Brain and Behavior behavioral symptoms cognitive deficit dysexecutive syndrome HD progression Huntington disease |
author_facet |
Simone Migliore Giulia D’Aurizio Sabrina Maffi Consuelo Ceccarelli Giovanni Ristori Silvia Romano Anna Castaldo Caterina Mariotti Giuseppe Curcio Ferdinando Squitieri |
author_sort |
Simone Migliore |
title |
Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional study |
title_short |
Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional study |
title_full |
Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional study |
title_fullStr |
Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional study |
title_full_unstemmed |
Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional study |
title_sort |
cognitive and behavioral associated changes in manifest huntington disease: a retrospective cross‐sectional study |
publisher |
Wiley |
series |
Brain and Behavior |
issn |
2162-3279 |
publishDate |
2021-07-01 |
description |
Abstract Introduction Behavioral and cognitive changes can be observed across all Huntington disease (HD) stages. Our multicenter and retrospective study investigated the association between cognitive and behavioral scale scores in manifest HD, at three different yearly timepoints. Methods We analyzed cognitive and behavioral domains by the Unified Huntington's Disease Rating Scale (UHDRS) and by the Problem Behaviors Assessment Short Form (PBA‐s), at three different yearly times of life (t0 or baseline, t1 after one year, t2 after two years), in 97 patients with manifest HD (mean age 48.62 ± 13.1), from three ENROLL‐HD Centers. In order to test the disease progression, we also examined patients’ motor and functional changes by the UHDRS, overtime. Results The severity of apathy and of perseveration/obsession was associated with the severity of the cognitive decline (p < .0001), regardless of the yearly timepoint. The score of irritability significantly and positively correlated with perseveration errors in the verbal fluency test at t0 (r = .34; p = .001), while the psychosis significantly and negatively correlated with the information processing speed at t0 (r = −.21; p = .038) and significantly and positively correlated with perseveration errors in the verbal fluency test at t1 (r = .35; p < .0001). The disease progression was confirmed by the significant worsening of the UHDRS‐Total Motor Score (TMS) and of the UHDRS‐Total Functional Capacity (TFC) scale score after two‐year follow‐up (p < .0001). Conclusion Although the progression of abnormal behavioral manifestations cannot be predicted in HD, the severity of apathy and perseveration/obsessions are significantly associated with the severity of the cognitive function impairment, thus contributing, together, to the disease development and to patients’ loss of independence, in addition to the neurological manifestations. This cognitive‐behavior pattern determines a common underlying deficit depending on a dysexecutive syndrome. |
topic |
behavioral symptoms cognitive deficit dysexecutive syndrome HD progression Huntington disease |
url |
https://doi.org/10.1002/brb3.2151 |
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