Disentangling the neurobiological bases of temporal impulsivity in Huntington's disease

dc.contributor.authorPardina Torner, Helena
dc.contributor.authorPaepe, Audrey E. de
dc.contributor.authorGarcía Gorro, Clara
dc.contributor.authorRodríguez Dechicha, Nadia
dc.contributor.authorVaquer, Irene
dc.contributor.authorCalopa, Matilde
dc.contributor.authorRuíz Idiago, Jesús
dc.contributor.authorMareca, Celia
dc.contributor.authorDiego Balaguer, Ruth de
dc.contributor.authorCámara, Estela
dc.date.accessioned2024-05-15T09:17:54Z
dc.date.available2024-05-15T09:17:54Z
dc.date.issued2024-03-01
dc.date.updated2024-05-08T12:07:54Z
dc.description.abstractBackgroundDespite its impact on daily life, impulsivity in Huntington's disease (HD) is understudied as a neuropsychiatric symptom. Our aim is to characterize temporal impulsivity in HD and to disentangle the white matter correlate associated with impulsivity.MethodsForty-seven HD individuals and 36 healthy controls were scanned and evaluated for temporal impulsivity using a delay-discounting (DD) task and complementary Sensitivity to Punishment and Sensitivity to Reward Questionnaire. Diffusion tensor imaging was employed to characterize the structural connectivity of three limbic tracts: the uncinate fasciculus (UF), the accumbofrontal tract (NAcc-OFC), and the dorsolateral prefrontal cortex connectig the caudate nucleus (DLPFC-cn). Multiple linear regression analyses were applied to analyze the relationship between impulsive behavior and white matter microstructural integrity.ResultsOur results revealed altered structural connectivity in the DLPC-cn, the NAcc-OFC and the UF in HD individuals. At the same time, the variability in structural connectivity of these tracts was associated with the individual differences in temporal impulsivity. Specifically, increased structural connectivity in the right NAcc-OFC and reduced connectivity in the left UF were associated with higher temporal impulsivity scores.ConclusionsThe present findings highlight the importance of investigating the spectrum of temporal impulsivity in HD. As, while less prevalent than other psychiatric features, this symptom is still reported to significantly impact the quality of life of patients and caregivers. This study provides evidence that individual differences observed in temporal impulsivity may be explained by variability in limbic frontostriatal tracts, while shedding light on the role of sensitivity to reward in modulating impulsive behavior through the selection of immediate rewards. This study investigates individual differences in temporal impulsivity by using a delay discounting task and, its relationship with white matter connectivity. Our findings reveal significant alterations in the microstructure of key tracts of interest, including the right DLPF-Ccn, bilateral uncinate fasciculus and the left accumbo-frontal tract, in individuals with HD. Furthermore, we observed that variability in the structural connectivity in specific tracts is associated with individual differences in temporal impulsivity. image
dc.format.extent12 p.
dc.format.mimetypeapplication/pdf
dc.identifier.issn2162-3279
dc.identifier.pmid38450912
dc.identifier.urihttps://hdl.handle.net/2445/211289
dc.language.isoeng
dc.publisherWiley
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1002/brb3.3335
dc.relation.ispartofBrain and Behavior, 2024, vol. 14, num. 3
dc.relation.urihttps://doi.org/10.1002/brb3.3335
dc.rightscc by (c) Pardina Torner, Helena et al, 2024
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationConducta compulsiva
dc.subject.classificationMalalties neurodegeneratives
dc.subject.otherCompulsive behavior
dc.subject.otherNeurodegenerative Diseases
dc.titleDisentangling the neurobiological bases of temporal impulsivity in Huntington's disease
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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