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Extrastriatal degeneration correlates with deficits in the motor domain subscales of the UHDRS.
Galvez, Victor; Ramírez-García, Gabriel; Hernandez-Castillo, Carlos R; Bayliss, Leo; Díaz, Rosalinda; Lopez-Titla, María Margarita; Campos-Romo, Aurelio; Fernandez-Ruiz, Juan.
Afiliación
  • Galvez V; Instituto de Neuroetología, Universidad Veracruzana, Mexico; Unidad Periférica de Neurociencias, Facultad de Medicina, Universidad Nacional Autónoma de México, Instituto Nacional de Neurología y Neurocirugía "MVS", Mexico; Universidad Panamericana, Escuela de Psicología, Laboratorio de Neurociencias
  • Ramírez-García G; Unidad Periférica de Neurociencias, Facultad de Medicina, Universidad Nacional Autónoma de México, Instituto Nacional de Neurología y Neurocirugía "MVS", Mexico.
  • Hernandez-Castillo CR; CONACYT - Instituto de Neuroetología, Universidad Veracruzana, Mexico.
  • Bayliss L; Instituto Nacional de Neurología y Neurocirugía "Manuel Velasco Suarez", Mexico.
  • Díaz R; Laboratorio de Neuropsicología, Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico.
  • Lopez-Titla MM; Imágenes Cerebrales, Servicios Clínicos, Instituto Nacional de Psiquiatría "Ramón de la Fuente Muñiz", Mexico.
  • Campos-Romo A; Unidad Periférica de Neurociencias, Facultad de Medicina, Universidad Nacional Autónoma de México, Instituto Nacional de Neurología y Neurocirugía "MVS", Mexico.
  • Fernandez-Ruiz J; Instituto de Neuroetología, Universidad Veracruzana, Mexico; Laboratorio de Neuropsicología, Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico; Facultad de Psicología, Universidad Veracruzana, Mexico. Electronic address: jfr@unam.mx.
J Neurol Sci ; 385: 22-29, 2018 02 15.
Article en En | MEDLINE | ID: mdl-29406908
ABSTRACT

INTRODUCTION:

Striatal degeneration has significant behavioral effects in patients with Huntington's disease (HD). However, there is scant evidence of the possible contribution of extrastriatal regions to the motor alterations assessed within the different domains of the Unified Huntington's Disease Rating Scale (UHDRS).

OBJECTIVE:

Analyze if extrastriatal grey matter decrease in patients with HD correlates with motor performance assessed with the UHDRS and its different domains.

METHOD:

Twenty-two molecular diagnosed patients with incipient HD, and twenty-two control participants matched for sex and age participated in this study. Voxel-based morphometry (VBM) analyses were done to identify grey matter decrease in the HD patients, and its relationship with the motor deterioration measured with the UHDRS motor scale. To further explore this relationship, a principal component analysis (PCA) was done on the UHDRS domains scores. Then the average of each component was used as a covariate in a VBM analysis. Finally, individual sub-scores from each domain were also tested for correlations with the VBM results.

RESULTS:

In addition to the striatal degeneration, the VBM analysis showed significant negative correlations between the global UHDRS scores and the cerebellum, insula and precuneus atrophy. The UHDRS PCA showed component-related negative correlations suggesting a specific impact of individual degnerations. Further analyses with the individual sub-scores showed more specific corelations, including chorea, with right caudate and left posterior cingulate gyrus; ocular pursuit, with left precentral gyrus, left superior temporal gyrus, cerebellum culmen and right temporal lobe. Saccadic movements with left postcentral gyrus and left middle occipital gyrus.

CONCLUSION:

In the early stages of HD, it is possible to find correlations between behavioral alterations as measured with the UHDRS motor domains, and extrastriatal regions, including specific areas of the cerebellum, and insular, parietal and frontal cortices. These areas could contribute to the HD related impairments along with the classical deficits associated with the striatal degeneration.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Huntington / Sustancia Gris / Trastornos Mentales / Degeneración Nerviosa Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurol Sci Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Huntington / Sustancia Gris / Trastornos Mentales / Degeneración Nerviosa Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurol Sci Año: 2018 Tipo del documento: Article
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