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1.
Cogn Behav Neurol ; 35(4): 247-254, 2022 12 01.
Artículo en Inglés | MEDLINE | ID: mdl-36149396

RESUMEN

BACKGROUND: Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a monogenic small-vessel disease that is characterized by a wide range of neurologic and neuropsychological impairments. Constructional impairments have been reported in some cases but have never been assessed systematically. OBJECTIVE: To evaluate constructional abilities and their cognitive and neural correlates in nondemented individuals with CADASIL. METHOD: Thirty individuals with CADASIL who were not affected by clinically relevant cognitive deterioration and 30 healthy controls (HC) underwent an extensive cognitive assessment and paper-and-pencil visuoconstructional tasks in order to detect constructional impairments. Performance on the visuoconstructional tasks was correlated with the cognitive assessment scores and with quantitative indices of regional gray matter atrophy (obtained via FreeSurfer image analysis) and white matter involvement. RESULTS: The individuals with CADASIL achieved significantly lower scores on the cognitive assessment compared with the HC. Poor visuoconstructional abilities were observed in seven (23.3%) of the individuals with CADASIL when performing the copy drawing task and in nine (30%) when performing the Rey Complex Figure Test. Logistic regression revealed that visuoconstructional impairments were significantly associated with scores on the Frontal Assessment Battery and the Attentional Matrices Test. Morphometric results revealed that scores on the visuoconstructional tasks were related to gray matter atrophy of the left frontal lobe and right parietal lobe. CONCLUSION: Impairments on visuoconstructional tasks are quite common in individuals with CADASIL, even in the lack of clinically relevant cognitive deterioration, and are critically related to frontal and parietal atrophy.


Asunto(s)
CADASIL , Leucoencefalopatías , Adulto , Humanos , CADASIL/diagnóstico por imagen , CADASIL/patología , Infarto Cerebral , Leucoencefalopatías/diagnóstico por imagen , Leucoencefalopatías/patología , Lóbulo Frontal , Atrofia/patología , Imagen por Resonancia Magnética
2.
Neurosci Lett ; 506(1): 116-20, 2012 Jan 06.
Artículo en Inglés | MEDLINE | ID: mdl-22079340

RESUMEN

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) may involve many target organs with relevant variability among affected individuals. We performed a multi-organ assessment tapping nervous system, skeletal muscle and cardiovascular system in thirty-nine individuals belonging to 16 families from Central Italy sharing the same R1006C CADASIL mutation. Stroke prevalence was larger in female patients (66.7%) than in males (23.8%); high levels of CKemia were quite frequent (21.6%) and were related to a myopathy without mitochondrial alterations; several individuals had atrial septal aneurysm (10.3%). No specific relationships between common cardiovascular risk factors and clinical manifestations were found. The present systematic study thus identified several gender-related, myopathic and cardiovascular peculiarities of R1006C mutation. This kind of comprehensive approach is necessary to define clinical course, prognosis and treatment options for a multi-organ disease such as CADASIL.


Asunto(s)
Arginina/genética , CADASIL/genética , Cisteína/genética , Salud de la Familia , Mutación/genética , Receptores Notch/genética , Adulto , Anciano , Anciano de 80 o más Años , CADASIL/sangre , CADASIL/complicaciones , CADASIL/diagnóstico , Anomalías Cardiovasculares/etiología , Colesterol/metabolismo , Creatina Quinasa/sangre , Progresión de la Enfermedad , Electromiografía , Femenino , Frecuencia de los Genes , Genotipo , Humanos , Italia , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Músculo Esquelético/fisiopatología , Conducción Nerviosa , Neurofisiología , Pruebas Neuropsicológicas , Fenotipo , Receptor Notch3 , Tomografía Computarizada por Rayos X
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