Strategic white matter tracts for processing speed deficits in age-related small vessel disease

Autor: Stefan Ropele, Martin Dichgans, Lukas Pirpamer, Benno Gesierich, Reinhold Schmidt, Stephan Seiler, Edith Hofer, Mariya Gonik, Edouard Duchesnay, Eric Jouvent, Marco Duering, Hugues Chabriat
Rok vydání: 2014
Předmět:
Male
Trail Making Test
Disease
physiopathology [Brain]
computer.software_genre
Brain mapping
blood supply [Brain]
Lesion
White matter
methods [Brain Mapping]
Leukoencephalopathies
pathology [Brain]
Region of interest
Voxel
medicine
Humans
ddc:610
physiopathology [Cerebral Small Vessel Diseases]
Aged
physiopathology [Leukoencephalopathies]
Brain Mapping
pathology [Leukoencephalopathies]
Brain
etiology [Cognition Disorders]
Anatomy
instrumentation [Brain Mapping]
Middle Aged
Hyperintensity
etiology [Leukoencephalopathies]
medicine.anatomical_structure
Cerebral Small Vessel Diseases
complications [Cerebral Small Vessel Diseases]
physiopathology [Cognition Disorders]
pathology [Cerebral Small Vessel Diseases]
pathology [Cognition Disorders]
Female
Neurology (clinical)
medicine.symptom
Cognition Disorders
Psychology
Neuroscience
computer
Zdroj: Neurology 82(22), 1946-1950 (2014). doi:10.1212/WNL.0000000000000475
ISSN: 1526-632X
0028-3878
DOI: 10.1212/wnl.0000000000000475
Popis: Objective: Cerebral small vessel disease is the most common cause of vascular cognitive impairment and typically manifests with slowed processing speed. We investigated the impact of lesion location on processing speed in age-related small vessel disease. Methods: A total of 584 community-dwelling elderly underwent brain MRI followed by segmentation of white matter hyperintensities. Processing speed was determined by the timed measure of the Trail Making Test part B. The impact of the location of white matter hyperintensities was assessed by voxel-based lesion-symptom mapping and graph-based statistical models on regional lesion volumes in major white matter tracts. Results: Voxel-based lesion-symptom mapping identified multiple voxel clusters where the presence of white matter hyperintensities was associated with slower performance on the Trail Making Test part B. Clusters were located bilaterally in the forceps minor and anterior thalamic radiation. Region of interest–based Bayesian network analyses on lesion volumes within major white matter tracts depicted the same tracts as direct predictors for an impaired Trail Making Test part B performance. Conclusions: Our findings highlight damage to frontal interhemispheric and thalamic projection fiber tracts harboring frontal-subcortical neuronal circuits as a predictor for processing speed performance in age-related small vessel disease.
Databáze: OpenAIRE