Widespread White Matter Aberrations Are Associated with Phonemic Verbal Fluency Impairment in Chronic Traumatic Brain Injury.


Journal

Journal of neurotrauma
ISSN: 1557-9042
Titre abrégé: J Neurotrauma
Pays: United States
ID NLM: 8811626

Informations de publication

Date de publication:
01 04 2020
Historique:
pubmed: 22 10 2019
medline: 20 8 2021
entrez: 22 10 2019
Statut: ppublish

Résumé

Microstructural white matter (WM) disruption and resulting abnormal structural connectivity form a potential underlying pathology in traumatic brain injury (TBI). Herein, to determine the potential mechanism of cognitive deterioration in TBI, we examined the association of damage to specific WM tracts with cognitive function in TBI patients. We recruited 18 individuals with mild-to-moderate/severe TBI in the chronic phase and 17 age-matched controls. We determined the pattern of WM aberrations in TBI using tract-based spatial statistics (TBSS) and then examined the relationship between cognitive impairment and WM damage using the threshold-free cluster enhancement correction in TBSS. TBSS analysis showed that TBI patients exhibited WM aberrations in a wide range of brain regions. In the majority of these regions, lower fractional anisotropy (FA) largely overlapped with increased radial diffusivity, but not with axial diffusivity. Further, voxel-wise correction in TBSS demonstrated that higher FA values were associated with better performance in the phonemic verbal fluency task (VFT) in widespread WM regions, but not with the semantic VFT. Despite variation in the magnitude and location of brain injury between individual cases, chronic TBI patients exhibited widespread WM aberrations. We confirmed the findings of previous studies that WM integrity is lower across the spectrum of TBI severity in chronic subjects compared to controls. Further, phonemic VFT may be a more sensitive cognitive measure of executive dysfunction associated with WM aberrations in TBI compared with semantic VFT.

Identifiants

pubmed: 31631743
doi: 10.1089/neu.2019.6751
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

975-981

Auteurs

Bun Yamagata (B)

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Ryo Ueda (R)

Department of Radiological Sciences, Graduate School of Health Sciences, Tokyo Metropolitan University, Tokyo, Japan.
Office of Radiation Technology, Keio University Hospital, Tokyo, Japan.

Kumiko Tasato (K)

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Yuta Aoki (Y)

Medical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.

Shogo Hotta (S)

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Jinichi Hirano (J)

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Akihiro Takamiya (A)

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Shutaro Nakaaki (S)

Department of Psychiatry and Cognitive-Behavioral Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Hajime Tabuchi (H)

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Masaru Mimura (M)

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

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