White matter endophenotype candidates for ADHD: a diffusion imaging tractography study with sibling design.


Journal

Psychological medicine
ISSN: 1469-8978
Titre abrégé: Psychol Med
Pays: England
ID NLM: 1254142

Informations de publication

Date de publication:
05 2020
Historique:
pubmed: 23 5 2019
medline: 11 5 2021
entrez: 23 5 2019
Statut: ppublish

Résumé

Brain structural alterations are frequently observed in probands with attention-deficit/hyperactivity disorder (ADHD). Here we examined the microstructural integrity of 76 white matter tracts among unaffected siblings of patients with ADHD to evaluate the potential familial risk and its association with clinical and neuropsychological manifestations. The comparison groups included medication-naïve ADHD probands (n = 50), their unaffected siblings (n = 50) and typically developing controls (n = 50, age-and-sex matched with ADHD probands). Whole brain tractography was reconstructed automatically by tract-based analysis of diffusion spectrum imaging (DSI). Microstructural properties of white matter tracts were represented by the values of generalized fractional anisotropy (GFA), fractional anisotropy (FA), mean diffusivity (MD), radial diffusivity (RD) and axial diffusivity (AD). Compared to the control group, ADHD probands showed higher AD values in the perpendicular fasciculus, superior longitudinal fasciculus I, corticospinal tract, and corpus callosum. The AD values of unaffected siblings were in the intermediate position between those of the ADHD and control groups. These AD values were significantly associated with ADHD symptoms, sustained attention and working memory, for all white matter tracks evaluated except for the perpendicular fasciculus. Higher FA and lower RD values in the right frontostriatal tract connecting ventrolateral prefrontal cortex (FS-VLPFC) were associated with better performance in spatial span only in the unaffected sibling group. Abnormal AD values of specific white matter tracts among unaffected siblings of ADHD probands suggest the presence of familial risk in this population. The right FS-VLPFC may have a role in preventing the expression of the ADHD-related behavioral phenotype. NCT01682915.

Sections du résumé

BACKGROUND
Brain structural alterations are frequently observed in probands with attention-deficit/hyperactivity disorder (ADHD). Here we examined the microstructural integrity of 76 white matter tracts among unaffected siblings of patients with ADHD to evaluate the potential familial risk and its association with clinical and neuropsychological manifestations.
METHODS
The comparison groups included medication-naïve ADHD probands (n = 50), their unaffected siblings (n = 50) and typically developing controls (n = 50, age-and-sex matched with ADHD probands). Whole brain tractography was reconstructed automatically by tract-based analysis of diffusion spectrum imaging (DSI). Microstructural properties of white matter tracts were represented by the values of generalized fractional anisotropy (GFA), fractional anisotropy (FA), mean diffusivity (MD), radial diffusivity (RD) and axial diffusivity (AD).
RESULTS
Compared to the control group, ADHD probands showed higher AD values in the perpendicular fasciculus, superior longitudinal fasciculus I, corticospinal tract, and corpus callosum. The AD values of unaffected siblings were in the intermediate position between those of the ADHD and control groups. These AD values were significantly associated with ADHD symptoms, sustained attention and working memory, for all white matter tracks evaluated except for the perpendicular fasciculus. Higher FA and lower RD values in the right frontostriatal tract connecting ventrolateral prefrontal cortex (FS-VLPFC) were associated with better performance in spatial span only in the unaffected sibling group.
CONCLUSIONS
Abnormal AD values of specific white matter tracts among unaffected siblings of ADHD probands suggest the presence of familial risk in this population. The right FS-VLPFC may have a role in preventing the expression of the ADHD-related behavioral phenotype.
CLINICALTRIALS.GOV NUMBER
NCT01682915.

Identifiants

pubmed: 31115278
pii: S0033291719001120
doi: 10.1017/S0033291719001120
doi:

Banques de données

ClinicalTrials.gov
['NCT01682915']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1203-1213

Auteurs

Huey-Ling Chiang (HL)

Department of Psychiatry, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
Department of Psychiatry, Far Eastern Memorial Hospital, New Taipei City, Taiwan.

Yung-Chin Hsu (YC)

Institute of Medical Device and Imaging, National Taiwan University College of Medicine, Taipei, Taiwan.
AcroViz Technology Inc., Taipei, Taiwan.

Chi-Yuan Shang (CY)

Department of Psychiatry, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.

Wen-Yih Isaac Tseng (WI)

Institute of Medical Device and Imaging, National Taiwan University College of Medicine, Taipei, Taiwan.
Molecular Imaging Center, National Taiwan University, Taipei, Taiwan.

Susan Shur-Fen Gau (SS)

Department of Psychiatry, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
Graduate Institute of Clinical Medicine, and Graduate Institute of Brain and Mind Sciences, National Taiwan University College of Medicine, Taipei, Taiwan.

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Classifications MeSH