Microstructural Alterations in Bipolar and Major Depressive Disorders: A Diffusion Kurtosis Imaging Study.

bipolar disorder diffusion kurtosis imaging major depressive disorder mean kurtosis microstructural alterations

Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
10 2020
Historique:
received: 15 01 2020
revised: 06 04 2020
accepted: 06 04 2020
pubmed: 25 4 2020
medline: 15 5 2021
entrez: 25 4 2020
Statut: ppublish

Résumé

Identifying structural and functional abnormalities in bipolar (BD) and major depressive disorders (MDD) is important for understanding biological processes. Diffusion kurtosis imaging (DKI) may be able to detect the brain's microstructural alterations in BD and MDD and any differences between the two. Prospective. In all, 16 BD patients, 19 MDD patients, and 20 age- and gender-matched healthy volunteers. DKI at 3.0T. The major DKI indices of the brain were compared voxel-by-voxel among the three groups. Significantly different voxels were tested for correlation with clinical variables (ie, Young Mania Rating Scale [YMRS], 17-item Hamilton Depression Rating Scale [17-HDRS], Montgomery-Åsberg Depression Rating Scale, total disease duration, duration of current episode, and the number of past manic/depressive episodes). The performance of the DKI indices in identifying microstructural alterations was estimated. One-way analysis of variance (ANOVA) was used for group comparison of DKI indices. The performance of these indices in detecting microstructural alterations was determined by receiver operating characteristic (ROC) analysis. Pearson's product-moment correlation analyses were used to test the correlations of these indices with clinical variables. DKI revealed widespread microstructural alterations across the brain in each disorder (P < 0.05). Some were significantly different between the two disorders. Mean kurtosis (MK) in the gray matter of the right inferior parietal lobe was able to distinguish BD and MDD with an accuracy of 0.906. A strong correlation was revealed between MK in that region and YMRS in BD patients (r = -0.641, corrected P = 0.042) or 17-HDRS in MDD patients (r = -0.613, corrected P = 0.030). There were also strong correlations between a few other DKI indices and disease duration (r = -0.676 or 0.626, corrected P < 0.05). DKI detected microstructural brain alterations in BD and MDD. Its indices may be useful to distinguish the two disorders or to reflect disease severity and duration. 2 TECHNICAL EFFICACY STAGE: 3 J. Magn. Reson. Imaging 2020;52:1187-1196.

Sections du résumé

BACKGROUND
Identifying structural and functional abnormalities in bipolar (BD) and major depressive disorders (MDD) is important for understanding biological processes.
HYPOTHESIS
Diffusion kurtosis imaging (DKI) may be able to detect the brain's microstructural alterations in BD and MDD and any differences between the two.
STUDY TYPE
Prospective.
SUBJECTS
In all, 16 BD patients, 19 MDD patients, and 20 age- and gender-matched healthy volunteers.
FIELD STRENGTH/SEQUENCE
DKI at 3.0T.
ASSESSMENT
The major DKI indices of the brain were compared voxel-by-voxel among the three groups. Significantly different voxels were tested for correlation with clinical variables (ie, Young Mania Rating Scale [YMRS], 17-item Hamilton Depression Rating Scale [17-HDRS], Montgomery-Åsberg Depression Rating Scale, total disease duration, duration of current episode, and the number of past manic/depressive episodes). The performance of the DKI indices in identifying microstructural alterations was estimated.
STATISTICAL TESTS
One-way analysis of variance (ANOVA) was used for group comparison of DKI indices. The performance of these indices in detecting microstructural alterations was determined by receiver operating characteristic (ROC) analysis. Pearson's product-moment correlation analyses were used to test the correlations of these indices with clinical variables.
RESULTS
DKI revealed widespread microstructural alterations across the brain in each disorder (P < 0.05). Some were significantly different between the two disorders. Mean kurtosis (MK) in the gray matter of the right inferior parietal lobe was able to distinguish BD and MDD with an accuracy of 0.906. A strong correlation was revealed between MK in that region and YMRS in BD patients (r = -0.641, corrected P = 0.042) or 17-HDRS in MDD patients (r = -0.613, corrected P = 0.030). There were also strong correlations between a few other DKI indices and disease duration (r = -0.676 or 0.626, corrected P < 0.05).
DATA CONCLUSION
DKI detected microstructural brain alterations in BD and MDD. Its indices may be useful to distinguish the two disorders or to reflect disease severity and duration.
LEVEL OF EVIDENCE
2 TECHNICAL EFFICACY STAGE: 3 J. Magn. Reson. Imaging 2020;52:1187-1196.

Identifiants

pubmed: 32329208
doi: 10.1002/jmri.27174
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1187-1196

Informations de copyright

© 2020 International Society for Magnetic Resonance in Medicine.

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Auteurs

Daisuke Sawamura (D)

Department of Biomarker Imaging Science, Graduate School of Medical Science and Engineering, Hokkaido University, Sapporo, Japan.
Department of Functioning and Disability, Faculty of Health Sciences, Hokkaido University, Sapporo, Japan.

Hisashi Narita (H)

Department of Psychiatry, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Naoki Hashimoto (N)

Department of Psychiatry, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Shin Nakagawa (S)

Department of Psychiatry, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Hiroyuki Hamaguchi (H)

Department of Biomarker Imaging Science, Graduate School of Medical Science and Engineering, Hokkaido University, Sapporo, Japan.
Department of Radiological Technology, Hokkaido University Hospital, Sapporo, Japan.

Noriyuki Fujima (N)

Department of Diagnostic and Interventional Radiology, Hokkaido University Hospital, Sapporo, Japan.
Department of Radiology, Boston Medical Center, Boston University School of Medicine, Boston, Massachusetts, USA.

Kohsuke Kudo (K)

Department of Diagnostic and Interventional Radiology, Hokkaido University Hospital, Sapporo, Japan.
Global Station for Quantum Medical Science and Engineering, Global Institution for Collaborative Research and Education, Hokkaido University, Sapporo, Japan.

Hiroki Shirato (H)

Global Station for Quantum Medical Science and Engineering, Global Institution for Collaborative Research and Education, Hokkaido University, Sapporo, Japan.
Global Center for Biomedical Science and Engineering, Faculty of Medicine, Hokkaido University, Sapporo, Japan.

Khin K Tha (KK)

Department of Biomarker Imaging Science, Graduate School of Medical Science and Engineering, Hokkaido University, Sapporo, Japan.
Department of Diagnostic and Interventional Radiology, Hokkaido University Hospital, Sapporo, Japan.
Global Station for Quantum Medical Science and Engineering, Global Institution for Collaborative Research and Education, Hokkaido University, Sapporo, Japan.
Global Center for Biomedical Science and Engineering, Faculty of Medicine, Hokkaido University, Sapporo, Japan.

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