White matter abnormalities in depression: A categorical and phenotypic diffusion MRI study

Mood depressive disorder is one of the most disabling chronic diseases with a high rate of everyday life disability that affects 350 million people around the world. Recent advances in neuroimaging have reported widespread structural abnormalities, suggesting a dysfunctional frontal-limbic circuit i...

Full description

Bibliographic Details
Main Authors: Julie Coloigner, Jean-Marie Batail, Olivier Commowick, Isabelle Corouge, Gabriel Robert, Christian Barillot, Dominique Drapier
Format: Article
Language:English
Published: Elsevier 2019-01-01
Series:NeuroImage: Clinical
Online Access:http://www.sciencedirect.com/science/article/pii/S2213158219300609
id doaj-7d60d3a863064a6998a794e2babcf036
record_format Article
collection DOAJ
language English
format Article
sources DOAJ
author Julie Coloigner
Jean-Marie Batail
Olivier Commowick
Isabelle Corouge
Gabriel Robert
Christian Barillot
Dominique Drapier
spellingShingle Julie Coloigner
Jean-Marie Batail
Olivier Commowick
Isabelle Corouge
Gabriel Robert
Christian Barillot
Dominique Drapier
White matter abnormalities in depression: A categorical and phenotypic diffusion MRI study
NeuroImage: Clinical
author_facet Julie Coloigner
Jean-Marie Batail
Olivier Commowick
Isabelle Corouge
Gabriel Robert
Christian Barillot
Dominique Drapier
author_sort Julie Coloigner
title White matter abnormalities in depression: A categorical and phenotypic diffusion MRI study
title_short White matter abnormalities in depression: A categorical and phenotypic diffusion MRI study
title_full White matter abnormalities in depression: A categorical and phenotypic diffusion MRI study
title_fullStr White matter abnormalities in depression: A categorical and phenotypic diffusion MRI study
title_full_unstemmed White matter abnormalities in depression: A categorical and phenotypic diffusion MRI study
title_sort white matter abnormalities in depression: a categorical and phenotypic diffusion mri study
publisher Elsevier
series NeuroImage: Clinical
issn 2213-1582
publishDate 2019-01-01
description Mood depressive disorder is one of the most disabling chronic diseases with a high rate of everyday life disability that affects 350 million people around the world. Recent advances in neuroimaging have reported widespread structural abnormalities, suggesting a dysfunctional frontal-limbic circuit involved in the pathophysiological mechanisms of depression. However, a variety of different white matter regions has been implicated and is sought to suffer from lack of reproducibility of such categorical-based biomarkers. These inconsistent results might be attributed to various factors: actual categorical definition of depression as well as clinical phenotype variability. In this study, we 1/ examined WM changes in a large cohort (114 patients) compared to a healthy control group and 2/ sought to identify specific WM alterations in relation to specific depressive phenotypes such as anhedonia (i.e. lack of pleasure), anxiety and psychomotor retardation –three core symptoms involved in depression. Consistent with previous studies, reduced white matter was observed in the genu of the corpus callosum extending to the inferior fasciculus and posterior thalamic radiation, confirming a frontal-limbic circuit abnormality. Our analysis also reported other patterns of increased fractional anisotropy and axial diffusivity as well as decreased apparent diffusion coefficient and radial diffusivity in the splenium of the corpus callosum and posterior limb of the internal capsule. Moreover, a positive correlation between FA and anhedonia was found in the superior longitudinal fasciculus as well as a negative correlation in the cingulum. Then, the analysis of the anxiety and diffusion metric revealed that increased anxiety was associated with greater FA values in genu and splenium of corpus callosum, anterior corona radiata and posterior thalamic radiation. Finally, the motor retardation analysis showed a correlation between increased Widlöcher depressive retardation scale scores and reduced FA in the body and genu of the corpus callosum, fornix, and superior striatum. Through this twofold approach (categorical and phenotypic), this study has underlined the need to move forward to a symptom-based research area of biomarkers, which help to understand the pathophysiology of mood depressive disorders and to stratify precise phenotypes of depression with targeted therapeutic strategies. Keywords: Diffusion-weighted imaging, Voxel-based analysis, Fractional anisotropy value, Depression, Categorical and phenotypic approach
url http://www.sciencedirect.com/science/article/pii/S2213158219300609
work_keys_str_mv AT juliecoloigner whitematterabnormalitiesindepressionacategoricalandphenotypicdiffusionmristudy
AT jeanmariebatail whitematterabnormalitiesindepressionacategoricalandphenotypicdiffusionmristudy
AT oliviercommowick whitematterabnormalitiesindepressionacategoricalandphenotypicdiffusionmristudy
AT isabellecorouge whitematterabnormalitiesindepressionacategoricalandphenotypicdiffusionmristudy
AT gabrielrobert whitematterabnormalitiesindepressionacategoricalandphenotypicdiffusionmristudy
AT christianbarillot whitematterabnormalitiesindepressionacategoricalandphenotypicdiffusionmristudy
AT dominiquedrapier whitematterabnormalitiesindepressionacategoricalandphenotypicdiffusionmristudy
_version_ 1724826816658538496
spelling doaj-7d60d3a863064a6998a794e2babcf0362020-11-25T02:30:55ZengElsevierNeuroImage: Clinical2213-15822019-01-0122White matter abnormalities in depression: A categorical and phenotypic diffusion MRI studyJulie Coloigner0Jean-Marie Batail1Olivier Commowick2Isabelle Corouge3Gabriel Robert4Christian Barillot5Dominique Drapier6Univ Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, Empenn ERL U-1228, F-35000 Rennes, France; Corresponding author at : Unité Empenn U1228, INSERM, INRIA, Université Rennes I, IRISA, UMR CNRS 6074 Campus de Beaulieu 35042 Rennes Cedex, France.Univ Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, Empenn ERL U-1228, F-35000 Rennes, France; Centre Hospitalier Guillaume Régnier, Academic Psychiatry Department, 35703 Rennes, France; Univ of Rennes, “Behavior and Basal Ganglia” research unit (EA 4712), Rennes, FranceUniv Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, Empenn ERL U-1228, F-35000 Rennes, FranceUniv Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, Empenn ERL U-1228, F-35000 Rennes, FranceUniv Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, Empenn ERL U-1228, F-35000 Rennes, France; Centre Hospitalier Guillaume Régnier, Academic Psychiatry Department, 35703 Rennes, France; Univ of Rennes, “Behavior and Basal Ganglia” research unit (EA 4712), Rennes, FranceUniv Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, Empenn ERL U-1228, F-35000 Rennes, FranceCentre Hospitalier Guillaume Régnier, Academic Psychiatry Department, 35703 Rennes, France; Univ of Rennes, “Behavior and Basal Ganglia” research unit (EA 4712), Rennes, FranceMood depressive disorder is one of the most disabling chronic diseases with a high rate of everyday life disability that affects 350 million people around the world. Recent advances in neuroimaging have reported widespread structural abnormalities, suggesting a dysfunctional frontal-limbic circuit involved in the pathophysiological mechanisms of depression. However, a variety of different white matter regions has been implicated and is sought to suffer from lack of reproducibility of such categorical-based biomarkers. These inconsistent results might be attributed to various factors: actual categorical definition of depression as well as clinical phenotype variability. In this study, we 1/ examined WM changes in a large cohort (114 patients) compared to a healthy control group and 2/ sought to identify specific WM alterations in relation to specific depressive phenotypes such as anhedonia (i.e. lack of pleasure), anxiety and psychomotor retardation –three core symptoms involved in depression. Consistent with previous studies, reduced white matter was observed in the genu of the corpus callosum extending to the inferior fasciculus and posterior thalamic radiation, confirming a frontal-limbic circuit abnormality. Our analysis also reported other patterns of increased fractional anisotropy and axial diffusivity as well as decreased apparent diffusion coefficient and radial diffusivity in the splenium of the corpus callosum and posterior limb of the internal capsule. Moreover, a positive correlation between FA and anhedonia was found in the superior longitudinal fasciculus as well as a negative correlation in the cingulum. Then, the analysis of the anxiety and diffusion metric revealed that increased anxiety was associated with greater FA values in genu and splenium of corpus callosum, anterior corona radiata and posterior thalamic radiation. Finally, the motor retardation analysis showed a correlation between increased Widlöcher depressive retardation scale scores and reduced FA in the body and genu of the corpus callosum, fornix, and superior striatum. Through this twofold approach (categorical and phenotypic), this study has underlined the need to move forward to a symptom-based research area of biomarkers, which help to understand the pathophysiology of mood depressive disorders and to stratify precise phenotypes of depression with targeted therapeutic strategies. Keywords: Diffusion-weighted imaging, Voxel-based analysis, Fractional anisotropy value, Depression, Categorical and phenotypic approachhttp://www.sciencedirect.com/science/article/pii/S2213158219300609