학술논문

Variability of white matter anatomy in the subcallosal cingulate area
Document Type
article
Source
Human Brain Mapping. 42(7)
Subject
Biological Psychology
Biomedical and Clinical Sciences
Clinical Sciences
Psychology
Mental Health
Serious Mental Illness
Depression
Brain Disorders
Clinical Research
Major Depressive Disorder
Neurosciences
Aetiology
2.1 Biological and endogenous factors
Adult
Corpus Callosum
Depressive Disorder
Major
Diffusion Tensor Imaging
Gyrus Cinguli
Humans
Nerve Net
Prefrontal Cortex
Ventral Striatum
White Matter
anatomy
depression
probabilistic Tractography
subcallosal cingulate
Cognitive Sciences
Experimental Psychology
Biological psychology
Cognitive and computational psychology
Language
Abstract
The subcallosal cingulate (SCC) area is a putative hub in the brain network underlying depression. Deep brain stimulation (DBS) targeting a particular subregion of SCC, identified as the intersection of forceps minor (FM), uncinate fasciculus (UCF), cingulum and fronto-striatal fiber bundles, may be critical to a therapeutic response in patients with severe, treatment-resistant forms of major depressive disorder (MDD). The pattern and variability of the white matter anatomy and organization within SCC has not been extensively characterized across individuals. The goal of this study is to investigate the variability of white matter bundles within the SCC that structurally connect this region with critical nodes in the depression network. Structural and diffusion data from 100 healthy subjects from the Human Connectome Project database were analyzed. Anatomically defined SCC regions were used as seeds to perform probabilistic tractography and to estimate the connectivity from the SCC to subject-specific target areas believed to be involved in the pathology of MDD including ventral striatum (VS), UCF, anterior cingulate cortex (ACC), and medial prefrontal cortex (mPFC). Four distinct areas of connectivity were identified within SCC across subjects: (a) postero-lateral SCC connectivity to medial temporal regions via UCF, (b) postero-medial connectivity to VS, (c) superior-medial connectivity to ACC via cingulum bundle, and (d) antero-lateral connectivity to mPFC regions via forceps minor. Assuming white matter connectivity is critical to therapeutic response, the improved anatomic understanding of SCC as well as an appreciation of the intersubject variability are critical to developing optimized therapeutic targeting for SCC DBS.