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Human habenula segmentation using myelin content

Authors :
Kim, Joo-won
Kim, Joo-won
Naidich, Thomas P.
Ely, Benjamin A.
Yacoub, Essa
De Martino, Federico
Fowkes, Mary E.
Goodman, Wayne K.
Xu, Junqian
Kim, Joo-won
Kim, Joo-won
Naidich, Thomas P.
Ely, Benjamin A.
Yacoub, Essa
De Martino, Federico
Fowkes, Mary E.
Goodman, Wayne K.
Xu, Junqian
Source :
Neuroimage vol.130 (2016) date: 2016-04-15 p.145-156 [ISSN 1053-8119]
Publication Year :
2016

Abstract

The habenula consists of a pair of small epithalamic nuclei located adjacent to the dorsomedial thalamus. Despite increasing interest in imaging the habenula due to its critical role in mediating subcortical reward circuitry, in vivo neuroimaging research targeting the human habenula has been limited by its small size and low anatomical contrast. In this work, we have developed an objective semi-automated habenula segmentation scheme consisting of histogram-based thresholding, region growing, geometric constraints, and partial volume estimation steps. This segmentation schemewas designed around in vivo 3 T myelin-sensitive images, generated by taking the ratio of high-resolution T1w over T2w images. Due to the high myelin content of the habenula, the contrast-to-noise ratio with the thalamus in the in vivo 3 T myelin-sensitive images was significantly higher than the T1wor T2wimages alone. In addition, in vivo 7 T myelin-sensitive images (T1wover T2*w ratio images) and ex vivo proton density-weighted images, along with histological evidence from the literature, strongly corroborated the in vivo 3 T habenulamyelin contrast used in the proposed segmentation scheme. The proposed segmentation scheme represents a step toward a scalable approach for objective segmentation of the habenula suitable for both morphological evaluation and habenula seed region selection in functional and diffusion MRI applications.

Details

Database :
OAIster
Journal :
Neuroimage vol.130 (2016) date: 2016-04-15 p.145-156 [ISSN 1053-8119]
Notes :
DOI: 10.1016/j.neuroimage.2016.01.048, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1050391702
Document Type :
Electronic Resource