Literature DB >> 24463571

Normal centrolineal myelination of the callosal splenium reflects the development of the cortical origin and size of its commissural fibers.

Matthew T Whitehead1, Anand Raju, Asim F Choudhri.   

Abstract

INTRODUCTION: Commissural white matter fibers comprising the callosal splenium are diverse. Subsections of the splenium myelinate at different times, in a centrolineal manner. The aims of this study are to depict the normal callosal splenium myelination pattern and to distinguish the transient age-related mid splenium hypointensity from pathology.
METHODS: We reviewed 131 consecutive brain MRIs in patients between ages 3 and 6 months from a single academic children's hospital. Patients that were preterm, hydrocephalic, and/or had volume loss were excluded. Fifty total MR exams that included T1-weighted MR imaging (T1WI), T2-weighted MR imaging (T2WI), and diffusion tensor imaging (DTI) were reviewed. Regions of callosal splenium myelination manifested by T1 and T2 shortening were evaluated. Tractography was performed with seeds placed over the posterior, mid, and anterior splenium to define the origin, destination, and course of traversing fibers.
RESULTS: Splenium signal varied significantly from 3 to 6 months, with distinct age-related trends. On T1WI, the splenium was hypointense at 3 months (12/13), centrally hypointense/peripherally hyperintense at 4 months (15/16), and hyperintense at 6 months (10/11). Tractography revealed three distinct white matter tract populations: medial occipital (posterior); precuneus, posterior cingulate, and medial temporal (middle); and postcentral gyri (anterior).
CONCLUSION: Specific commissural fiber components of the splenium myelinate at different times. The transient developmental mid splenium hypointensity on T1WI corresponds to tracts from the associative cortex, principally the precuneus. Heterogeneous splenium signal alteration in patients ages 3-6 months is a normal developmental phenomenon that should not be confused with pathologic lesions.

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Year:  2014        PMID: 24463571     DOI: 10.1007/s00234-014-1323-5

Source DB:  PubMed          Journal:  Neuroradiology        ISSN: 0028-3940            Impact factor:   2.804


  15 in total

1.  Fiber composition of the human corpus callosum.

Authors:  F Aboitiz; A B Scheibel; R S Fisher; E Zaidel
Journal:  Brain Res       Date:  1992-12-11       Impact factor: 3.252

2.  Progression of corpus callosum diffusion-tensor imaging values during a period of signal changes consistent with myelination.

Authors:  James M Provenzale; Jared Isaacson; Steven Chen
Journal:  AJR Am J Roentgenol       Date:  2012-06       Impact factor: 3.959

3.  Topography of the human corpus callosum revisited--comprehensive fiber tractography using diffusion tensor magnetic resonance imaging.

Authors:  Sabine Hofer; Jens Frahm
Journal:  Neuroimage       Date:  2006-07-18       Impact factor: 6.556

4.  Axon overproduction and elimination in the corpus callosum of the developing rhesus monkey.

Authors:  A S LaMantia; P Rakic
Journal:  J Neurosci       Date:  1990-07       Impact factor: 6.167

5.  Early postnatal development of corpus callosum and corticospinal white matter assessed with quantitative tractography.

Authors:  J H Gilmore; W Lin; I Corouge; Y S K Vetsa; J K Smith; C Kang; H Gu; R M Hamer; J A Lieberman; G Gerig
Journal:  AJNR Am J Neuroradiol       Date:  2007-10       Impact factor: 3.825

6.  Diffusion tensor imaging to evaluate commissural disconnection after corpus callosotomy.

Authors:  Asim F Choudhri; Matthew T Whitehead; Amy L McGregor; Stephanie L Einhaus; Frederick A Boop; James W Wheless
Journal:  Neuroradiology       Date:  2013-10-10       Impact factor: 2.804

7.  Normal postnatal development of the corpus callosum as demonstrated by MR imaging.

Authors:  A J Barkovich; B O Kjos
Journal:  AJNR Am J Neuroradiol       Date:  1988 May-Jun       Impact factor: 3.825

8.  The corpus callosum, the other great forebrain commissures, and the septum pellucidum: anatomy, development, and malformation.

Authors:  Charles Raybaud
Journal:  Neuroradiology       Date:  2010-04-27       Impact factor: 2.804

9.  Cytological and quantitative characteristics of four cerebral commissures in the rhesus monkey.

Authors:  A S Lamantia; P Rakic
Journal:  J Comp Neurol       Date:  1990-01-22       Impact factor: 3.215

10.  Mapping infant brain myelination with magnetic resonance imaging.

Authors:  Sean C L Deoni; Evelyne Mercure; Anna Blasi; David Gasston; Alex Thomson; Mark Johnson; Steven C R Williams; Declan G M Murphy
Journal:  J Neurosci       Date:  2011-01-12       Impact factor: 6.167

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  1 in total

1.  Convergence of Cortical, Thalamocortical, and Callosal Pathways during Human Fetal Development Revealed by Diffusion MRI Tractography.

Authors:  Rongpin Wang; Molly Wilkinson; Tara Kane; Emi Takahashi
Journal:  Front Neurosci       Date:  2017-11-01       Impact factor: 4.677

  1 in total

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