Rationale and Objectives
Phase difference enhanced (PADRE) imaging technique can selectively enhanced the phase difference between the target and surrounding tissue. Our purpose is to assess the delineations of the optic radiation and primary visual cortex (stria of Gennari) using PADRE.
Materials and Methods
The subjects were 6 healthy volunteers. Axial and coronal high-spatial resolution PADRE images were acquired covering the entire optic radiation using a 3T magnetic resonance system. Two radiologists evaluated the PADRE and susceptibility-weighted imaging (SWI)-like images for the delineation of four layers at the optic radiation (tapetum, internal sagittal stratum, external sagittal stratum, and adjacent white matter) on the basis of the anatomic appearances of the cadaveric specimens stained with Bodian’s method and Kluver-Barrera method. The radiologists also assessed the delineations of the stria of Gennari on PADRE and SWI-like images.
Results
In all 6 healthy subjects, the PADRE images clearly identified the four layers at the optic radiation, as well as the stria of Gennari, which were difficult to appreciate in SWI-like images. The anatomic appearances of the optic radiation on PADRE images were more similar to those seen in the specimens stained with Kluver-Barrera method than with Bodian’s method.
Conclusion
The PADRE technique can delineate the four layers at the optic radiation and the stria of Gennari; the differences in myelin densities can also be enhanced. The PADRE technique may have the potential to reinforce the clinical utility of MRI in the diagnosis of diseases that affect the optic radiation and primary visual cortex.
The primary visual cortex is the first cortical area to receive visual input, which is characterized by an easily identifiable anatomical landmark: the stria of Gennari. The optic radiation is a fiber tract, which begins at the lateral geniculate nucleus, passes through the temporal and parietal lobes, and terminates in the primary visual cortex. In the specimens stained using Bodian’s method, the tapetum, internal sagittal stratum, external sagittal stratum, and adjacent white matter are seen as four layers parallel to the wall of the lateral ventricle at the level of the posterior trigone .
Haacke et al designed a high-spatial-resolution three-dimensional (3D) fast low-angle shot magnetic resonance (MR) imaging technique that can enhance subtle differences in the subvoxel magnetic heterogeneities . This technique is called susceptibility-weighted imaging (SWI), and is obtained by multiplication of the phase and magnitude images. The phase images can provide excellent image contrast and reveal anatomical structures that are not visible on the corresponding magnitude images.
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Materials and methods
MR Imaging
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The PADRE Technique
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Subjects and Histological Specimens
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Image Interpretation
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A Patient with Glioblastoma
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Results
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Discussion
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References
1. Kitajima M., Korogi Y., Takahashi M., et. al.: MR signal intensity of the optic radiation. Am J Neuroradiol 1996; 17: pp. 1379-1383.
2. Haacke E.M., Ayaz M., Khan A., et. al.: Establishing a baseline phase behavior in magnetic resonance imaging to determine normal vs. abnormal iron content in the brain. J Magn Reson Imaging 2007; 26: pp. 256-264.
3. Haacke E.M., Cheng N.Y., House M.J., et. al.: Imaging iron stores in the brain using magnetic resonance imaging. Magn Reson Imaging 2005; 23: pp. 1-25.
4. Haacke E.M., Xu Y., Cheng Y.C., et. al.: Susceptibility weighted imaging (SWI). Magn Reson Med 2004; 52: pp. 612-618.
5. Mori N., Miki Y., Kasahara S., et. al.: Susceptibility-weighted imaging at 3 Tesla delineates the optic radiation. Invest Radiol 2009; 44: pp. 140-145.
6. Kakeda S., Korogi Y., Yoneda T., et. al.: A novel tract imaging technique of the brainstem using phase difference enhanced imaging: normal anatomy and initial experience in multiple system atrophy. Eur Radiol 2011; 21: pp. 2202-2210.
7. Yoneda T.: Triple-layer appearance of human cerebral cortices on phase-difference enhanced imaging using 3D principle of echo shifting with a train of observations (PRESTO) sequence. ProcIntl Soc Mag Reson 2009; 17: pp. 27.
8. Burgel U., Mecklenburg I., Blohm U., et. al.: Histological visualization of long fiber tracts in the white matter of adult human brains. J Hirnforsch 1997; 38: pp. 397-404.
9. Li T.Q., van Gelderen P., Merkle H., et. al.: Extensive heterogeneity in white matter intensity in high-resolution T2*-weighted MRI of the human brain at 7.0 T. Neuroimage 2006; 32: pp. 1032-1040.
10. Duyn J.H., van Gelderen P., Li T.Q., et. al.: High-field MRI of brain cortical substructure based on signal phase. Proc Natl Acad Sci U S A 2007; 104: pp. 11796-11801.
11. Zhong K., Leupold J., von Elverfeldt D., et. al.: The molecular basis for gray and white matter contrast in phase imaging. Neuroimage 2008; 40: pp. 1561-1566.
12. Hammond K.E., Lupo J.M., Xu D., et. al.: Development of a robust method for generating 7.0 T multichannel phase images of the brain with application to normal volunteers and patients with neurological diseases. Neuroimage 2008; 39: pp. 1682-1692.
13. Taoka T., Sakamoto M., Nakagawa H., et. al.: Diffusion tensor tractography of the Meyer loop in cases of temporal lobe resection for temporal lobe epilepsy: correlation between postsurgical visual field defect and anterior limit of Meyer loop on tractography. Am J Neuroradiol 2008; 29: pp. 1329-1334.
14. Van Buren J.M., Baldwin M.: The architecture of the optic radiation in the temporal lobe of man. Brain 1958; 81: pp. 15-40.
15. Boyd J.D., Matsubara J.A.: Repositioning the stria of Gennari [abstract]. Abstr Soc Neurosci 2005;
16. Duyn J.H., van Gelderen P., Li T.Q., et. al.: High-field MRI of brain cortical substructure based on signal phase. Proc Natl Acad Sci U S A 2007; 104: pp. 11796-11801.
17. Griswold M.A., Jakob P.M., Nittka M., et. al.: Partially parallel imaging with localized sensitivities (PILS). Magn Reson Med 2000; 44: pp. 602-609.