Diffusion properties of NAA in human corpus callosum as studied with diffusion tensor spectroscopy
Jaymin Upadhyay
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Program in Neuroscience, Boston University, Boston, Massachusetts
Search for more papers by this authorKevin Hallock
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Search for more papers by this authorKelley Erb
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Search for more papers by this authorDae-Shik Kim
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Search for more papers by this authorCorresponding Author
Itamar Ronen
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Department of Anatomy and Neurobiology, 715 Albany St., Boston University School of Medicine, Boston, MA 02118===Search for more papers by this authorJaymin Upadhyay
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Program in Neuroscience, Boston University, Boston, Massachusetts
Search for more papers by this authorKevin Hallock
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Search for more papers by this authorKelley Erb
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Search for more papers by this authorDae-Shik Kim
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Search for more papers by this authorCorresponding Author
Itamar Ronen
Center for Biomedical Imaging, Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts
Department of Anatomy and Neurobiology, 715 Albany St., Boston University School of Medicine, Boston, MA 02118===Search for more papers by this authorAbstract
In diffusion tensor imaging (DTI) the anisotropic movement of water is exploited to characterize microstructure. One confounding issue of DTI is the presence of intra- and extracellular components contributing to the measured diffusivity. This causes an ambiguity in determining the underlying cause of diffusion properties, particularly the fractional anisotropy (FA). In this study an intracellular constituent, N-acetyl aspartate (NAA), was used to probe intracellular diffusion, while water molecules were used to probe the combined intra- and extracellular diffusion. NAA and water diffusion measurements were made in anterior and medial corpus callosum (CC) regions, which are referred to as R1 and R2, respectively. FA(NAA) was found to be greater than FA(Water) in both CC regions, thus indicating a higher degree of anisotropy within the intracellular space in comparison to the combined intra- and extracellular spaces. A decreasing trend in the FA of NAA and water was observed between R1 and R2, while the radial diffusivity (RD) for both molecules increased. The increase in RD(NAA) is particularly significant, thus explaining the more significant decrease in FA(NAA) between the two regions. It is suggested that diffusion tensor spectroscopy of NAA can potentially be used to further characterize microscopic anatomic organization in white matter. Magn Reson Med 58:1045–1053, 2007. © 2007 Wiley-Liss, Inc.
REFERENCES
- 1 Le Bihan D, Breton E, Lallemand D, Grenier P, Cabanis E, Laval-Jeantet M. MR imaging of intravoxel incoherent motions: application to diffusion and perfusion in neurologic disorders. Radiology 1986; 161: 401–407.
- 2 Basser PJ. Inferring microstructural features and the physiological state of tissues from diffusion-weighted images. NMR Biomed 1995; 8: 333–344.
- 3 Moseley ME, Kucharczyk J, Mintorovitch J, Cohen Y, Kurhanewicz J, Derugin N, Asgari H, Norman D. Diffusion-weighted MR imaging of acute stroke: correlation with T2-weighted and magnetic susceptibility-enhanced MR imaging in cats. AJNR Am J Neuroradiol 1990; 11: 423–429.
- 4 Basser PJ, Pajevic S, Pierpaoli C, Duda J, Aldroubi A. In vivo fiber tractography using DT-MRI data. Magn Reson Med 2000; 44: 625–632.
- 5 Le Bihan D. Molecular diffusion, tissue microdynamics and microstructure. NMR Biomed 1995; 8: 375–386.
- 6 Song SK, Yoshino J, Le TQ, Lin SJ, Sun SW, Cross AH, Armstrong RC. Demyelination increases radial diffusivity in corpus callosum of mouse brain. Neuroimage 2005; 26: 132–140.
- 7 Moonen CT, van Zijl PC, Le Bihan D, DesPres D. In vivo NMR diffusion spectroscopy: 31P application to phosphorus metabolites in muscle. Magn Reson Med 1990; 13: 467–477.
- 8 Merboldt KD, Horstermann D, Hanicke W, Bruhn H, Frahm J. Molecular self-diffusion of intracellular metabolites in rat brain in vivo investigated by localized proton NMR diffusion spectroscopy. Magn Reson Med 1993; 29: 125–129.
- 9 Wick M, Nagatomo Y, Prielmeier F, Frahm J. Alteration of intracellular metabolite diffusion in rat brain in vivo during ischemia and reperfusion. Stroke 1995; 26: 1930–1933; discussion 1934.
- 10 Nicolay K, Braun KP, Graaf RA, Dijkhuizen RM, Kruiskamp MJ. Diffusion NMR spectroscopy. NMR Biomed 2001; 14: 94–111.
- 11 Abe O, Okubo T, Hayashi N, Saito N, Iriguchi N, Shirouzu I, Kojima Y, Masumoto T, Ohtomo K, Sasaki Y. Temporal changes of the apparent diffusion coefficients of water and metabolites in rats with hemispheric infarction: experimental study of transhemispheric diaschisis in the contralateral hemisphere at 7 Tesla. J Cereb Blood Flow Metab 2000; 20: 726–735.
- 12 Dreher W, Busch E, Leibfritz D. Changes in apparent diffusion coefficients of metabolites in rat brain after middle cerebral artery occlusion measured by proton magnetic resonance spectroscopy. Magn Reson Med 2001; 45: 383–389.
- 13 Kroenke CD, Ackerman JJ, Yablonskiy DA. On the nature of the NAA diffusion attenuated MR signal in the central nervous system. Magn Reson Med 2004; 52: 1052–1059.
- 14 Ellegood J, Hanstock CC, Beaulieu C. Trace apparent diffusion coefficients of metabolites in human brain using diffusion weighted magnetic resonance spectroscopy. Magn Reson Med 2005; 53: 1025–1032.
- 15 Harada M, Uno M, Hong F, Hisaoka S, Nishitani H, Matsuda T. Diffusion-weighted in vivo localized proton MR spectroscopy of human cerebral ischemia and tumor. NMR Biomed 2002; 15: 69–74.
- 16 Posse S, Cuenod CA, Le Bihan D. Human brain: proton diffusion MR spectroscopy. Radiology 1993; 188: 719–725.
- 17 Ellegood J, Hanstock CC, Beaulieu C. Diffusion tensor spectroscopy (DTS) of human brain. Magn Reson Med 2006; 55: 1–8.
- 18 Nadler JV, Cooper JR. N-acetyl-L-aspartic acid content of human neural tumours and bovine peripheral nervous tissues. J Neurochem 1972; 19: 313–319.
- 19 Burri R, Bigler P, Straehl P, Posse S, Colombo JP, Herschkowitz N. Brain development: 1H magnetic resonance spectroscopy of rat brain extracts compared with chromatographic methods. Neurochem Res 1990; 15: 1009–1016.
- 20 Urenjak J, Williams SR, Gadian DG, Noble M. Proton nuclear magnetic resonance spectroscopy unambiguously identifies different neural cell types. J Neurosci 1993; 13: 981–989.
- 21 Aboitiz F, Scheibel AB, Fisher RS, Zaidel E. Fiber composition of the human corpus callosum. Brain Res 1992; 598: 143–153.
- 22 Witelson SF. Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study. Brain 1989; 112(Pt 3): 799–835.
- 23 Nunes RG, Jezzard P, Clare S. Investigations on the efficiency of cardiac-gated methods for the acquisition of diffusion-weighted images. J Magn Reson 2005; 177: 102–110.
- 24 Tomasch J. Size, distribution, and number of fibres in the human corpus callosum. Anat Rec 1954; 119: 119–135.
- 25 Waxman SG. Conduction in myelinated, unmyelinated, and demyelinated fibers. Arch Neurol 1977; 34: 585–589.
- 26 Assaf Y, Basser PJ. Composite hindered and restricted model of diffusion (CHARMED) MR imaging of the human brain. Neuroimage 2005; 27: 48–58.
- 27 Song SK, Sun SW, Ramsbottom MJ, Chang C, Russell J, Cross AH. Dysmyelination revealed through MRI as increased radial (but unchanged axial) diffusion of water. Neuroimage 2002; 17: 1429–1436.
- 28 Beaulieu C, Allen PS. Determinants of anisotropic water diffusion in nerves. Magn Reson Med 1994; 31: 394–400.
- 29 Zhai G, Lin W, Wilber KP, Gerig G, Gilmore JH. Comparisons of regional white matter diffusion in healthy neonates and adults performed with a 3.0-T head-only MR imaging unit. Radiology 2003; 229: 673–681.
- 30 Chepuri NB, Yen YF, Burdette JH, Li H, Moody DM, Maldjian JA. Diffusion anisotropy in the corpus callosum. AJNR Am J Neuroradiol 2002; 23: 803–808.
- 31 Shin YW, Kim DJ, Ha TH, Park HJ, Moon WJ, Chung EC, Lee JM, Kim IY, Kim SI, Kwon JS. Sex differences in the human corpus callosum: diffusion tensor imaging study. Neuroreport 2005; 16: 795–798.
- 32 Hasan KM, Gupta RK, Santos RM, Wolinsky JS, Narayana PA. Diffusion tensor fractional anisotropy of the normal-appearing seven segments of the corpus callosum in healthy adults and relapsing-remitting multiple sclerosis patients. J Magn Reson Imaging 2005; 21: 735–743.
- 33 Pfefferbaum A, Adalsteinsson E, Sullivan EV. Dysmorphology and microstructural degradation of the corpus callosum: interaction of age and alcoholism. Neurobiol Aging 2005; 27: 994–1009.