Development of chemical exchange saturation transfer at 7T

Chemical exchange saturation transfer (CEST) MRI is a molecular imaging method that has previously been successful at reporting variations in tissue protein and glycogen contents and pH. We have implemented amide proton transfer (APT), a specific form of chemical exchange saturation transfer imaging, at high field (7T) and used it to study healthy human subjects and patients with multiple sclerosis. The effects of static field inhomogeneities were mitigated using a water saturation shift referencing method to center each z‐spectrum on a voxel‐by‐voxel basis. Contrary to results obtained at lower fields, APT imaging at 7T revealed significant contrast between white and gray matters, with a higher APT signal apparent within the white matter. Preliminary studies of multiple sclerosis showed that the APT asymmetry varied with the type of lesion examined. An increase in APT asymmetry relative to healthy tissue was found in some lesions. These results indicate the potential utility of APT at high field as a noninvasive biomarker of white matter pathology, providing complementary information to other MRI methods in current clinical use. Magn Reson Med, 2011. © 2011 Wiley‐Liss, Inc.

[1]  Hans Lassmann,et al.  Inflammatory central nervous system demyelination: Correlation of magnetic resonance imaging findings with lesion pathology , 1997, Annals of neurology.

[2]  Jaco J. M. Zwanenburg,et al.  Fluid attenuated inversion recovery (FLAIR) MRI at 7.0 Tesla: comparison with 1.5 and 3.0 Tesla , 2009, European Radiology.

[3]  F. Barkhof,et al.  Histopathologic correlate of hypointense lesions on T1-weighted spin-echo MRI in multiple sclerosis , 1998, Neurology.

[4]  Jinyuan Zhou,et al.  Amide proton transfer (APT) contrast for imaging of brain tumors , 2003, Magnetic resonance in medicine.

[5]  Jinyuan Zhou,et al.  Quantitative description of the asymmetry in magnetization transfer effects around the water resonance in the human brain , 2007, Magnetic resonance in medicine.

[6]  Klaus-Armin Nave,et al.  Myelin Biology and Disorders , 2004 .

[7]  Jinyuan Zhou,et al.  Detection of the Ischemic Penumbra Using pH-Weighted MRI , 2007, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[8]  Xavier Golay,et al.  Amide proton transfer imaging of human brain tumors at 3T , 2006, Magnetic resonance in medicine.

[9]  R. Balaban,et al.  Magnetization transfer contrast (MTC) and tissue water proton relaxation in vivo , 1989, Magnetic resonance in medicine.

[10]  R. Bryant,et al.  The dynamics of water-protein interactions. , 1996, Annual review of biophysics and biomolecular structure.

[11]  R V Mulkern,et al.  The general solution to the Bloch equation with constant rf and relaxation terms: application to saturation and slice selection. , 1993, Medical physics.

[12]  Jinyuan Zhou,et al.  Optimization of the irradiation power in chemical exchange dependent saturation transfer experiments. , 2005, Journal of magnetic resonance.

[13]  D. Altman,et al.  STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT , 1986, The Lancet.

[14]  Roland Martin,et al.  The immunopathogenesis of multiple sclerosis. , 2002, Journal of rehabilitation research and development.

[15]  Robert S. Balaban,et al.  NMR imaging of labile proton exchange , 1990 .

[16]  Jinyuan Zhou,et al.  Practical data acquisition method for human brain tumor amide proton transfer (APT) imaging , 2008, Magnetic resonance in medicine.

[17]  A. Beckett,et al.  AKUFO AND IBARAPA. , 1965, Lancet.

[18]  Hans Lassmann,et al.  Cellular Damage and Repair in Multiple Sclerosis , 2004 .

[19]  J M Bland,et al.  Statistical methods for assessing agreement between two methods of clinical measurement , 1986 .

[20]  D. Sodickson,et al.  Ultimate intrinsic signal‐to‐noise ratio for parallel MRI: Electromagnetic field considerations , 2003, Magnetic resonance in medicine.

[21]  Jinyuan Zhou,et al.  Using the amide proton signals of intracellular proteins and peptides to detect pH effects in MRI , 2003, Nature Medicine.

[22]  Bennett A Landman,et al.  Water saturation shift referencing (WASSR) for chemical exchange saturation transfer (CEST) experiments , 2009, Magnetic resonance in medicine.

[23]  R S Balaban,et al.  A new class of contrast agents for MRI based on proton chemical exchange dependent saturation transfer (CEST). , 2000, Journal of magnetic resonance.

[24]  Peter C M van Zijl,et al.  MRI detection of glycogen in vivo by using chemical exchange saturation transfer imaging (glycoCEST) , 2007, Proceedings of the National Academy of Sciences.

[25]  Jinyuan Zhou,et al.  Amide proton transfer imaging of 9L gliosarcoma and human glioblastoma xenografts , 2008, NMR in biomedicine.

[26]  G H Glover,et al.  An extended two‐point dixon algorithm for calculating separate water, fat, and B0 images , 1997, Magnetic resonance in medicine.

[27]  J A Frank,et al.  Perfusion imaging with compensation for asymmetric magnetization transfer effects , 1996, Magnetic resonance in medicine.

[28]  Alain Pitiot,et al.  Magnetization transfer phenomenon in the human brain at 7 T , 2010, NeuroImage.

[29]  Susumu Mori,et al.  Mechanism of magnetization transfer during on‐resonance water saturation. A new approach to detect mobile proteins, peptides, and lipids , 2003, Magnetic resonance in medicine.

[30]  Jinyuan Zhou,et al.  Chemical exchange saturation transfer imaging and spectroscopy , 2006 .