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T2-Weighted Fast MR Imaging with True FISP Versus HASTE

Comparative Efficacy in the Evaluation of Normal Fetal Brain Maturation

Hsiao-Wen Chung1,2, Cheng-Yu Chen2, Robert A. Zimmerman3, Kwo-Wei Lee2, Chueng-Chen Lee2 and Shy-Chi Chin2

1 Department of Electrical Engineering, National Taiwan University, No. 1, Section 4, Roosevelt Rd., Taipei, Taiwan 10764, Republic of China.
2 Department of Radiology, Tri-Service General Hospital and National Defense Medical Center, No. 8, Section 3, Ting-Chou Rd., Taipei, Taiwan 100, Republic of China.
3 Department of Radiology, The Children's Hospital of Philadelphia, 34th St. and Civic Center Blvd., Philadelphia, PA 19104.



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Fig. 1A. Brainstem myelination in normal fetus at 22 weeks' gestation. Magnified axial half-Fourier acquisition single-shot turbo spin-echo MR image at mid pons level shows that, compared with supratentorial brain where myelination has not begun and no point-spread-function blurring is seen, myelination of pontine tegmentum (arrowheads) is blurred because of T2 decay in myelinated white matter.

 


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Fig. 1B. Brainstem myelination in normal fetus at 22 weeks' gestation. Magnified axial fast MR image with steady-state free precession at same level as A shows early brainstem myelination.

 


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Fig. 2A. Neuronal migration in normal fetus at 22 weeks' gestation. Magnified coronal half-Fourier acquisition single-shot turbo spin-echo MR image shows four-layer pattern of cerebral mantle comprising, from inner to outer layers, germinal matrix, row of migrating neurons, intermediate zone, and immature cortex. Arrows indicate boundaries between layers.

 


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Fig. 2B. Neuronal migration in normal fetus at 22 weeks' gestation. Magnified coronal fast MR image with steady-state free precession at same level as A shows comparable imaging quality in supratentorial anatomy depiction during second trimester. Arrows indicate boundaries between layers.

 


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Fig. 3A. Perirolandic myelination in normal fetus at 33 weeks' gestation. Magnified axial half-Fourier acquisition single-shot turbo spinecho MR image suffers from severe blurring along phase-encoding direction (arrows). Myelination was distorted by blurring and hence was less conspicuous.

 


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Fig. 3B. Perirolandic myelination in normal fetus at 33 weeks' gestation. Magnified axial fast MR image with steady-state free precession at same level as A clearly shows early perirolandic myelination as hypointense signal (arrowheads). Note that fat-water boundary was conspicuously delineated in this image because of out-phase nature of TE (2.3 msec) in gradient-echo images.

 


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Fig. 4. Graph shows theoretic signal change as function of T1/T2 for fast imaging with steady-state precession (true FISP), plotted for three excitation flip angles using formula in literature [11, 13]. Scale on x-axis corresponds to myelination process that causes increase of T1/T2 from 2500/400 msec (approximately 6.3%) to 900/80 msec (approximately 11.3%). For 70° flip angle (solid line) used in this study, myelinated white matter has signal intensity of 50% less than that in nonmyelinated white matter in true FISP images. This decreasing change provides conspicuous contrast in true FISP images, revealing myelination as low-signal-intensity areas. Dotted line=30° flip angle, dashed line=50° flip angle.

 


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Fig. 5. Graph shows effect of steady-state-free-precession (SSFP) angle in one TR on signal of fast imaging with steady-state free precession at 70° flip angle plotted for (from top to bottom) cerebral spinal fluid, nonmyelinated white matter, adult gray matter, and adult white matter. Note that if 180° phase alternation is used for radiofrequency excitation, signal is relatively uniform for all brain tissues with about ± 90° tolerance in SSFP angle. With automatic shimming, a line width of 64 Hz at 1.5 T, measured at one tenth of maximum, was routinely achievable. Banding-free images can thus be obtained at TR of 8.0 msec or less. Also note significant signal difference between nonmyelinated and myelinated white matter because of changes in T1/T2, which provides poor contrast between adult gray and white matter.

 

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