Quantitative Assessment of Normal Fetal Brain Myelination Using Fast Macromolecular Proton Fraction Mapping

被引:33
作者
Yarnykh, V. L. [1 ,2 ]
Prihod'ko, I. Y. [3 ]
Savelov, A. A. [3 ]
Korostyshevskaya, A. M. [3 ]
机构
[1] Univ Washington, Dept Radiol, 850 Republican St,Room 255, Seattle, WA 98109 USA
[2] Tomsk State Univ, Res Inst Biol & Biophys, Tomsk, Russia
[3] Russian Acad Sci, Inst Int Tomog Ctr, Siberian Branch, Novosibirsk, Russia
基金
俄罗斯科学基金会;
关键词
IN-VIVO; MULTIPLE-SCLEROSIS; HIGH-RESOLUTION; MR; MODEL; MATURATION; DEMYELINATION; CEREBRUM; INFANTS; FETUSES;
D O I
10.3174/ajnr.A5668
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND PURPOSE: Fast macromolecular proton fraction mapping is a recently emerged MRI method for quantitative myelin imaging. Our aim was to develop a clinically targeted technique for macromolecular proton fraction mapping of the fetal brain and test its capability to characterize normal prenatal myelination. MATERIALS AND METHODS: This prospective study included 41 pregnant women (gestational age range, 18-38 weeks) without abnormal findings on fetal brain MR imaging performed for clinical indications. A fast fetal brain macromolecular proton fraction mapping protocol was implemented on a clinical 1.5T MR imaging scanner without software modifications and was performed after a clinical examination with an additional scan time of <5 minutes. 3D macromolecular proton fraction maps were reconstructed from magnetization transfer-weighted, T1-weighted, and proton density-weighted images by the single-point method. Mean macromolecular proton fraction in the brain stem, cerebellum, and thalamus and frontal, temporal, and occipital WM was compared between structures and pregnancy trimesters using analysis of variance. Gestational age dependence of the macromolecular proton fraction was assessed using the Pearson correlation coefficient (r). RESULTS: The mean macromolecular proton fraction in the fetal brain structures varied between 2.3% and 4.3%, being 5-fold lower than macromolecular proton fraction in adult WM. The macromolecular proton fraction in the third trimester was higher compared with the second trimester in the brain stem, cerebellum, and thalamus. The highest macromolecular proton fraction was observed in the brain stem, followed by the thalamus, cerebellum, and cerebral WM. The macromolecular proton fraction in the brain stem, cerebellum, and thalamus strongly correlated with gestational age (r = 0.88, 0.80, and 0.73; P < .001). No significant correlations were found for cerebral WM regions. CONCLUSIONS: Myelin is the main factor determining macromolecular proton fraction in brain tissues. Macromolecular proton fraction mapping is sensitive to the earliest stages of the fetal brain myelination and can be implemented in a clinical setting.
引用
收藏
页码:1341 / 1348
页数:8
相关论文
共 33 条
[1]   Semiquantitative assessment of myelination using magnetic resonance imaging in normal fetal brains [J].
Abe, S ;
Takagi, K ;
Yamamoto, T ;
Okuhata, Y ;
Kato, T .
PRENATAL DIAGNOSIS, 2004, 24 (05) :352-357
[2]   Morphometric assessment of collagen accumulation in germinal matrix vessels of premature human neonates [J].
Anstrom, JA ;
Thore, CR ;
Moody, DM ;
Challa, VR ;
Block, SM ;
Brown, WR .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2005, 31 (02) :181-190
[3]   3D in utero quantification of T2*relaxation times in human fetal brain tissues for age optimized structural and functional MRI [J].
Blazejewska, Anna I. ;
Seshamani, Sharmishtaa ;
McKown, Susan K. ;
Caucutt, Jason S. ;
Dighe, Manjiri ;
Gatenby, Christopher ;
Studholme, Colin .
MAGNETIC RESONANCE IN MEDICINE, 2017, 78 (03) :909-916
[4]  
Brisse H, 1997, AM J NEURORADIOL, V18, P1491
[5]   T2-weighted fast MR imaging with true FISP versus HASTE: Comparative efficacy in the evaluation of normal fetal brain maturation [J].
Chung, HW ;
Chen, CY ;
Zimmerman, RA ;
Lee, KW ;
Lee, CC ;
Chin, SC .
AMERICAN JOURNAL OF ROENTGENOLOGY, 2000, 175 (05) :1375-1380
[6]   Signal-to-noise measurements in magnitude images from NMR phased arrays [J].
Constantinides, CD ;
Atalar, E ;
McVeigh, ER .
MAGNETIC RESONANCE IN MEDICINE, 1997, 38 (05) :852-857
[7]   MYELINATION IN NEONATAL BRAIN [J].
GILLES, FH .
HUMAN PATHOLOGY, 1976, 7 (03) :244-248
[8]  
GIRARD N, 1995, AM J NEURORADIOL, V16, P407
[9]   THE RICIAN DISTRIBUTION OF NOISY MRI DATA [J].
GUDBJARTSSON, H ;
PATZ, S .
MAGNETIC RESONANCE IN MEDICINE, 1995, 34 (06) :910-914
[10]  
HASEGAWA M, 1992, BRAIN DEV-JPN, V14, P1