White and gray matter development in human fetal, newborn and pediatric brains

被引:292
作者
Huang, Hao
Zhang, Jiangyang
Wakana, Setsu
Zhang, Weihong
Ren, Tianbo
Richards, Linda J.
Yarowsky, Paul
Donohue, Pamela
Graham, Ernest
van Zijl, Peter C. M.
Mori, Susumu
机构
[1] Johns Hopkins Univ, Sch Med, Dept Radiol, Baltimore, MD 21205 USA
[2] Kennedy Krieger Inst, FM Kirby Ctr Funct Magnet Resonance Imaging, Baltimore, MD 21205 USA
[3] Univ Maryland, Dept Anat & Neurobiol, Baltimore, MD 21201 USA
[4] Univ Queensland, Dept Anat & Dev Biol, St Lucia, Qld 4072, Australia
[5] Univ Maryland, Dept Pharmacol & Expt Therapeut, Baltimore, MD 21201 USA
[6] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
[7] Johns Hopkins Univ, Sch Med, Dept Gynecol & Obstet, Baltimore, MD 21205 USA
关键词
DTI; brain development; atlas; neonate; PVL;
D O I
10.1016/j.neuroimage.2006.06.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Brain anatomy is characterized by dramatic growth from the end of the second trimester through the neonatal stage. The characterization of normal axonal growth of the white matter tracts has not been well-documented to date and could provide important clues to understanding the extensive inhomogeneity of white matter injuries in cerebral palsy (CP) patients. However, anatomical studies of human brain development during this period are surprisingly scarce and histology-based atlases have become available only recently. Diffusion tensor magnetic resonance imaging (DTMRI) can reveal detailed anatomy of white matter. We acquired diffusion tensor images (DTI) of postmortem fetal brain samples and in vivo neonates and children. Neural structures were annotated in two-dimensional (2D) slices, segmented, measured, and reconstructed three-dimensionally (3D). The growth status of various white matter tracts was evaluated on cross-sections at 19-20 gestational weeks, and compared with 0-month-old neonates and 5- to 6-year-old children. Limbic, commissural, association, and projection white matter tracts and gray matter structures were illustrated in 3D and quantitatively characterized to assess their dynamic changes. The overall pattern of the time courses for the development of different white matter is that limbic fibers develop first and association fibers last and commissural and projection fibers are forming from anterior to posterior part of the brain. The resultant DTNIRI-based 3D human brain data will be a valuable resource for human brain developmental study and will provide reference standards for diagnostic radiology of premature newborns. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:27 / 38
页数:12
相关论文
共 39 条
[1]  
Barkovich A. J., 2000, PEDIAT NEUROIMAGING
[2]   MR DIFFUSION TENSOR SPECTROSCOPY AND IMAGING [J].
BASSER, PJ ;
MATTIELLO, J ;
LEBIHAN, D .
BIOPHYSICAL JOURNAL, 1994, 66 (01) :259-267
[3]  
Bayer S. A., 2005, The Human Brain During the Second Trimester
[4]  
Bayer S. A., 2004, HUMAN BRAIN 3 TRIMES
[5]   Virtual in vivo interactive dissection of white matter fasciculi in the human brain [J].
Catani, M ;
Howard, RJ ;
Pajevic, S ;
Jones, DK .
NEUROIMAGE, 2002, 17 (01) :77-94
[6]   Axonal development in the cerebral white matter of the human fetus and infant [J].
Haynes, RL ;
Borenstein, NS ;
Desilva, TM ;
Folkerth, RD ;
Liu, LG ;
Volpe, JJ ;
Kinney, HC .
JOURNAL OF COMPARATIVE NEUROLOGY, 2005, 484 (02) :156-167
[7]   Pediatric diffusion tensor imaging: Normal database and observation of the white matter maturation in early childhood [J].
Hermoye, L ;
Saint-Maitin, C ;
Cosnard, G ;
Lee, SK ;
Kim, J ;
Nassogne, MC ;
Menten, R ;
Clapuyt, P ;
Donohue, PK ;
Hua, KG ;
Wakana, S ;
Jiang, HY ;
van Zijl, PCM ;
Mori, S .
NEUROIMAGE, 2006, 29 (02) :493-504
[8]   Diffusion tensor imaging of periventricular leukomalacia shows affected sensory cortex white matter pathways [J].
Hoon, AH ;
Lawrie, WT ;
Melhem, ER ;
Reinhardt, EM ;
van Zijl, PCM ;
Solaiyappan, M ;
Jiang, H ;
Johnston, MV ;
Mori, S .
NEUROLOGY, 2002, 59 (05) :752-756
[9]  
Huppi P S, 2001, Semin Neonatol, V6, P195, DOI 10.1053/siny.2001.0039
[10]  
Hüppi PS, 1998, PEDIATR RES, V44, P584