Quantitative magnetic resonance imaging of brain development in premature and mature newborns

被引:534
作者
Hüppi, PS
Warfield, S
Kikinis, R
Barnes, PD
Zientara, GP
Jolesz, FA
Tsuji, MK
Volpe, JJ
机构
[1] Brigham & Womens Hosp, Joint Program Neonatol, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, MRI Div, Boston, MA 02115 USA
[4] Childrens Hosp, Dept Radiol, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Childrens Hosp, Dept Neurol, Boston, MA USA
关键词
D O I
10.1002/ana.410430213
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Definition in the living premature infant of the anatomical and temporal characteristics of development of critical brain structures is crucial for insight into the time of greatest vulnerability of such brain structures. We used three-dimensional magnetic resonance imaging (3D MRI) and image-processing algorithms to quantitate total brain volume and total volumes of cerebral gray matter (GM), unmyelinated white matter (WM), myelinated WM, and cerebrospinal fluid (CSF) in 78 premature and mature newborns (postconceptional age, 29-41 weeks). Total brain tissue volume was shown to increase linearly at a rate of 22 ml/wk. Total GM showed a linear increase in relative intracranial volume of approximately 1.4% or 15 mi in absolute volume per week. The pronounced increase in total GM reflected primarily a fourfold increase in cortical GM. Unmyelinated WM was found to be the most prominent brain tissue class in the preterm infant younger than 36 weeks of postconceptional age. Although minimal myelinated WM was present in the preterm infant at 29 weeks, between 35 and 41 weeks an abrupt fivefold increase in absolute volume of myelinated WM was documented. Extracerebral and intraventricular CSF was readily quantitated by this technique and found to change minimally. The application of 3D MRI and tissue segmentation to the study of human infant brain from 29 to 41 weeks of postconceptional age has provided new insights into cerebral cortical development and myelination and has for the first time provided means of quantitative assessment in vivo of early human brain development.
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页码:224 / 235
页数:12
相关论文
共 43 条
[1]   TECHNIQUES FOR MEASURING SULCAL GYRAL PATTERNS IN THE BRAIN AS VISUALIZED THROUGH MAGNETIC-RESONANCE SCANNING - BRAINPLOT AND BRAINMAP [J].
ANDREASEN, NC ;
HARRIS, G ;
CIZADLO, T ;
ARNDT, S ;
OLEARY, DS ;
SWAYZE, V ;
FLAUM, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) :93-97
[2]  
BARKOVICH AJ, 1992, AM J NEURORADIOL, V13, P447
[3]  
CAVINESS VS, 1992, BRAIN DEV-JPN, V14, pS80
[4]   GYRAL DEVELOPMENT OF HUMAN-BRAIN [J].
CHI, JG ;
DOOLING, EC ;
GILLES, FH .
ANNALS OF NEUROLOGY, 1977, 1 (01) :86-93
[5]   MRI - STABILITY OF 3 SUPERVISED SEGMENTATION TECHNIQUES [J].
CLARKE, LP ;
VELTHUIZEN, RP ;
PHUPHANICH, S ;
SCHELLENBERG, JD ;
ARRINGTON, JA ;
SILBIGER, M .
MAGNETIC RESONANCE IMAGING, 1993, 11 (01) :95-106
[6]   QUANTITATIVE GROWTH AND DEVELOPMENT OF HUMAN BRAIN [J].
DOBBING, J ;
SANDS, J .
ARCHIVES OF DISEASE IN CHILDHOOD, 1973, 48 (10) :757-767
[7]  
DOROVINIZIS K, 1977, ARCH PATHOL LAB MED, V101, P192
[8]  
EVRARD P, 1992, BIOL NEONATE, V61, P1
[9]   MAGNETIC-RESONANCE IMAGING-BASED BRAIN MORPHOMETRY - DEVELOPMENT AND APPLICATION TO NORMAL SUBJECTS [J].
FILIPEK, PA ;
KENNEDY, DN ;
CAVINESS, VS ;
ROSSNICK, SL ;
SPRAGGINS, TA ;
STAREWICZ, PM .
ANNALS OF NEUROLOGY, 1989, 25 (01) :61-67
[10]  
FRIEDMAN JH, 1975, IEEE T COMPUT, V24, P1000, DOI 10.1109/T-C.1975.224110