Abnormal brain microstructure and metabolism in small-for-gestational-age term fetuses with normal umbilical artery Doppler

被引:68
作者
Sanz-Cortes, M. [1 ,2 ]
Figueras, F. [1 ,2 ]
Bargallo, N. [3 ]
Padilla, N. [1 ,2 ]
Amat-Roldan, I. [1 ,2 ]
Gratacos, E. [1 ,2 ]
机构
[1] Univ Barcelona, Hosp Clin, Inst Invest Biomed August Pi & Sunyer IDIBAPS, ICGON,Fetal Perinatal Med Res Grp, E-08028 Barcelona, Spain
[2] ISCIII, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Barcelona, Spain
[3] Hosp Clin Barcelona, Dept Radiol, Barcelona, Spain
关键词
diffusion weighted imaging; DWI; growth restriction; inositol; magnetic resonance spectroscopy; MRS; SGA; small-for-gestational-age; MAGNETIC-RESONANCE SPECTROSCOPY; INTRAUTERINE GROWTH RESTRICTION; H-1 MR SPECTROSCOPY; NORMAL FETAL-BRAIN; BIRTH-WEIGHT; IN-UTERO; INFANTS; MATURATION; POPULATION; CHILDREN;
D O I
10.1002/uog.7724
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Objectives To assess microstructural and metabolic brain differences between small-for-gestational age (SGA) and appropriate-for-gestational age (AGA) fetuses at 37 weeks' gestation by magnetic resonance imaging (MRI) spectroscopy and diffusion weighted imaging. Methods Eight SGA and five matched AGA singleton fetuses, all with normal umbilical artery Doppler, were evaluated using MRI at 37 weeks to measure markers of brain microstructure and metabolism. The metabolic spectrum of N-acetyl-aspartate/choline, choline/creatine, inositol/choline and creatine/choline ratios in the left frontal lobe and the apparent diffusion coefficient from the right and left basal ganglia and frontal and occipital lobes, pyramidal tract and corpus callosum were analyzed and compared. Results As compared with controls, SGA fetuses showed a significant increase in inositol/choline ratio (SGA, 0.57 vs. AGA, 0.25; P = 0.04) and significantly higher ADC values in the pyramidal tract (SGA, 119.87 x 10(-5) mm(2)/s vs. AGA, 105.11 x 10(-5) mm(2)/s; P = 0.04). Conclusions SGA fetuses with normal umbilical artery Doppler present microstructural and metabolic brain changes, suggesting the existence of an abnormal in-utero brain development in fetuses with this condition. Copyright (C) 2010 ISUOG. Published by John Wiley e. Sons, Ltd.
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页码:159 / 165
页数:7
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