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2.
AJNR Am J Neuroradiol ; 34(10): 2026-33, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23703146

ABSTRACT

BACKGROUND AND PURPOSE: Abnormal cerebral microstructure has been documented in term neonates with congenital heart disease, portending risk for injury and poor neurodevelopmental outcome. Our hypothesis was that preterm neonates with congenital heart disease would demonstrate diffuse cerebral microstructural abnormalities when compared with critically ill neonates without congenital heart disease. A secondary aim was to identify any association between microstructural abnormalities, white matter injury (eg, punctate white matter lesions), and other clinical variables, including heart lesions. MATERIALS AND METHODS: With the use of tract-based spatial statistics, an unbiased, voxelwise method for analyzing diffusion tensor imaging data, we compared 21 preterm neonates with congenital heart disease with 2 cohorts of neonates without congenital heart disease: 28 term and 27 preterm neonates, identified from the same neonatal intensive care unit. RESULTS: Compared with term neonates without congenital heart disease, preterm neonates with congenital heart disease had microstructural abnormalities in widespread regions of the central white matter. However, 42% of the preterm neonates with congenital heart disease had punctate white matter lesions. When neonates with punctate white matter lesions were excluded, microstructural abnormalities remained only in the splenium. Preterm neonates with congenital heart disease had similar microstructure to preterm neonates without congenital heart disease. CONCLUSIONS: Diffuse microstructural abnormalities were observed in preterm neonates with congenital heart disease, strongly associated with punctate white matter lesions. Independently, regional vulnerability of the splenium, a structure associated with visual spatial function, was observed in all preterm neonates with congenital heart disease.


Subject(s)
Brain Diseases/mortality , Brain Diseases/pathology , Brain/abnormalities , Diffusion Tensor Imaging , Heart Defects, Congenital/mortality , Infant, Premature , Cohort Studies , Corpus Callosum/pathology , Critical Illness/mortality , Humans , Incidence , Infant, Newborn , Infant, Premature, Diseases/mortality , Infant, Premature, Diseases/pathology , Intensive Care, Neonatal , Leukoencephalopathies/mortality , Leukoencephalopathies/pathology , Longitudinal Studies , Magnetic Resonance Imaging , Nerve Fibers, Myelinated/pathology , Retrospective Studies , Risk Factors , Survival Rate
3.
AJNR Am J Neuroradiol ; 30(9): 1787-91, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19541779

ABSTRACT

BACKGROUND AND PURPOSE: To date, very limited attention has been given to ocular abnormalities or growth parameters detected by fetal MR imaging. Our objective was to retrospectively determine the relationship between different parameters of eye development and estimated gestational age in the human fetus by use of fetal MR imaging. MATERIALS AND METHODS: A retrospective study was performed to measure the transverse diameter, interocular distance, and lens diameter of the globes of 127 fetuses who had a morphologically normal central nervous system. Multiple single-shot T2 fast spin-echo images were obtained with a 1.5T magnet by use of contiguous 3-mm intervals in at least 2 orthogonal planes. Loess curves were fitted to explore the relationship between gestational age and each of the 3 measurements of interest. Different models were compared statistically to determine the model of best fit. RESULTS: For each variable of interest, the "best" model of eye growth was a quadratic function. Specifically, lens growth seems to plateau after 36 weeks of gestation, interocular distance plateaus after 36 weeks of gestation, and globe growth plateaus after 42 weeks of gestation. CONCLUSIONS: The lens, orbit, and interocular distance growth of the fetus can be demonstrated on fetal MR imaging. All 3 measurements suggest a quadratic model of growth, which indicates slowing of growth toward the end of gestation.


Subject(s)
Eye/anatomy & histology , Eye/embryology , Gestational Age , Magnetic Resonance Imaging/methods , Prenatal Diagnosis/methods , Eye/growth & development , Female , Humans , Male
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