Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 12 de 12
Filter
1.
Ultrasound Obstet Gynecol ; 57(5): 769-775, 2021 05.
Article in English | MEDLINE | ID: mdl-32202689

ABSTRACT

OBJECTIVE: Fetal cerebrovascular resistance is influenced by several factors in the setting of intact autoregulation to allow for normal cerebral blood flow and oxygenation. Maternal hyperoxygenation (MH) allows for acute alterations in fetal physiology and can be a tool to test cerebrovascular reactivity in late-gestation fetuses. In this study, we utilized MH to evaluate cerebrovascular reactivity in fetuses with specific congenital heart disease (CHD). METHODS: This was a cross-sectional study of fetuses with complex CHD compared to controls without CHD. CHD cases were grouped according to physiology into: left-sided obstructive lesion (LSOL), right-sided obstructive lesion (RSOL) or dextro-transposition of the great arteries (d-TGA). Subjects underwent MH testing during the third-trimester fetal echocardiogram. The pulsatility index (PI) was calculated for the fetal middle cerebral artery (MCA), umbilical artery (UA) and branch pulmonary artery (PA). The change in PI from baseline to during MH was compared between each CHD group and controls. RESULTS: Sixty pregnant women were enrolled (CHD, n = 43; control, n = 17). In the CHD group, there were 27 fetuses with LSOL, seven with RSOL and nine with d-TGA. Mean gestational age was 33.9 (95% CI, 33.6-34.2) weeks. At baseline, MCA-PI Z-score was lowest in the LSOL group (-1.8 (95% CI, -2.4 to -1.2)) compared with the control group (-0.8 (95% CI, -1.3 to -0.3)) (P = 0.01). In response to MH, MCA-PI Z-score increased significantly in the control and d-TGA groups but did not change significantly in the LSOL and RSOL groups. The change in MCA-PI Z-score was significantly higher in the control group than in the LSOL group (0.9 (95% CI, 0.42-1.4) vs 0.12 (95% CI, -0.21 to 0.45); P = 0.03). This difference was more pronounced in the LSOL subgroup with retrograde aortic arch flow. Branch PA-PI decreased significantly in response to MH in all groups, with no difference in the change from baseline to MH between the groups, while UA-PI was unchanged during MH compared with at baseline. CONCLUSIONS: The fetal cerebrovascular response to MH varies based on the underlying CHD diagnosis, suggesting that cardiovascular physiology may influence the autoregulatory capacity of the fetal brain. Further studies are needed to determine the clinical implications of these findings on long-term neurodevelopment in these at-risk children. © 2020 International Society of Ultrasound in Obstetrics and Gynecology.


Subject(s)
Cerebrovascular Circulation , Fetal Therapies/methods , Heart Defects, Congenital/embryology , Oxygen Inhalation Therapy/methods , Placental Circulation , Adaptation, Physiological , Adult , Case-Control Studies , Cross-Sectional Studies , Echocardiography , Female , Fetus/embryology , Fetus/physiopathology , Gestational Age , Heart Defects, Congenital/diagnostic imaging , Heart Defects, Congenital/physiopathology , Humans , Middle Cerebral Artery/diagnostic imaging , Middle Cerebral Artery/embryology , Middle Cerebral Artery/physiopathology , Pregnancy , Pregnancy Trimester, Third , Pulmonary Artery/diagnostic imaging , Pulmonary Artery/embryology , Pulmonary Artery/physiopathology , Pulsatile Flow , Ultrasonography, Prenatal , Umbilical Arteries/diagnostic imaging , Umbilical Arteries/embryology , Umbilical Arteries/physiopathology
2.
AJNR Am J Neuroradiol ; 39(11): 2140-2147, 2018 11.
Article in English | MEDLINE | ID: mdl-30337433

ABSTRACT

BACKGROUND AND PURPOSE: Differences in structural brain connectivity that underlie inattention have been previously investigated in adolescents with attention deficit/hyperactivity disorder, but not in the context of premature birth, which is often associated with attentional problems. The purpose of this study was to identify the neural correlates of attentional problems in adolescents born prematurely and determine neonatal predictors of those neural correlates and attention problems. MATERIALS AND METHODS: The study included 24 adolescents (12.5 ± 1.8 years of age; 12 girls, 12 boys) who were born prematurely and underwent MR imaging of the brain and cognitive assessment, both shortly after birth and as adolescents. Structural connectivity was assessed at adolescence using diffusion tensor imaging and tractography. RESULTS: Of the 24 subjects, 12 had attention deficits. A set of axonal pathways connecting the frontal, parietal, temporal, and occipital lobes had significantly lower fractional anisotropy in subjects with attentional problems. The temporoparietal connection between the left precuneus and left middle temporal gyrus was the most significantly underconnected interlobar axonal pathway. Low birth weight and ventriculomegaly, but not white matter injury or intraventricular hemorrhage on neonatal MR imaging, predicted temporoparietal hypoconnectivity in adolescence. However, neither birth weight nor other neonatal characteristics were associated with attention deficits directly. CONCLUSIONS: We identified an aberrant structural brain connectivity pattern, involving temporoparietal hypoconnectivity, in prematurely born adolescents with attentional problems. We also identified birth weight as a potential neonatal predictor of the temporoparietal hypoconnectivity. These findings add to our understanding of the neural basis and etiology of inattention in adolescents after premature birth.


Subject(s)
Attention Deficit Disorder with Hyperactivity/pathology , Brain/pathology , Neural Pathways/pathology , Premature Birth , Adolescent , Attention Deficit Disorder with Hyperactivity/etiology , Brain Mapping/methods , Child , Diffusion Tensor Imaging , Female , Humans , Infant, Newborn , Male , Pregnancy
4.
Phys Rev E ; 93(2): 023201, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26986426

ABSTRACT

The Yukawa one-component plasma (OCP) model is a paradigm for describing plasmas that contain one component of interest and one or more other components that can be treated as a neutralizing, screening background. In appropriately scaled units, interactions are characterized entirely by a screening parameter, κ. As a result, systems of similar κ show the same dynamics, regardless of the underlying parameters (e.g., density and temperature). We demonstrate this behavior using ultracold neutral plasmas (UNPs) created by photoionizing a cold (T≤10 mK) gas. The ions in UNP systems are well described by the Yukawa model, with the electrons providing the screening. Creation of the plasma through photoionization can be thought of as a rapid quench of the interaction potential from κ=∞ to a final κ value set by the electron density and temperature. We demonstrate experimentally that the postquench dynamics are universal in κ over a factor of 30 in density and an order of magnitude in temperature. Results are compared with molecular-dynamics simulations. We also demonstrate that features of the postquench kinetic energy evolution, such as disorder-induced heating and kinetic-energy oscillations, can be used to determine the plasma density and the electron temperature.


Subject(s)
Plasma Gases/chemistry , Electrons , Hot Temperature , Kinetics , Molecular Dynamics Simulation
5.
Phys Rev Lett ; 109(18): 185008, 2012 Nov 02.
Article in English | MEDLINE | ID: mdl-23215292

ABSTRACT

Collisional relaxation of Coulomb systems is studied in the strongly coupled regime. We use an optical pump-probe approach to manipulate and monitor the dynamics of ions in an ultracold neutral plasma, which allows direct measurement of relaxation rates in a regime where common Landau-Spitzer theory breaks down. Numerical simulations confirm the experimental results and display non-Markovian dynamics at early times.

6.
AJNR Am J Neuroradiol ; 32(2): E21-2, 2011 Feb.
Article in English | MEDLINE | ID: mdl-20075085

ABSTRACT

Fetal diffusion MR imaging was performed in 3 fetuses with CHD. ADC values in the periatrial WM, thalamus, and basal ganglia were compared with those in a control population of fetuses. Diffusivity in the periatrial WM and thalamus was higher for the fetuses with CHD compared with controls. These observations support the finding of abnormal in utero brain development in fetuses with CHD.


Subject(s)
Diffusion Magnetic Resonance Imaging/methods , Fetal Diseases/pathology , Heart Defects, Congenital/complications , Leukoencephalopathies/pathology , Thalamus/abnormalities , Agenesis of Corpus Callosum , Corpus Callosum/pathology , Female , Humans , Leukoencephalopathies/congenital , Leukoencephalopathies/etiology , Pregnancy , Prenatal Diagnosis/methods , Severity of Illness Index , Thalamus/pathology
7.
Brain Struct Funct ; 215(3-4): 255-63, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21046152

ABSTRACT

The waiting period of subplate evolution is a critical phase for the proper formation of neural connections in the brain. During this time, which corresponds to 15 to 24 postconceptual weeks (PCW) in the human fetus, thalamocortical and cortico-cortical afferents wait in and are in part guided by molecules embedded in the extracellular matrix of the subplate. Recent advances in fetal MRI techniques now allow us to study the developing brain anatomy in 3D from in utero imaging. We describe a reliable segmentation protocol to delineate the boundaries of the subplate from T2-W MRI. The reliability of the protocol was evaluated in terms of intra-rater reproducibility on a subset of the subjects. We also present the first 3D quantitative analyses of temporal changes in subplate volume, thickness, and contrast from 18 to 24 PCW. Our analysis shows that firstly, global subplate volume increases in proportion with the supratentorial volume; the subplate remained approximately one-third of supratentorial volume. Secondly, we found both global and regional growth in subplate thickness and a linear increase in the median and maximum subplate thickness through the waiting period. Furthermore, we found that posterior regions--specifically the occipital pole, ventral occipito-temporal region, and planum temporale--of the developing brain underwent the most statistically significant increases in subplate thickness. During this period, the thickest region was the developing somatosensory/motor cortex. The subplate growth patterns reported here may be used as a baseline for comparison to abnormal fetal brain development.


Subject(s)
Fetal Development/physiology , Fetus/embryology , Motor Cortex/embryology , Neurons, Afferent/cytology , Somatosensory Cortex/embryology , Adult , Brain Mapping , Female , Gestational Age , Humans , Imaging, Three-Dimensional , Magnetic Resonance Imaging , Morphogenesis , Motor Cortex/cytology , Pregnancy , Reproducibility of Results , Somatosensory Cortex/cytology
8.
Phys Rev Lett ; 105(6): 065004, 2010 Aug 06.
Article in English | MEDLINE | ID: mdl-20867986

ABSTRACT

We photoionize laser-cooled atoms with a laser beam possessing spatially periodic intensity modulations to create ultracold neutral plasmas with controlled density perturbations. Laser-induced fluorescence imaging reveals that the density perturbations oscillate in space and time, and the dispersion relation of the oscillations matches that of ion acoustic waves, which are long-wavelength, electrostatic, density waves.

9.
J Thorac Cardiovasc Surg ; 140(3): 550-7, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20434174

ABSTRACT

OBJECTIVE: Preoperative brain injury, particularly stroke and white matter injury, is common in neonates with congenital heart disease. The objective of this study was to determine the risk of hemorrhage or extension of preoperative brain injury with cardiac surgery. METHODS: This dual-center prospective cohort study recruited 92 term neonates, 62 with transposition of the great arteries and 30 with single ventricle physiology, from 2 tertiary referral centers. Neonates underwent brain magnetic resonance imaging scans before and after cardiac surgery. RESULTS: Brain injury was identified in 40 (43%) neonates on the preoperative magnetic resonance imaging scan (median 5 days after birth): stroke in 23, white matter injury in 21, and intraventricular hemorrhage in 7. None of the brain lesions presented clinically with overt signs or seizures. Preoperative brain injury was associated with balloon atrial septostomy (P = .003) and lowest arterial oxygen saturation (P = .007); in a multivariable model, only the effect of balloon atrial septostomy remained significant when adjusting for lowest arterial oxygen saturation. On postoperative magnetic resonance imaging in 78 neonates (median 21 days after birth), none of the preoperative lesions showed evidence of extension or hemorrhagic transformation (0/40 [95% confidence interval: 0%-7%]). The presence of preoperative brain injury was not a significant risk factor for acquiring new injury on postoperative magnetic resonance imaging (P = .8). CONCLUSIONS: Clinically silent brain injuries identified preoperatively in neonates with congenital heart disease, including stroke, have a low risk of progression with surgery and cardiopulmonary bypass and should therefore not delay clinically indicated cardiac surgery. In this multicenter cohort, balloon atrial septostomy remains an important risk factor for preoperative brain injury, particularly stroke.


Subject(s)
Brain/pathology , Cardiac Surgical Procedures , Heart Defects, Congenital/surgery , Intracranial Hemorrhages/complications , Stroke/complications , British Columbia , Cardiac Surgical Procedures/adverse effects , Catheterization/adverse effects , Disease Progression , Female , Heart Defects, Congenital/blood , Heart Defects, Congenital/complications , Humans , Infant, Newborn , Intracranial Hemorrhages/blood , Intracranial Hemorrhages/pathology , Logistic Models , Magnetic Resonance Imaging , Male , Oxygen/blood , Prospective Studies , Risk Assessment , Risk Factors , San Francisco , Stroke/blood , Stroke/pathology , Time Factors , Treatment Outcome
10.
Brain Pathol ; 15(3): 250-60, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16196392

ABSTRACT

Perinatal brain injury may result in widespread deficits in visual, motor and cognitive systems suggesting disrupted brain development. Neurosensory and cognitive impairment are observed at increasing frequency with decreasing gestational ages, suggesting a unique vulnerability of the developing brain. The peak of human subplate neuron development coincides with the gestational ages of highest vulnerability to perinatal brain injury in the premature infant. At the same time, human thalamocortical connections are forming and being refined by activity-dependent mechanisms during critical periods. Subplate neurons are the first cortical neurons to mature and are selectively vulnerable to early hypoxic-ischemic brain injury in animal models. Timing of subplate neuron death determines the resulting defect in thalamocortical development: very early excitotoxic subplate neuron death results in failure of thalamocortical innervation, while later subplate neuron death interferes with the refinement of thalamocortical connections into mature circuits. We suggest that subplate neuron injury may be a central component of perinatal brain injury resulting in specific neurodevelopmental consequences.


Subject(s)
Cerebral Cortex/growth & development , Cerebral Cortex/pathology , Neuronal Plasticity/physiology , Neurons/pathology , Premature Birth/pathology , Animals , Female , Humans , Infant, Newborn , Neurons/cytology , Pregnancy
11.
J Neurosci ; 21(14): 5121-9, 2001 Jul 15.
Article in English | MEDLINE | ID: mdl-11438587

ABSTRACT

Subplate neurons of mammalian neocortex undergo pronounced cell death postnatally, long after they have matured and become incorporated into functional cortical circuits. They express the p75 neurotrophin receptor (p75NTR), which is known to signal cell death in some types of neurons via the activation of sphingomyelinase and the concomitant increase in the sphingolipid ceramide. To evaluate the role of p75NTR in subplate neurons, they were immunopurified and cultured in vitro. Contrary to its known function as a death receptor, ligand binding to p75NTR promotes subplate neuron survival. Moreover, p75NTR-dependent survival is blocked by inhibition of ceramide synthesis and rescued by addition of its precursor sphingomyelin. Inhibition of Trk signaling does not block survival, nor is Trk signaling alone sufficient to promote survival. Thus, ligand-dependent p75NTR regulation of the ceramide pathway mediates survival in certain neurons and may represent an important target for neuroprotective drugs in degenerative diseases involving p75NTR-expressing neurons, such as Alzheimer's disease.


Subject(s)
Cell Survival/physiology , Neurons/metabolism , Receptors, Nerve Growth Factor/metabolism , Signal Transduction/physiology , Animals , Antibodies/pharmacology , Brain-Derived Neurotrophic Factor/pharmacology , Bromodeoxyuridine , Cell Separation , Cell Survival/drug effects , Cells, Cultured , Dose-Response Relationship, Drug , Immunosorbent Techniques , In Situ Hybridization , Neocortex , Neurons/cytology , Neurons/drug effects , Rats , Rats, Long-Evans , Receptor Protein-Tyrosine Kinases/metabolism , Receptor, Nerve Growth Factor , Receptors, Nerve Growth Factor/antagonists & inhibitors , Signal Transduction/drug effects , Sphingolipids/metabolism
12.
Proc Natl Acad Sci U S A ; 96(23): 13491-5, 1999 Nov 09.
Article in English | MEDLINE | ID: mdl-10557348

ABSTRACT

Ocular dominance column formation in visual cortex depends on both the presence of subplate neurons and the endogenous expression of neurotrophins. Here we show that deletion of subplate neurons, which supply glutamatergic inputs to visual cortex, leads to a paradoxical increase in brain-derived neurotrophic factor mRNA in the same region of visual cortex in which ocular dominance columns are absent. Subplate neuron ablation also increases glutamic acid decarboxylase-67 levels, indicating an alteration in cortical inhibition. These observations imply a role for this special class of neurons in modulating activity-dependent competition by regulating levels of neurotrophins and excitability within a developing cortical circuit.


Subject(s)
Brain-Derived Neurotrophic Factor/metabolism , Dominance, Cerebral , Neurons/physiology , Visual Cortex/physiology , Base Sequence , Brain-Derived Neurotrophic Factor/genetics , DNA Primers , In Situ Hybridization , Kainic Acid/pharmacology , Neurons/drug effects , Neurons/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Visual Cortex/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...