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1. |
Visual Processing in Infants and Children Studied Using Functional MRI |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 135-140
ERNST MARTIN,
PHILIPP JOERI,
THOMAS LOENNEKER,
DIMITRIOS EKATODRAMIS,
DEBORAH VITACCO,
JUERGEN HENNIG,
VALENTINE MARCAR,
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摘要:
We studied the development of visual processing in 58 children, ranging from 1 d to 12 y of age (median age 29 mo), using functional magnetic resonance imaging. All but nine children had either been sedated using chloral hydrate (n= 12) or pentobarbital (n= 28). Nine children were studied under a full halothane/N2O:O2anesthesia. In the first postnatal month, 30% of the neonates showed a positive blood oxygenation level-dependent (BOLD) contrast signal, whereas, for infants between the ages of 1 mo and 1 y, 27% did so. Thirty-one percent of children between 1 and 6 y of age and 71% of children aged 6 y and above showed a positive BOLD contrast signal change to our visual stimulation paradigm.Besides the usual positive BOLD contrast signal change, we also noted that a large portion of the children measured displayed a negative BOLD contrast signal change. This negative BOLD contrast signal change was observed in 30% of children up to 1 mo of age, in 27% between 1 mo and 1 y of age, in 47% between 1 and 6 y of age, and in 14% of children 6 y and older. In the children in which we observed a negative correlating BOLD contrast signal change, the locus was more anterior and more lateral than the positive BOLD contrast signal, placing it in the secondary visual cortical area. The results indicate that when using functional magnetic resonance imaging on children, the primary visual cortical area does not respond functionally in the same manner as that of the adult until 1.5 y of age. This supports earlier clinical and electrophysiologic findings that different cortical mechanisms seem to contribute to visual perception at different times postnatally.
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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2. |
Perinatal Myocardial DNA and Protein Changes in the Lamb: Effect of Cortisol in the Fetus |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 141-146
ABRAHAM RUDOLPH,
CHRISTINE ROMAN,
VERONIQUE GOURNAY,
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摘要:
Myocardial growth during fetal life is accomplished by proliferation of the number of myocytes (hyperplasia). Shortly after birth, normal growth of the heart is predominantly due to increase in cell size (hypertrophy), and myocytes largely lose the capability to replicate. This change is characterized by a decrease in myocardial DNA concentration and an increase in protein/DNA concentration ratio. Among many of the events associated with birth is an increase in plasma cortisol concentrations in the few days before delivery of the fetus. To determine the possible role of cortisol in the postnatal change in myocardial growth, we measured DNA and protein concentrations in the free walls of the left (LV) and right (RV) ventricles in normal fetal lambs, normal newborn lambs, and in fetal lambs in which cortisone was infused for 72-80 h into the left coronary artery, which we showed does not perfuse the RV free wall. Normally, fetal RV DNA is higher than LV DNA concentration, and DNA/protein ratio is lower in RV than in LV. It is suggested that this could be related to the greater load on the RV. Postnatally, protein concentrations increase progressively, but DNA remains the same in both ventricles, and protein/DNA ratios increase. Cortisol, infused to achieve normal prenatal levels in LV myocardium, markedly decreases LV DNA without affecting RV DNA concentrations. The present study indicates that cortisol inhibits myocyte replication and that cortisol simulates the change in myocardial growth pattern normally occurring after birth. It raises concerns regarding prenatal administration of glucocorticoids to mothers to mature the fetal lungs before preterm delivery.
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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3. |
Interpreting the13C-Urea Breath Test among a Large Population of Young Children from a Developing Country |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 147-151
JULIAN THOMAS,
ANNE DALE,
MARILYN HARDING,
W. COWARD,
TIMOTHY COLE,
PETER SULLIVAN,
DAVID CAMPBELL,
BRYAN WARREN,
LAWRENCE WEAVER,
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摘要:
The13C-urea breath test is a noninvasive tool for the diagnosis of gastricHelicobacter pyloriinfection. However, it has not been validated in young children from the developing world, where infection is very common.13C urea breath tests were performed on 1532 occasions on 247 Gambian infants and children aged from 3 to 48 mo. The means and variances of the separate sub-populations of13C enrichment results contained within the overall dataset were estimated by a Genstat procedure using the EM algorithm, thereby identifying a cut-off value to discriminate positive from negative results. To illustrate the appropriateness of this calculated cut-off value,13C urea breath tests were performed upon a small group of 14 patients aged 6 to 28 mo undergoing diagnostic upper endoscopy. Fixed gastric antral biopsies were examined to identifyH. pylori. Two sub-populations were identified within the large dataset. A cut-off value of 5.47 δ‰ relative to Pee Dee Belemnite limestone above baseline at 30 min identified 95% of the normally distributed negative sub-population and 99.4% of the log normal distributed positive sub-population. Comparison with endoscopic data confirmed that this cut-off value was appropriate for this population, as 7/7 children withoutH. pylorion their gastric biopsies had negative urea breath tests, and 6/7 children with gastricH. pyloricolonization had positive urea breath tests. These findings confirm the value of the urea breath test as a diagnostic tool in young children from developing countries. They also offer a way to calculate the most appropriate cut-off value for use in different populations and the likelihood that it will correctly assign any value into the appropriate sub-population, without the need for endoscopy.
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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4. |
Developmental Expression of NADPH Phagocytic Oxidase Components in Mouse Embryos |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 152-157
ROBERT BAEHNER,
SHARON MILLAR-GROFF,
PABLO BRINGAS,
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摘要:
We wished to determine when each of the four NADPH oxidase components p22 phagocytic oxidase (phox), gp91 phox, p47 phox, p67 phox is first expressed embryologically and whether the expression pattern occurs in a consistent temporal sequence or whether the four genes are expressed simultaneously. A deficiency of any one of them results in chronic granulomatous disease (CGD). mRNA transcripts and protein expression for p22 phox, gp91 phox, p47 phox, p67 phox was monitored in murine embryos at time of implantation (E5.5) until E 11.5, and in fetal liver, spleen, and limb bone marrow from E 14 until term (E 19). We observed that mRNA was first expressed for p22 phox at E 5.5, for p67 phox at E 7.0 and for p47 phox at E 7.5 before the onset of yolk sac hematopoiesis (E 8.0). gp91 Phox mRNA was first expressed at E 9.0. However, only p22 phox protein was expressed in circulating hemacytoblast by E 9.0. No other embryonic tissue contained phox proteins either before or after the establishment of hemocytoblastic circulation. The four specific mRNA transcripts and phox proteins were expressed in nests of developing granulocytes in liver by E 14 and the expression continued in the liver at E 16 and E 19. Spleen and limb bone marrow showed inconsistent results. Cord blood neutrophils contained all phox proteins. These studies confirm that the four CGD-related phox mRNA components of NADPH oxidase are expressed early in embryonic development and the expression occurs in a consistent sequential fashion but only p22 phox protein appears in embryonic hemocytoblast.
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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5. |
Hematologic Involvement in Mitochondrial Cytopathies in Childhood: A Retrospective Study of Bone Marrow Smears |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 158-162
BRIGITTE BADER-MEUNIER,
FRANÇOISE MIÉLOT,
JEANINE BRETON-GORIUS,
ELISABETH CRAMER,
JOSETTE GUICHARD,
PIERRE LANDRIEU,
JEAN-PAUL DOMMERGUES,
GIL TCHERNIA,
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摘要:
We retrospectively analyzed the bone marrow (BM) smears of 10 children with mitochondrial cytopathies. Light microscopic examination showed large and coalescent cytoplasmic vacuolization of some BM precursors in nine cases, including two children with normal peripheral blood counts and four with sideroblastic anemia. BM ultrastructural study showed abnormal mitochondria in the erythroid lineage in all three children studied. Ultrastructural studies in two cases revealed a population of giant mitochondria with abnormal ultrastructure coexisting with a population of normal mitochondria in proerythroblasts, basophil erythroblasts, and less commonly in more mature erythroblasts. In a third child, mitochondria were normal in size with cristae either absent or exhibiting abnormal longitudinal orientation. Heteroplasmic segregation of mitochondria during cell division could account for the finding of a double population of cells on ultrastructural examination. These features suggest that cytologic and ultrastructural BM examination could be useful for the diagnosis of mitochondrial disorders. That is, when large and coalescent cytoplasmic vacuoles of BM precursor cells are present, the clinician should search for mitochondrial cytopathy in a child with unexplained cytopenia(s).
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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6. |
Analysis and Characterization of Hematopoietic Progenitor Cells from Fetal Bone Marrow, Adult Bone Marrow, Peripheral Blood, and Cord Blood |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 163-169
AI WU,
MARIA MICHEJDA,
AMITABHA MAZUMDER,
KENNETH MEEHAN,
FREDERICK MENENDEZ,
JEAN-GILLES TCHABO,
REBECCA SLACK,
MARK JOHNSON,
JOSEPH BELLANTI,
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摘要:
Hematopoietic stem cell transplantation has been increasingly used to replace a defective hematopoietic system and to treat various genetic defects as well as malignant diseases. However, the limitations of conventional bone marrow transplantation have stimulated an intense interest in exploring the use of alternative sources of hematopoietic stem cells, including peripheral blood mononuclear cells (PBMC) and cord blood (CB). A major investigative effort of our laboratory has been focused on evaluating fetal bone marrow (FBM) for transplantation. The current study compares and characterizes the functional and phenotypic characteristics of FBM, CB, adult bone marrow (ABM), and PBMC by clonogenicity assays, immunogenicity, and the quantification of progenitor cells. There was a striking difference in the proportion of CD34+cells in FBM, ABM, PBMC, and CB (24.6%, 2.1%, 0.5%, and 2.0%, respectively). The clonogenic potential, as measured by colony forming unit in culture (CFU-C) assay, was significantly higher in FBM when compared with ABM, PBMC, and CB (202.5, 73.5, 40.8, and 65.5 colonies/105cells, respectively). There was a significant decrease in proliferative responsiveness in mixed lymphocyte reaction (MLR) assay of FBM and CB compared with ABM and PBMC. These observations indicate that each source of hematopoietic stem cells has different intrinsic properties closely correlated with ontogenetic age that is a vital determinant for phenotypic characteristics, lineage commitments, immunogenicity, and proliferative potentials.
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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7. |
Severe Congenital Hypothyroidism Due to a Homozygous Mutation of the βTSH Gene |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 170-173
HEIKE BIEBERMANN,
KLAUS-PETER LIESENKÖTTER,
MICHAEL EMEIS,
MICHAEL OBLADEN,
ANNETTE GRÜTERS,
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摘要:
Isolated TSH deficiency leading to hypothyroidism seems to be a rare condition, escaping the diagnosis by neonatal screening programs, which are based on the primary determination of TSH. This is the first report of a case with an autosomal recessive TSH defect caused by a homozygous mutation of the βTSH gene that was diagnosed in the early neonatal period. Hypothyroidism in the first child of apparently unrelated parents was suspected because of the classical symptoms of congenital hypothyroidism, which were fully expressed already on the 11th day of life. Routine neonatal TSH-screening on the 4th day of life had been normal, but subsequent determination of serum thyroid hormone levels revealed almost undetectable levels and thyroid hormone substitution was immediately started. Because there was no indication for other pituitary hormone deficiencies, sequence analysis of the βTSH gene was initiated. A homozygous T deletion in codon 105 was found resulting in a change of a highly conserved cysteine to valine followed by eight altered amino acids and a premature stop codon due to the frame-shift. This altered βTSH is a biologically inactive peptide. Because of the early development of severe symptoms, it is possible that this altered TSH suppresses the physiologic constitutive activity of the unliganded TSH receptor. Rapid molecular diagnosis in this patient clarified the diagnosis without additional endocrine and imaging studies and it is concluded, that symptoms of hypothyroidism in the neonatal period should result always in an immediate comprehensive work-up of thyroid function including molecular genetic studies irrespective of the screening result.
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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8. |
Surface Hydrophobicity Is Increased in the Ileum and Proximal Colon of Cystic Fibrosis Mice |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 174-178
CATHERINE CHUNG,
LAWRENCE VAN HOOF,
ZDENKA POLICOVA,
SATTI BEHARRY,
PHILIP SHERMAN,
A. NEUMANN,
PETER DURIE,
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摘要:
Patients with cystic fibrosis (CF) have abnormal concentrations and composition of electrolytes and macromolecules in gastrointestinal secretions. Such alterations could change intestinal surface properties, such as surface hydrophobicity, and may influence the adhesion of macromolecules, bacteria, or microbial toxins to the intestinal surface. The objective of this study was to compare the surface hydrophobicity of the gastrointestinal tract in wild type and CF mice. We used axisymmetric drop shape analysis-contact diameter to determine surface hydrophobicity by measuring contact angles of sessile water droplets placed onto epithelial surfaces. In wild type mice, there were no differences in contact angles between the duodenum, upper jejunum, lower jejunum, and ileum. The contact angle of the gastric mucosa was lower than the rest of the gastrointestinal tract. Contact angles of the proximal colon and distal colon were both higher than that of the gastric mucosa and those of the small intestinal sections. In CF mice, contact angles along the gastrointestinal tract followed the same pattern as in wild type mice. However, contact angles in the ileum and proximal colon of CF mice were greater than those from wild type mice. This study of the murine intestine showed regional differences in surface hydrophobicity comparable to those observed in other mammalian species. In addition, we showed that the ileum and proximal colon of CF mice were more hydrophobic than the corresponding segments in wild type mice. These observations are of potential clinical relevance because patients with CF exhibit clinical manifestations of gastrointestinal disease primarily in the ileum and proximal colon.
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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9. |
Effects of Dexamethasone on Meconium Aspiration Syndrome in Newborn Piglets |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 179-183
AMIR KHAN,
FATEN SHABAREK,
JAMES KUTCHBACK,
KEVIN LALLY,
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摘要:
We examined the effects of dexamethasone on lung function in a piglet model of meconium aspiration syndrome. We induced lung injury in 10 newborn piglets (age 5 ± 0.2 d) with 4 mL/kg body weight of 20% sterile human meconium in normal saline given via tracheostomy. Ventilator management was aimed at maintaining comparable values of end tidal carbon dioxide, Hb saturation, and arterial blood gases. Lung function was assessed using a BICORE CP100 neonatal monitor. Five piglets received 0.5 mg/kg of dexamethasone 2 and 8 h after meconium administration, whereas control piglets received normal saline at similar times. Ventilator settings, oxygen requirements, and lung compliance were similar between groups at the start of the study. Two hours after the instillation of meconium, there was marked lung dysfunction in both groups as evidenced by increased oxygen requirements [fraction of inspired oxygen (FiO2) 0.98 ± 0.01versusFiO20.21 ± 0,p< 0.0001] and reduced lung compliance (0.35 ± 0.03versus0.8 ± 0.03 mL · kg-1· cm-1H2O,p< 0.0001). Administration of dexamethasone resulted in lower oxygen requirements (FiO20.27 ± 0.01versusFiO21.0 ± 0.0,p< 0.00001), lower oxygenation index (2.17 ± 0.17versus22.64 ± 3.39,p< 0.0001), ventilatory efficiency index (0.30 ± 0.01versus0.07 ± 0.01,p< 0.0001), and improved lung compliance (0.68 ± 0.04versus0.34 ± 0.05 mL · kg-1· cm-1H2O,p< 0.001) compared with the control group. In summary, a two-dose course of 0.5 mg/kg of dexamethasone improved blood gases and lung function in a piglet model of meconium aspiration syndrome.
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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10. |
Indomethacin Improves Oxygen-Induced Retinopathy in the Mouse |
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Pediatric Research,
Volume 46,
Issue 2,
1999,
Page 184-188
BHARAT NANDGAONKAR,
TOMAS ROTSCHILD,
KUN YU,
ROSEMARY HIGGINS,
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摘要:
Retinopathy of prematurity is a disease commonly affecting extremely premature babies. Indomethacin is widely used in the perinatal period. The goal of the present study was to test the hypothesis that indomethacin will improve retinopathy in a mouse model when administered during the period of injury (hyperoxia exposure) to the developing retinal vasculature. C57BL6 mice pups were exposed to 75% oxygen from postnatal d 7 through 12. Indomethacin was administered along with the oxygen exposure as a single subcutaneous dose of 0.5 mg/kg/d for 5 d. Animals were killed on postnatal d 17 through 20. The severity of retinopathy was assessed by a retinopathy scoring system of fluorescein-conjugated dextran-perfused retinal flat mounts and by quantitation of extraretinal nuclei by use of periodic acid-Schiff-stained retinal sections. Animals that received indomethacin during hyperoxia exposure had a significantly lower median (25th, 75th quartile) retinopathy score 5 (4.5, 6) compared with animals that received oxygen [8 (7.5, 10)]. Animals given indomethacin during hyperoxia exposure had a significantly lower extraretinal nuclei count per section (13.3 ± 4.6) (mean ± SD) compared with animals that were oxygen exposed (41.9 ± 14.7). Indomethacin did not affect the normal development of the retinal vasculature or the growth of the animals. The data show that indomethacin improves oxygen-induced retinopathy when administered concurrently with the injury phase without affecting the normal retinal development or growth of the animals.
ISSN:0031-3998
出版商:OVID
年代:1999
数据来源: OVID
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