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1. |
Dietary Management of Acute Diarrhoea in Children: Effect of Fermented and Amylase-Digested Weaning Foods on Intestinal Permeability |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 235-241
Willumsen* Juana,
Darling* Jonathan,
Kitundu† Jesse,
Kingamkono‡ Rose,
Msengi† Abel,
Mduma‡ Benedicta,
Sullivan* Keith,
Tomkins* Andrew,
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摘要:
Background:There is a strong relationship between diarrhoea, malnutrition, and intestinal integrity. To investigate the effect of different dietary treatment on intestinal permeability during acute diarrhoea, 87 Tanzanian children aged 6-25 months were recruited to this study when admitted to hospital.Methods:Children with acute diarrhoea were rehydrated and then randomly assigned to one of three dietary treatment groups: a conventional low-energy density porridge, a high-energy density amylase digested porridge (AMD), or a high-energy density amylase digested and then fermented porridge (FAD). Lactulose/mannitol permeability tests were performed on admission, at 3 days, and at follow-up 2 and 4 weeks after discharge. The lactulose/mannitol (L/M) ratios were compared between dietary treatment groups and to a group of age-matched, healthy control subjects.Results:Children with diarrhoea had higher L/M ratios (geometric mean 0.85, 95% CI 0.68-1.05) compared with control subjects (0.14, 0.12-0.17) on admission. There was a significant difference in the change in L/M ratio between admission and 3 days between dietary treatment groups in favour of the FAD group (p < 0.05).Conclusions:Dietary treatment and intestinal damage at admission explain 13.5% of the variation in L/M ratio, but when age at admission and age at weaning are included as covariants, 21.9% is explained. FAD porridge seems to be more effective in the treatment of intestinal permeability than AMD or conventional porridge. Urinary lactose concentrations in spot urine samples taken prior to the permeability test were also measured. There was a significant correlation with the L/M ratio (correlation coefficient = 0.62, p < 0.001).
ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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2. |
Simplified Preparation of a Refined Milk Formula Comparable to Rat's Milk: Influence of the Formula on Development of the Gut and Brain in Artificially Reared Rat Pups |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 242-252
Kanno Takahiro,
Koyanagi Namiko,
Katoku Youli,
Yonekubo Akie,
Yajima Takaji,
Kuwata Tamotsu,
Kitagawa* Hiroshi,
Harada† Etsumori,
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摘要:
Background:Milk formulas for artificially reared (AR) rat pups are mostly based on complex cow's milk products, prepared by laborious and time-consuming processes. The aim of this study was to develop a simplified procedure for preparing a refined formula and to examine its influences on gut and brain development.Methods:The formula comprised a combination of purified cow's casein and whey proteins, five kinds of edible oil, minerals, and vitamins. Detailed analyses showed that the composition of macro- and micro-nutrients, osmolarity, and pH of the new formula closely resembled those of rat's milk. Rat pups, each with an intragastric cannula implanted at age 5 days, were artificially reared for the following 10-15 days.Results:The body weight gain of AR pups matched that of mother-reared (MR) pups. Histoplanimetrical analyses showed that the small intestine in AR pups was more developed in relation to area of a transverse section, number and length of villi, and thickness of tunica muscularis than that of MR pups. Fat components in the formula influenced the fatty acid composition and the cholesterol-to-phospholipid ratio in the small intestinal microvillus membrane (MVM) of AR pups, but not the MVM fluidity. Brain weight was not significantly different between the two groups at age 15-20 days.Conclusion:This formula is useful for artificial rearing of rats and for identifying dietary components contributing to metabolic adaptation during the suckling period.
ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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3. |
NOTICES |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 252-252
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ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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4. |
Intussusception: A 9-Year Survey (1986-1995) |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 253-256
Eshel,
G. Barr,
J. Heyman,
E. Tauber,
T. Klin,
B. Vinograd,
I. Starinsky*,
R. Lahat,
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摘要:
Background:Acute intussusception has different clinical features in various parts of the world. The goal of this study was to determine the clinical presentation in different ethnic groups in Israel.Methods:A retrospective chart review of a 9-year period (1985-1995) was carried out at a university medical center. Data extracted included age, sex, ethnic origin, presenting symptoms and signs, the type of enema (barium or air), and the success rate of non-surgical reduction of the intussusception.Results:Ninety patients suffering from intestinal obstruction due to acute intussusception were admitted. The triad of intermittent screaming attacks, lethargy, and vomiting was observed in 37.5% of study subjects. The majority of patients were admitted during the warmer months of the year. The average age of the patients was 7.8 ± 3.7 months; 70% of them were between the ages of 4 and 9 months and 92.5% under 1 year of age. The female-to-male ratio was 1:2.1. Air enema was superior to the barium enema in achieving reduction (p < 0.01). The incidence in the Jewish population was similar to that observed in other surveys, and twice that found in the Arab population in our region (p < 0.05).Conclusions:The overall clinical presentation of acute intussusception found in our study does not differ from other studies. The lower incidence of acute intussusception found in the Arab population can be explained by ethnic, genetic, or nutritional factors.
ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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5. |
Lactose Maldigestion in Breast-Feeding Gambian Infants |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 257-263
Northrop-Clewes,
C. Lunn*,
P. Downes*,
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摘要:
Background:The ability of breast-feeding infants to utilize lactose, the major carbohydrate in breast-milk, is dependent on the presence of the enzyme lactase (E.C.3.2.1.108). Lactase is located in the brush border of the small intestine and because of its exposed position it is extremely vulnerable to pathogenic damage. Breast-fed Gambian infants have poor growth associated with intestinal damage beyond 3-4 months. The aim of this study was to assess the ability of Gambian infants aged 2-15 months (N = 113) to digest lactose and to see how this varied with age, intestinal permeability, and growth performance.Methods:Lactose maldigestion was estimated by monthly measurements of urinary lactose and lactulose following an oral dose of the latter.Results:Both urinary lactose excretion and lactulose maldigestion increased with age (p < 0.0001 ANOVA). Up to 6 months the mean urinary lactose: lactulose excretion ratio was within the quoted normal range (< 0.4). Beyond this age, mean values were hypolactasic. Lactose maldigestion was related to poor growth in both weight and length (r =-0.04, p < 0.0001, after age correction). Althogh a major part of this relationship was a reflection of the previously reported correlation between intestinal permeability and growth, more than 30% of the association was in addition to the permeability effect. Possible explanations are discussed.Conclusions:Moderate-to-severe hypolactasia does occur in breast-fed Gambian infants and is related to poorer-than-expected growth. However, this does not mean that breast milk intake should be reduced as the nutritional and immunological benefits of breast milk continue to outweigh any disadvantages.
ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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6. |
Vitamin A Concentration in the Liver Decreases with Age in Patients with Cystic Fibrosis |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 264-270
Lindblad*∥,
Anders Diczfalusy†,
Uif Hultcrantz‡,
Rolf Thorell§,
Anders Strandvik∥,
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摘要:
Background:Vitamin A deficiency is a common manifestation in cystic fibrosis (CF), but high levels of vitamin A in the liver have also been described. High levels of vitamin A in the liver are toxic, while normal levels might be protective against liver damage. In order to investigate whether liver damage in patients with CF is related to vitamin A content of the liver, vitamin A status was investigated in 15 patients with CF aged 8 to 34 years.Methods:Liver biopsy was performed on clinical indication and the vitamin A concentration in the liver was determined as retinylpalmitate. Serum levels of retinol and retinol-binding protein were investigated on the morning of the biopsy. Eight patients had morphologic signs of cirrhosis. Eight patinets had been on treatment with ursodeoxycholic acid for 1 to 3 years. All but three patients had been on vitamin A supplementation for years.Results:Five patients had serum concentrations of retinol below the reference range and seven patients had decreased serum levels of retinol-binding protein. There was a strong correlation between serum levels of retinol and retinol-binding protein (rs= 0.90, p = 0.01), but no correlations with age, Shwachamn score, or genotype. Six of the patients had vitamin A concentrations in the liver <40 μg/g wet weight, and the concentrations decreased significantly with age (rs= 0.77, p = 0.01), without correlation to clinical score or liver disease. There was no indication of hypervitaminosis, although younger patients had been or were being treated with vitamin A in fat-water emulsion.Conclusions:Our results indicate that the risk of vitamin a deficiency in cystic fibrosis increases with age. The data do not support the view that patients are at risk for hypervitaminosis by long-term supplementation with vitamin A. No correlation was found between the severity of liver disease and the vitamin A content in the liver.
ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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7. |
Fecal α1-Antitrypsin in Newborn Infants |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 271-275
Keller*†,
Klaus-Michael Knobel‡,
Richard Ewe‡,
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摘要:
Background:Fecal α1-antitrypsin is used as a marker for intestinal protein loss reflecting increased intestinal permeability. Exact data of fecal α1-antitrypsin in newborn infants are not available.Methods:30 healthy mature neonates and three infants with impaired gastrointestinal passage due to stenoses and atresia respectively, were investigated during the first days of life. The amniotic fluid of 13 and the serum of 17 infants was available. α1-antitrypsin was determined using the radial immunodiffusion method.Results:Normal newborns showed mean fecal α1-antitrypsin levels (±SD) of 2061 ± 817 mg/dl (day 1), 1186 ± 720 mg/dl (day 2), 308 ± 380 (day 3), 35 ± 27 (day 5), and 27 ± 21 mg/dl (day 6). Two infants with esophageal atresia presented a much lower pattern, and one with annular pancreas had a fecal α1-antitrypsin pattern comparable with that of normal babies. Serum α1-antitrypsin was normal (275 ± 52 mg/dl), and amniotic fluid contained 20 ± 12 mg/dl α1-antitrypsin.Conclusions:The pattern of neonatal fecal α1-antitrypsin content appears to reflect the meconium clearance of the gut rather than intestinal permeability and “gut closure.” We hypothesize that the origin of increased fecal α1-antitrypsin is the result of accumulated secretions from bile, the pancreas, and the duodenum, but α1-antitrypsin originating from swallowed amniotic fluid during pregnancy may play an additional role.
ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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8. |
Hepatocellular Adenomas in Glycogen Storage Disease Type I and III: A Series of 43 Patients and Review of the Literature |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 276-279
Labrune,
Philippe Trioche,
Pascale Duvaltier,
Isabelle Chevalier,
Paquita Odièvre,
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摘要:
Background:Hepatocellular adenomas may develop in patients with glycogen storage disease types I and III, and the malignant degeneration of adenomas in hepatocellular carcinoma has been reported in ten cases. The aim of this work was to study the characteristics of hepatic adenomas in a large series of 43 patients with glycogen storage disease types I and III and to determine the optimal means of follow-up.Methods:The charts of 43 patients with glycogen storage disease type I and III were studied. In all these patients, abdominal ultrasonography and the determination of serum α-fetoprotein had been performed yearly and serum concentrations of several proteins were determined once.Results:51.8% of patients with type I and 25% of patients with type III glycogen storage disease had hepatic adenomas at the time of the study. The male to female ratio was 2 to 1 in type I, and no female had adenomas in type III. No evidence of malignant transformation was observed during the follow-up period. Serum concentrations of several proteins were significantly higher in patients with hepatic adenomas than in patients without such lesions.Conclusions:In patients with glycogen storage disease type I and III, the determination of α-fetoprotein serum concentration has to be combined with yearly hepatic ultrasound examinations. Other investigations such as CT scan should be considered when the size of any adenoma increases. The malignant transformation of hepatocellular adenoma into hepatocellular carcinoma remains a rare event.
ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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9. |
Plasma Vitamin K1and PIVKA-II After Oral Administration of Mixed-Micellar or Cremophor EL-solubilized Preparations of Vitamin K1to Normal Breast-Fed Newborns |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 280-284
Schubiger,
G. Grüter*,
J. Shearer†,
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摘要:
Background:Vitamin K1prophylaxis in neonates is required for prevention of vitamin K1deficiency bleeding. Although intramuscular administration of vitamin K1is safe, this invasive method is not generally accepted. We therefore examined the pharmacokinetics of two orally administered vitamin K1preparations in normal, fully breast-fed newborns.Methods:Within 1 hour of birth, each baby was randomized to a 2 mg dose of either a conventional Cremophor EL-solubilized preparation of vitamin K1(Konakion drops, F. Hoffmann-La Roche, n = 16), or a new mixed-micellar preparation of vitamin K1(Konakion MM, F. Hoffmann-La Roche, n = 14). The concentrations of vitamin K1, des-γ-carboxyprothrombin (PIVKA-II), and total bound bilirubin were measured in plasma samples taken at 24 hours, 4 days, and 24 days after birth.Results:The median concentration of plasma vitamin K1was higher at all three time points in the group that received the mixed-micellar preparation, but the difference was only significant (p < 0.05) at 4 days. At 24 hours and 4 days, PIVKA-II was detectable in a significantly lower proportions of infants receiving the new mixed-micellar preparation than those receiving the Cremophor EL preparation (21% vs. 75% at 24 hours, p < 0.05 and 14% vs. 50% at 4 days, p < 0.05). None of the infants in the study had detectable PIVKA-II levels 24 days after birth.Conclusions:Our results suggest that when given orally, the mixed-micellar preparation is superior to the conventional formulation because it increases plasma vitamin K1concentrations to higher levels, suggesting superior bioavailability, and decreases PIVKA-II concentrations more efficiently, suggesting a faster pharmacodynamic response.
ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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10. |
Fecal Polyamine Concentration in Children with and without Nutrient Malabsorption |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 24,
Issue 3,
1997,
Page 285-288
Forget*,
P. Sinaasappel†,
M. Bouquet†,
J. Deutz‡,
N. Smeets*,
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摘要:
Background:Fermentation products of malabsorbed nutrients are thought to be responsible for intestinal adaptation following small bowel resection in rats. It has been suggested that either short-chain fatty acids or polyamines (mainly putrescine and cadaverine) could be the fermentation products involved. There are no data available on fecal polyamine content in humans. The present study compared the fecal polyamine concentrations in children with and without malabsorption.Methods:Sixteen (8 girls, 8 boys) malabsorption patients (cystic fibrosis: 13, short bowel syndrome: 2, biliary atresia: 1) with a mean age of 8 years were compared to 17 (9 girls, 8 boys) sick children without malabsorption (mean age 5.7 years). Three-day fecal collections were performed and analyzed for fat and polyamine concentrations. High-performance liquid chromatography (HPLC) was used for the measurement of polyamine concentrations.Results:Mean and SEM for fecal fat excretion was 13.4 ± 2.5 g/day and 1.5 ± 0.3 g/day in the malabsorption and control group respectively. Median fecal cadaverine and putrescine concentrations were 3723 μmol.kg-1feces and 4737 μmol.kg-1feces for the malabsorption group and 114 μmol.kg-1feces and 306 μmol.kg-1feces for the control group (p < 0.007 and < 0.00001 respectively). No significant differences were found for fecal spermine and spermidine concentrations between the two groups.Conclusions:Children with malabsorption show very high fecal putrescine and cadaverine concentrations. Our results support the hypothesis that fecal polyamines could be important.
ISSN:0277-2116
出版商:OVID
年代:1997
数据来源: OVID
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