Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
País como assunto
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
J Pediatr Gastroenterol Nutr ; 70(5): 580-585, 2020 05.
Artigo em Inglês | MEDLINE | ID: mdl-31899733

RESUMO

BACKGROUND: Noninvasive and accurate methods to monitor inflammatory bowel disease are required. As a planned ancillary study of the prospective ImageKids cohort, we aimed to assess the performance of fecal calprotectin (FC) with comparison to 3 fecal inflammatory markers; S100A12 (FA12), tumor pyruvate kinase isoenzyme type M2 (FM2PK) and fecal osteoprotegerin (FOPG) as indicators of a number of disease characteristics. METHODS: The ImageKids study was a multicenter study designed to develop 2 magnetic resonance enterography-based measures for children with Crohn disease (6-18 years old). All patients underwent magnetic resonance enterography, a complete ileocolonoscopic evaluation and provided a fecal sample. Fecal samples were assay for FC, FA12, FM2PK, and FOPG by ELISA. RESULTS: One-hundred fifty-six children provided 190 fecal samples. Median (interquartile range) for fecal makers were FC, 602 (181-1185) µg/g; FA12, 21 (3-109) µg/g; FM2PK, 16 (2-20) U/mL; and FOPG, 125 (125-312) µg/g. All markers correlated with simple endoscopic severity index for Crohn disease and with other constructs of disease activity, but FC had the highest overall correlations. FA12, however, predicted mucosal healing with significantly higher specificity (87% vs 70%, P = 0.004) and equivalent sensitivity (91% vs 90%) compared to FC. CONCLUSION: This study has confirmed that FC is useful, and overall best, marker to monitor mucosal inflammation in inflammatory bowel disease. FA12, however, appears to be a more suitable maker for prediction of mucosal healing in children.


Assuntos
Doença de Crohn , Adolescente , Biomarcadores/análise , Criança , Colonoscopia , Doença de Crohn/diagnóstico , Fezes/química , Humanos , Inflamação , Complexo Antígeno L1 Leucocitário , Estudos Prospectivos , Índice de Gravidade de Doença
2.
J Pediatr Gastroenterol Nutr ; 61(4): 411-4, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-25883058

RESUMO

OBJECTIVES: Vitamin D deficiency is common in children with inflammatory bowel disease (IBD). The aim of this study was to determine the safety and efficacy of stoss therapy on vitamin D levels during a period of 6 months in children with IBD and vitamin D deficiency (<50 nmol/L). METHODS: A retrospective chart review was undertaken, focusing upon children managed in the IBD clinic at Sydney Children's Hospital between 2006 and 2010. Those with a 25-hydroxyvitamin D (25-OHD) level <50 nmol/L and those who received stoss therapy were included in this study. RESULTS: A total of 76 children received stoss therapy. There was a significant and sustained increase in 25-OHD levels at all of the time points compared with baseline (40.8 ±â€Š7.5 nmol/L), 1 month (145.6 ±â€Š51.8 nmol/L), 3 months (87.1 ±â€Š28.4 nmol/L), and 6 months 69.2 ±â€Š31.3 nmol/L). There were no significant changes in serum calcium, phosphate, or parathyroid hormone at any time points. CONCLUSIONS: Stoss therapy safely and effectively achieved and maintained a level of 25-OHD >50 nmol/L during 6 months in these children with IBD. Further prospective studies are now required to confirm this finding and establish whether this intervention has other benefits.


Assuntos
Calcifediol/sangue , Colecalciferol/administração & dosagem , Suplementos Nutricionais , Doenças Inflamatórias Intestinais/fisiopatologia , Deficiência de Vitamina D/dietoterapia , Adolescente , Calcifediol/metabolismo , Criança , Pré-Escolar , Colecalciferol/efeitos adversos , Colecalciferol/metabolismo , Colecalciferol/uso terapêutico , Estudos de Coortes , Colite Ulcerativa/fisiopatologia , Doença de Crohn/fisiopatologia , Suplementos Nutricionais/efeitos adversos , Feminino , Seguimentos , Hospitais Pediátricos , Humanos , Masculino , Prontuários Médicos , New South Wales , Ambulatório Hospitalar , Estudos Retrospectivos , Deficiência de Vitamina D/complicações , Deficiência de Vitamina D/etiologia , Deficiência de Vitamina D/metabolismo
SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa