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1.
Eur J Pediatr ; 168(9): 1069-74, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19066956

RESUMO

BACKGROUND: Neutropenia and/or neutrophil dysfunction are part of glycogen storage disease type 1b (GSD1b) phenotype. Recent studies indicated that activation of apoptosis and increased reactive oxygen species are implicated in the pathogenesis of neutropenia in GSD1b. METHODS: We studied seven GSD1b patients over a 2-year-period to evaluate the efficacy of vitamin E, a known antioxidant, in preventing or improving the clinical manifestations associated with neutropenia and neutrophil dysfunction. Frequency and severity of infections, neutrophil counts and function, ileocolonoscopy and intestinal histology, were monitored. During the first year, patients did not assume vitamin E; during the second year of the study, vitamin E supplementation was added to their therapeutic regimens. RESULTS: During vitamin E supplementation, the mean values of neutrophil counts were significantly higher (p < 0.05) and neutrophil counts lower than 500/mm(3) were found less frequently (p < 0.05); the frequency and severity of infections, mouth ulcers and perianal lesions, was reduced (p < 0.05); ileocolonoscopy and histology showed a mild improvement. Vitamin E supplementation did not result in changes in neutrophil function. CONCLUSIONS: These results suggest that vitamin E supplementation might be beneficial in GSD1b patients and may alleviate disease manifestations associated with neutropenia.


Assuntos
Infecções Bacterianas/epidemiologia , Infecções Bacterianas/prevenção & controle , Doença de Depósito de Glicogênio Tipo I/tratamento farmacológico , Neutropenia/tratamento farmacológico , Vitamina E/uso terapêutico , Adolescente , Adulto , Antiporters/genética , Criança , Pré-Escolar , Análise Mutacional de DNA , Feminino , Doença de Depósito de Glicogênio Tipo I/genética , Humanos , Masculino , Proteínas de Transporte de Monossacarídeos/genética , Mutação Puntual/genética , Estudos Prospectivos , Resultado do Tratamento , Adulto Jovem
2.
J Inherit Metab Dis ; 29(1): 186-9, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16601889

RESUMO

We report a 3-year-old Italian patient with the hyperornithinaemia, hyperammonaemia, homocitrullinuria (HHH) syndrome who presented with neurological deterioration after an intercurrent infection. Hyperammonaemia, coagulopathy and moderate hypertransaminasaemia were detected on hospital admission. Severe hepatocellular necrosis with hypertransaminasaemia (aspartate aminotransferase 20,000 UI/L, alanine aminotransferase 18,400 UI/L) and coagulopathy (PT < 5%) rapidly developed within few days, prompting evaluation for liver transplantation. A protein-restricted diet and arginine supplementation were immediately started, with a rapid improvement of the patient's neurological conditions and normalization of liver function tests and blood ammonia. The diagnosis of HHH syndrome was based on the presence of the typical metabolic abnormalities. Molecular analysis of the SLC25A15 gene showed that the patient was heterozygous for two novel mutations (G113C and M273K). The diagnosis of HHH syndrome should be considered in patients with fulminant hepatitis-like presentations. Early identification and treatment of these patients can be life-saving and can avoid liver transplantation.


Assuntos
Citrulina/análogos & derivados , Hepatite/diagnóstico , Hiperamonemia/complicações , Erros Inatos do Metabolismo/complicações , Ornitina/urina , Alanina Transaminase/sangue , Sistemas de Transporte de Aminoácidos Básicos , Arginina/uso terapêutico , Aspartato Aminotransferases/sangue , Pré-Escolar , Citrulina/sangue , Citrulina/urina , Dieta com Restrição de Proteínas , Humanos , Hiperamonemia/diagnóstico , Fígado/patologia , Masculino , Erros Inatos do Metabolismo/diagnóstico , Proteínas de Transporte da Membrana Mitocondrial , Ornitina/sangue , Proteínas/genética , Síndrome
3.
Chemosphere ; 50(8): 959-66, 2003 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-12531700

RESUMO

Olive-mill wastewater (OMW), an effluent of olive oil extraction process, is annually produced in huge amounts in olive growing areas. An interesting option for its disposal is the spreading on agricultural land, provided that phytotoxic effects are neutralized. The objective of the present investigation was to evaluate the potential of an enzyme-based treatment in removing OMW phytotoxicity. To this aim, germinability experiments on durum wheat (Triticum durum Desf. cv. Duilio) were conducted in the presence of different dilutions of raw or enzyme-treated OMW. OMW treatment with laccase resulted in a 65% and 86% reduction in total phenols and ortho-diphenols respectively, due their polymerization as revealed by size-exclusion chromatography. Raw OMW exerted a significant concentration-dependent inhibition on the germinability of durum wheat seeds which was evident up to a dilution rate of 1:8. When the effluent was treated with a fungal laccase, germinability was increased by 57% at a 1:8 dilution and by 94% at a 1:2 dilution, as compared to the same dilutions using untreated OMW. The treatment with laccase also decreased the mean germination time by about 1 day as compared to untreated controls. These results show that germinability inhibition due to OMW can be reduced effectively using fungal laccase, suggesting that phenols are the main determinants of its phytotoxicity.


Assuntos
Conservação dos Recursos Naturais , Fenóis/efeitos adversos , Fenóis/metabolismo , Óleos de Plantas , Triticum/crescimento & desenvolvimento , Eliminação de Resíduos Líquidos/métodos , Fertilizantes , Indústria Alimentícia , Fungos/enzimologia , Germinação , Lacase , Azeite de Oliva , Oxirredutases/farmacologia , Sementes/crescimento & desenvolvimento
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