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1.
Mol Nutr Food Res ; 55(8): 1266-70, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21710563

RESUMEN

Celiac disease (CD) is a gluten-sensitive enteropathy with an immune basis. We established the immune reactivity of the alcohol-soluble fraction from two minor cereals (tef and millet) and two pseudocereals (amaranth and quinoa) which are believed to be nontoxic based on taxonomy. Grains were examined in intestinal T-cell lines (iTCLs), cultures of duodenal explants from HLA-DQ2(+) CD patients and HLA-DQ8 transgenic mice for signs of activation. Our data indicated that tef, millet, amaranth, and quinoa did not show any immune cross-reactivity toward wheat gliadin, and therefore confirming their safety in the diet of CD patients.


Asunto(s)
Enfermedad Celíaca/etiología , Grano Comestible/inmunología , Proteínas de Plantas/inmunología , Alcoholes , Amaranthus/inmunología , Secuencia de Aminoácidos , Animales , Chenopodium quinoa/inmunología , Reacciones Cruzadas , Glútenes , Humanos , Interferón gamma/biosíntesis , Ratones , Ratones Transgénicos , Datos de Secuencia Molecular , Panicum/inmunología , Extractos Vegetales/inmunología , Proteínas de Plantas/química , Alineación de Secuencia
2.
Am J Gastroenterol ; 100(11): 2583-91, 2005 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-16279916

RESUMEN

OBJECTIVES: Our objectives were to assess the beneficial and harmful effects of milk thistle (MT) or MT constituents versus placebo or no intervention in patients with alcoholic liver disease and/or hepatitis B and/or C liver diseases. METHODS: Randomized clinical trials studying patients with alcoholic and/or hepatitis B or C liver diseases were included (December 2003). The randomized clinical trials were evaluated by components of methodological quality. RESULTS: Thirteen randomized clinical trials assessed MT in 915 patients with alcoholic and/or hepatitis B or C liver diseases. The methodological quality was low: only 23% of the trials reported adequate allocation concealment and only 46% were considered double blind. MT versus placebo or no intervention for a median duration of 6 months had no significant effects on all-cause mortality (relative risk (RR) 0.78, 95% confidence interval (CI) 0.53-1.15), complications of liver disease, or liver histology. Liver-related mortality was significantly reduced by MT in all trials (RR 0.50, 95% CI 0.29-0.88), but not in high-quality trials (RR 0.57, 95% CI 0.28-1.19). MT was not associated with a significantly increased risk of adverse events. CONCLUSIONS: Based on high-quality trials, MT does not seem to significantly influence the course of patients with alcoholic and/or hepatitis B or C liver diseases. MT could potentially affect liver injury. Adequately conducted randomized clinical trials on MT versus placebo may be needed.


Asunto(s)
Hepatitis B/tratamiento farmacológico , Hepatitis C/tratamiento farmacológico , Hepatitis Alcohólica/tratamiento farmacológico , Fitoterapia , Preparaciones de Plantas/uso terapéutico , Ensayos Clínicos Controlados Aleatorios como Asunto , Silybum marianum , Causas de Muerte , Método Doble Ciego , Humanos , Placebos , Ensayos Clínicos Controlados Aleatorios como Asunto/normas , Proyectos de Investigación/normas , Factores de Tiempo , Resultado del Tratamiento
3.
J Clin Gastroenterol ; 39(4): 291-7, 2005 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-15758622

RESUMEN

GOALS: Therapy for active ulcerative colitis (UC) usually involves rectal formulations of corticosteroids (CS), which are characterized by the risk of systemic steroid-related adverse effects. BACKGROUND: To compare the efficacy and safety of the topically acting CS beclomethasone dipropionate (BDP) versus mesalamine (5-ASA) in the treatment of active UC. STUDY: Patients with mild to moderate distal active UC were randomized to a 6-week treatment with BDP 3 mg enema o.d. or 5-ASA 1 g enema daily in a single-blind, multicenter, parallel-group, controlled study. The primary efficacy variable was the decrease in Disease Activity Index (DAI) score. Safety variables were adrenal function, monitoring of adverse events, vital signs, and laboratory parameters. RESULTS: A total of 217 patients were enrolled and treated with BDP (n = 111) or 5-ASA (n = 106). A significant decrease in the DAI score (P < 0.05) was observed in both treatment groups, with a clinical remission rate of 36.7% in the BDP group and of 29.2% in the 5-ASA group. Both treatments were well tolerated. No changes from baseline in morning cortisol levels were observed in the BDP group. CONCLUSIONS: BDP administered as a rectal enema over a 6-week treatment period was efficacious and safe in patients with active UC, without interference with pituitary adrenal axis.


Asunto(s)
Antiinflamatorios no Esteroideos/administración & dosificación , Beclometasona/administración & dosificación , Colitis Ulcerosa/tratamiento farmacológico , Glucocorticoides/administración & dosificación , Mesalamina/administración & dosificación , Administración Tópica , Adolescente , Adulto , Anciano , Biomarcadores/sangre , Sedimentación Sanguínea , Colitis Ulcerosa/sangre , Colitis Ulcerosa/patología , Colonoscopía , Recuento de Eritrocitos , Femenino , Estudios de Seguimiento , Humanos , Mucosa Intestinal/patología , Recuento de Leucocitos , Masculino , Persona de Mediana Edad , Inducción de Remisión , Estudios Retrospectivos , Seguridad , Índice de Severidad de la Enfermedad , Método Simple Ciego , Resultado del Tratamiento
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