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1.
J Pediatr Gastroenterol Nutr ; 39(2): 153-7, 2004 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-15269619

RESUMEN

OBJECTIVES: Investigate whether fecal neopterin concentration (a potential marker of gut inflammation) in Gambian children with enteropathy was associated with growth failure. Secondary outcome measures tested the associations between Giardia lamblia infestation, fecal neopterin and lactulose mannitol absorption ratio(L:M), a measure of intestinal permeability. METHODS: Seventy-two children had height and weight measured every 6 to 8 weeks until 15 months of age in a rural Gambian village. L:M ratio, a measure of small intestinal permeability and fecal neopterin were measured at these times. Stool was examined by immunofluorescence and light microscope for Giardia cysts. RESULTS: Long-term height and weight gains were negatively associated with mean subject fecal neopterin concentration (r = -0.29 and -0.36, respectively; P < 0.001). There was no correlation between fecal neopterin and intestinal permeability or history of diarrhea. Of 72 children studied, 19 had Giardia cysts in stool and 38 had negative stool examinations. Infected children had a mean of 0.7 days of diarrhea/week (95% confidence interval [CI], 0.31-1.03) versus 0.8 days/week (95% CI, 0.71-0.85) in uninfected children. No difference in growth was detected between those with positive or negative fecal smears. Mean L:M ratio was the same in both groups (0.31; 95% CI, 0.26-0.34). CONCLUSIONS: Consistent with the theory that intestinal inflammation in tropical infants may impair growth, fecal neopterin concentrations were inversely associated with growth. Factors other than Giardia are causing enteropathy and growth failure in Gambian infants.


Asunto(s)
Desarrollo Infantil , Heces/química , Heces/parasitología , Giardia lamblia , Giardiasis/complicaciones , Trastornos del Crecimiento/etiología , Neopterin/análisis , Animales , Estatura , Peso Corporal , Femenino , Gambia , Giardiasis/epidemiología , Indicadores de Salud , Humanos , Lactante , Absorción Intestinal , Intestino Delgado/metabolismo , Intestino Delgado/parasitología , Intestino Delgado/patología , Lactulosa/metabolismo , Masculino , Manitol/metabolismo , Recuento de Huevos de Parásitos , Permeabilidad , Salud Rural
2.
Am J Pathol ; 163(6): 2407-12, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14633612

RESUMEN

Some findings suggest an infectious factor in cardiac myxoma and certain histopathological features indicate herpes simplex virus type 1 (HSV-1) infection. We hypothesized that HSV-1 may be involved in the pathogenesis of cardiac myxoma. Paraffin-embedded tissue samples from 17 patients with atrial myxoma were investigated for HSV-1 antigen by immunohistochemistry and viral genomic DNA by nested polymerase chain reaction. The histogenesis and oncogenesis of atrial myxoma were assessed by the expression of calretinin, Ki67, and p53 protein, respectively. Autopsy myocardial samples, including endocardium from 12 patients who died by accident or other conditions, were used for comparison. HSV-1 antigen was detected in atrial myxoma from 12 of 17 patients: 8 of these 12 samples were positive also for HSV-1 DNA. No HSV-1 antigen or DNA was found in tissue from the comparison group. Antigens of HSV-2, varicella-zoster virus, Epstein-Barr virus, and cytomegalovirus were not found in atrial myxoma. Calretinin was found in myxoma cells of all 17 cases but Ki67 was present only in smooth muscle cells or infiltrating cells in some cases. p53 was not detectable in any myxoma. Most infiltrating cells were cytotoxic T lymphocytes. These data suggest that HSV-1 infection is associated with some cases of sporadic atrial myxoma and that these may result from a chronic inflammatory lesion of endocardium.


Asunto(s)
Neoplasias Cardíacas/virología , Herpes Simple/complicaciones , Herpesvirus Humano 1 , Mixoma/virología , Adolescente , Adulto , Anciano , Antígenos Virales/análisis , Calbindina 2 , ADN/genética , Femenino , Atrios Cardíacos , Neoplasias Cardíacas/inmunología , Neoplasias Cardíacas/metabolismo , Neoplasias Cardíacas/patología , Herpesvirus Humano 1/genética , Herpesvirus Humano 1/inmunología , Humanos , Antígeno Ki-67/metabolismo , Masculino , Persona de Mediana Edad , Mixoma/inmunología , Mixoma/metabolismo , Mixoma/patología , Reacción en Cadena de la Polimerasa , Proteína G de Unión al Calcio S100/metabolismo , Proteína p53 Supresora de Tumor/metabolismo
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