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1.
Anatol J Cardiol ; 16(9): 655-61, 2016 09.
Artículo en Inglés | MEDLINE | ID: mdl-27488747

RESUMEN

OBJECTIVE: Atrial fibrillation (AF) is the most common arrhythmia following coronary artery by-pass graft surgery (CABG). The value of SYNTAX score to predict postoperative atrial fibrillation (PoAF) has not been clearly addressed. We aimed to evaluate this relationship in patients undergoing isolated CABG. METHODS: This study was designed as a single-center, non-randomized, observational, prospective study. Ninety-four patients undergoing isolated on-pump CABG, who had sinus rhythm and were older than 18 years, were enrolled. Demographic characteristics of the patients were recorded; SYNTAX score was calculated preoperatively for each patient. The univariate and multivariate logistic regression analysis were used to determine for predictors of PoAF. RESULTS: The median SYNTAX score of the enrolled patients was 21, (56-5). PoAF was observed in 31 (33.3%) patients. Univariate logistic regression showed that age, chronic obstructive pulmonary disease (COPD), red blood cell distribution width (RDW), urea, initial troponin I, peak postoperative troponin I, interventricular septum, left atrial diameter, and SYNTAX score were significantly associated with the frequency of PoAF following CABG. An independent association was identified with age [ß: 0.088, p:0.023, OR: 1.092, 95% CI (1.012-1.179)], COPD [(ß: 2.222, p:0.003, OR: 9.228, 95% CI (2.150-39.602)], and SYNTAX score [(ß: 0.130, p:0.002, OR: 1.139, 95% CI (1.050-1.235)]. CONCLUSION: This study showed that a higher SYNTAX score was related to more frequent PoAF in patients undergoing isolated on-pump CABG.


Asunto(s)
Fibrilación Atrial/diagnóstico , Puente de Arteria Coronaria/efectos adversos , Adulto , Fibrilación Atrial/etiología , Biomarcadores/análisis , Humanos , Complicaciones Posoperatorias , Periodo Posoperatorio , Estudios Prospectivos , Análisis de Regresión , Medición de Riesgo , Factores de Riesgo
2.
Gastroenterology ; 148(1): 126-136.e6, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-25307862

RESUMEN

BACKGROUND & AIMS: We previously established long-term, 3-dimensional culture of organoids from mouse tissues (intestine, stomach, pancreas, and liver) and human intestine and pancreas. Here we describe conditions required for long-term 3-dimensional culture of human gastric stem cells. The technology can be applied to study the epithelial response to infection with Helicobacter pylori. METHODS: We generated organoids from surgical samples of human gastric corpus. Culture conditions were developed based on those for the mouse gastric and human intestinal systems. We used microinjection to infect the organoids with H pylori. Epithelial responses were measured using microarray and quantitative polymerase chain reaction analyses. RESULTS: Human gastric cells were expanded indefinitely in 3-dimensional cultures. We cultured cells from healthy gastric tissues, single-sorted stem cells, or tumor tissues. Organoids maintained many characteristics of their respective tissues based on their histology, expression of markers, and euploidy. Organoids from healthy tissue expressed markers of 4 lineages of the stomach and self-organized into gland and pit domains. They could be directed to specifically express either lineages of the gastric gland, or the gastric pit, by addition of nicotinamide and withdrawal of WNT. Although gastric pit lineages had only marginal reactions to bacterial infection, gastric gland lineages mounted a strong inflammatory response. CONCLUSIONS: We developed a system to culture human gastric organoids. This system can be used to study H pylori infection and other gastric pathologies.


Asunto(s)
Células Epiteliales/microbiología , Infecciones por Helicobacter/microbiología , Helicobacter pylori/patogenicidad , Células Madre/microbiología , Estómago/microbiología , Adulto , Anciano , Anciano de 80 o más Años , Biomarcadores/metabolismo , Técnicas de Cultivo de Célula , Linaje de la Célula , Proliferación Celular , Separación Celular , Células Cultivadas , Células Epiteliales/efectos de los fármacos , Células Epiteliales/inmunología , Células Epiteliales/metabolismo , Células Epiteliales/patología , Femenino , Mucosa Gástrica/metabolismo , Regulación de la Expresión Génica , Infecciones por Helicobacter/inmunología , Infecciones por Helicobacter/metabolismo , Infecciones por Helicobacter/patología , Helicobacter pylori/inmunología , Humanos , Masculino , Persona de Mediana Edad , Niacinamida/farmacología , Organoides , Fenotipo , Ploidias , Células Madre/efectos de los fármacos , Células Madre/inmunología , Células Madre/metabolismo , Células Madre/patología , Estómago/efectos de los fármacos , Estómago/inmunología , Estómago/patología , Factores de Tiempo , Proteínas Wnt/metabolismo
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