8 research outputs found

    Detection and Analysis of Anomalies in People Density and Mobility Through Wireless Smartphone Tracking

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    One of the challenges of this century is to use the data that a smart-city provides to make life easier for its inhabitants. Speci cally, within the area of urban mobility, the possibility of detecting anomalies in the movement of pedestrians and vehicles is an issue of vital importance for the planning and administration of a city. The aim of this paper is to propose a methodology to detect the movement of people from the information transmitted by their smart mobile devices, analyze these data, and be able to detect or recognize anomalies in their behavior. In order to validate this methodology, different experiments have been carried out based on real data aiming to extract knowledge, as well as obtaining a characterisation of the anomalies detected. The use of this methodology might help the city policy makers to better manage their mobility and transport resources.This work was supported by in part by the Dirección General de Tråfico under Project SPIP2017-02116, in part by the Ministerio de Ciencia, Innovación y Universidades under Grant RTI2018-102002-A-I00, in part by the Ministerio español de Economía y Competitividad under Grant TIN2017-85727-C4-2-P, in part by the FEDER under Grant TEC2015-68752, and in part by the FEDER y Junta de Andalucía under Project B-TIC-402-UGR18

    N-acetyl cysteine reverts the proinflammatory state induced by cigarette smoke extract in lung Calu-3 cells

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    Chronic obstructive pulmonary disease (COPD) and cystic fibrosis (CF) are lethal pulmonary diseases. Cigarette consumption is the main cause for development of COPD, while CF is produced by mutations in the CFTR gene. Although these diseases have a different etiology, both share a CFTR activity impairment and proinflammatory state even under sterile conditions. The aim of this work was to study the extent of the protective effect of the antioxidant N-acetylcysteine (NAC) over the proinflammatory state (IL-6 and IL-8), oxidative stress (reactive oxygen species, ROS), and CFTR levels, caused by Cigarette Smoke Extract (CSE) in Calu-3 airway epithelial cells. CSE treatment (100 ”g/ml during 24 h) decreased CFTR mRNA expression and activity, and increased the release of IL-6 and IL-8. The effect on these cytokines was inhibited by N-acetyl cysteine (NAC, 5 mM) or the NF-kB inhibitor, IKK-2 (10 ”M). CSE treatment also increased cellular and mitochondrial ROS levels. The cellular ROS levels were normalized to control values by NAC treatment, although significant effects on mitochondrial ROS levels were observed only at short times (5ÂŽ) and effects on CFTR levels were not observed. In addition, CSE reduced the mitochondrial NADH-cytochrome c oxidoreductase (mCx I-III) activity, an effect that was not reverted by NAC. The reduced CFTR expression and the mitochondrial damage induced by CSE could not be normalized by NAC treatment, evidencing the need for a more specific reagent. In conclusion, CSE causes a sterile proinflammatory state and mitochondrial damage in Calu-3 cells that was partially recovered by NAC treatment. Keywords: Cigarette smoke extract, Mitochondria, CFTR, ROS, COPD, Cystic fibrosi

    Estudio sobre algoritmos genéticos en la nube y el modelo de programación MapReduce

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    Este trabajo presenta el proyecto fin de carrera “Estudio sobre algoritmos genĂ©ticos en la nube y el modelo de programaciĂłn MapReduce”. Durante el desarrollo de este proyecto se investigĂł en el uso y aplicaciĂłn de Algoritmos GenĂ©ticos en distintos entornos de Cloud Computing, como el MapReduce o virtualizaciĂłn de instancias. Se ejecutaron distintas configuraciones de parĂĄmetros del algoritmo (como el tamaño de poblaciĂłn o el tipo de crossover) en distintas instancias de Amazon Web Services. Los resultados muestran el efecto de estos parĂĄmetros al tipo de instancia utilizada.This paper shows the final degree project “A study of genetic algorithms in the cloud and the MapReduce model”. During the development of this project the usage and application of genetic algorithms in different Cloud Computing environments was investigated, such as MapReduce or virtualization. Different parameter configurations, such as the population size or crossover type, were launched in different instances of Amazon Web Services. Results show the effect of these parameters to the different types of used instances.Universidad de Granada: Departamento de Arquitectura y TecnologĂ­a de Computadores; Vicerrectorado para la GarantĂ­a de la Calidad.Financiado con los proyectos EvOrq (TIC-3903), Beca FPU AP2009-2942, ANY-SELF (TIN2011-28627-C04-02) y CANUBE (Proyecto 83 CEI-BIOTIC)

    The expression of the mitochondrial encoded gene ND4 is downregulated in cystic fibrosis

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    Abstract: Cystic fibrosis (CF) is a disease produced by mutations in the CFTR channel. We have previously reported that the CFTR chloride transport activity regulates the differential expression of several genes, including SRC. Here we report that MT-ND4, a mitochondrial gene encoding a subunit of the mitochondrial Complex I (mtCx-I), is also a CFTR-dependent gene. A reduced expression of MT-ND4 was observed in CFDE cells (derived from a CF patient) when compared to CFDE cells ectopically expressing wild type CFTR. The differential expression of MT-ND4 in CF was confirmed by PCR. In situ hybridizations of deparaffinized human lung tissue slices derived from wt-CFTR or CF patients also showed downregulation of ND4 in CF. In addition, glibenclamide or CFTR(inh)-172 (CFTR chloride transport inhibitors) reduced MT-ND4 expression in cells expressing wt CFTR. These results suggest that the CFTR chloride transport activity indirectly up-regulates MT-ND4 expression

    Second Colombian Consensus on the Management of Post-menopausal Osteoporosis: 2017 Update

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    La AsociaciĂłn Colombiana de Osteoporosis y Metabolismo Mineral se reuniĂł a principios de 2017 para actualizar el Consenso Colombiano de Osteoporosis, elaborado por primera vez en 2005, un paso que se considerĂł necesario en vista del subdiagnĂłstico de esta enfermedad, el impacto esperado del envejecimiento poblacional y los cambios en el tratamiento farmacolĂłgico que ha habido desde entonces. Se seleccionĂł un equipo tĂ©cnico con especialistas de mĂșltiples ĂĄreas y amplia trayectoria, repartidos en 4 grupos de trabajo: definiciĂłn y epidemiologĂ­a, diagnĂłstico, tratamiento farmacolĂłgico y medidas no farmacolĂłgicas. Luego de una revisiĂłn de la literatura cientĂ­fica, en reuniones de trabajo se generaron las definiciones y recomendaciones que se resumen en este documento.The Colombian Osteoporosis and Mineral Metabolism Association met in early 2017 to update the Colombian Consensus on Osteoporosis. This was first issued in 2005, and is seen as a necessary step in view of the underdiagnosed status of this disease, and the expected impact of population ageing. A technical team was formed with specialists with long experience across multiple disciplines, who were assigned to four working groups: definitions and epidemiology, diagnosis, pharmacological treatment, and non-pharmacological treatment. After a scientific literature review and a series of meetings, the definitions and recommendations are summarised in this article

    Alternative forms of portal vein revascularization in liver transplant recipients with complex portal vein thrombosis

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    Background & Aims: Complex portal vein thrombosis (PVT) is a challenge in liver transplantation (LT). Extra-anatomical approaches to portal revascularization, including renoportal (RPA), left gastric vein (LGA), pericholedochal vein (PCA), and cavoportal (CPA) anastomoses, have been described in case reports and series. The RP4LT Collaborative was created to record cases of alternative portal revascularization performed for complex PVT. Methods: An international, observational web registry was launched in 2020. Cases of complex PVT undergoing first LT performed with RPA, LGA, PCA, or CPA were recorded and updated through 12/2021. Results: A total of 140 cases were available for analysis: 74 RPA, 18 LGA, 20 PCA, and 28 CPA. Transplants were primarily performed with whole livers (98%) in recipients with median (IQR) age 58 (49-63) years, model for end-stage liver disease score 17 (14–24), and cold ischemia 431 (360-505) minutes. Post-operatively, 49% of recipients developed acute kidney injury, 16% diuretic-responsive ascites, 9% refractory ascites (29% with CPA, p <0.001), and 10% variceal hemorrhage (25% with CPA, p = 0.002). After a median follow-up of 22 (4-67) months, patient and graft 1-/3-/5-year survival rates were 71/67/61% and 69/63/57%, respectively. On multivariate Cox proportional hazards analysis, the only factor significantly and independently associated with all-cause graft loss was non-physiological portal vein reconstruction in which all graft portal inflow arose from recipient systemic circulation (hazard ratio 6.639, 95% CI 2.159-20.422, p = 0.001). Conclusions: Alternative forms of portal vein anastomosis achieving physiological portal inflow (i.e., at least some recipient splanchnic blood flow reaching transplant graft) offer acceptable post-transplant results in LT candidates with complex PVT. On the contrary, non-physiological portal vein anastomoses fail to resolve portal hypertension and should not be performed. Impact and implications: Complex portal vein thrombosis (PVT) is a challenge in liver transplantation. Results of this international, multicenter analysis may be used to guide clinical decisions in transplant candidates with complex PVT. Extra-anatomical portal vein anastomoses that allow for at least some recipient splanchnic blood flow to the transplant allograft offer acceptable results. On the other hand, anastomoses that deliver only systemic blood flow to the allograft fail to resolve portal hypertension and should not be performed

    Evaluation of a quality improvement intervention to reduce anastomotic leak following right colectomy (EAGLE): pragmatic, batched stepped-wedge, cluster-randomized trial in 64 countries

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    Background Anastomotic leak affects 8 per cent of patients after right colectomy with a 10-fold increased risk of postoperative death. The EAGLE study aimed to develop and test whether an international, standardized quality improvement intervention could reduce anastomotic leaks. Methods The internationally intended protocol, iteratively co-developed by a multistage Delphi process, comprised an online educational module introducing risk stratification, an intraoperative checklist, and harmonized surgical techniques. Clusters (hospital teams) were randomized to one of three arms with varied sequences of intervention/data collection by a derived stepped-wedge batch design (at least 18 hospital teams per batch). Patients were blinded to the study allocation. Low- and middle-income country enrolment was encouraged. The primary outcome (assessed by intention to treat) was anastomotic leak rate, and subgroup analyses by module completion (at least 80 per cent of surgeons, high engagement; less than 50 per cent, low engagement) were preplanned. Results A total 355 hospital teams registered, with 332 from 64 countries (39.2 per cent low and middle income) included in the final analysis. The online modules were completed by half of the surgeons (2143 of 4411). The primary analysis included 3039 of the 3268 patients recruited (206 patients had no anastomosis and 23 were lost to follow-up), with anastomotic leaks arising before and after the intervention in 10.1 and 9.6 per cent respectively (adjusted OR 0.87, 95 per cent c.i. 0.59 to 1.30; P = 0.498). The proportion of surgeons completing the educational modules was an influence: the leak rate decreased from 12.2 per cent (61 of 500) before intervention to 5.1 per cent (24 of 473) after intervention in high-engagement centres (adjusted OR 0.36, 0.20 to 0.64; P &lt; 0.001), but this was not observed in low-engagement hospitals (8.3 per cent (59 of 714) and 13.8 per cent (61 of 443) respectively; adjusted OR 2.09, 1.31 to 3.31). Conclusion Completion of globally available digital training by engaged teams can alter anastomotic leak rates. Registration number: NCT04270721 (http://www.clinicaltrials.gov)
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