1,744 research outputs found

    The Sigma Commutator from Lattice QCD

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    As a direct source of information on chiral symmetry breaking within QCD, the sigma commutator is of considerable importance. Since hadron structure is a non-perturbative problem, numerical calculations on a space-time lattice are currently the only rigorous approach. With recent advances in the calculation of hadron masses within full QCD, it is of interest to see whether the sigma commutator can be calculated directly from the dependence of the nucleon mass on the input quark mass. We show that, provided the correct chiral behaviour of QCD is respected in the extrapolation to realistic quark masses, one can indeed obtain a fairly reliable determination of the sigma commutator using present lattice data. For two-flavour dynamical fermion QCD the sigma commutator lies between 45 and 55 MeV based on recent data from CP-PACS and UKQCD.Comment: 4 pages, 3 figures, uses espcrc1.sty and epsfig.sty. Contribution to the proceedings of the International Conference on Quark Nuclear Physics held in Adelaide Feb. 200

    Chiral Nonanalytic Behaviour: The Edinburgh Plot

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    The Edinburgh Plot is a scale independent way of presenting lattice QCD calculations over a wide range of quark masses. In this sense it is appealing as an indicator of how the approach to physical quark masses is progressing. The difficulty remains that even the most state of the art calculations are still at quark masses that are too heavy to apply dimensionally-regulated chiral perturbation theory. We present a method allowing predictions of the behaviour of the Edinburgh plot, in both the continuum, and on the lattice.Comment: 3 pages, 4 figures, Lattice2002(Spectrum

    Baryon Mass Extrapolation

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    Consideration of the analytical properties of pion-induced baryon self-energies leads to new functional forms for the extrapolation of light baryon masses. These functional forms reproduce the leading non-analytic behavior of chiral perturbation theory, the correct heavy-quark limit and have the advantage of containing information on the extended structure of hadrons. The forms involve only three unknown parameters which may be optimized by fitting to present lattice data. Recent dynamical fermion results from CP-PACS and UK-QCD are extrapolated using these new functional forms. We also use these functions to probe the limit of the chiral perturbative regime and shed light on the applicability of chiral perturbation theory to the extrapolation of present lattice QCD results.Comment: LATTICE99 (QCD Spectrum and Quark Masses

    Chiral Corrections to Baryon Masses Calculated within Lattice QCD

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    Consideration of the analytic properties of pion-induced baryon self energies leads to new functional forms for the extrapolation of light baryon masses. These functional forms reproduce the leading non-analytic behavior of chiral perturbation theory, the correct non-analytic behavior at the NπN \pi threshold and the appropriate heavy-quark limit. They involve only three unknown parameters, which may be obtained by fitting lattice QCD data. Recent dynamical fermion results from CP-PACS and UKQCD are extrapolated using these new functional forms. We also use these functions to probe the limit of applicability of chiral perturbation theory.Comment: 4 pages, 2 figures, Contribution to the Proceedings of the 15th Particles and Nuclei International Conference (PANIC 99), Uppsala, Sweden, June 10-16, 199

    What treatments relieve arthritis and fatigue associated with systemic lupus erythematosus?

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    Q: What treatments relieve arthritis and fatigue associated with systemic lupus erythematosus? A: Hydroxychloroquine and chloroquine improve the arthritis associated with mild systemic lupus erythematosus (SLE)--producing a 50% reduction in arthritis flares and articular involvement--and have few adverse effects (strength of recommendation [SOR]: a, systematic review of randomized controlled trials [RCTs]). Methotrexate reduces arthralgias by as much as 79%, but produces adverse effects in up to 70% of patients (SOR: b, systematic review of RCTs with limited patient-oriented evidence). Nonsteroidal anti-inflammatory drugs (NSAIDs) and corticosteroids are often used for SLE joint pain (SOR: c, expert opinion). Omega-3 fatty acids may reduce arthritis symptoms by about 35% (SOR: b, RCTs with inconsistent evidence). Abatacept and dehydroepiandrosterone don't produce clinically meaningful improvements in fatigue associated with SLE, and abatacept causes significant adverse effects (SOR: b, posthoc analysis of a single RCT). Aerobic exercise may help fatigue (SOR: b, systematic review with inconsistent evidence)

    Visualisation of BioPAX Networks using BioLayout Express (3D).

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    BioLayout Express (3D) is a network analysis tool designed for the visualisation and analysis of graphs derived from biological data. It has proved to be powerful in the analysis of gene expression data, biological pathways and in a range of other applications. In version 3.2 of the tool we have introduced the ability to import, merge and display pathways and protein interaction networks available in the BioPAX Level 3 standard exchange format. A graphical interface allows users to search for pathways or interaction data stored in the Pathway Commons database. Queries using either gene/protein or pathway names are made via the cPath2 client and users can also define the source and/or species of information that they wish to examine. Data matching a query are listed and individual records may be viewed in isolation or merged using an 'Advanced' query tab. A visualisation scheme has been defined by mapping BioPAX entity types to a range of glyphs. Graphs of these data can be viewed and explored within BioLayout as 2D or 3D graph layouts, where they can be edited and/or exported for visualisation and editing within other tools

    From Isotopes to TK Interviews: Towards Interdisciplinary Research in Fort Resolution and the Slave River Delta, Northwest Territories

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    Evolving research in Fort Resolution and the Slave River Delta, Northwest Territories, aims to improve understanding of how the natural ecosystem functions and responds to various environmental stressors, as well as to enhance the stewardship of natural resources and the capacity of local residents to respond to change. We seek to integrate approaches that span the natural and social sciences and traditional knowledge understandings of change, employing a research design developed in response to the concerns of a northern community. In doing so, we have strived for a research process that is collaborative, interdisciplinary, policy-oriented, and reflective of northern priorities. These elements characterize the new northern research paradigm increasingly promoted by various federal funding agencies, northern partners, and communities. They represent a holistic perspective in the pursuit of solutions to address complex environmental and socioeconomic concerns about impacts of climate change and resource development on northern societies. However, efforts to fulfill the objectives of this research paradigm are associated with a host of on-the-ground challenges. These challenges include (but are not restricted to) developing effective community partnerships and collaboration and documenting change through interdisciplinary approaches. Here we provide an overview of the components that comprise our interdisciplinary research program and offer an accounting of our formative experiences in confronting these challenges

    Risk factors for malaria infection prevalence and household vector density between mass distribution campaigns of long-lasting insecticidal nets in North-western Tanzania.

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    BACKGROUND: Long-lasting insecticidal nets (LLINs) are the most widely deployed vector control intervention in sub-Saharan Africa to prevent malaria. Recent reports indicate selection of pyrethroid insecticide resistance is widespread in mosquito vectors. This paper explores risk factors associated with malaria infection prevalence and vector density between mass distribution campaigns, changes in net coverage, and loss of protection in an area of high pyrethroid resistance in Northwest Tanzania. METHODS: A cross sectional malaria survey of 3456 children was undertaken in 2014 in Muleba district, Kagera region west of Lake Victoria. Vector density was assessed using indoor light traps and outdoor tent traps. Anophelines were identified to species using PCR and tested for Plasmodium falciparum circumsporozoite protein. Logistic regression was used to identify household and environmental factors associated with malaria infection and regression binomial negative for vector density. RESULTS: LLIN use was 27.7%. Only 16.9% of households had sufficient nets to cover all sleeping places. Malaria infection was independently associated with access to LLINs (OR: 0.57; 95% CI 0.34-0.98). LLINs less than 2 years old were slightly more protective than older LLINs (53 vs 65% prevalence of infection); however, there was no evidence that LLINs in good condition (hole index < 65) were more protective than LLINs, which were more holed. Other risk factors for malaria infection were age, group, altitude and house construction quality. Independent risk factors for vector density were consistent with malaria outcomes and included altitude, wind, livestock, house quality, open eaves and LLIN usage. Indoor collections comprised 4.6% Anopheles funestus and 95.4% Anopheles gambiae of which 4.5% were Anopheles arabiensis and 93.5% were Anopheles gambiae sensu stricto. CONCLUSION: Three years after the mass distribution campaign and despite top-ups, LLIN usage had declined considerably. While children living in households with access to LLINs were at lower risk of malaria, infection prevalence remained high even among users of LLINs in good condition. While effort should be made to maintain high coverage between campaigns, distribution of standard pyrethroid-only LLINs appears insufficient to prevent malaria transmission in this area of intense pyrethroid resistance

    A Randomized Trial of Albumin Infusions in Hospitalized Patients with Cirrhosis

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    BACKGROUND Infection and increased systemic inflammation cause organ dysfunction and death in patients with decompensated cirrhosis. Preclinical studies provide support for an antiinflammatory role of albumin, but confirmatory large-scale clinical trials are lacking. Whether targeting a serum albumin level of 30 g per liter or greater in these patients with repeated daily infusions of 20% human albumin solution, as compared with standard care, would reduce the incidences of infection, kidney dysfunction, and death is unknown. METHODS We conducted a randomized, multicenter, open-label, parallel-group trial involving hospitalized patients with decompensated cirrhosis who had a serum albumin level of less than 30 g per liter at enrollment. Patients were randomly assigned to receive either targeted 20% human albumin solution for up to 14 days or until discharge, whichever came first, or standard care. Treatment commenced within 3 days after admission. The composite primary end point was new infection, kidney dysfunction, or death between days 3 and 15 after the initiation of treatment. RESULTS A total of 777 patients underwent randomization, and alcohol was reported to be a cause of cirrhosis in most of these patients. A median total infusion of albumin of 200 g (interquartile range, 140 to 280) per patient was administered to the targeted albumin group (increasing the albumin level to ≥30 g per liter), as compared with a median of 20 g (interquartile range, 0 to 120) per patient administered to the standard-care group (adjusted mean difference, 143 g; 95% confidence interval [CI], 127 to 158.2). The percentage of patients with a primary end-point event did not differ significantly between the targeted albumin group (113 of 380 patients [29.7%]) and the standard-care group (120 of 397 patients [30.2%]) (adjusted odds ratio, 0.98; 95% CI, 0.71 to 1.33; P=0.87). A time-to-event analysis in which data were censored at the time of discharge or at day 15 also showed no significant between-group difference (hazard ratio, 1.04; 95% CI, 0.81 to 1.35). More severe or life-threatening serious adverse events occurred in the albumin group than in the standard-care group. CONCLUSIONS In patients hospitalized with decompensated cirrhosis, albumin infusions to increase the albumin level to a target of 30 g per liter or more was not more beneficial than the current standard care in the United Kingdom. (Funded by the Health Innovation Challenge Fund; ATTIRE EudraCT number, 2014-002300-24. opens in new tab; ISRCT number, N14174793. opens in new tab.
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