122 research outputs found

    Multidetector computed tomography angiography for assessment of in-stent restenosis: meta-analysis of diagnostic performance

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    <p>Abstract</p> <p>Background</p> <p>Multi-detector computed tomography angiography (MDCTA)of the coronary arteries after stenting has been evaluated in multiple studies.</p> <p>The purpose of this study was to perform a structured review and meta-analysis of the diagnostic performance of MDCTA for the detection of in-stent restenosis in the coronary arteries.</p> <p>Methods</p> <p>A Pubmed and manual search of the literature on in-stent restenosis (ISR) detected on MDCTA compared with conventional coronary angiography (CA) was performed. Bivariate summary receiver operating curve (SROC) analysis, with calculation of summary estimates was done on a stent and patient basis. In addition, the influence of study characteristics on diagnostic performance and number of non-assessable segments (NAP) was investigated with logistic meta-regression.</p> <p>Results</p> <p>Fourteen studies were included. On a stent basis, Pooled sensitivity and specificity were 0.82(0.72–0.89) and 0.91 (0.83–0.96). Pooled negative likelihood ratio and positive likelihood ratio were 0.20 (0.13–0.32) and 9.34 (4.68–18.62) respectively. The exclusion of non-assessable stents and the strut thickness of the stents had an influence on the diagnostic performance. The proportion of non-assessable stents was influenced by the number of detectors, stent diameter, strut thickness and the use of an edge-enhancing kernel.</p> <p>Conclusion</p> <p>The sensitivity of MDTCA for the detection of in-stent stenosis is insufficient to use this test to select patients for further invasive testing as with this strategy around 20% of the patients with in-stent stenosis would be missed. Further improvement of scanner technology is needed before it can be recommended as a triage instrument in practice. In addition, the number of non-assessable stents is also high.</p

    Processing of Genome 5β€² Termini as a Strategy of Negative-Strand RNA Viruses to Avoid RIG-I-Dependent Interferon Induction

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    Innate immunity is critically dependent on the rapid production of interferon in response to intruding viruses. The intracellular pathogen recognition receptors RIG-I and MDA5 are essential for interferon induction by viral RNAs containing 5β€² triphosphates or double-stranded structures, respectively. Viruses with a negative-stranded RNA genome are an important group of pathogens causing emerging and re-emerging diseases. We investigated the ability of genomic RNAs from substantial representatives of this virus group to induce interferon via RIG-I or MDA5. RNAs isolated from particles of Ebola virus, Nipah virus, Lassa virus, and Rift Valley fever virus strongly activated the interferon-beta promoter. Knockdown experiments demonstrated that interferon induction depended on RIG-I, but not MDA5, and phosphatase treatment revealed a requirement for the RNA 5β€² triphosphate group. In contrast, genomic RNAs of Hantaan virus, Crimean-Congo hemorrhagic fever virus and Borna disease virus did not trigger interferon induction. Sensitivity of these RNAs to a 5β€² monophosphate-specific exonuclease indicates that the RIG-I-activating 5β€² triphosphate group was removed post-transcriptionally by a viral function. Consequently, RIG-I is unable to bind the RNAs of Hantaan virus, Crimean-Congo hemorrhagic fever virus and Borna disease virus. These results establish RIG-I as a major intracellular recognition receptor for the genome of most negative-strand RNA viruses and define the cleavage of triphosphates at the RNA 5β€² end as a strategy of viruses to evade the innate immune response

    ABO Blood Group and the Risk of Hepatocellular Carcinoma: A Case-Control Study in Patients with Chronic Hepatitis B

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    BACKGROUND: Studies have observed an association between the ABO blood group and risk of certain malignancies. However, no studies of the association with hepatocellular carcinoma (HCC) risk are available. We conducted this hospital-based case-control study to examine the association with HCC in patients with chronic hepatitis B (CHB). METHODS: From January 2004 to December 2008, a total of 6275 consecutive eligible patients with chronic hepatitis B virus (HBV) infection were recruited. 1105 of them were patients with HBV-related HCC and 5,170 patients were CHB without HCC. Multivariate logistic regression models were used to investigate the association between the ABO blood group and HCC risk. RESULTS: Compared with subjects with blood type O, the adjusted odds ratio (AOR) for the association of those with blood type A and HCC risk was 1.39 [95% confidence interval (CI), 1.05-1.83] after adjusting for age, sex, type 2 diabetes, cirrhosis, hepatitis B e antigen, and HBV DNA. The associations were only statistically significant [AOR (95%CI)β€Š=β€Š1.56(1.14-2.13)] for men, for being hepatitis B e antigen positive [AOR (95%CI)β€Š=β€Š4.92(2.83-8.57)], for those with cirrhosis [AOR (95%CI), 1.57(1.12-2.20)], and for those with HBV DNA≀10(5)copies/mL [AOR (95%CI), 1.58(1.04-2.42)]. Stratified analysis by sex indicated that compared with those with blood type O, those with blood type B also had a significantly high risk of HCC among men, whereas, those with blood type AB or B had a low risk of HCC among women. CONCLUSIONS: The ABO blood type was associated with the risk of HCC in Chinese patients with CHB. The association was gender-related

    Rare-earth/transition-metal magnets at finite temperature: Self-interaction-corrected relativistic density functional theory in the disordered local moment picture

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    Atomic-scale computational modeling of technologically relevant permanent magnetic materials faces two key challenges. First, a material's magnetic properties depend sensitively on temperature, so the calculations must account for thermally induced magnetic disorder. Second, the most widely used permanent magnets are based on rare-earth elements, whose highly localized 4f electrons are poorly described by standard electronic structure methods. Here, we take two established theories, the disordered local moment picture of thermally induced magnetic disorder and self-interaction-corrected density functional theory, and devise a computational framework to overcome these challenges. Using this approach, we calculate magnetic moments and Curie temperatures of the rare-earth cobalt (RECo5) family for RE = Y-Lu. The calculations correctly reproduce the experimentally measured trends across the series and confirm that, apart from the hypothetical compound EuCo5, SmCo5 has the strongest magnetic properties at high temperature. An order-parameter analysis demonstrates that varying the RE has a surprisingly strong effect on the Co-Co magnetic interactions determining the Curie temperature, even when the lattice parameters are kept fixed. We propose the origin of this behavior is a small contribution to the density from f-character electrons located close to the Fermi level

    Ab initio calculations of temperature-dependent magnetostriction of Fe and A2 Fe1-xGax within the disordered local moment picture

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    The fully relativistic disordered local moment (DLM) theory is used to perform calculations of the magnetic torque of tetragonally distorted Fe and fully disordered (A2)Fe1-xGax(0≀x≀0.2) alloys to describe the temperature dependence of their magnetoelasticity. The finite-temperature magnetoelasticity, in particular the magnetoelastic constant B1, is obtained within DLM theory by studying the response of the magnetic torque generated by the magnetocrystalline anisotropy to the application of a tetragonal strain. Calculations of B1 have been performed on bcc Fe across its ferromagnetic temperature range. Our results show good qualitative agreement with experiment, in particular reproducing the anomalous, nonmonotonic thermal behavior of bcc Fe's magnetostriction, which has been largely unexplained for more than 50 years. The method has also been used to calculate the finite-temperature magnetoelasticity of the A2 phase of Fe1-xGax alloys as a starting point for further investigations into the giant magnetostriction of Galfenol alloys. Our calculations show that homogeneously doping bcc Fe with Ga does not produce an enhancement in magnetostriction and that the nonmonotonic temperature dependence and significant volume dependence are suppressed by increasing Ga content

    Spin orientation and magnetostriction of Tb1βˆ’xDyxFe2 from first principles

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    The optimal amount of dysprosium in the highly magnetostrictive rare-earth compounds Tb1βˆ’xDyxFe2 for room-temperature applications has long been known to be x = 0.73 (Terfenol-D). Here, we derive this value from first principles by calculating the easy magnetization direction and magnetostriction as a function of composition and temperature. We use crystal-field coefficients obtained within density-functional theory to construct phenomenological anisotropy and magnetoelastic constants. The temperature dependence of these constants is obtained from disordered-local-moment calculations of the rare-earth magnetic order parameter. Our calculations find the critical Dy concentration required to switch the magnetization direction at room temperature to be xc = 0.78, with magnetostrictions Ξ»111 = 2700 and Ξ»100 = βˆ’430 ppm, close to the Terfenol-D values
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