217 research outputs found

    Interpretable Diabetic Retinopathy Diagnosis based on Biomarker Activation Map

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    Deep learning classifiers provide the most accurate means of automatically diagnosing diabetic retinopathy (DR) based on optical coherence tomography (OCT) and its angiography (OCTA). The power of these models is attributable in part to the inclusion of hidden layers that provide the complexity required to achieve a desired task. However, hidden layers also render algorithm outputs difficult to interpret. Here we introduce a novel biomarker activation map (BAM) framework based on generative adversarial learning that allows clinicians to verify and understand classifiers decision-making. A data set including 456 macular scans were graded as non-referable or referable DR based on current clinical standards. A DR classifier that was used to evaluate our BAM was first trained based on this data set. The BAM generation framework was designed by combing two U-shaped generators to provide meaningful interpretability to this classifier. The main generator was trained to take referable scans as input and produce an output that would be classified by the classifier as non-referable. The BAM is then constructed as the difference image between the output and input of the main generator. To ensure that the BAM only highlights classifier-utilized biomarkers an assistant generator was trained to do the opposite, producing scans that would be classified as referable by the classifier from non-referable scans. The generated BAMs highlighted known pathologic features including nonperfusion area and retinal fluid. A fully interpretable classifier based on these highlights could help clinicians better utilize and verify automated DR diagnosis.Comment: 12 pages, 8 figure

    Diversity and structure of soil bacterial communities in the Fildes Region (maritime Antarctica) as revealed by 454 pyrosequencing

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    This study assessed the diversity and composition of bacterial communities in four different soils (human-, penguin-, seal-colony impacted soils and pristine soil) in the Fildes Region (King George Island, Antarctica) using 454 pyrosequencing with bacterial-specific primers targeting the 16S rRNA gene. Proteobacteria, Actinobacteria, Acidobacteria, and Verrucomicrobia were abundant phyla in almost all the soil samples. The four types of soils were significantly different in geochemical properties and bacterial community structure. Thermotogae, Cyanobacteria, Fibrobacteres, Deinococcus-Thermus, and Chlorobi obviously varied in their abundance among the 4 soil types. Considering all the samples together, members of the genera Gaiella, Chloracidobacterium, Nitrospira, Polaromonas, Gemmatimonas, Sphingomonas and Chthoniobacter were found to predominate, whereas members of the genera Chamaesiphon, Herbaspirillum, Hirschia, Nevskia, Nitrosococcus, Rhodococcus, Rhodomicrobium, and Xanthomonas varied obviously in their abundance among the four soil types. Distance-based redundancy analysis revealed that pH (p < 0.01), phosphate phosphorus (p < 0.01), organic carbon (p < 0.05), and organic nitrogen (p < 0.05) were the most significant factors that correlated with the community distribution of soil bacteria. To our knowledge, this is the first study to explore the soil bacterial communities in human-, penguin-, and seal- colony impacted soils from ice-free areas in maritime Antarctica using high-throughput pyrosequencing

    Incidence and Risk of QTc Interval Prolongation among Cancer Patients Treated with Vandetanib: A Systematic Review and Meta-analysis

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    Vandetanib is a multikinase inhibitor that is under assessment for the treatment of various cancers. QTc interval prolongation is one of the major adverse effects of this drug, but the reported incidence varies substantially among clinical trials. We performed a systematic review and meta-analysis to obtain a better understanding in the risk of QTc interval prolongation among cancer patients administered vandetanib.Eligible studies were phase II and III prospective clinical trials that involved cancer patients who were prescribed vandetanib 300 mg/d and that included data on QTc interval prolongation. The overall incidence and risk of QTc interval prolongation were calculated using random-effects or fixed-effects models, depending on the heterogeneity of the included studies. Nine trials with 2,188 patients were included for the meta-analysis. The overall incidence of all-grade and high-grade QTc interval prolongation was 16.4% (95% CI, 8.1-30.4%) and 3.7% (8.1-30.4%), respectively, among non-thyroid cancer patients, and 18.0% (10.7-28.6%) and 12.0% (4.5-28.0%), respectively, among thyroid cancer patients. Patients with thyroid cancer who had longer treatment duration also had a higher incidence of high-grade events, with a relative risk of 3.24 (1.57-6.71), than patients who had non-thyroid cancer. Vandetanib was associated with a significantly increased risk of all-grade QTc interval prolongation with overall Peto odds ratios of 7.26 (4.36-12.09) and 5.70 (3.09-10.53) among patients with non-thyroid cancer and thyroid cancer, respectively, compared to the controls.Treatment with vandetanib is associated with a significant increase in the overall incidence and risk of QTc interval prolongation. Different cancer types and treatment durations may affect the risk of developing high-grade QTc interval prolongation

    The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters

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    It has been long considered that zinc homeostasis in bacteria is maintained by export systems and uptake systems, which are separately controlled by their own regulators and the uptake systems are negatively regulated by Zur which binds to an about 30-bp AT-rich sequence known as Zur-box present in its target promoters to block the entry of RNA polymerase. Here, we demonstrated in vivo and in vitro that in addition to act as a repressor of putative Zn2+-uptake systems, the Zur of the bacterial phytopathogen Xanthomonas campestris pathovar campestris (Xcc) acts as an activator of a Zn2+ efflux pump. The Xcc Zur binds to a similar Zur-box with ∼30-bp AT-rich sequence in the promoters of the genes encoding putative Zn2+-uptake systems but a 59-bp GC-rich sequence with a 20-bp inverted repeat overlapping the promoter's −35 to −10 sequence of the gene encoding a Zn2+-export system. Mutagenesis of the inverted repeat sequence resulted in abolishment of the in vitro binding and the in vivo and in vitro activation of the export gene's promoter by Zur. These results reveal that the Xcc Zur functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters

    Steroids in the Treatment of IgA Nephropathy to the Improvement of Renal Survival: A Systematic Review and Meta-Analysis

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    Studies have shown that steroids can improve kidney survival and decrease the risk of proteinuria in patients with Immunoglobulin A nephropathy, but the overall benefit of steroids in the treatment of Immunoglobulin A nephropathy remains controversial. The aim of this study was to evaluate the benefits and risks of steroids for renal survival in adults with Immunoglobulin A nephropathy.We searched the Cochrane Renal Group Specialized Register, Cochrane Controlled Trial Registry, MEDLINE and EMBASE databases. All eligible studies were measuring at least one of the following outcomes: end-stage renal failure, doubling of serum creatinine and urinary protein excretion. Fifteen relevant trials (n = 1542) that met our inclusion criteria were identified. In a pooled analysis, steroid therapy was associated with statistically significant reduction of the risk in end-stage renal failure (RR: 0.46, 95% CI: 0.27 to 0.79), doubling of serum creatinine (RR = 0.34, 95%CI = 0.15 to 0.77) and reduced urinary protein excretion (MD = −0.47g/day, 95%CI = −0.64 to −0.31).We identified that steroid therapy was associated with a decrease of proteinuria and with a statistically significant reduction of the risk in end-stage renal failure. Moreover, subgroup analysis also suggested that long-term steroid therapy had a higher efficiency than standard and short term therapy

    Measurement of Branching Ratios for ηc\eta_c Hadronic Decays

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    In a sample of 58 million J/ψJ/\psi events collected with the BES II detector, the process J/ψγηc\psi\to\gamma\eta_c is observed in five decay channels: ηcK+Kπ+π\eta_c \to K^+K^-\pi^+\pi^-, π+ππ+π\pi^+\pi^-\pi^+\pi^-, K±KS0πK^\pm K^0_S \pi^\mp (with KS0π+πK^0_S\to\pi^+\pi^-), ϕϕ\phi\phi (with ϕK+K\phi\to K^+K^-) and ppˉp\bar{p}. From these signals, we determine Br(J/ψγηc)×Br(ηcK+Kπ+π)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to K^+K^-\pi^+\pi^-) =(1.5±0.2±0.2)×104=(1.5\pm0.2\pm0.2)\times10^{-4}, Br(J/ψγηc)×Br(ηcπ+ππ+π)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to \pi^+\pi^-\pi^+\pi^-) =(1.3±0.2±0.4)×104=(1.3\pm0.2\pm0.4)\times10^{-4}, Br(J/ψγηc)×Br(ηcK±KS0π)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to K^\pm K_{S}^{0}\pi^\mp) =(2.2±0.3±0.5)×104=(2.2\pm0.3\pm0.5)\times10^{-4}, Br(J/ψγηc)×Br(ηcϕϕ)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to \phi\phi) =(3.3±0.6±0.6)×105=(3.3\pm0.6\pm0.6)\times10^{-5} and Br(J/ψγηc)×Br(ηcppˉ)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to p\bar{p}) =(1.9±0.3±0.3)×105=(1.9\pm0.3\pm0.3)\times10^{-5}.Comment: 8 pages, 1 figures and 4 table. Submitted to Phys. Lett.

    Partial Wave Analyses of J/ψγK+KJ/\psi\to\gamma K^+K^- and γKS0KS0\gamma K^0_SK^0_S

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    Results are presented on J/ψJ/\psi radiative decays to K+KK^+K^- and KS0KS0K^0_SK^0_S based on a sample of 58M J/ψJ/\psi events taken with the BES II detector. A partial wave analysis is carried out using the relativistic covariant tensor amplitude method in the 1-2 GeV mass range. There is conspicuous production due to the f2(1525)f'_2(1525) and f0(1710)f_0(1710). The latter peaks at a mass of 1740±425+101740\pm 4^{+10}_{-25} MeV with a width of 1668+510+15166{^{+5}_{-8}}{^{+15}_{-10}} MeV. Spin 0 is strongly preferred over spin 2. For the f2(1525)f'_2(1525), the helicity amplitude ratios are determined to be x2=1.00±0.280.36+1.06x^2 = 1.00\pm0.28^{+1.06}_{-0.36} and y2=0.44±0.080.56+0.10y^2 = 0.44\pm{0.08}^{+0.10}_{-0.56}.Comment: 16 pages, 5 figure

    Measurement of Inclusive Monmentum Spectra and Multiplicity Distributions of Charged Particles at s25\sqrt{s}\sim 2-5 GeV

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    Inclusive momentum spectra and multiplicity distributions of charged particles measured with BESII detector at center of mass energies of 2.2,2.6,3.0,3.2,4.6 and 4.8 GeV are presented. Values of the second binomial moment, R2R_2, obtained from the multiplicity distributions are reported. These results are compared with both experimental data from high energy e+ee^+e^-, epep and ppˉp\bar{p} experiments and QCD calculations.Comment: 9 pages, 7 figures, 3 tables, it will be submitted to PR
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