Measuring the aspect ratio renormalization of anisotropic-lattice gluons

Using tadpole inproved actions we investigate the consistency between different methods of measuring the aspect ratio renormalization of anisotropic-lattice gluons for bare aspect ratios \chi_0=4,6,10 and inverse lattice spacing in the range a_s^{-1}=660-840 MeV. The tadpole corrections to the action, which are established self-consistently, are defined for two cases, mean link tadpoles in Landau gauge and gauge invariant mean plaquette tadpoles. Parameters in the latter case exhibited no dependence on the spatial lattice size, L, while in the former, parameters showed only a weak dependence on L easily extrapolated to L=\infty. The renormalized anisotropy \chi_R was measured using both the torelon dispersion relation and the sideways potential method. We found good agreement between these different approaches. Any discrepancy was at worst 3-4% which is consistent with the effect of lattice artifacts that for the torelon we estimate as O(\a_Sa_s^2/R^2) where R is the flux-tube radius. We also present some new data that suggests that rotational invariance is established more accurately for the mean-link action than the plaquette action.Comment: LaTeX 18 pages including 7 figure

Measurement of hybrid content of heavy quarkonia using lattice NRQCD

Using lowest-order lattice NRQCD to create heavy meson propagators and applying the spin-dependent interaction, $c_B^{} \frac{-g}{2m_q}\vec\sigma\cdot\vec{B}$, at varying intermediate time slices, we compute the off-diagonal matrix element of the Hamiltonian for the quarkonium-hybrid two-state system. Thus far, we have results for one set of quenched lattices with an interpolation in quark mass to match the bottomonium spectrum. After diagonalization of the two-state Hamiltonian, we find the ground state of the $\Upsilon$ to show a $0.0035(1)c_B^2$ (with $c_B^2 \sim 1.5-3.1$) probability admixture of hybrid, $|b\bar{b}g>$.Comment: 11 pages, 4 figures, to appear in Phys Rev

Hybrid configuration content of heavy S-wave mesons

We use the non-relativistic expansion of QCD (NRQCD) on the lattice to study the lowest hybrid configuration contribution to the ground state of heavy S-wave mesons. Using lowest-order lattice NRQCD to create the heavy-quark propagators, we form a basis of ``unperturbed'' S-wave and hybrid states. We then apply the lowest-order coupling of the quark spin and chromomagnetic field at an intermediate time slice to create ``mixed'' correlators between the S-wave and hybrid states. From the resulting amplitudes, we extract the off-diagonal element of our two-state Hamiltonian. Diagonalizing this Hamiltonian gives us the admixture of hybrid configuration within the meson ground state. The present effort represents a continuation of previous work: the analysis has been extended to include lattices of varying spacings, source operators having better overlap with the ground states, and the pseudoscalar (along with the vector) channel. Results are presented for bottomonium ($\Upsilon$, $\eta_b^{}$) using three different sets of quenched lattices. We also show results for charmonium ($J/\psi$, $\eta_c^{}$) from one lattice set, although we note that the non-relativistic approximation is not expected to be very good in this case.Comment: 9 pages, 7 figures, version to appear in Phys Rev

Lower serum IgA is associated with COPD exacerbation risk in SPIROMICS

Background Decreased but measurable serum IgA levels (70 mg/dL) have been associated with risk for infections in some populations, but are unstudied in COPD. This study tested the hypothesis that subnormal serum IgA levels would be associated with exacerbation risk in COPD. Methods Data were analyzed from 1,049 COPD participants from the observational cohort study SPIROMICS (535 (51%) women; mean age 66.1 (SD 7.8), 338 (32%) current smokers) who had baseline serum IgA measured using the Myriad RBM biomarker discovery platform. Exacerbation data was collected prospectively (mean 944.3 (SD 281.3) days), and adjusted linear, logistic and zero-inflated negative binomial regressions were performed. Results Mean IgA was 269.1 mg/dL (SD 150.9). One individual had deficient levels of serum IgA (<7 mg/dL) and 25 (2.4%) had IgA level 70 mg/dL. Participants with IgA 70 mg/dL were younger (62 vs. 66 years, p = 0.01) but otherwise similar to those with higher IgA. In adjusted models, IgA 70 mg/dL was associated with higher exacerbation incidence rates (IRR 1.71, 95% CI 1.01-2.87, p = 0.044) and greater risk for any severe exacerbation (OR 2.99, 95% CI 1.30-6.94, p = 0.010). In adjusted models among those in the lowest decile (<120 mg/ dL), each 10 mg/dL decrement in IgA (analyzed continuously) was associated with more exacerbations during follow-up (β 0.24, 95% CI 0.017-0.46, p = 0.035). Conclusions Subnormal serum IgA levels were associated with increased risk for acute exacerbations, supporting mildly impaired IgA levels as a contributing factor in COPD morbidity. Additionally, a dose-response relationship between lower serum IgA and number of exacerbations was found among individuals with serum IgA in the lowest decile, further supporting the link between serum IgA and exacerbation risk. Future COPD studies should more comprehensively characterize immune status to define the clinical relevance of these findings and their potential for therapeutic correction

Should science educators deal with the science/religion issue?

I begin by examining the natures of science and religion before looking at the ways in which they relate to one another. I then look at a number of case studies that centre on the relationships between science and religion, including attempts to find mechanisms for divine action in quantum theory and chaos theory, creationism, genetic engineering and the writings of Richard Dawkins. Finally, I consider some of the pedagogical issues that would need to be considered if the science/religion issue is to be addressed in the classroom. I conclude that there are increasing arguments in favour of science educators teaching about the science/religion issue. The principal reason for this is to help students better to learn science. However, such teaching makes greater demands on science educators than has generally been the case. Certain of these demands are identified and some specific suggestions are made as to how a science educator might deal with the science/religion issue. © 2008 Taylor & Francis

Alignment of inhaled chronic obstructive pulmonary disease therapies with published strategies :analysis of the Global Initiative for Chronic Obstructive Lung Disease recommendations in SpiroMics

Rationale: Despite awareness of chronic obstructive pulmonary disease (COPD) treatment recommendations, uptake is poor. The Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS) spans 2010-2016, providing an opportunity to assess integration of 2011 Global Initiative for Obstructive Lung Disease (GOLD) treatment strategies over time in a large observational cohort study. Objectives: To evaluate how COPD treatment aligns with 2011 GOLD strategies and determine factors associated with failure to align with recommendations. Methods: Information on inhaled medication use collected via questionnaire annually for 4 years was compiled into therapeutic classes (long-acting antimuscarinic agent, long-acting b-agonist, inhaled corticosteroids [ICS], and combinations thereof). Medications were not modified by SPIROMICS investigators. 2011 GOLD COPD categories A, B, C, and D were assigned. Alignment of inhaler regimen with first-/second-line GOLD recommendations was determined, stratifying into recommendation aligned or nonaligned. Recommendation-nonaligned participants were further stratified into overuse and underuse categories. Results: Of 1,721 participants with COPD, at baseline, 52% of regimens aligned with GOLD recommendations. Among participants with nonaligned regimens, 46% reported underuse, predominately owing to lack of long-acting inhalers in GOLD category D. Of the 54% reporting overuse, 95% were treated with nonindicated ICS-containing regimens. Among 431 participants with 4 years of follow-up data, recommendation alignment did not change over time. When we compared 2011 and 2017 recommendations, we found that 47% did not align with either set of recommendations, whereas 35% were in alignment with both recommendations. Conclusions: Among SPIROMICS participants with COPD, nearly 50% reported inhaler regimens that did not align with GOLD recommendations. Nonalignment was driven largely by overuse of ICS regimens in milder disease and lack of long-acting inhalers in severe disease

Clinical significance of bronchodilator responsiveness evaluated by forced vital capacity in COPD: SPIROMICS cohort analysis

Objective: Bronchodilator responsiveness (BDR) is prevalent in COPD, but its clinical implications remain unclear. We explored the significance of BDR, defined by post-bronchodilator change in FEV1 (BDRFEV1) as a measure reflecting the change in flow and in FVC (BDRFVC)reflecting the change in volume. Methods: We analyzed 2974 participants from a multicenter observational study designed to identify varying COPD phenotypes (SPIROMICS). We evaluated the association of BDR with baseline clinical characteristics, rate of prospective exacerbations and mortality using negative binomial regression and Cox proportional hazards models. Results: A majority of COPD participants exhibited BDR (52.7%). BDRFEV1 occurred more often in earlier stages of COPD, while BDRFVC occurred more frequently in more advanced disease. When defined by increases in either FEV1 or FVC, BDR was associated with a self-reported history of asthma, but not with blood eosinophil counts. BDRFVC was more prevalent in subjects with greater emphysema and small airway disease on CT. In a univariate analysis, BDRFVC was associated with increased exacerbations and mortality, although no significance was found in a model adjusted for post-bronchodilator FEV1. Conclusion: With advanced airflow obstruction in COPD, BDRFVC is more prevalent in comparison to BDRFEV1 and correlates with the extent of emphysema and degree of small airway disease. Since these associations appear to be related to the impairment of FEV1,BDRFVC itself does not define a distinct phenotype nor can it be more predictive of outcomes, but it can offer additional insights into the pathophysiologic mechanism in advanced COPD. Clinical trials registration: ClinicalTrials.gov: NCT01969344T4