85 research outputs found
Field evidence for the upwind velocity shift at the crest of low dunes
Wind topographically forced by hills and sand dunes accelerates on the upwind
(stoss) slopes and reduces on the downwind (lee) slopes. This secondary wind
regime, however, possesses a subtle effect, reported here for the first time
from field measurements of near-surface wind velocity over a low dune: the wind
velocity close to the surface reaches its maximum upwind of the crest. Our
field-measured data show that this upwind phase shift of velocity with respect
to topography is found to be in quantitative agreement with the prediction of
hydrodynamical linear analysis for turbulent flows with first order closures.
This effect, together with sand transport spatial relaxation, is at the origin
of the mechanisms of dune initiation, instability and growth.Comment: 13 pages, 6 figures. Version accepted for publication in
Boundary-Layer Meteorolog
Hypertension and type 2 diabetes: What family physicians can do to improve control of blood pressure - an observational study
Background: The prevalence of type 2 diabetes is rising, and most of these patients also have hypertension,
substantially increasing the risk of cardiovascular morbidity and mortality. The majority of these patients do not
reach target blood pressure levels for a wide variety of reasons. When a literature review provided no clear focus
for action when patients are not at target, we initiated a study to identify characteristics of patients and providers
associated with achieving target BP levels in community-based practice.
Methods: We conducted a practice- based, cross-sectional observational and mailed survey study. The setting was
the practices of 27 family physicians and nurse practitioners in 3 eastern provinces in Canada. The participants
were all patients with type 2 diabetes who could understand English, were able to give consent, and would be
available for follow-up for more than one year. Data were collected from each patient’s medical record and from
each patient and physician/nurse practitioner by mailed survey. Our main outcome measures were overall blood
pressure at target (< 130/80), systolic blood pressure at target, and diastolic blood pressure at target. Analysis
included initial descriptive statistics, logistic regression models, and multivariate regression using hierarchical
nonlinear modeling (HNLM).
Results: Fifty-four percent were at target for both systolic and diastolic pressures. Sixty-two percent were at systolic
target, and 79% were at diastolic target. Patients who reported eating food low in salt had higher odds of
reaching target blood pressure. Similarly, patients reporting low adherence to their medication regimen had lower
odds of reaching target blood pressure.
Conclusions: When primary care health professionals are dealing with blood pressures above target in a patient
with type 2 diabetes, they should pay particular attention to two factors. They should inquire about dietary salt
intake, strongly emphasize the importance of reduction, and refer for detailed counseling if necessary. Similarly,
they should inquire about adherence to the medication regimen, and employ a variety of patient-oriented
strategies to improve adherence
Engineering and characterisation of chimeric monoclonal antibody 806 (ch806) for targeted immunotherapy of tumours expressing de2-7 EGFR or amplified EGFR
We report the generation of a chimeric monoclonal antibody (ch806) with specificity for an epitope on the epidermal growth factor receptor (EGFR) that is different from that targeted by all other anti-EGFR therapies. Ch806 antibody is reactive to both de2-7 and overexpressed wild-type (wt) EGFR but not native EGFR expressed in normal tissues at physiological levels. Ch806 was stably expressed in CHO (DHFR −/−) cells and purified for subsequent characterisation and validated for use in preliminary immunotherapy investigations. Ch806 retained the antigen binding specificity and affinity of the murine parental antibody. Furthermore, ch806 displayed enhanced antibody-dependent cellular cytotoxicity against target cells expressing the 806 antigen in the presence of human effector cells. Ch806 was successfully radiolabelled with both iodine-125 and indium-111 without loss of antigen binding affinity or specificity. The radioimmunoconjugates were stable in the presence of human serum at 37°C for up to 9 days and displayed a terminal half-life (T1/2β) of approximately 78 h in nude mice. Biodistribution studies undertaken in BALB/c nude mice bearing de2-7 EGFR-expressing or amplified EGFR-expressing xenografts revealed that 125I-labelled ch806 failed to display any significant tumour retention. However, specific and prolonged tumour localisation of' 111In-labelled ch806 was demonstrated with uptake of 31%ID g−1 and a tumour to blood ratio of 5 : 1 observed at 7 days postinjection. In vivo therapy studies with ch806 demonstrated significant antitumour effects on established de2-7 EGFR xenografts in BALB/c nude mice compared to control, and both murine 806 and the anti-EGFR 528 antibodies. These results support a potential therapeutic role of ch806 in the treatment of suitable EGFR-expressing tumours, and warrants further investigation of the potential of ch806 as a therapeutic agent
Transmission of Vibrio cholerae Is Antagonized by Lytic Phage and Entry into the Aquatic Environment
Cholera outbreaks are proposed to propagate in explosive cycles powered by hyperinfectious Vibrio cholerae and quenched by lytic vibriophage. However, studies to elucidate how these factors affect transmission are lacking because the field experiments are almost intractable. One reason for this is that V. cholerae loses the ability to culture upon transfer to pond water. This phenotype is called the active but non-culturable state (ABNC; an alternative term is viable but non-culturable) because these cells maintain the capacity for metabolic activity. ABNC bacteria may serve as the environmental reservoir for outbreaks but rigorous animal studies to test this hypothesis have not been conducted. In this project, we wanted to determine the relevance of ABNC cells to transmission as well as the impact lytic phage have on V. cholerae as the bacteria enter the ABNC state. Rice-water stool that naturally harbored lytic phage or in vitro derived V. cholerae were incubated in a pond microcosm, and the culturability, infectious dose, and transcriptome were assayed over 24 h. The data show that the major contributors to infection are culturable V. cholerae and not ABNC cells. Phage did not affect colonization immediately after shedding from the patients because the phage titer was too low. However, V. cholerae failed to colonize the small intestine after 24 h of incubation in pond water—the point when the phage and ABNC cell titers were highest. The transcriptional analysis traced the transformation into the non-infectious ABNC state and supports models for the adaptation to nutrient poor aquatic environments. Phage had an undetectable impact on this adaptation. Taken together, the rise of ABNC cells and lytic phage blocked transmission. Thus, there is a fitness advantage if V. cholerae can make a rapid transfer to the next host before these negative selective pressures compound in the aquatic environment
Comparison of 16S ribosomal RNA gene sequence analysis and conventional culture in the environmental survey of a hospital
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Chronic obstructive pulmonary disease (COPD) is characterized by reduced lung function and is the third leading cause of death globally. Through genome-wide association discovery in 48,943 individuals, selected from extremes of the lung function distribution in UK Biobank, and follow-up in 95,375 individuals, we increased the yield of independent signals for lung function from 54 to 97. A genetic risk score was associated with COPD susceptibility (odds ratio per 1 s.d. of the risk score (∼6 alleles) (95% confidence interval) = 1.24 (1.20-1.27), P = 5.05 × 10‾⁴⁹), and we observed a 3.7-fold difference in COPD risk between individuals in the highest and lowest genetic risk score deciles in UK Biobank. The 97 signals show enrichment in genes for development, elastic fibers and epigenetic regulation pathways. We highlight targets for drugs and compounds in development for COPD and asthma (genes in the inositol phosphate metabolism pathway and CHRM3) and describe targets for potential drug repositioning from other clinical indications.This work was funded by a Medical Research Council (MRC) strategic award to M.D.T., I.P.H., D.S. and L.V.W. (MC_PC_12010). This research has been conducted using the UK Biobank Resource under application 648. This article presents independent research funded partially by the National Institute for Health Research (NIHR). The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the UK Department of Health. This research used the ALICE and SPECTRE High-Performance Computing Facilities at the University of Leicester. Additional acknowledgments and funding details can be found in the Supplementary Note
WSES guidelines for management of Clostridium difficile infection in surgical patients
In the last two decades there have been dramatic changes in the epidemiology of Clostridium difficile infection (CDI), with increases in incidence and severity of disease in many countries worldwide. The incidence of CDI has also increased in surgical patients. Optimization of management of C difficile, has therefore become increasingly urgent. An international multidisciplinary panel of experts prepared evidenced-based World Society of Emergency Surgery (WSES) guidelines for management of CDI in surgical patients.Peer reviewe
WSES guidelines for management of Clostridium difficile infection in surgical patients
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