500 research outputs found
Cooperative multithreading on embedded multiprocessor architectures enables energy-scalable design
Effect of Galectin 3 on Aldosterone-Associated Risk of Cardiovascular Mortality in Patients Undergoing Coronary Angiography
Recent experimental studies have suggested that galectin-3 has an interaction with aldosterone, and modifies its adverse effects. We therefore aimed to elucidate whether the relationship between plasma aldosterone concentrations (PACs) and long-term fatal cardiovascular (CV) events would depend on plasma galectin-3 levels. A total of 2,457 patients (median age: 63.5 [interquartile range (IQR) = 56.3 to 70.6] years, 30.1% women) from the LUdwigshafen RIsk and Cardiovascular Health study, with a median follow-up of 9.9 (IQR = 8.5 to 10.7) years, were included. We tested the interaction between aldosterone and galectin-3 for CV-mortality using a multivariate Cox proportional hazard model, reporting hazard ratios (HRs) with 95% confidence intervals (95%CIs). Adjustments for multiple CV risk factors as well as medication use were included. Mean PAC was 79.0 (IQR = 48.0 to 124.0) pg/ml and there were 558 (16.8%) CV deaths. There was a significant interaction between PAC and galectin-3 (p = 0.021). When stratifying patients by the median galectin-3, there was a significant association between aldosterone and CV-mortality for those above (HR per 1 standard deviation = 1.14; 95%CI [1.01 to 1.30], p = 0.023), but not below the cut-off value (HR per 1 standard deviation = 1.00; 95%CI [0.87 to 1.15], p = 0.185). In conclusion, the current study demonstrates for the first time a modifying effect of galectin-3 on the association between aldosterone and CV-mortality risk in humans. These findings indicate that galectin-3 is an intermediate between aldosterone and adverse outcomes
Vitamin D testing and treatment: a narrative review of current evidence
Vitamin D testing and treatment is a subject of controversial scientific discussions, and it is challenging to navigate through the expanding vitamin D literature with heterogeneous and partially opposed opinions and recommendations. In this narrative review, we aim to provide an update on vitamin D guidelines and the current evidence on the role of vitamin D for human health with its subsequent implications for patient care and public health issues. Vitamin D is critical for bone and mineral metabolism, and it is established that vitamin D deficiency can cause rickets and osteomalacia. While many guidelines recommend target serum 25-hydroxyvitamin D (25[OH]D) concentrations of ≥50 nmol/L (20 ng/mL), the minimum consensus in the scientific community is that serum 25(OH)D concentrations below 25–30 nmol/L (10–12 ng/mL) must be prevented and treated. Using this latter threshold of serum 25(OH)D concentrations, it has been documented that there is a high worldwide prevalence of vitamin D deficiency that may require public health actions such as vitamin D food fortification. On the other hand, there is also reason for concern that an exploding rate of vitamin D testing and supplementation increases costs and might potentially be harmful. In the scientific debate on vitamin D, we should consider that nutrient trials differ from drug trials and that apart from the opposed positions regarding indications for vitamin D treatment we still have to better characterize the precise role of vitamin D for human health
Anticipated climate and land-cover changes reveal refuge areas for Borneo's orang-utans
Habitat loss and climate change pose a double jeopardy for many threatened taxa, making the identification of optimal
habitat for the future a conservation priority. Using a case study of the endangered Bornean orang-utan, we identify
environmental refuges by integrating bioclimatic models with projected deforestation and oil-palm agriculture
suitability from the 1950s to 2080s. We coupled a maximum entropy algorithm with information on habitat needs to
predict suitable habitat for the present day and 1950s. We then projected to the 2020s, 2050s and 2080s in models
incorporating only land-cover change, climate change or both processes combined. For future climate, we incorporated
projections from four model and emission scenario combinations. For future land cover, we developed spatial
deforestation predictions from 10 years of satellite data. Refuges were delineated as suitable forested habitats identified
by all models that were also unsuitable for oil palm – a major threat to tropical biodiversity. Our analyses indicate
that in 2010 up to 260 000 km2 of Borneo was suitable habitat within the core orang-utan range; an 18–24%
reduction since the 1950s. Land-cover models predicted further decline of 15–30% by the 2080s. Although habitat
extent under future climate conditions varied among projections, there was majority consensus, particularly in northeastern
and western regions. Across projections habitat loss due to climate change alone averaged 63% by 2080, but
74% when also considering land-cover change. Refuge areas amounted to 2000–42 000 km2 depending on thresholds
used, with 900–17 000 km2 outside the current species range. We demonstrate that efforts to halt deforestation could
mediate some orang-utan habitat loss, but further decline of the most suitable areas is to be expected given projected
changes to climate. Protected refuge areas could therefore become increasingly important for ongoing translocation
efforts. We present an approach to help identify such areas for highly threatened species given environmental
changes expected this century
The proton and deuteron F_2 structure function at low Q^2
Measurements of the proton and deuteron structure functions are
presented. The data, taken at Jefferson Lab Hall C, span the four-momentum
transfer range GeV, and Bjorken values from 0.009 to
0.45, thus extending the knowledge of to low values of at low .
Next-to-next-to-leading order calculations using recent parton distribution
functions start to deviate from the data for GeV at the low and
high -values. Down to the lowest value of , the structure function is
in good agreement with a parameterization of based on data that have been
taken at much higher values of or much lower values of , and which is
constrained by data at the photon point. The ratio of the deuteron and proton
structure functions at low remains well described by a logarithmic
dependence on at low .Comment: 3 figures, submitted pape
Longitudinal-Transverse Separations of Structure Functions at Low for Hydrogen and Deuterium
We report on a study of the longitudinal to transverse cross section ratio,
, at low values of and , as determined from
inclusive inelastic electron-hydrogen and electron-deuterium scattering data
from Jefferson Lab Hall C spanning the four-momentum transfer range 0.06 GeV. Even at the lowest values of , remains
nearly constant and does not disappear with decreasing , as expected. We
find a nearly identical behaviour for hydrogen and deuterium.Comment: 4 pages, 2 gigure
Measurements of electron-proton elastic cross sections for
We report on precision measurements of the elastic cross section for
electron-proton scattering performed in Hall C at Jefferson Lab. The
measurements were made at 28 unique kinematic settings covering a range in
momentum transfer of 0.4 5.5 . These measurements
represent a significant contribution to the world's cross section data set in
the range where a large discrepancy currently exists between the ratio of
electric to magnetic proton form factors extracted from previous cross section
measurements and that recently measured via polarization transfer in Hall A at
Jefferson Lab.Comment: 17 pages, 18 figures; text added, some figures replace
The effect of vitamin D supplementation on plasma non-oxidised PTH in a randomised clinical trial
Objective: PTH can be oxidised in vivo, rendering it biologically inactive. Non-oxidised PTH (n-oxPTH) may therefore give a better image of the hormonal status of the patient. While vitamin D supplementation decreases total PTH (tPTH) concentration, the effect on n-oxPTH concentration is unexplored. We investigated the effect of vitamin D on n-oxPTH concentration in comparison to tPTH and compared the correlations between parameters of calcium, bone and lipid metabolism with n-oxPTH and tPTH.
Methods: N-oxPTH was measured in 108 vitamin D-insufficient (25(O H)D <75 nmol/L) hypertensive patients, treated with vitamin D (2800 IE daily) or placebo for 8 weeks in the Styrian Vitamin D Hypertension Trial (NCT02136771). We calculated the treatment effect and performed correlation analyses of n-oxPTH and tPTH with parameters of calcium, bone and lipid metabolism and oxidative stress.
Results: After treatment, compared to placebo, 25(OH)D concentrations increased, tPTH decreased by 9% (P < 0.001), n-oxPTH by 7% (P = 0.025) and the ratio of n-oxPTH/tPTH increased (P = 0.027). Changes in phosphate and HDL concentration correlated with changes in n-oxPTH, but not tPTH.
Conclusions: tPTH and n-oxPTH decrease upon vitamin D supplementation. Our study suggests that vitamin D supplementation reduces the oxidation of PTH, as we observed a small but significant increase in the non-oxidised proportion of PTH upon treatment. In addition, we found that changes in phosphate and HDL concentration showed a relationship with changes in n-oxPTH, but not tPTH. This may be explained by the biological activity of n-oxPTH. Further research should be carried out to establish the clinical relevance of n-oxPTH
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