3,479 research outputs found
Two Welsh surveys of blood lead and blood pressure.
The relationship between blood pressure and blood lead was examined in two population samples. One of these consisted of 1137 men aged 49 to 65 years, the other of 865 men and 856 women aged 18 to 64 years. Neither population had any known important exposure to lead, and the 95% ranges of blood lead levels were 6 to 26 micrograms/100 mL and 6 to 23 micrograms/mL in the men and 5 to 18 micrograms/100 mL in the women. No significant relationship between blood pressure and blood lead was detected in either of the population samples, and the regression coefficients suggest that if there were a real effect, then the mean difference in blood pressure per 10 micrograms difference in blood lead is likely to be 0.7 mm Hg in both systolic and diastolic pressures. In the survey of 1137 men, the rise in blood pressure was measured during the cold pressor test. This test is likely to be affected if lead were to affect neurogenic mediators of blood pressure. The mean change in systolic pressure was 24 mm Hg and the 95% range was -6 to 60 mm Hg, but there was no evidence of any association with blood lead level
The CP-violating asymmetry in \eta\to\pi^+ \pi^- e^+e^-
We study the CP-violating asymmetry {\cal A}_{\rm CP}, which arises, in
\eta\to\pi^+\pi^- e^+e^-, from the angular correlation of the e^+ e^- and
\pi^+\pi^- planes due to the interference between the magnetic and electric
decay amplitudes. With the phenomenologically determined magnetic amplitude and
branching ratio as input, the asymmetry, induced by the electric bremsstrahlung
amplitude through the CP-violating decay \eta\to\pi^+\pi^-, and by an
unconventional tensor type operator, has been estimated respectively. The upper
bound of {\cal A}_{\rm CP} from the former is about 10^{-3}, and the asymmetry
from the latter might be up to O(10^{-2}). One can therefore expect that this
CP asymmetry would be an interesting CP-violating observable for the future
precise measurements in the \eta factories.Comment: LaTeX, 6 pages. One reference corrected, and some new references
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Vitamin D intake and risk of CVD and all-cause mortality: evidence from the Caerphilly Prospective Cohort Study
OBJECTIVE:
Prospective data on the associations between vitamin D intake and risk of CVD and all-cause mortality are limited and inconclusive. The aim of the present study was to investigate the associations between vitamin D intake and CVD risk and all-cause mortality in the Caerphilly Prospective Cohort Study.
DESIGN:
The associations of vitamin D intake with CVD risk markers were examined cross-sectionally at baseline and longitudinally at 5-year, 10-year and >20-year follow-ups. In addition, the predictive value of vitamin D intake for CVD events and all-cause mortality after >20 years of follow-up was examined. Logistic regression and general linear regression were used for data analysis.
SETTING:
Participants in the UK.
SUBJECTS:
Men (n 452) who were free from CVD and type 2 diabetes at recruitment.
RESULTS:
Higher vitamin D intake was associated with increased HDL cholesterol (P=0·003) and pulse pressure (P=0·04) and decreased total cholesterol:HDL cholesterol (P=0·008) cross-sectionally at baseline, but the associations were lost during follow-up. Furthermore, higher vitamin D intake was associated with decreased concentration of plasma TAG at baseline (P=0·01) and at the 5-year (P=0·01), but not the 10-year examination. After >20 years of follow-up, vitamin D was not associated with stroke (n 72), myocardial infarctions (n 142), heart failure (n 43) or all-cause mortality (n 281), but was positively associated with increased diastolic blood pressure (P=0·03).
CONCLUSIONS:
The study supports associations of higher vitamin D intake with lower fasting plasma TAG and higher diastolic blood pressure
AMI-LA Observations of the SuperCLASS Super-cluster
We present a deep survey of the SuperCLASS super-cluster - a region of sky
known to contain five Abell clusters at redshift - performed using
the Arcminute Microkelvin Imager (AMI) Large Array (LA) at 15.5GHz. Our
survey covers an area of approximately 0.9 square degrees. We achieve a nominal
sensitivity of Jy beam toward the field centre, finding 80
sources above a threshold. We derive the radio colour-colour
distribution for sources common to three surveys that cover the field and
identify three sources with strongly curved spectra - a high-frequency-peaked
source and two GHz-peaked-spectrum sources. The differential source count (i)
agrees well with previous deep radio source count, (ii) exhibits no evidence of
an emerging population of star-forming galaxies, down to a limit of 0.24mJy,
and (iii) disagrees with some models of the 15GHz source population.
However, our source count is in agreement with recent work that provides an
analytical correction to the source count from the SKADS Simulated Sky,
supporting the suggestion that this discrepancy is caused by an abundance of
flat-spectrum galaxy cores as-yet not included in source population models.Comment: 17 pages, 14 figures, 3 tables. Accepted for publication in MNRA
K^+ -> pi^+pi^0e^+e^-: a novel short-distance probe
We study the decay K^+ -> pi^+ pi^0 e^+ e^-, currently under analysis by the
NA62 Collaboration at CERN. In particular, we provide a detailed analysis of
the Dalitz plot for the long-distance, gamma^*-mediated, contributions
(Bremsstrahlung, direct emission and its interference). We also examine a set
of asymmetries to isolate genuine short-distance effects. While we show that
charge asymmetries are not required to test short distances, they provide the
best environment for its detection. This constitutes by itself a strong
motivation for NA62 to study K^- decays in the future. We therefore provide a
detailed study of different charge asymmetries and the corresponding estimated
signals. Whenever possible, we make contact with the related processes K^+ ->
pi^+ pi^0 gamma and K_L -> pi^+ pi^- e^+ e^- and discuss the advantages of K^+
-> pi^+ pi^0 e^+ e^- over them.Comment: 25 pages, 6 figure
A Single Dose of the DENV-1 Candidate Vaccine rDEN1Δ30 Is Strongly Immunogenic and Induces Resistance to a Second Dose in a Randomized Trial
Dengue is an emerging infectious disease that has become the most important arboviral infection worldwide. There are four serotypes of dengue virus, DENV-1, DENV-2, DENV-3, and DENV-4, each capable of causing the full spectrum of disease. rDEN1Δ30 is a live attenuated investigational vaccine for the prevention of DENV-1 illness and is also a component of an investigational tetravalent DENV vaccine currently in Phase I evaluation. A single subcutaneous dose of rDEN1Δ30 was previously shown to be safe and immunogenic in healthy adults. In the current randomized placebo-controlled trial, 60 healthy flavivirus-naive adults were randomized to receive 2 doses of rDEN1Δ30 (N = 50) or placebo (N = 10), either on study days 0 and 120 (cohort 1) or 0 and 180 (cohort 2). We sought to evaluate the safety and immunogenicity of this candidate vaccine in 50 additional vaccinees and to test whether the humoral immune response could be boosted by a second dose administered 4 or 6 months after the first dose. The first dose of vaccine was well tolerated, infected 47/50 vaccinees and induced seroconversion in 46/50 vaccinees. Irrespective of dosing interval, the second dose of vaccine was also well tolerated but did not induce any detectable viremia or ≥4-fold rise in serum neutralizing antibody titer.Only five subjects had an anamnestic antibody response detectable by ELISA following a second dose of vaccine, demonstrating that the vaccine induced sterilizing humoral immunity in most vaccinees for at least six months following primary vaccination.The promising safety and immunogenicity profile of this vaccine confirms its suitability for inclusion in a tetravalent dengue vaccine
Sun exposure and melanoma risk at different latitudes: a pooled analysis of 5700 cases and 7216 controls
Background Melanoma risk is related to sun exposure; we have investigated risk variation by tumour site and latitude
Does \u2018bigger\u2019mean \u2018better\u2019? Pitfalls and shortcuts associated with big data for social research
\u2018Big data is here to stay.\u2019 This key statement has a double value: is an assumption as well as the reason why a theoretical reflection is needed. Furthermore, Big data is something that is gaining visibility and success in social sciences even, overcoming the division between humanities and computer sciences. In this contribution some considerations on the presence and the certain persistence of Big data as a socio-technical assemblage will be outlined. Therefore, the intriguing opportunities for social research linked to such interaction between practices and technological development will be developed. However, despite a promissory rhetoric, fostered by several scholars since the birth of Big data as a labelled concept, some risks are just around the corner. The claims for the methodological power of bigger and bigger datasets, as well as increasing speed in analysis and data collection, are creating a real hype in social research. Peculiar attention is needed in order to avoid some pitfalls. These risks will be analysed for what concerns the validity of the research results \u2018obtained through Big data. After a pars distruens, this contribution will conclude with a pars construens; assuming the previous critiques, a mixed methods research design approach will be described as a general proposal with the objective of stimulating a debate on the integration of Big data in complex research projecting
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