34 research outputs found
Exploring flavor structure of supersymmetry breaking from rare B decays and unitarity triangle
We study effects of supersymmetric particles in various rare B decay
processes as well as in the unitarity triangle analysis. We consider three
different supersymmetric models, the minimal supergravity, SU(5) SUSY GUT with
right-handed neutrinos, and the minimal supersymmetric standard model with U(2)
flavor symmetry. In the SU(5) SUSY GUT with right-handed neutrinos, we consider
two cases of the mass matrix of the right-handed neutrinos. We calculate direct
and mixing-induced CP asymmetries in the b to s gamma decay and CP asymmetry in
B_d to phi K_S as well as the B_s--anti-B_s mixing amplitude for the unitarity
triangle analysis in these models. We show that large deviations are possible
for the SU(5) SUSY GUT and the U(2) model. The pattern and correlations of
deviations from the standard model will be useful to discriminate the different
SUSY models in future B experiments.Comment: revtex4, 36 pages, 10 figure
The integrated Sachs-Wolfe imprints of cosmic superstructures: a problem for \Lambda CDM
A crucial diagnostic of the \Lambda CDM cosmological model is the integrated
Sachs-Wolfe (ISW) effect of large-scale structure on the cosmic microwave
background (CMB). The ISW imprint of superstructures of size \sim100\;h^{-1}
Mpc at redshift has been detected with significance,
however it has been noted that the signal is much larger than expected. We
revisit the calculation using linear theory predictions in \Lambda CDM
cosmology for the number density of superstructures and their radial density
profile, and take possible selection effects into account. While our expected
signal is larger than previous estimates, it is still inconsistent by
with the observation. If the observed signal is indeed due to the
ISW effect then huge, extremely underdense voids are far more common in the
observed universe than predicted by \Lambda CDM.Comment: 3 figures. v3: minor additions for clearer explanations, conclusions
unchanged. Version to be published in JCA
SUSY breaking mediation mechanisms and (g-2)_\mu, B -> X_s \gamma, B -> X_{s} l^+ l^- and B_s -> \mu^+ \mu^-
We show that there are qualitative differences in correlations among
, , and in various SUSY breaking mediation mechanisms: minimal supergravity
(mSUGRA), gauge mediation (GMSB), anomaly mediation (AMSB), gaugino mediation
(MSB), weakly and strongly interacting string theories, and
brane models. After imposing the direct search limits on the Higgs boson and
SUSY particle search limits and branching ratio, we find all
the scenarios can accommodate the in the range of
(a few tens), and predict that the branching ratio for can differ from the standard model (SM) prediction by
but no more. On the other hand, the is sensitive to the
SUSY breaking mediation mechanisms through the pseudoscalar and stop masses
( and ), and the stop mixing angle. In the GMSB with a
small messenger number, the AMSB, the MSB and the noscale scenarios,
one finds that , which is
below the search limit at the Tevatron Run II. Only the mSUGRA or string
inspired models can generate a large branching ratio for this decay.Comment: 40 pages, 21 figures (to appear in JHEP
Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry.
BACKGROUND: The Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF) is an ongoing prospective noninterventional registry, which is providing important information on the baseline characteristics, treatment patterns, and 1-year outcomes in patients with newly diagnosed non-valvular atrial fibrillation (NVAF). This report describes data from Indian patients recruited in this registry. METHODS AND RESULTS: A total of 52,014 patients with newly diagnosed AF were enrolled globally; of these, 1388 patients were recruited from 26 sites within India (2012-2016). In India, the mean age was 65.8 years at diagnosis of NVAF. Hypertension was the most prevalent risk factor for AF, present in 68.5% of patients from India and in 76.3% of patients globally (P < 0.001). Diabetes and coronary artery disease (CAD) were prevalent in 36.2% and 28.1% of patients as compared with global prevalence of 22.2% and 21.6%, respectively (P < 0.001 for both). Antiplatelet therapy was the most common antithrombotic treatment in India. With increasing stroke risk, however, patients were more likely to receive oral anticoagulant therapy [mainly vitamin K antagonist (VKA)], but average international normalized ratio (INR) was lower among Indian patients [median INR value 1.6 (interquartile range {IQR}: 1.3-2.3) versus 2.3 (IQR 1.8-2.8) (P < 0.001)]. Compared with other countries, patients from India had markedly higher rates of all-cause mortality [7.68 per 100 person-years (95% confidence interval 6.32-9.35) vs 4.34 (4.16-4.53), P < 0.0001], while rates of stroke/systemic embolism and major bleeding were lower after 1 year of follow-up. CONCLUSION: Compared to previously published registries from India, the GARFIELD-AF registry describes clinical profiles and outcomes in Indian patients with AF of a different etiology. The registry data show that compared to the rest of the world, Indian AF patients are younger in age and have more diabetes and CAD. Patients with a higher stroke risk are more likely to receive anticoagulation therapy with VKA but are underdosed compared with the global average in the GARFIELD-AF. CLINICAL TRIAL REGISTRATION-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01090362
Global, regional, and national age-sex-specific mortality and life expectancy, 1950–2017: a systematic analysis for the Global Burden of Disease Study 2017
BACKGROUND:
Assessments of age-specific mortality and life expectancy have been done by the UN Population Division, Department of Economics and Social Affairs (UNPOP), the United States Census Bureau, WHO, and as part of previous iterations of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD). Previous iterations of the GBD used population estimates from UNPOP, which were not derived in a way that was internally consistent with the estimates of the numbers of deaths in the GBD. The present iteration of the GBD, GBD 2017, improves on previous assessments and provides timely estimates of the mortality experience of populations globally.
METHODS:
The GBD uses all available data to produce estimates of mortality rates between 1950 and 2017 for 23 age groups, both sexes, and 918 locations, including 195 countries and territories and subnational locations for 16 countries. Data used include vital registration systems, sample registration systems, household surveys (complete birth histories, summary birth histories, sibling histories), censuses (summary birth histories, household deaths), and Demographic Surveillance Sites. In total, this analysis used 8259 data sources. Estimates of the probability of death between birth and the age of 5 years and between ages 15 and 60 years are generated and then input into a model life table system to produce complete life tables for all locations and years. Fatal discontinuities and mortality due to HIV/AIDS are analysed separately and then incorporated into the estimation. We analyse the relationship between age-specific mortality and development status using the Socio-demographic Index, a composite measure based on fertility under the age of 25 years, education, and income. There are four main methodological improvements in GBD 2017 compared with GBD 2016: 622 additional data sources have been incorporated; new estimates of population, generated by the GBD study, are used; statistical methods used in different components of the analysis have been further standardised and improved; and the analysis has been extended backwards in time by two decades to start in 1950.
FINDINGS:
Globally, 18·7% (95% uncertainty interval 18·4–19·0) of deaths were registered in 1950 and that proportion has been steadily increasing since, with 58·8% (58·2–59·3) of all deaths being registered in 2015. At the global level, between 1950 and 2017, life expectancy increased from 48·1 years (46·5–49·6) to 70·5 years (70·1–70·8) for men and from 52·9 years (51·7–54·0) to 75·6 years (75·3–75·9) for women. Despite this overall progress, there remains substantial variation in life expectancy at birth in 2017, which ranges from 49·1 years (46·5–51·7) for men in the Central African Republic to 87·6 years (86·9–88·1) among women in Singapore. The greatest progress across age groups was for children younger than 5 years; under-5 mortality dropped from 216·0 deaths (196·3–238·1) per 1000 livebirths in 1950 to 38·9 deaths (35·6–42·83) per 1000 livebirths in 2017, with huge reductions across countries. Nevertheless, there were still 5·4 million (5·2–5·6) deaths among children younger than 5 years in the world in 2017. Progress has been less pronounced and more variable for adults, especially for adult males, who had stagnant or increasing mortality rates in several countries. The gap between male and female life expectancy between 1950 and 2017, while relatively stable at the global level, shows distinctive patterns across super-regions and has consistently been the largest in central Europe, eastern Europe, and central Asia, and smallest in south Asia. Performance was also variable across countries and time in observed mortality rates compared with those expected on the basis of development.
INTERPRETATION:
This analysis of age-sex-specific mortality shows that there are remarkably complex patterns in population mortality across countries. The findings of this study highlight global successes, such as the large decline in under-5 mortality, which reflects significant local, national, and global commitment and investment over several decades. However, they also bring attention to mortality patterns that are a cause for concern, particularly among adult men and, to a lesser extent, women, whose mortality rates have stagnated in many countries over the time period of this study, and in some cases are increasing