109 research outputs found
Investigation on serum hormonal parameters (ghrelin, corticosterone, insulin, t3 and t4) in chronic mild stress rat model of depression
Measurement of asymmetries and branching-fraction ratios for and with using Belle and Belle II data
We measure asymmetries and branching-fraction ratios for and decays with , where
is a superposition of and . We use the full data set of the
Belle experiment, containing pairs, and data from the
Belle~II experiment, containing pairs, both collected
in electron-positron collisions at the resonance. Our results
provide model-independent information on the unitarity triangle angle .Comment: 26 pages, 8 figure
Tests of light-lepton universality in angular asymmetries of decays
We present the first comprehensive tests of light-lepton universality in the
angular distributions of semileptonic \Bz-meson decays to charged spin-1
charmed mesons. We measure five angular-asymmetry observables as functions of
the decay recoil that are sensitive to lepton-universality-violating
contributions. We use events where one neutral \B is fully reconstructed in
\PUpsilonFourS{} \to\B\overline{B} decays in data corresponding to \lumion
integrated luminosity from electron-positron collisions collected with the
\belletwo detector. We find no significant deviation from the standard model
expectations
Search for an invisible in a final state with two muons and missing energy at Belle II
The extension of the standard model predicts the existence
of a lepton-flavor-universality-violating boson that couples only
to the heavier lepton families. We search for such a through its
invisible decay in the process . We use a
sample of electron-positron collisions at a center-of-mass energy of 10.58GeV
collected by the Belle II experiment in 2019-2020, corresponding to an
integrated luminosity of 79.7fb. We find no excess over the expected
standard-model background. We set 90-confidence-level upper limits on the
cross section for this process as well as on the coupling of the model, which
ranges from at low masses to 1 at
masses of 8
Measurement of the branching fraction and asymmetry of decays using pairs in Belle II data
We report measurements of the branching fraction and asymmetry in
decays reconstructed at Belle II in an
electron-positron collision sample containing
pairs. We measure a branching fraction \mathcal{B}(\Bpipi) =
(1.38 \pm 0.27 \pm 0.22) \times 10^{-6} and a asymmetry \Acp(\Bpipi)
= 0.14 \pm 0.46 \pm 0.07, where the first uncertainty is statistical and the
second is systematic
Measurement of branching fractions and direct asymmetries for and decays at Belle II
We report measurements of the branching fractions and direct
asymmetries of the decays , , , and , and use these for testing the standard
model through an isospin-based sum rule. In addition, we measure the branching
fraction and direct asymmetry of the decay and
the branching fraction of the decay . The data are
collected with the Belle II detector from collisions at the
resonance produced by the SuperKEKB asymmetric-energy collider
and contain bottom-antibottom meson pairs. Signal yields are
determined in two-dimensional fits to background-discriminating variables, and
range from 500 to 3900 decays, depending on the channel. We obtain for the sum rule, in agreement with the standard model
expectation of zero and with a precision comparable to the best existing
determinations
Burden of disease scenarios for 204 countries and territories, 2022–2050: a forecasting analysis for the Global Burden of Disease Study 2021
Background: Future trends in disease burden and drivers of health are of great interest to policy makers and the public at large. This information can be used for policy and long-term health investment, planning, and prioritisation. We have expanded and improved upon previous forecasts produced as part of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) and provide a reference forecast (the most likely future), and alternative scenarios assessing disease burden trajectories if selected sets of risk factors were eliminated from current levels by 2050. Methods: Using forecasts of major drivers of health such as the Socio-demographic Index (SDI; a composite measure of lag-distributed income per capita, mean years of education, and total fertility under 25 years of age) and the full set of risk factor exposures captured by GBD, we provide cause-specific forecasts of mortality, years of life lost (YLLs), years lived with disability (YLDs), and disability-adjusted life-years (DALYs) by age and sex from 2022 to 2050 for 204 countries and territories, 21 GBD regions, seven super-regions, and the world. All analyses were done at the cause-specific level so that only risk factors deemed causal by the GBD comparative risk assessment influenced future trajectories of mortality for each disease. Cause-specific mortality was modelled using mixed-effects models with SDI and time as the main covariates, and the combined impact of causal risk factors as an offset in the model. At the all-cause mortality level, we captured unexplained variation by modelling residuals with an autoregressive integrated moving average model with drift attenuation. These all-cause forecasts constrained the cause-specific forecasts at successively deeper levels of the GBD cause hierarchy using cascading mortality models, thus ensuring a robust estimate of cause-specific mortality. For non-fatal measures (eg, low back pain), incidence and prevalence were forecasted from mixed-effects models with SDI as the main covariate, and YLDs were computed from the resulting prevalence forecasts and average disability weights from GBD. Alternative future scenarios were constructed by replacing appropriate reference trajectories for risk factors with hypothetical trajectories of gradual elimination of risk factor exposure from current levels to 2050. The scenarios were constructed from various sets of risk factors: environmental risks (Safer Environment scenario), risks associated with communicable, maternal, neonatal, and nutritional diseases (CMNNs; Improved Childhood Nutrition and Vaccination scenario), risks associated with major non-communicable diseases (NCDs; Improved Behavioural and Metabolic Risks scenario), and the combined effects of these three scenarios. Using the Shared Socioeconomic Pathways climate scenarios SSP2-4.5 as reference and SSP1-1.9 as an optimistic alternative in the Safer Environment scenario, we accounted for climate change impact on health by using the most recent Intergovernmental Panel on Climate Change temperature forecasts and published trajectories of ambient air pollution for the same two scenarios. Life expectancy and healthy life expectancy were computed using standard methods. The forecasting framework includes computing the age-sex-specific future population for each location and separately for each scenario. 95% uncertainty intervals (UIs) for each individual future estimate were derived from the 2·5th and 97·5th percentiles of distributions generated from propagating 500 draws through the multistage computational pipeline. Findings: In the reference scenario forecast, global and super-regional life expectancy increased from 2022 to 2050, but improvement was at a slower pace than in the three decades preceding the COVID-19 pandemic (beginning in 2020). Gains in future life expectancy were forecasted to be greatest in super-regions with comparatively low life expectancies (such as sub-Saharan Africa) compared with super-regions with higher life expectancies (such as the high-income super-region), leading to a trend towards convergence in life expectancy across locations between now and 2050. At the super-region level, forecasted healthy life expectancy patterns were similar to those of life expectancies. Forecasts for the reference scenario found that health will improve in the coming decades, with all-cause age-standardised DALY rates decreasing in every GBD super-region. The total DALY burden measured in counts, however, will increase in every super-region, largely a function of population ageing and growth. We also forecasted that both DALY counts and age-standardised DALY rates will continue to shift from CMNNs to NCDs, with the most pronounced shifts occurring in sub-Saharan Africa (60·1% [95% UI 56·8–63·1] of DALYs were from CMNNs in 2022 compared with 35·8% [31·0–45·0] in 2050) and south Asia (31·7% [29·2–34·1] to 15·5% [13·7–17·5]). This shift is reflected in the leading global causes of DALYs, with the top four causes in 2050 being ischaemic heart disease, stroke, diabetes, and chronic obstructive pulmonary disease, compared with 2022, with ischaemic heart disease, neonatal disorders, stroke, and lower respiratory infections at the top. The global proportion of DALYs due to YLDs likewise increased from 33·8% (27·4–40·3) to 41·1% (33·9–48·1) from 2022 to 2050, demonstrating an important shift in overall disease burden towards morbidity and away from premature death. The largest shift of this kind was forecasted for sub-Saharan Africa, from 20·1% (15·6–25·3) of DALYs due to YLDs in 2022 to 35·6% (26·5–43·0) in 2050. In the assessment of alternative future scenarios, the combined effects of the scenarios (Safer Environment, Improved Childhood Nutrition and Vaccination, and Improved Behavioural and Metabolic Risks scenarios) demonstrated an important decrease in the global burden of DALYs in 2050 of 15·4% (13·5–17·5) compared with the reference scenario, with decreases across super-regions ranging from 10·4% (9·7–11·3) in the high-income super-region to 23·9% (20·7–27·3) in north Africa and the Middle East. The Safer Environment scenario had its largest decrease in sub-Saharan Africa (5·2% [3·5–6·8]), the Improved Behavioural and Metabolic Risks scenario in north Africa and the Middle East (23·2% [20·2–26·5]), and the Improved Nutrition and Vaccination scenario in sub-Saharan Africa (2·0% [–0·6 to 3·6]). Interpretation: Globally, life expectancy and age-standardised disease burden were forecasted to improve between 2022 and 2050, with the majority of the burden continuing to shift from CMNNs to NCDs. That said, continued progress on reducing the CMNN disease burden will be dependent on maintaining investment in and policy emphasis on CMNN disease prevention and treatment. Mostly due to growth and ageing of populations, the number of deaths and DALYs due to all causes combined will generally increase. By constructing alternative future scenarios wherein certain risk exposures are eliminated by 2050, we have shown that opportunities exist to substantially improve health outcomes in the future through concerted efforts to prevent exposure to well established risk factors and to expand access to key health interventions. Funding: Bill & Melinda Gates Foundation
Search for a resonance in events with the Belle II experiment
We report the first search for a non-standard-model resonance decaying into
pairs in events in
the 3.6-10 GeV/ mass range. We use a 62.8 fb sample of
collisions collected at a center-of-mass energy of 10.58 GeV by the Belle II
experiment at the SuperKEKB collider. The analysis probes three different
models predicting a spin-1 particle coupling only to the heavier lepton
families, a Higgs-like spin-0 particle that couples preferentially to charged
leptons (leptophilic scalar), and an axion-like particle, respectively. We
observe no evidence for a signal and set exclusion limits at 90% confidence
level on the product of cross section and branching fraction into pairs,
ranging from 0.7 fb to 24 fb, and on the couplings of these processes. We
obtain world-leading constraints on the couplings for the leptophilic scalar
model for masses above 6.5 GeV/ and for the axion-like particle model over
the entire mass range
Measurement of asymmetries in decays with Belle II
We present a measurement of time-dependent rate asymmetries in decays to search for non-standard-model physics in transitions. The data sample is collected with the Belle II
detector at the SuperKEKB asymmetric-energy collider in 2019-2022
and contains bottom-antibottom mesons from
resonance decays. We reconstruct signal events and
extract the charge-parity () violating parameters from a fit to the
distribution of the proper-decay-time difference of the two mesons. The
measured direct and mixing-induced asymmetries are
and , respectively, where the first
uncertainties are statistical and the second are systematic. The results are
compatible with the asymmetries observed in
transitions
Observation of decays using the 2019-2022 Belle II data sample
We present a measurement of the branching fractions of four decay modes. The measurement is based on data from
SuperKEKB electron-positron collisions at the resonance
collected with the Belle II detector and corresponding to an integrated
luminosity of . The event yields are extracted from fits
to the distributions of the difference between expected and observed meson
energy to separate signal and background, and are efficiency-corrected as a
function of the invariant mass of the system. We find the branching
fractions to be: where the first uncertainty is statistical and
the second systematic. These results include the first observation of
, , and decays and a significant improvement in the precision
of compared to previous measurements
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