2,740 research outputs found
The Diagnosis and Management of Nonalcoholic Fatty Liver Disease: Practice Guidance from the American Association for the Study of Liver Diseases
This guidance provides a data-supported approach to the diagnostic, therapeutic, and preventive aspects of NAFLD care. A âGuidanceâ document is different from a âGuideline.â Guidelines are developed by a multidisciplinary panel of experts and rate the quality (level) of the evidence and the strength of each recommendation using the Grading of Recommendations, Assessment Development, and Evaluation (GRADE) system. A guidance document is developed by a panel of experts in the topic, and guidance statements, not recommendations, are put forward to help clinicians understand and implement the most recent evidence
Measurement of an excess in the yield of J/ at very low in Pb-Pb collisions at = 2.76 TeV
We report on the first measurement of an excess in the yield of J/ at
very low transverse momentum ( GeV/) in peripheral hadronic
Pb-Pb collisions at = 2.76 TeV, performed by ALICE at the
CERN LHC. Remarkably, the measured nuclear modification factor of J/ in
the rapidity range reaches about 7 (2) in the range 0-0.3
GeV/ in the 70-90% (50-70%) centrality class. The J/ production cross
section associated with the observed excess is obtained under the hypothesis
that coherent photoproduction of J/ is the underlying physics mechanism.
If confirmed, the observation of J/ coherent photoproduction in Pb-Pb
collisions at impact parameters smaller than twice the nuclear radius opens new
theoretical and experimental challenges and opportunities. In particular,
coherent photoproduction accompanying hadronic collisions may provide insight
into the dynamics of photoproduction and nuclear reactions, as well as become a
novel probe of the Quark-Gluon Plasma.Comment: 18 pages, 3 captioned figures, 1 table, authors from page 13,
published version, figures at
http://aliceinfo.cern.ch/ArtSubmission/node/191
Body mass index trajectories in young adulthood predict nonâ alcoholic fatty liver disease in middle age: The CARDIA cohort study
Background & AimsNonâ alcoholic fatty liver disease is an epidemic. Identifying modifiable risk factors for nonâ alcoholic fatty liver disease development is essential to design effective prevention programmes. We tested whether 25â year patterns of body mass index change are associated with midlife nonâ alcoholic fatty liver disease.MethodsIn all, 4423 participants from Coronary Artery Risk Development in Young Adults, a prospective populationâ based biracial cohort (age 18â 30), underwent body mass index measurement at baseline (1985â 1986) and 3 or more times over 25Ă years. At Year 25, 3115 had liver fat assessed by nonâ contrast computed tomography. Nonâ alcoholic fatty liver disease was defined as liver attenuation â ¤40 Hounsfield Units after exclusions. Latent mixture modelling identified 25â year trajectories in body mass index per cent change (%Ă ) from baseline.ResultsWe identified four distinct trajectories of BMI%Ă : stable (26.2% of cohort, 25â year BMI %Ă Ă =Ă 3.1%), moderate increase (46.0%, BMI%Ă Ă =Ă 21.7%), high increase (20.9%, BMI%Ă Ă =Ă 41.9%) and extreme increase (6.9%, BMI%Ă Ă =Ă 65.9%). Y25 nonâ alcoholic fatty liver disease prevalence was higher in groups with greater BMI %Ă : 4.1%, 9.3%, 13.0%, and 17.6%, respectively (Pâ trend <.0001). In multivariable analyses, participants with increasing BMI%Ă had increasingly greater odds of nonâ alcoholic fatty liver disease compared to the stable group: OR: 3.35 (95% CI: 2.07â 5.42), 7.80 (4.60â 13.23) and 12.68 (6.68â 24.09) for moderate, high and extreme body mass index increase, respectively. Associations were only moderately attenuated when adjusted for baseline or Y25 body mass index.ConclusionsTrajectories of weight gain during young adulthood are associated with greater nonâ alcoholic fatty liver disease prevalence in midlife independent of metabolic covariates and baseline or concurrent body mass index highlighting the importance of weight maintenance throughout adulthood as a target for primary nonâ alcoholic fatty liver disease prevention.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/142937/1/liv13603.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/142937/2/liv13603_am.pd
First measurement of production in pp collisions at = 7 TeV
The production of the charm-strange baryon is measured for
the first time at the LHC via its semileptonic decay into e
in pp collisions at TeV with the ALICE detector. The transverse
momentum () differential cross section multiplied by the branching
ratio is presented in the interval 1 8 GeV/ at
mid-rapidity, 0.5. The transverse momentum dependence of the
baryon production relative to the D meson production is
compared to predictions of event generators with various tunes of the
hadronisation mechanism, which are found to underestimate the measured
cross-section ratio.Comment: 22 pages, 6 captioned figures, 1 table, authors from page 17,
published version, figures at
http://aliceinfo.cern.ch/ArtSubmission/node/412
Constraining the magnitude of the Chiral Magnetic Effect with Event Shape Engineering in Pb-Pb collisions at = 2.76$ TeV
In ultrarelativistic heavy-ion collisions, the event-by-event variation of
the elliptic flow reflects fluctuations in the shape of the initial state
of the system. This allows to select events with the same centrality but
different initial geometry. This selection technique, Event Shape Engineering,
has been used in the analysis of charge-dependent two- and three-particle
correlations in Pb-Pb collisions at TeV. The
two-particle correlator ,
calculated for different combinations of charges and , is
almost independent of (for a given centrality), while the three-particle
correlator
scales almost linearly both with the event and charged-particle
pseudorapidity density. The charge dependence of the three-particle correlator
is often interpreted as evidence for the Chiral Magnetic Effect (CME), a parity
violating effect of the strong interaction. However, its measured dependence on
points to a large non-CME contribution to the correlator. Comparing the
results with Monte Carlo calculations including a magnetic field due to the
spectators, the upper limit of the CME signal contribution to the
three-particle correlator in the 10-50% centrality interval is found to be
26-33% at 95% confidence level.Comment: 20 pages, 6 captioned figures, 1 tables, authors from page 15,
published version, figures at
http://aliceinfo.cern.ch/ArtSubmission/node/382
Twentyâ fiveâ year trajectories of insulin resistance and pancreatic Ă²â cell response and diabetes risk in nonalcoholic fatty liver disease
Background & AimsInsulin resistance is a risk marker for nonâ alcoholic fatty liver disease, and a risk factor for liver disease progression. We assessed temporal trajectories of insulin resistance and Ă²â cell response to serum glucose concentration throughout adulthood and their association with diabetes risk in nonâ alcoholic fatty liver disease.MethodsThree thousand and sixty participants from Coronary Artery Risk Development in Young Adults, a prospective biâ racial cohort of adults age 18â 30Ă years at baseline (1985â 1986; Y0) who completed up to 5 exams over 25Ă years and had fasting insulin and glucose measurement were included. At Y25 (2010â 2011), nonâ alcoholic fatty liver disease was assessed by noncontrast computed tomography after exclusion of other liver fat causes. Latent mixture modelling identified 25â year trajectories in homeostatic model assessment insulin resistance and Ă²â cell response homeostatic model assessmentâ Ă².ResultsThree distinct trajectories were identified, separately, for homeostatic model assessment insulin resistance (lowâ stable [47%]; moderateâ increasing [42%]; and highâ increasing [12%]) and homeostatic model assessmentâ Ă² (lowâ decreasing [16%]; moderateâ decreasing [63%]; and highâ decreasing [21%]). Y25 nonâ alcoholic fatty liver disease prevalence was 24.5%. Among nonâ alcoholic fatty liver disease, highâ increasing homeostatic model assessment insulin resistance (referent: lowâ stable) was associated with greater prevalent (OR 95% CIĂ =Ă 8.0, 2.0â 31.9) and incident (ORĂ =Ă 10.5, 2.6â 32.8) diabetes after multivariable adjustment including Y0 or Y25 homeostatic model assessment insulin resistance. In contrast, nonâ alcoholic fatty liver disease participants with lowâ decreasing homeostatic model assessmentâ Ă² (referent: highâ decreasing) had the highest odds of prevalent (ORĂ =Ă 14.1, 3.9â 50.9) and incident (ORĂ =Ă 10.3, 2.7â 39.3) diabetes.ConclusionTrajectories of insulin resistance and Ă²â cell response during young and middle adulthood are robustly associated with diabetes risk in nonâ alcoholic fatty liver disease. Thus, how persons with nonâ alcoholic fatty liver disease develop resistance to insulin provides important information about risk of diabetes in midlife above and beyond degree of insulin resistance at the time of nonâ alcoholic fatty liver disease assessment.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/146427/1/liv13747_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/146427/2/liv13747.pd
Prospects for at CERN in NA62
The NA62 experiment will begin taking data in 2015. Its primary purpose is a
10% measurement of the branching ratio of the ultrarare kaon decay , using the decay in flight of kaons in an unseparated
beam with momentum 75 GeV/c.The detector and analysis technique are described
here.Comment: 8 pages for proceedings of 50 Years of CP
Methyl donor deficient diets cause distinct alterations in lipid metabolism but are poorly representative of human NAFLD
Background: Non-alcoholic fatty liver disease (NAFLD) is a global health issue. Dietary methyl donor restriction is used to induce a NAFLD/non-alcoholic steatohepatitis (NASH) phenotype in rodents, however the extent to which this model reflects human NAFLD remains incompletely understood. To address this, we undertook hepatic transcriptional profiling of methyl donor restricted rodents and compared these to published human NAFLD datasets. Â Â Â Â Â Â Â Â Â Â Â Methods: Adult C57BL/6J mice were maintained on control, choline deficient (CDD) or methionine/choline deficient (MCDD) diets for four weeks; the effects on methyl donor and lipid biology were investigated by bioinformatic analysis of hepatic gene expression profiles followed by a cross-species comparison with human expression data of all stages of NAFLD. Results: Compared to controls, expression of the very low density lipoprotein (VLDL) packaging carboxylesterases (Ces1d, Ces1f, Ces3b) and the NAFLD risk allele Pnpla3 were suppressed in MCDD; with Pnpla3 and the liver predominant Ces isoform, Ces3b, also suppressed in CDD. With respect to 1-carbon metabolism, down-regulation of Chka, Chkb, Pcty1a, Gnmt and Ahcy with concurrent upregulation of Mat2a suggests a drive to maintain S-adenosylmethionine levels. There was minimal similarity between global gene expression patterns in either dietary intervention and any stage of human NAFLD, however some common transcriptomic changes in inflammatory, fibrotic and proliferative mediators were identified in MCDD, NASH and HCC. Conclusions: This study suggests suppression of VLDL assembly machinery may contribute to hepatic lipid accumulation in these models, but that CDD and MCDD rodent diets are minimally representative of human NAFLD at the transcriptional level
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