542 research outputs found

    Interleukin-1 beta single-nucleotide polymorphism\u27s C allele is associated with elevated risk of gastric cancer in helicobacter pylori-infected Peruvians

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    Particular alleles of the interleukin-1B (IL-1B) gene have been correlated with increased risk of atrophic gastritis and gastric cancer in the populations of East Asia and Europe. No such data exist from Peru, a developing country with a population genotypically different from others studied and with a high prevalence of Helicobacter pylori infection and gastric cancer. We conducted a case-control study comparing 334 hospitalized patients with atrophic gastritis or gastric cancer with 158 nonatrophic gastritis patients (controls). Conditional logistic regression analysis revealed that an increased risk of atrophic gastritis (odds ratio, 5.60) and gastric cancer (odds ratio, 2.36) was associated with the IL-1B-511 C allele. Our study is the first to establish this allele as a risk for these conditions. Given the high prevalence of H. pylori and recurrence rate after treatment, IL-1B-511 single-nucleotide polymorphism analysis may identify those individuals who would benefit most from robust H. pylori eradication efforts in Peru

    Dyspepsia Symptoms and Helicobacter pylori Infection, Nakuru, Kenya

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    The prevalence of Helicobacter pylori infection was studied in 138 patients with dyspepsia in a hospital in Nakuru, Kenya, and in 138 asymptomatic sex- and age-matched controls from the same population. Anti–H. pylori immunoglobulin (Ig) G was more prevalent in dyspeptic than asymptomatic persons (71% vs. 51%), particularly those <30 years old (71% vs. 38%). H. pylori seropositivity was associated with dyspepsia after adjusting for age, sex, and residence (urban or rural). Among adults, the association between H. pylori infection and dyspepsia remained after adjusting for the above factors and for educational attainment, family size, and manual occupation. H. pylori infection in asymptomatic residents of Nakuru, Kenya, was more prevalent in older persons, with a rate of 68%, than in those 31–40 years of age. However, young persons with dyspepsia had an unexpectedly high prevalence of H. pylori infection. H. pylori test-and-treat strategy should be considered in Kenyan patients with dyspepsia, particularly in persons <30 years of age

    Broad-Range Bacterial Detection and the Analysis of Unexplained Death and Critical Illness

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    Broad-range rDNA polymerase chain reaction (PCR) provides an alternative, cultivation-independent approach for identifying pathogens. In 1995, the Centers for Disease Control and Prevention initiated population-based surveillance for unexplained life-threatening infections (Unexplained Death and Critical Illness Project [UNEX]). To address the causes of UNEX cases, we examined 59 specimens from 46 cases by using broad-range bacterial 16S rDNA PCR and phylogenetic analysis of amplified sequences. Specimens from eight cases yielded sequences from Neisseria meningitidis (cerebrospinal fluid from two patients with meningitis), Streptococcus pneumoniae (cerebrospinal fluid from one patient with meningitis and pleural fluid from two patients with pneumonia), or Stenotrophomonas maltophilia (bone marrow aspirate from one patient with pneumonia). Streptococcus pneumoniae rDNA sequence microheterogeneity was found in one pleural fluid specimen, suggesting the presence of multiple strains. In conclusion, known bacterial pathogens cause some critical illnesses and deaths that fail to be explained with traditional diagnostic methods

    Myocarditis Outbreak among Adults, Illinois, 2003

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    An outbreak of myocarditis occurred among adults in Illinois in 2003. Diagnostic testing of myocardial tissues from 3 patients and comprehensive tests for enterovirus and adenovirus of other specimens from patients were inconclusive. Appropriate specimen collection from patients with idiopathic cardiomyopathy and further enhancement of diagnostic techniques are needed

    Surveillance for Unexplained Deaths and Critical Illnesses

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    Population-based surveillance for unexplained death and critical illness possibly due to infectious causes (UNEX) was conducted in four U.S. Emerging Infections Program sites (population 7.7 million) from May 1, 1995, to December 31, 1998, to define the incidence, epidemiologic features, and etiology of this syndrome. A case was defined as death or critical illness in a hospitalized, previously healthy person, 1 to 49 years of age, with infection hallmarks but no cause identified after routine testing. A total of 137 cases were identified (incidence rate 0.5 per 100,000 per year). Patients’ median age was 20 years, 72 (53%) were female, 112 (82%) were white, and 41 (30%) died. The most common clinical presentations were neurologic (29%), respiratory (27%), and cardiac (21%). Infectious causes were identified for 34 cases (28% of the 122 cases with clinical specimens); 23 (68%) were diagnosed by reference serologic tests, and 11 (32%) by polymerase chain reaction-based methods. The UNEX network model would improve U.S. diagnostic capacities and preparedness for emerging infections

    A measurement of ∆Γs

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    Using a dataset corresponding to 9 fb−1 of integrated luminosity collected with the LHCb detector between 2011 and 2018 in proton-proton collisions, the decay-time distributions of the decay modes Bs 0→J/ψη′ and Bs 0→J/ψπ+π− are studied. The decay-width difference between the light and heavy mass eigenstates of the Bs 0 meson is measured to be ∆Γs = 0.087 ± 0.012 ± 0.009 ps−1, where the first uncertainty is statistical and the second systematic

    Observation of the decays B(s)0Ds1(2536)K±B_{(s)}^{0}\to D_{s1}(2536)^{\mp}K^{\pm}

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    This paper reports the observation of the decays B(s)0Ds1(2536)K±B_{(s)}^{0}\to D_{s1}(2536)^{\mp}K^{\pm} using proton-proton collision data collected by the LHCb experiment, corresponding to an integrated luminosity of 9fb19\,\mathrm{fb}^{-1}. The branching fractions of these decays are measured relative to the normalisation channel B0D0K+KB^{0}\to \overline{D}^{0}K^{+}K^{-}. The Ds1(2536)D_{s1}(2536)^{-} meson is reconstructed in the D(2007)0K\overline{D}^{*}(2007)^{0}K^{-} decay channel and the products of branching fractions are measured to be B(Bs0Ds1(2536)K±)×B(Ds1(2536)D(2007)0K)=(2.49±0.11±0.12±0.25±0.06)×105,\mathcal{B}(B_{s}^{0}\to D_{s1}(2536)^{\mp}K^{\pm})\times\mathcal{B}(D_{s1}(2536)^{-}\to\overline{D}^{*}(2007)^{0}K^{-})=(2.49\pm0.11\pm0.12\pm0.25\pm0.06)\times 10^{-5}, B(B0Ds1(2536)K±)×B(Ds1(2536)D(2007)0K)=(0.510±0.021±0.036±0.050)×105.\mathcal{B}(B^{0}\to D_{s1}(2536)^{\mp}K^{\pm})\times\mathcal{B}(D_{s1}(2536)^{-}\to\overline{D}^{*}(2007)^{0}K^{-}) = (0.510\pm0.021\pm0.036\pm0.050)\times 10^{-5}. The first uncertainty is statistical, the second systematic, and the third arises from the uncertainty of the branching fraction of the B0D0K+KB^{0}\to \overline{D}^{0}K^{+}K^{-} normalisation channel. The last uncertainty in the Bs0B_{s}^{0} result is due to the limited knowledge of the fragmentation fraction ratio, fs/fdf_{s}/f_{d}. The significance for the Bs0B_{s}^{0} and B0B^{0} signals is larger than 10σ10\,\sigma. The ratio of the helicity amplitudes which governs the angular distribution of the Ds1(2536)D(2007)0KD_{s1}(2536)^{-}\to\overline{D}^{*}(2007)^{0}K^{-} decay is determined from the data. The ratio of the SS- and DD-wave amplitudes is found to be 1.11±0.15±0.061.11\pm0.15\pm 0.06 and its phase 0.70±0.09±0.040.70\pm0.09\pm 0.04 rad, where the first uncertainty is statistical and the second systematic.Comment: All figures and tables, along with machine-readable versions and any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2023-014.html (LHCb public pages

    Observation of strangeness enhancement with charmed mesons in high-multiplicity pPbp\mathrm{Pb} collisions at sNN=8.16\sqrt {s_{\mathrm{NN}}}=8.16\,TeV

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    The production of prompt Ds+D^+_{s} and D+D^+ mesons is measured by the LHCb experiment in proton-lead (pPbp\mathrm{Pb}) collisions in both the forward (1.5<y<4.01.5<y^*<4.0) and backward (5.0<y<2.5-5.0<y^*<-2.5) rapidity regions at a nucleon-nucleon center-of-mass energy of sNN=8.16\sqrt {s_{\mathrm{NN}}}=8.16\,TeV. The nuclear modification factors of both Ds+D^+_{s} and D+D^+ mesons are determined as a function of transverse momentum, pTp_{\mathrm{T}}, and rapidity. In addition, the Ds+D^+_{s} to D+D^+ cross-section ratio is measured as a function of the charged particle multiplicity in the event. An enhanced Ds+D^+_{s} to D+D^+ production in high-multiplicity events is observed for the whole measured pTp_{\mathrm{T}} range, in particular at low pTp_{\mathrm{T}} and backward rapidity, where the significance exceeds six standard deviations. This constitutes the first observation of strangeness enhancement in charm quark hadronization in high-multiplicity pPbp\mathrm{Pb} collisions. The results are also qualitatively consistent with the presence of quark coalescence as an additional charm quark hadronization mechanism in high-multiplicity proton-lead collisions.Comment: All figures and tables, along with machine-readable versions and any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2023-021.html (LHCb public pages

    Measurements of the branching fraction ratio B(ϕμ+μ)/B(ϕe+e)\cal{B}(\phi \to \mu^+\mu^-)/\cal{B}(\phi \to e^+e^-) with charm meson decays

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    Measurements of the branching fraction ratio B(ϕμ+μ)/B(ϕe+e){\cal{B}(\phi \to \mu^+ \mu^-)/\cal{B}(\phi\to e^+e^-)} with Ds+π+ϕ{D_{s}^{+} \to \pi^{+} \phi} and D+π+ϕ{D^{+} \to \pi^{+} \phi} decays, denoted RϕπsR^{s}_{\phi \pi} and RϕπdR^{d}_{\phi \pi}, are presented. The analysis is performed using a dataset corresponding to an integrated luminosity of 5.4fb1\,\rm{fb}^{-1} of pppp collision data collected with the LHCb experiment. The branching fractions are normalised with respect to the B+K+J/ψ(e+e){B^{+} \to K^{+} J/\psi(\to e^+e^-)} and B+K+J/ψ(μ+μ){B^{+} \to K^{+} J/\psi(\to \mu^+\mu^-)} decay modes. The combination of the results yields Rϕπ=1.022±0.012(stat)±0.048(syst). R_{\phi \pi} = 1.022 \pm 0.012 \,({\rm stat}) \, \pm 0.048 \,({\rm syst}). The result is compatible with previous measurements of the ϕ+\phi \to \ell^{+}\ell^{-} branching fractions and predictions based on the Standard Model.Comment: All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2023-038.html (LHCb public pages

    Search for CP\textit{CP} violation in the phase space of D0KS0K±πD^{0} \rightarrow K_{S}^{0} K^{\pm} \pi^{\mp} decays with the energy test

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    A search for CP\textit{CP} violation in D0KS0K+πD^{0} \rightarrow K_{S}^{0} K^{+} \pi^{-} and D0KS0Kπ+D^{0} \rightarrow K_{S}^{0} K^{-} \pi^{+} decays is reported. The search is performed using an unbinned model-independent method known as the energy test that probes local CP\textit{CP} violation in the phase space of the decays. The data analysed correspond to an integrated luminosity of 5.4 5.4~fb1^{-1} collected in proton-proton collisions by the LHCb experiment at a centre-of-mass energy of s=13\sqrt{s}=13~TeV, amounting to approximately 950000 and 620000 signal candidates for the D0KS0Kπ+D^{0} \rightarrow K_{S}^{0} K^{-} \pi^{+} and D0KS0K+πD^{0} \rightarrow K_{S}^{0} K^{+} \pi^{-} modes, respectively. The method is validated using D0Kπ+ππ+D^{0} \rightarrow K^{-} \pi^{+} \pi^{-} \pi^{+} and D0KS0π+πD^{0} \rightarrow K_{S}^{0} \pi^{+} \pi^{-} decays, where CP\textit{CP}-violating effects are expected to be negligible, and using background-enhanced regions of the signal decays. The results are consistent with CP\textit{CP} symmetry in both the D0KS0Kπ+D^{0} \rightarrow K_{S}^{0} K^{-} \pi^{+} and the D0KS0K+πD^{0} \rightarrow K_{S}^{0} K^{+} \pi^{-} decays, with pp-values for the hypothesis of no CP\textit{CP} violation of 70% and 66%, respectively.Comment: All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2023-019.html (LHCb public pages
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