529 research outputs found

    Signals of Unconventional E6_6 Models at e+ee^+e^- Colliders

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    Generation dependent discrete symmetries often appear in models derived from superstring theories. In particular, in the framework of E6_6 models the presence of such symmetries is required in order to allow for the radiative generation of naturally small neutrino masses. Recently it was shown that by imposing suitable generation dependent discrete symmetries, a class of models can be consistently constructed in which the three sets of known fermions in each generation do not have the same assignments with respect to the {\bf 27} representation of E6_6. In this scenario, the different embedding in the gauge group of the three generations implies in particular that the known charged leptons couple in a non--universal way to the new neutral gauge bosons (Zβ)(Z_\beta) present in these models. We exploit this fact to study the signature of this class of models at present and future e+ee^+e^- colliders. We show that some signals of deviation from lepton universality as well as some other discrepancies with the standard model predictions which have been observed at the TRISTAN collider in the production rate of μ\mu and τ\tau, can be accounted for if the ZβZ_\beta mass is not much heavier than 300 GeV. We also study the discovery limits for lepton universality violation of this type at LEP-2 and at the 500 GeV e+ee^+e^- Next Linear Collider (NLC). We show that models predicting unconventional assignments for the leptons will give an unmistakable signature, when the ZβZ_\beta mass is as heavy as 800\sim 800 GeV (LEP-2) and 2\sim 2 TeV (NLC).Comment: Plain Tex, 20 pages. 4 PostScript figures (uses `epsf.tex'). Modified file-format. No changes in the tex

    Unconventional superstring derived E6_{\bf 6} models and neutrino phenomenology

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    Conventional superstring derived E6_6 models can accommodate small neutrino masses if a discrete symmetry is imposed which forbids tree level Dirac neutrino masses but allows for radiative mass generation. Since the only possible symmetries of this kind are known to be generation dependent, we explore the possibility that the three sets of light states in each generation do not have the same assignments with respect to the 27 of E6E_6, leading to non universal gauge interactions under the additional U(1)U(1)' factors for the known fermions. We argue that models realising such a scenario are viable, with their structure being constrained mainly by the requirement of the absence of flavor changing neutral currents in the Higgs sector. Moreover, in contrast to the standard case, rank 6 models are not disfavoured with respect to rank 5. By requiring the number of light neutral states to be minimal, these models have an almost unique pattern of neutrino masses and mixings. We construct a model based on the unconventional assignment scenario in which (with a natural choice of the parameters) m_{\nut}\sim O(10)eV is generated at one loop, m_{\num} is generated at two loops and lies in a range interesting for the solar neutrino problem, and \nue remains massless. In addition, since baryon and lepton number are conserved, there is no proton decay in the model. To illustrate the non-standard phenomenology implied by our scheme we also discuss a second scenario in which an attempt for solving the solar neutrino puzzle with matter enhanced oscillations and practically massless neutrinos can be formulated, and in which peculiar effects for the \num --> \nut conversion of the upward-going atmospheric neutrinos could arise as well.Comment: Plain Tex, 33 pages, 3 PostScript figures (uses epsf.tex). Modified file-format. No changes in the tex

    Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort

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    Background: The human chromosomal region 9p21.3 has been shown to be strongly associated with Coronary Heart Disease (CHD) in several Genome-wide Association Studies (GWAS). Recently, this region has also been shown to be associated with Aggressive Periodontitis (AgP), strengthening the hypothesis that the established epidemiological association between periodontitis and CHD is caused by a shared genetic background, in addition to common environmental and behavioural risk factors. However, the size of the analyzed cohorts in this primary analysis was small compared to other association studies on complex diseases. Using our own AgP cohort, we attempted to confirm the described associations for the chromosomal region 9p21.3. Methods: We analyzed our cohort consisting of patients suffering from the most severe form of AgP, generalized AgP (gAgP) (n = 130) and appropriate periodontally healthy control individuals (n = 339) by genotyping four tagging SNPs (rs2891168, rs1333042, rs1333048 and rs496892), located in the chromosomal region 9p21.3, that have been associated with AgP. Results: The results confirmed significant associations between three of the four SNPs and gAgP. The combination of our results with those from the study which described this association for the first time in a meta-analysis of the four tagging SNPs produced clearly lower p-values compared with the results of each individual study. According to these results, the most plausible genetic model for the association of all four tested SNPs with gAgP seems to be the multiplicative one. Conclusion: We positively replicated the finding of an association between the chromosomal region 9p21.3 and gAgP. This result strengthens support for the hypothesis that shared susceptibility genes within this chromosomal locus might be involved in the pathogenesis of both CHD and gAgP

    Mortality profiles in a country facing epidemiological transition: An analysis of registered data

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    BACKGROUND: Sub-national analyses of causes of death and time-trends help to define public health policy priorities. They are particularly important in countries undergoing epidemiological transition like Peru. There are no studies exploring Peruvian national and regional characteristics of such epidemiological transition. We aimed to describe Peru's national and regional mortality profiles between 1996 and 2000. METHODS: Registered mortality data for the study period were corrected for under-registration following standardized methods. Main causes of death by age group and by geographical region were determined. Departmental mortality profiles were constructed to evaluate mortality transition, using 1996 data as baseline. Annual cumulative slopes for the period 1996-2000 were estimated for each department and region. RESULTS: For the study period non-communicable diseases explained more than half of all causes of death, communicable diseases more than one third, and injuries 10.8% of all deaths. Lima accounted for 32% of total population and 20% of total deaths. The Andean region, with 38% of Peru's population, accounted for half of all country deaths. Departmental mortality predominance shifted from communicable diseases in 1996 towards non-communicable diseases and injuries in 2000. Maternal and perinatal conditions, and nutritional deficiencies and nutritional anaemia declined markedly in all departments and regions. Infectious diseases decreased in all regions except Lima. In all regions acute respiratory infections are a leading cause of death, but their proportion ranged from 9.3% in Lima and Callao to 15.3% in the Andean region. Tuberculosis and injuries ranked high in Lima and the Andean region. CONCLUSION: Peruvian mortality shows a double burden of communicable and non-communicable, with increasing importance of non-communicable diseases and injuries. This challenges national and sub-national health system performance and policy making

    Antimicrobial resistance among migrants in Europe: a systematic review and meta-analysis

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    BACKGROUND: Rates of antimicrobial resistance (AMR) are rising globally and there is concern that increased migration is contributing to the burden of antibiotic resistance in Europe. However, the effect of migration on the burden of AMR in Europe has not yet been comprehensively examined. Therefore, we did a systematic review and meta-analysis to identify and synthesise data for AMR carriage or infection in migrants to Europe to examine differences in patterns of AMR across migrant groups and in different settings. METHODS: For this systematic review and meta-analysis, we searched MEDLINE, Embase, PubMed, and Scopus with no language restrictions from Jan 1, 2000, to Jan 18, 2017, for primary data from observational studies reporting antibacterial resistance in common bacterial pathogens among migrants to 21 European Union-15 and European Economic Area countries. To be eligible for inclusion, studies had to report data on carriage or infection with laboratory-confirmed antibiotic-resistant organisms in migrant populations. We extracted data from eligible studies and assessed quality using piloted, standardised forms. We did not examine drug resistance in tuberculosis and excluded articles solely reporting on this parameter. We also excluded articles in which migrant status was determined by ethnicity, country of birth of participants' parents, or was not defined, and articles in which data were not disaggregated by migrant status. Outcomes were carriage of or infection with antibiotic-resistant organisms. We used random-effects models to calculate the pooled prevalence of each outcome. The study protocol is registered with PROSPERO, number CRD42016043681. FINDINGS: We identified 2274 articles, of which 23 observational studies reporting on antibiotic resistance in 2319 migrants were included. The pooled prevalence of any AMR carriage or AMR infection in migrants was 25·4% (95% CI 19·1-31·8; I2 =98%), including meticillin-resistant Staphylococcus aureus (7·8%, 4·8-10·7; I2 =92%) and antibiotic-resistant Gram-negative bacteria (27·2%, 17·6-36·8; I2 =94%). The pooled prevalence of any AMR carriage or infection was higher in refugees and asylum seekers (33·0%, 18·3-47·6; I2 =98%) than in other migrant groups (6·6%, 1·8-11·3; I2 =92%). The pooled prevalence of antibiotic-resistant organisms was slightly higher in high-migrant community settings (33·1%, 11·1-55·1; I2 =96%) than in migrants in hospitals (24·3%, 16·1-32·6; I2 =98%). We did not find evidence of high rates of transmission of AMR from migrant to host populations. INTERPRETATION: Migrants are exposed to conditions favouring the emergence of drug resistance during transit and in host countries in Europe. Increased antibiotic resistance among refugees and asylum seekers and in high-migrant community settings (such as refugee camps and detention facilities) highlights the need for improved living conditions, access to health care, and initiatives to facilitate detection of and appropriate high-quality treatment for antibiotic-resistant infections during transit and in host countries. Protocols for the prevention and control of infection and for antibiotic surveillance need to be integrated in all aspects of health care, which should be accessible for all migrant groups, and should target determinants of AMR before, during, and after migration. FUNDING: UK National Institute for Health Research Imperial Biomedical Research Centre, Imperial College Healthcare Charity, the Wellcome Trust, and UK National Institute for Health Research Health Protection Research Unit in Healthcare-associated Infections and Antimictobial Resistance at Imperial College London
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