48 research outputs found

    Hidden Trigger for the Giant Starburst Arc in M 83?

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    The huge star formation events that occur at some galactic centers do not provide enough clues as to their origin, since the morphological signatures of the triggering mechanism are smeared out in the timescale of a few orbital revolutions of the galaxy core. Our high spatial resolution three-dimensional near-infrared spectroscopy for the first time reveals that a previously known hidden mass concentration is located exactly at the youngest end of a giant star-forming arc. This location, the inferred average cluster ages, and the dynamical times clearly indicate that the interloper has left behind a spur of violent star formation in M 83, in a transient event lasting less than one orbital revolution. The study of the origin (bar funneling or cannibalized satellite) and fate (black hole merging or giant stellar cluster) of this system could provide clues to the question of core growing and morphological evolution in grand-design spiral galaxies. In particular, our TreeSPH numerical modeling suggests that the two nuclei could coalesce, forming a single massive core in about 60 million years or less

    Discrimination of biclonal B-cell chronic lymphoproliferative neoplasias by tetraspanin antigen expression

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    This work was supported by Grants from MEC SAF2004-02900 (PAL) and SAF 2002-03096 (AO), Fondo de Investigación Sanitaria PI02-0585 (PAL), and Fundación Memoria Samuel Solórzano Barruso (PAL).Peer Reviewe

    The nearest extreme starburst: bubbles, young star clusters, and outflow in NGC 3256

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    In this Work we report, for the extreme starburst in the IR merger NGC 3256: (i) The detection of 4 galactic bubbles, associated with SN explosions.(ii) The first analysis of the spatial distribution of young star clusters (YSC) candidates.(iii) The kinematic study of the ionized gas in the core of of the main optical nucleus, performed with HST STIS spectra. The shape of the rotation curve and the emission line profile could be explained by the presence in the core of YSC with outflow.Comment: 5 pages, 5 figures, Contect Replac., accepted MN-RA

    A multiparameter flow cytometry immunophenotypic algorithm for the identification of newly diagnosed symptomatic myeloma with an MGUS-like signature and long-term disease control

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    GEM (Grupo Español de MM)/PETHEMA (Programa para el Estudio de la Terapéutica en Hemopatías Malignas) cooperative study group: et al.Achieving complete remission (CR) in multiple myeloma (MM) translates into extended survival, but two subgroups of patients fall outside this paradigm: cases with unsustained CR, and patients that do not achieve CR but return into a monoclonal gammopathy of undetermined significance (MGUS)-like status with long-term survival. Here, we describe a novel automated flow cytometric classification focused on the analysis of the plasma-cell compartment to identify among newly diagnosed symptomatic MM patients (N=698) cases with a baseline MGUS-like profile, by comparing them to MGUS (N=497) patients and validating the classification model in 114 smoldering MM patients. Overall, 59 symptomatic MM patients (8%) showed an MGUS-like profile. Despite achieving similar CR rates after high-dose therapy/autologous stem cell transplantation vs other MM patients, MGUS-like cases had unprecedented longer time-to-progression (TTP) and overall survival (OS; ∼60% at 10 years; P<0.001). Importantly, MGUS-like MM patients failing to achieve CR showed similar TTP (P=0.81) and OS (P=0.24) vs cases attaining CR. This automated classification also identified MGUS patients with shorter TTP (P=0.001, hazard ratio: 5.53) and ultra-high-risk smoldering MM (median TTP, 15 months). In summary, we have developed a biomarker that identifies a subset of symptomatic MM patients with an occult MGUS-like signature and an excellent outcome, independently of the depth of response.Peer Reviewe

    Minimal residual disease evaluation by flow cytometry is a complementary tool to cytogenetics for treatment decisions in acute myeloid leukaemia

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    For PETHEMA Programa para el Estudio de la Terapéutica en Hemopatías Malignas Cooperative Study Group.The clinical utility of minimal residual disease (MRD) analysis in acute myeloid leukaemia (AML) is not yet defined. We analysed the prognostic impact of MRD level at complete remision after induction therapy using multiparameter flow cytometry in 306 non-APL AML patients. First, we validated the prognostic value of MRD-thresholds we have previously proposed (≥0.1%; ≥0.01-0.1%; and <0.01), with a 5-year RFS of 38%, 50% and 71%, respectively (p = 0.002). Cytogenetics is the most relevant prognosis factor in AML, however intermediate risk cytogenetics represent a grey zone that require other biomarkers for risk stratification, and we show that MRD evaluation discriminate three prognostic subgroups (p = 0.03). Also, MRD assessments yielded relevant information on favourable and adverse cytogenetics, since patients with favourable cytogenetics and high MRD levels have poor prognosis and patients with adverse cytogenetics but undetectable MRD overcomes the adverse prognosis. Interestingly, in patients with intermediate or high MRD levels, intensification with transplant improved the outcome as compared with chemotherapy, while the type of intensification therapy did not influenced the outcome of patients with low MRD levels. Multivariate analysis revealed age, MRD and cytogenetics as independent variables. Moreover, a scoring system, easy in clinical practice, was generated based on MRD level and cytogenetics.This work was supported in part by Spanish grants from Fondo de Investigación Sanitaria-ISCIII (FIS 00/0023-03, PI12/02321), DGCYT (SAF 94- 0308, SAF2001-1687), Conserjería de Educación de Castilla y León (HUS416A12), and Red Temática de Investigación Cooperativa en Cáncer (RTICC-ISCIII) (RD12/0036/0069).Peer Reviewe

    Long-term effect of 2 intensive statin regimens on treatment and incidence of cardiovascular events in familial hypercholesterolemia : The SAFEHEART study

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    Funding: This study was supported by Fundación Hipercolesterolemia Familiar; Grant G03/181 Grant 08-2008 Centro Nacional de Investigaci?n Cardiovascular (CNIC).Background: Maximal doses of potent statins are the basement of treatment of familial hypercholesterolemia (FH). Little is known about the use of different statin regimens in FH. Objectives: The objectives of the study were to describe the treatment changes and low-density lipoprotein cholesterol (LDL-C) goal achievement with atorvastatin (ATV) and rosuvastatin (RV) in the SAFEHEART cohort, as well as to analyze the incidence of atherosclerotic cardiovascular events (ACVEs) and changes in the cardiovascular risk. Methods: SAFEHEART is a prospective follow-up nationwide cohort study in a molecularly defined FH population. The patients were contacted on a yearly basis to obtain relevant changes in life habits, medication, and ACVEs. Results: A total of 1939 patients were analyzed. Median follow-up was 6.6 years (5-10). The estimated 10-year risk according the SAFEHEART risk equation was 1.61 (0.67-3.39) and 1.22 (0.54-2.93) at enrollment for ATV and RV, respectively (P <.001). There were no significant differences at the follow-up: 1.29 (0.54-2.82) and 1.22 (0.54-2.76) in the ATV and RV groups, respectively (P =.51). Sixteen percent of patients in primary prevention with ATV and 18% with RV achieved an LDL-C <100 mg/dL and 4% in secondary prevention with ATV and 5% with RV achieved an LDL-C <70 mg/dL. The use of ezetimibe was marginally greater in the RV group. One hundred sixty ACVEs occurred during follow-up, being its incidence rate 1.1 events/100 patient-years in the ATV group and 1.2 in the RV group (P =.58). Conclusion: ATV and RV are 2 high-potency statins widely used in FH. Although the reduction in LDL-C levels was greater with RV than with ATV, the superiority of RV for reducing ACVEs was not demonstrated

    AINUR: Atlas of Images of NUclear Rings

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    We present the most complete atlas of nuclear rings to date. We include 113 rings found in 107 galaxies, six of which are elliptical galaxies, five are highly inclined disc galaxies, 18 are unbarred disc galaxies, and 78 are barred disc galaxies. Star-forming nuclear rings occur in 20% of disc galaxies with types between T=-3 and T=7. We aim to explore possible relationships between the size and morphology of the rings and various galactic parameters. We produce colour index and structure maps, as well as Halpha and Paalpha continuum-subtracted images from HST archival data. We derive ellipticity profiles from H-band 2MASS images in order to detect bars and find their metric parameters. We measure the non-axisymmetric torque parameter, Qg, and search for correlations between bar, ring metric parameters, and Qg. Our atlas of nuclear rings includes star-forming and dust rings. Nuclear rings span a range from a few tens of parsecs to a few kiloparsecs in radius. Star-forming nuclear rings can be found in a wide range of morphological types, from S0 to Sd, with a peak in the distribution between Sab and Sb, and without strong preference for barred galaxies. Dust nuclear rings are found in elliptical and S0 galaxies. For barred galaxies, the maximum radius that a nuclear ring can reach is a quarter of the bar radius. We found a nearly random distribution of PA offsets between nuclear rings and bars. There is some evidence that nuclear ring ellipticity is limited by bar ellipticity. We confirm that the maximum relative size of a star-forming nuclear ring is inversely proportional to the non-axisymmetric torque parameter, Qg, and that the origin of nuclear rings, even the ones in non-barred hosts, are closely linked to the existence of dynamical resonances.Comment: Accepted for publication in MNRAS. A full resolution version of the manuscript with high resolution figures can be found at http://www.iac.es/folleto/research/preprints

    Modifiable risk factors associated with prediabetes in men and women: A cross-sectional analysis of the cohort study in primary health care on the evolution of patients with prediabetes

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    Background: Prediabetes is a high-risk state for diabetes development, but little is known about the factors associated with this state. The aim of the study was to identify modifiable risk factors associated with the presence of prediabetes in men and women. Methods: Cohort Study in Primary Health Care on the Evolution of Patients with Prediabetes (PREDAPS-Study) is a prospective study on a cohort of 1184 subjects with prediabetes and another cohort of 838 subjects without glucose metabolism disorders. It is being conducted by 125 general practitioners in Spain. Data for this analysis were collected during the baseline stage in 2012. The modifiable risk factors included were: smoking habit, alcohol consumption, low physical activity, inadequate diet, hypertension, dyslipidemia, and obesity. To assess independent association between each factor and prediabetes, odds ratios (ORs) were estimated using logistic regression models. Results: Abdominal obesity, low plasma levels of high-density lipoprotein cholesterol (HDL-cholesterol), and hypertension were independently associated with the presence of prediabetes in both men and women. After adjusting for all factors, the respective ORs (95% Confidence Intervals) were 1.98 (1.41-2.79), 1.88 (1.23-2.88) and 1.86 (1.39-2.51) for men, and 1.89 (1.36-2.62), 1.58 (1.12-2.23) and 1.44 (1.07-1.92) for women. Also, general obesity was a risk factor in both sexes but did not reach statistical significance among men, after adjusting for all factors. Risky alcohol consumption was a risk factor for prediabetes in men, OR 1.49 (1.00-2.24). Conclusions: Obesity, low HDL-cholesterol levels, and hypertension were modifiable risk factors independently related to the presence of prediabetes in both sexes. The magnitudes of the associations were stronger for men than women. Abdominal obesity in both men and women displayed the strongest association with prediabetes. The findings suggest that there are some differences between men and women, which should be taken into account when implementing specific recommendations to prevent or delay the onset of diabetes in adult population
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