106 research outputs found

    Translation-covariant Markovian master equation for a test particle in a quantum fluid

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    A recently proposed master equation in the Lindblad form is studied with respect to covariance properties and existence of a stationary solution. The master equation describes the interaction of a test particle with a quantum fluid, the so-called Rayleigh gas, and is characterized by the appearance of a two-point correlation function known as dynamic structure factor, which reflects symmetry and statistical mechanics properties of the fluid. In the case of a free gas all relevant physical parameters, such as fugacity, ratio between the masses, momentum transfer and energy transfer are put into evidence, giving an exact expansion of the dynamic structure factor. The limit in which these quantities are small is then considered. In particular in the Brownian limit a Fokker-Planck equation is obtained in which the corrections due to quantum statistics can be explicitly evaluated and are given in terms of the Bose function g0(z)g_0 (z) and the Fermi function f0(z)f_0 (z).Comment: 18 pages, revtex, no figures, to appear in J. Math. Phy

    Mismatch repair SNPs and thyroid cancer susceptibility: a potential role for the MSH6 rs1042821 (Gly39Glu) polymorphism

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    Abstract of the Poster presented at the 3rd ESPT Conference (European Society of Pharmacogenomics and Personalised Therapy / European Society of Pharmacogenomics and Theranostics), 7-9 October 2015, Budapest

    Metrics and textural features of MRI diffusion to improve classification of pediatric posterior fossa tumors

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    BACKGROUND AND PURPOSE: Qualitative radiologic MR imaging review affords limited differentiation among types of pediatric posterior fossa brain tumors and cannot detect histologic or molecular subtypes, which could help to stratify treatment. This study aimed to improve current posterior fossa discrimination of histologic tumor type by using support vector machine classifiers on quantitative MR imaging features. MATERIALS AND METHODS: This retrospective study included preoperative MRI in 40 children with posterior fossa tumors (17 medulloblastomas, 16 pilocytic astrocytomas, and 7 ependymomas). Shape, histogram, and textural features were computed from contrast-enhanced T2WI and T1WI and diffusivity (ADC) maps. Combinations of features were used to train tumor-type-specific classifiers for medulloblastoma, pilocytic astrocytoma, and ependymoma types in separation and as a joint posterior fossa classifier. A tumor-subtype classifier was also produced for classic medulloblastoma. The performance of different classifiers was assessed and compared by using randomly selected subsets of training and test data. RESULTS: ADC histogram features (25th and 75th percentiles and skewness) yielded the best classification of tumor type (on average >95.8% of medulloblastomas, >96.9% of pilocytic astrocytomas, and >94.3% of ependymomas by using 8 training samples). The resulting joint posterior fossa classifier correctly assigned >91.4% of the posterior fossa tumors. For subtype classification, 89.4% of classic medulloblastomas were correctly classified on the basis of ADC texture features extracted from the Gray-Level Co-Occurence Matrix. CONCLUSIONS: Support vector machine–based classifiers using ADC histogram features yielded very good discrimination among pediatric posterior fossa tumor types, and ADC textural features show promise for further subtype discrimination. These findings suggest an added diagnostic value of quantitative feature analysis of diffusion MR imaging in pediatric neuro-oncology

    AnĂĄlise da estrutura fatorial da versĂŁo em portuguĂȘs da Escala de Auto-Silenciamento

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    This study focuses on the adaptation of the Portuguese version of the Escala de Autosilenciamiento [EAS, for its Portuguese acronym] (Neves, 2005) that has been designed to assess the use of cognitive schemas for self silencing in intimate relationships. Participants were 371 women with a mean age of 22.36 years (SD=2.69; Min=18; Max=31), who at that time were involved in affective relationships with an average duration of 39.65 months (SD=33.93; Min=10; Max=192).The exploratory factor analysis suggests a factor solution of three factors, where the first factor includes items from the silencing of the sef and divided self subscales. The second factor includes items from the care-giving subscale such as self-sacrifice. And the third factor includes items from the externalized self-perception subscale. Results of the confirmatory factor analysis show reliable global indices of fitness of the model, confirming the quality of the model in terms of adjustment to empirical data (X2/df=1.964, CFI=.862, GFI=.894, RMSEA=.051) compared to the original model. Implications for a further study of the construct validity of the scale are discussed.Este estudo se centra na adaptação da versĂŁo em portuguĂȘs da Escala de Auto-silenciamento (EAS; Neves, 2005) que estĂĄ desenhada para avaliar o uso de esquemas cognitivos de auto-silenciamento nas relaçÔes Ă­ntimas. Neste estudo participaram 371 mulheres, com uma idade mĂ©dia de 22,36 anos (DP = 2,69, mĂ­n. = 18, mĂĄx. = 31), que nessa Ă©poca estavam envolvidas em relaçÔes afetivas com uma duração mĂ©dia de 39,65 meses. (DP = 33,93, mĂ­n. = 0,10; mĂĄx. = 192). Uma anĂĄlise fatorial exploratĂłria posterior sugere uma solução de trĂȘs fatores, aonde o primeiro fator inclui os itens da sub-escala de silenciamento do self e do self dividido; o segundo inclui os itens da sub-escala de ProvisĂŁo de cuidados como o auto sacrifĂ­cio, e o terceiro inclui os itens da sub-escala de auto percepção externalizada. Os resultados da anĂĄlise fatorial confirmatĂłria mostram Ă­ndices gerais de adequação confiĂĄveis, o que confirma a qualidade do ajuste do modelo aos dados empĂ­ricos (X2/df = 1964, CFI = .862, GFI = 0,894, RMSEA = 0,051) em comparação com a teste original. Analisam-se as implicaçÔes para um estudo mĂĄs profundo da validez de constructo da escala.Este estudio se centra en la adaptaciĂłn de la versiĂłn en portuguĂ©s de la Escala de Autosilenciamiento (EAS; Neves, 2005) que estĂĄ diseñada para evaluar el uso de esquemas cognitivos de autosilenciamiento en las relaciones Ă­ntimas. En este estudio participaron 371 mujeres, con una edad media de 22,36 años (DP = 2,69, mĂ­n. = 18, mĂĄx. = 31), que en esa Ă©poca estaban involucradas en relaciones afectivas con una duraciĂłn promedio de 39,65 meses. (DP = 33,93, mĂ­n. = 0,10; mĂĄx. = 192). Un anĂĄlisis factorial exploratorio posterior sugiere una soluciĂłn de tres factores, donde el primer factor incluye los Ă­tems de la subescala de silenciamiento del self y del self dividido; el segundo incluye los Ă­tems de la subescala de ProvisiĂłn de cuidados como el autosacrificio, y el tercero incluye los Ă­tems de la subescala de autopercepciĂłn externalizada. Los resultados del anĂĄlisis factorial confirmatorio muestran Ă­ndices generales de adecuaciĂłn fiables, lo que confirma la calidad del ajuste del modelo a los datos empĂ­ricos (X2/df = 1964, CFI = .862, GFI = 0,894, RMSEA = 0,051) en comparaciĂłn con la prueba original. Se analizan las implicaciones para un estudio mĂĄs profundo de la validez de constructo de la escala

    Why Are Outcomes Different for Registry Patients Enrolled Prospectively and Retrospectively? Insights from the Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF).

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    Background: Retrospective and prospective observational studies are designed to reflect real-world evidence on clinical practice, but can yield conflicting results. The GARFIELD-AF Registry includes both methods of enrolment and allows analysis of differences in patient characteristics and outcomes that may result. Methods and Results: Patients with atrial fibrillation (AF) and ≄1 risk factor for stroke at diagnosis of AF were recruited either retrospectively (n = 5069) or prospectively (n = 5501) from 19 countries and then followed prospectively. The retrospectively enrolled cohort comprised patients with established AF (for a least 6, and up to 24 months before enrolment), who were identified retrospectively (and baseline and partial follow-up data were collected from the emedical records) and then followed prospectively between 0-18 months (such that the total time of follow-up was 24 months; data collection Dec-2009 and Oct-2010). In the prospectively enrolled cohort, patients with newly diagnosed AF (≀6 weeks after diagnosis) were recruited between Mar-2010 and Oct-2011 and were followed for 24 months after enrolment. Differences between the cohorts were observed in clinical characteristics, including type of AF, stroke prevention strategies, and event rates. More patients in the retrospectively identified cohort received vitamin K antagonists (62.1% vs. 53.2%) and fewer received non-vitamin K oral anticoagulants (1.8% vs . 4.2%). All-cause mortality rates per 100 person-years during the prospective follow-up (starting the first study visit up to 1 year) were significantly lower in the retrospective than prospectively identified cohort (3.04 [95% CI 2.51 to 3.67] vs . 4.05 [95% CI 3.53 to 4.63]; p = 0.016). Conclusions: Interpretations of data from registries that aim to evaluate the characteristics and outcomes of patients with AF must take account of differences in registry design and the impact of recall bias and survivorship bias that is incurred with retrospective enrolment. Clinical Trial Registration: - URL: http://www.clinicaltrials.gov . Unique identifier for GARFIELD-AF (NCT01090362)

    Improved risk stratification of patients with atrial fibrillation: an integrated GARFIELD-AF tool for the prediction of mortality, stroke and bleed in patients with and without anticoagulation.

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    OBJECTIVES: To provide an accurate, web-based tool for stratifying patients with atrial fibrillation to facilitate decisions on the potential benefits/risks of anticoagulation, based on mortality, stroke and bleeding risks. DESIGN: The new tool was developed, using stepwise regression, for all and then applied to lower risk patients. C-statistics were compared with CHA2DS2-VASc using 30-fold cross-validation to control for overfitting. External validation was undertaken in an independent dataset, Outcome Registry for Better Informed Treatment of Atrial Fibrillation (ORBIT-AF). PARTICIPANTS: Data from 39 898 patients enrolled in the prospective GARFIELD-AF registry provided the basis for deriving and validating an integrated risk tool to predict stroke risk, mortality and bleeding risk. RESULTS: The discriminatory value of the GARFIELD-AF risk model was superior to CHA2DS2-VASc for patients with or without anticoagulation. C-statistics (95% CI) for all-cause mortality, ischaemic stroke/systemic embolism and haemorrhagic stroke/major bleeding (treated patients) were: 0.77 (0.76 to 0.78), 0.69 (0.67 to 0.71) and 0.66 (0.62 to 0.69), respectively, for the GARFIELD-AF risk models, and 0.66 (0.64-0.67), 0.64 (0.61-0.66) and 0.64 (0.61-0.68), respectively, for CHA2DS2-VASc (or HAS-BLED for bleeding). In very low to low risk patients (CHA2DS2-VASc 0 or 1 (men) and 1 or 2 (women)), the CHA2DS2-VASc and HAS-BLED (for bleeding) scores offered weak discriminatory value for mortality, stroke/systemic embolism and major bleeding. C-statistics for the GARFIELD-AF risk tool were 0.69 (0.64 to 0.75), 0.65 (0.56 to 0.73) and 0.60 (0.47 to 0.73) for each end point, respectively, versus 0.50 (0.45 to 0.55), 0.59 (0.50 to 0.67) and 0.55 (0.53 to 0.56) for CHA2DS2-VASc (or HAS-BLED for bleeding). Upon validation in the ORBIT-AF population, C-statistics showed that the GARFIELD-AF risk tool was effective for predicting 1-year all-cause mortality using the full and simplified model for all-cause mortality: C-statistics 0.75 (0.73 to 0.77) and 0.75 (0.73 to 0.77), respectively, and for predicting for any stroke or systemic embolism over 1 year, C-statistics 0.68 (0.62 to 0.74). CONCLUSIONS: Performance of the GARFIELD-AF risk tool was superior to CHA2DS2-VASc in predicting stroke and mortality and superior to HAS-BLED for bleeding, overall and in lower risk patients. The GARFIELD-AF tool has the potential for incorporation in routine electronic systems, and for the first time, permits simultaneous evaluation of ischaemic stroke, mortality and bleeding risks. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier for GARFIELD-AF (NCT01090362) and for ORBIT-AF (NCT01165710)

    Two-year outcomes of patients with newly diagnosed atrial fibrillation: results from GARFIELD-AF.

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    AIMS: The relationship between outcomes and time after diagnosis for patients with non-valvular atrial fibrillation (NVAF) is poorly defined, especially beyond the first year. METHODS AND RESULTS: GARFIELD-AF is an ongoing, global observational study of adults with newly diagnosed NVAF. Two-year outcomes of 17 162 patients prospectively enrolled in GARFIELD-AF were analysed in light of baseline characteristics, risk profiles for stroke/systemic embolism (SE), and antithrombotic therapy. The mean (standard deviation) age was 69.8 (11.4) years, 43.8% were women, and the mean CHA2DS2-VASc score was 3.3 (1.6); 60.8% of patients were prescribed anticoagulant therapy with/without antiplatelet (AP) therapy, 27.4% AP monotherapy, and 11.8% no antithrombotic therapy. At 2-year follow-up, all-cause mortality, stroke/SE, and major bleeding had occurred at a rate (95% confidence interval) of 3.83 (3.62; 4.05), 1.25 (1.13; 1.38), and 0.70 (0.62; 0.81) per 100 person-years, respectively. Rates for all three major events were highest during the first 4 months. Congestive heart failure, acute coronary syndromes, sudden/unwitnessed death, malignancy, respiratory failure, and infection/sepsis accounted for 65% of all known causes of death and strokes for <10%. Anticoagulant treatment was associated with a 35% lower risk of death. CONCLUSION: The most frequent of the three major outcome measures was death, whose most common causes are not known to be significantly influenced by anticoagulation. This suggests that a more comprehensive approach to the management of NVAF may be needed to improve outcome. This could include, in addition to anticoagulation, interventions targeting modifiable, cause-specific risk factors for death. CLINICAL TRIAL REGISTRATION: http://www.clinicaltrials.gov. Unique identifier: NCT01090362

    Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry.

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    BACKGROUND: The Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF) is an ongoing prospective noninterventional registry, which is providing important information on the baseline characteristics, treatment patterns, and 1-year outcomes in patients with newly diagnosed non-valvular atrial fibrillation (NVAF). This report describes data from Indian patients recruited in this registry. METHODS AND RESULTS: A total of 52,014 patients with newly diagnosed AF were enrolled globally; of these, 1388 patients were recruited from 26 sites within India (2012-2016). In India, the mean age was 65.8 years at diagnosis of NVAF. Hypertension was the most prevalent risk factor for AF, present in 68.5% of patients from India and in 76.3% of patients globally (P < 0.001). Diabetes and coronary artery disease (CAD) were prevalent in 36.2% and 28.1% of patients as compared with global prevalence of 22.2% and 21.6%, respectively (P < 0.001 for both). Antiplatelet therapy was the most common antithrombotic treatment in India. With increasing stroke risk, however, patients were more likely to receive oral anticoagulant therapy [mainly vitamin K antagonist (VKA)], but average international normalized ratio (INR) was lower among Indian patients [median INR value 1.6 (interquartile range {IQR}: 1.3-2.3) versus 2.3 (IQR 1.8-2.8) (P < 0.001)]. Compared with other countries, patients from India had markedly higher rates of all-cause mortality [7.68 per 100 person-years (95% confidence interval 6.32-9.35) vs 4.34 (4.16-4.53), P < 0.0001], while rates of stroke/systemic embolism and major bleeding were lower after 1 year of follow-up. CONCLUSION: Compared to previously published registries from India, the GARFIELD-AF registry describes clinical profiles and outcomes in Indian patients with AF of a different etiology. The registry data show that compared to the rest of the world, Indian AF patients are younger in age and have more diabetes and CAD. Patients with a higher stroke risk are more likely to receive anticoagulation therapy with VKA but are underdosed compared with the global average in the GARFIELD-AF. CLINICAL TRIAL REGISTRATION-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01090362
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