86 research outputs found

    Analysis of arterial sub-trees affected by Pulmonary Emboli

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    ©2004 SPIE--The International Society for Optical Engineering. One print or electronic copy may be made for personal use only. Systematic reproduction and distribution, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper are prohibited. The electronic version of this article is the complete one and can be found online at: http://dx.doi.org/10.1117/12.535993DOI: 10.1117/12.535993Presented at Medical imaging 2004. Image processing : 16-19 February 2004, San Diego, California, USA.Although Pulmonary Embolism (PE) is one of the most common causes of unexpected death in the U.S., it may also be one of the most preventable. Images acquired from 16-slice Computed Tomography (CT) machines of contrast-injected patients provide sufficient resolution for the localization and analysis of emboli located in segmental and sub-segmental arteries. After a PE is found, it is difficult to assess the local characteristics of the affected arterial tree without automation. We propose a method to compute characteristics of the local arterial tree given the location of a PE. The computed information localizes the portion of the arterial tree that is affected by the embolism. Our method is based on the segmentation of the arteries and veins followed by a localized tree computation at the given site. The method determines bifurcation points and the remaining arterial tree. A preliminary segmentation method is also demonstrated to locally eliminate over-segmentation of the arterial tree. The final result can then be used assess the affected lung volume and arterial supply. Initial tests revealed a good ability to compute local tree characteristics of selected sites

    Mathematical modeling of thermal power plant's boiler air-gas flow path regulation modes

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    В работе предлагаются математические модели газовоздушного тракта котла и механизмов собственных нужд ТЭС. С использованием табличных и графических представлений напорных характеристик серийных вентиляторов и дымососов получены эквивалентные соотношения для сети механизмов. Исследована задача нахождения оптимальных параметров управления для группы центробежных механизмов, обеспечивающих работу газовоздушного тракта котла. Исследовано влияние разрежения в топке котла на режим работы его вспомогательных механизмов. Приводятся результаты моделирования для типичных последовательно-параллельных соединений механизмов в гидравлических сетях ТЭС.The paper presents a mathematical model for thermal power plant's boiler air-gas flow paths and auxiliaries. With application of production fans' and flue gas extractor fans' head-capacity curves and tables, equivalent relations for the net of the mechanisms are obtained. A problem of determining the optimal control parameters for a group of centrifugal mechanisms in the air-gas path is studied. The effect of the boiler furnace draft on its auxiliaries operation is analyzed. The results of mathematical modeling for typical serial and parallel connections of the mechanisms in the thermal power plant hydraulic network are given

    West Nile Virus Encephalitis and Myocarditis in Wolf and Dog

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    In the third season (2002) of the West Nile virus epidemic in the United States, two canids (wolf and dog) were diagnosed with West Nile virus encephalitis and myocarditis with similarities to known affected species (humans, horses, and birds). The West Nile virus infections were confirmed by immunohistochemistry and polymerase chain reaction

    Does Proximity to Retailers Influence Alcohol and Tobacco Use Among Latino Adolescents?

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    Despite decades of research surrounding determinants of alcohol and tobacco (A&T) use among adolescents, built environment influences have only recently been explored. This study used ordinal regression on 205 Latino adolescents to explore the influence of the built environment (proximity to A&T retailers) on A&T use, while controlling for recognized social predictors. The sample was 45% foreign-born. A&T use was associated with distance from respondents’ home to the nearest A&T retailer (−), acculturation (+), parents’ consistent use of contingency management (−), peer use of A&T (+), skipping school (+), attending school in immediate proximity to the US/Mexico border (+), and the interaction between the distance to the nearest retailer and parents’ consistent use of contingency management (+). The association between decreasing distance to the nearest A&T retailer and increased A&T use in Latino adolescents reveals an additional risk behavior determinant in the US–Mexico border region

    A genome-wide association study of marginal zone lymphoma shows association to the HLA region

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    Marginal zone lymphoma (MZL) is the third most common subtype of B-cell non-Hodgkin lymphoma. Here we perform a two-stage GWAS of 1,281 MZL cases and 7,127 controls of European ancestry and identify two independent loci near BTNL2 (rs9461741, P - 3.95 x 10(-15)) and HLA-B (rs2922994, P - 2.43 x 10(-9)) in the HLA region significantly associated with MZL risk. This is the first evidence that genetic variation in the major histocompatibility complex influences MZL susceptibility

    Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

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    Genetic association studies have identified 21 loci associated with atopic dermatitis risk predominantly in populations of European ancestry. To identify further susceptibility loci for this common, complex skin disease, we performed a meta-analysis of >15 million genetic variants in 21,399 cases and 95,464 controls from populations of European, African, Japanese and Latino ancestry, followed by replication in 32,059 cases and 228,628 controls from 18 studies. We identified ten new risk loci, bringing the total number of known atopic dermatitis risk loci to 31 (with new secondary signals at four of these loci). Notably, the new loci include candidate genes with roles in the regulation of innate host defenses and T cell function, underscoring the important contribution of (auto)immune mechanisms to atopic dermatitis pathogenesis

    Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

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    Background Huntington's disease is caused by a CAG repeat expansion in the huntingtin gene, HTT. Age at onset has been used as a quantitative phenotype in genetic analysis looking for Huntington's disease modifiers, but is hard to define and not always available. Therefore, we aimed to generate a novel measure of disease progression and to identify genetic markers associated with this progression measure. Methods We generated a progression score on the basis of principal component analysis of prospectively acquired longitudinal changes in motor, cognitive, and imaging measures in the 218 indivduals in the TRACK-HD cohort of Huntington's disease gene mutation carriers (data collected 2008–11). We generated a parallel progression score using data from 1773 previously genotyped participants from the European Huntington's Disease Network REGISTRY study of Huntington's disease mutation carriers (data collected 2003–13). We did a genome-wide association analyses in terms of progression for 216 TRACK-HD participants and 1773 REGISTRY participants, then a meta-analysis of these results was undertaken. Findings Longitudinal motor, cognitive, and imaging scores were correlated with each other in TRACK-HD participants, justifying use of a single, cross-domain measure of disease progression in both studies. The TRACK-HD and REGISTRY progression measures were correlated with each other (r=0·674), and with age at onset (TRACK-HD, r=0·315; REGISTRY, r=0·234). The meta-analysis of progression in TRACK-HD and REGISTRY gave a genome-wide significant signal (p=1·12 × 10−10) on chromosome 5 spanning three genes: MSH3, DHFR, and MTRNR2L2. The genes in this locus were associated with progression in TRACK-HD (MSH3 p=2·94 × 10−8 DHFR p=8·37 × 10−7 MTRNR2L2 p=2·15 × 10−9) and to a lesser extent in REGISTRY (MSH3 p=9·36 × 10−4 DHFR p=8·45 × 10−4 MTRNR2L2 p=1·20 × 10−3). The lead single nucleotide polymorphism (SNP) in TRACK-HD (rs557874766) was genome-wide significant in the meta-analysis (p=1·58 × 10−8), and encodes an aminoacid change (Pro67Ala) in MSH3. In TRACK-HD, each copy of the minor allele at this SNP was associated with a 0·4 units per year (95% CI 0·16–0·66) reduction in the rate of change of the Unified Huntington's Disease Rating Scale (UHDRS) Total Motor Score, and a reduction of 0·12 units per year (95% CI 0·06–0·18) in the rate of change of UHDRS Total Functional Capacity score. These associations remained significant after adjusting for age of onset. Interpretation The multidomain progression measure in TRACK-HD was associated with a functional variant that was genome-wide significant in our meta-analysis. The association in only 216 participants implies that the progression measure is a sensitive reflection of disease burden, that the effect size at this locus is large, or both. Knockout of Msh3 reduces somatic expansion in Huntington's disease mouse models, suggesting this mechanism as an area for future therapeutic investigation
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