77 research outputs found

    Distance spectral conditions for IDID-factor-critical and fractional [a,b][a, b]-factor of graphs

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    Let G=(V(G),E(G))G=(V(G), E(G)) be a graph with vertex set V(G)V(G) and edge set E(G)E(G). A graph is IDID-factor-critical if for every independent set II of GG whose size has the same parity as V(G)|V(G)|, GIG-I has a perfect matching. For two positive integers aa and bb with aba\leq b, let hh: E(G)[0,1]E(G)\rightarrow [0, 1] be a function on E(G)E(G) satisfying aeEG(vi)h(e)ba\leq\sum _{e\in E_{G}(v_{i})}h(e)\leq b for any vertex viV(G)v_{i}\in V(G). Then the spanning subgraph with edge set EhE_{h}, denoted by G[Eh]G[E_{h}], is called a fractional [a,b][a, b]-factor of GG with indicator function hh, where Eh={eE(G)h(e)>0}E_{h}=\{e\in E(G)\mid h(e)>0\} and EG(vi)={eE(G)eE_{G}(v_{i})=\{e\in E(G)\mid e is incident with viv_{i} in GG\}. A graph is defined as a fractional [a,b][a, b]-deleted graph if for any eE(G)e\in E(G), GeG-e contains a fractional [a,b][a, b]-factor. For any integer k1k\geq 1, a graph has a kk-factor if it contains a kk-regular spanning subgraph. In this paper, we firstly give a distance spectral radius condition of GG to guarantee that GG is IDID-factor-critical. Furthermore, we provide sufficient conditions in terms of distance spectral radius and distance signless Laplacian spectral radius for a graph to contain a fractional [a,b][a, b]-factor, fractional [a,b][a, b]-deleted-factor and kk-factor.Comment: 10 page

    Gardy Loo 2010 Fall

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    https://commons.lib.jmu.edu/gardyloo201019/1015/thumbnail.jp

    Experimental investigation of the two-phase local heat transfer coefficients for condensation of R134a in a micro-structured plate heat exchanger

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    Plate heat exchangers are widely used for two-phase heat transfer in the industrial applications, and recently more attention has been paid to the plate heat exchangers with enhanced surface due to their better heat transfer performance. In this paper, the local condensation heat transfer coefficients are studied using R134a in a micro-structured plate heat exchanger. In order to obtain a more accurate prediction model, a series of measurements are conducted under various operating conditions. The mass flux of R134a varied from 47 kg/m2s to 77 kg/m2s, the saturation pressure in the condenser ranged from 6.32 bar to 8.95 bar, and the value of the heat flux was between 13 kW/m2 and 22 kW/m2. The local two-phase Nusselt number increases with the increase of the mass flux. As the saturation pressure increases, the local two-phase Nusselt number increase at the beginning of the condensation and decrease at the end of the condensation. However, the effect of heat flux on local heat transfer is irregular, due to the interaction of these parameters in the experiment. Comparing with the unstructured plate heat exchanger, R134a condenses faster at the beginning of the process in the micro-sturctured plate heat exchanger, and the local heat transfer performs better when the vapor quality is lower. Combing with the phenomenon that the overall heat flux in micro-structured plate is larger under the same working conditions, it shows that the overall heat transfer of the micro-structured plate is improved, but the local heat transfer uprades only at lower vapor qualities. A new correlation is developed, it predicts all the experimental data within the root mean square error 10%, and a new correlation for the waterside is suggested as well. © 2021, The Author(s)

    Lipidomic landscape of lipokines in adipose tissue derived extracellular vesicles

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    Introduction: Adipose tissue-derived extracellular vesicles (EVs-AT) are recognized as critical mediators of metabolic alterations in obesity-related diseases. However, few studies have focused on the role of lipids within EVs-AT in the development of obesity-related diseases.Methods: In this study, we performed a targeted lipidomic analysis to compare the lipidome of EVs secreted by inguinal white adipose tissue (EVs-iWAT), epididymal white adipose tissue (EVs-eWAT), and interscapular brown adipose tissue (EVs-BAT) in lean and obese mice.Results: We uncovered a comprehensive lipidomic map, revealing the diversity and specific lipid sorting in EVs-iWAT, EVs-eWAT, and EVs-BAT in obesity. Biological function analyses suggested that lipids encapsulated within EVs-AT of obese individuals might correlate with metabolism, pro-inflammatory response, and insulin resistance. These effects were particularly pronounced in EVs-eWAT and EVs-BAT.Conclusion: Our findings indicated that EVs-AT serves as novel carriers for lipokines, thereby mediating the biological functions of EVs-AT. This study holds promise for the identification of new biomarkers for obesity-related diseases and the development of new strategies to combat metabolic diseases

    An improvement of sufficient condition for kk-leaf-connected graphs

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    For integer k2,k\geq2, a graph GG is called kk-leaf-connected if V(G)k+1|V(G)|\geq k+1 and given any subset SV(G)S\subseteq V(G) with S=k,|S|=k, GG always has a spanning tree TT such that SS is precisely the set of leaves of T.T. Thus a graph is 22-leaf-connected if and only if it is Hamilton-connected. In this paper, we present a best possible condition based upon the size to guarantee a graph to be kk-leaf-connected, which not only improves the results of Gurgel and Wakabayashi [On kk-leaf-connected graphs, J. Combin. Theory Ser. B 41 (1986) 1-16] and Ao, Liu, Yuan and Li [Improved sufficient conditions for kk-leaf-connected graphs, Discrete Appl. Math. 314 (2022) 17-30], but also extends the result of Xu, Zhai and Wang [An improvement of spectral conditions for Hamilton-connected graphs, Linear Multilinear Algebra, 2021]. Our key approach is showing that an (n+k1)(n+k-1)-closed non-kk-leaf-connected graph must contain a large clique if its size is large enough. As applications, sufficient conditions for a graph to be kk-leaf-connected in terms of the (signless Laplacian) spectral radius of GG or its complement are also presented.Comment: 15 pages, 2 figure

    Transforming unstructured digital clinical notes for improved health literacy

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    Purpose – Clinical notes typically contain medical jargons and specialized words and phrases that are complicated and technical to most people, which is one of the most challenging obstacles in health information dissemination to consumers by healthcare providers. The authors aim to investigate how to leverage machine learning techniques to transform clinical notes of interest into understandable expressions. Design/methodology/approach – The authors propose a natural language processing pipeline that is capable of extracting relevant information from long unstructured clinical notes and simplifying lexicons by replacing medical jargons and technical terms. Particularly, the authors develop an unsupervised keywords matching method to extract relevant information from clinical notes. To automatically evaluate completeness of the extracted information, the authors perform a multi-label classification task on the relevant texts. To simplify lexicons in the relevant text, the authors identify complex words using a sequence labeler and leverage transformer models to generate candidate words for substitution. The authors validate the proposed pipeline using 58,167 discharge summaries from critical care services. Findings – The results show that the proposed pipeline can identify relevant information with high completeness and simplify complex expressions in clinical notes so that the converted notes have a high level of readability but a low degree of meaning change. Social implications – The proposed pipeline can help healthcare consumers well understand their medical information and therefore strengthen communications between healthcare providers and consumers for better care. Originality/value – An innovative pipeline approach is developed to address the health literacy problem confronted by healthcare providers and consumers in the ongoing digital transformation process in the healthcare industry

    Risk factors for the development of hepatocellular carcinoma (HCC) in chronic hepatitis B virus (HBV) infection:a systematic review and meta-analysis

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    Hepatocellular carcinoma (HCC) is one of the leading contributors to cancer mortality worldwide and is a leading cause of death in individuals with chronic hepatitis B virus (HBV) infection. It is uncertain how the presence of other metabolic factors and comorbidities influences HCC risk in HBV. Therefore, we performed a systematic literature review and meta‐analysis to seek evidence for significant associations. MEDLINE, EMBASE and Web of Science databases were searched from 1 January 2000 to 24 June 2020 for studies investigating associations of metabolic factors and comorbidities with HCC risk in individuals with chronic HBV infection, written in English. We extracted data for meta‐analysis and generated pooled effect estimates from a fixed‐effects model. Pooled estimates from a random‐effects model were also generated if significant heterogeneity was present. We identified 40 observational studies reporting on associations of diabetes mellitus (DM), hypertension, dyslipidaemia and obesity with HCC risk. Only DM had a sufficient number of studies for meta‐analysis. DM was associated with >25% increase in hazards of HCC (fixed‐effects hazards ratio [HR] 1.26, 95% confidence interval (CI) 1.20–1.32, random‐effects HR 1.36, 95% CI 1.23–1.49). This association was attenuated towards the null in a sensitivity analysis restricted to studies adjusted for metformin use. In conclusion, in adults with chronic HBV infection, DM is a significant risk factor for HCC, but further investigation of the influence of antidiabetic drug use and glycaemic control on this association is needed. Enhanced screening of individuals with HBV and diabetes may be warranted

    Estimating the epidemiology of chronic Hepatitis B Virus (HBV) infection in the UK: what do we know and what are we missing?

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    Background: HBV is the leading global cause of cirrhosis and primary liver cancer. However, the UK HBV population has not been well characterised, and estimates of UK HBV prevalence and/or incidence vary widely between sources. We aimed to i) extract and summarise existing national HBV prevalence estimates, ii) add a new estimate based on primary care data, and; iii) critique data sources from which estimates were derived. Methods: We undertook a narrative review, searching for national estimates of CHB case numbers in the UK (incorporating incidence, prevalence and/or test positivity data) across a range of overlapping sources, including governmental body reports, publications from independent bodies (including medical charities and non-governmental organisations) and articles in peer-reviewed scientific journals. An alternative proxy for population prevalence was obtained via the UK antenatal screening programme which achieves over 95% coverage of pregnant women. We also searched for diagnoses of HBV in the QResearch primary care database based on laboratory tests and standardised coding. Results: We identified six CHB case number estimates, of which three reported information concerning population subgroups, including number of infected individuals across age, sex and ethnicity categories. Estimates among sources reporting prevalence varied from 0.27% to 0.73%, congruent with an estimated antenatal CHB prevalence of <0.5%. Our estimate, based on QResearch data, suggests a population prevalence of ~0.05%, reflecting a substantial underestimation based on primary care records. Discussion: Estimates varied by sources of error, bias and missingness, data linkage, and “blind spots” in HBV diagnoses testing/registration. The UK HBV burden is likely to be concentrated in vulnerable populations who may not be well represented in existing datasets including those experiencing socioeconomic deprivation and/or homelessness, ethnic minorities and people born in high-prevalence countries. This could lead to under- or over-estimation of population prevalence estimation. Multi-agency collaboration is required to fill evidence gaps

    Estimating the epidemiology of chronic Hepatitis B Virus (HBV) infection in the UK: what do we know and what are we missing?

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    Background: HBV is the leading global cause of cirrhosis and primary liver cancer. However, the UK HBV population has not been well characterised, and estimates of UK HBV prevalence and/or incidence vary widely between sources. We summarised datasets that are available to represent UK CHB epidemiology, considering differences between sources, and discussing deficiencies in current estimates. Methods: We searched for estimates of CHB case numbers in the UK (incorporating incidence and/or prevalence-like data) across a range of available sources, including UK-wide reports from government bodies, publications from independent bodies (including medical charities and non-governmental organisations) and articles in peer-reviewed scientific journals to collate estimated positivity rates. An alternative proxy for population prevalence was obtained via the UK antenatal screening programme which achieves over 95% coverage of pregnant women. Results: We identified six CHB case number estimates, of which three reported information concerning population subgroups, including number of infected individuals across age, sex and ethnicity categories. Estimates among sources reporting prevalence varied from 0.27% to 0.73%, congruent with an estimated antenatal CHB prevalence of <0.5%. Discussion: Estimates varied by sources of error, bias and missingness, data linkage, and substantial “blind spots” in consistent testing and registration of HBV diagnoses. The HBV burden in the UK is likely to be concentrated in vulnerable populations who may not be well represented in existing datasets including those experiencing socioeconomic deprivation, ethnic minorities, people experiencing homelessness and people born in high-prevalence countries. Together, these factors could lead to either under- or over-estimation of overall prevalence, and additional efforts are required to provide estimates that best reflect the whole population. Multi-parameter evidence synthesis and back-calculation model methods similar to those used to generate estimates of HCV ad HIV population-wide prevalence may be applicable to HBV

    Prevalence of Low Bone Mass and Osteoporosis in Ireland: the Dual‐Energy X‐Ray Absorptiometry (DXA) Health Informatics Prediction (HIP) Project

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    Osteoporosis is a common disease that has a significant impact on patients, healthcare systems, and society. World Health Organization (WHO) diagnostic criteria for postmenopausal women were established in 1994 to diagnose low bone mass (osteopenia) and osteoporosis using dual‐energy X‐ray absorptiometry (DXA)‐measured bone mineral density (BMD) to help understand the epidemiology of osteoporosis, and identify those at risk for fracture. These criteria may also apply to men ≥50 years, perimenopausal women, and people of different ethnicity. The DXA Health Informatics Prediction (HIP) project is an established convenience cohort of more than 36,000 patients who had a DXA scan to explore the epidemiology of osteoporosis and its management in the Republic of Ireland where the prevalence of osteoporosis remains unknown. In this article we compare the prevalence of a DXA classification low bone mass (T‐score < −1.0) and of osteoporosis (T‐score ≤ −2.5) among adults aged ≥40 years without major risk factors or fractures, with one or more major risk factors, and with one or more major osteoporotic fractures. A total of 33,344 subjects met our study inclusion criteria, including 28,933 (86.8%) women; 9362 had no fractures or major risk factors, 14,932 had one or more major clinical risk factors, and 9050 had one or more major osteoporotic fractures. The prevalence of low bone mass and osteoporosis increased significantly with age overall. The prevalence of low bone mass and osteoporosis was significantly greater among men and women with major osteoporotic fractures than healthy controls or those with clinical risk factors. Applying our results to the national population census figure of 5,123,536 in 2022 we estimate between 1,039,348 and 1,240,807 men and women aged ≥50 years have low bone mass, whereas between 308,474 and 498,104 have osteoporosis. These data are important for the diagnosis of osteoporosis in clinical practice, and national policy to reduce the illness burden of osteoporosis. © 2023 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research. Abstract Osteoporosis prevalence in Republic of Irelan
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