41 research outputs found

    Anti-embolism devices therapy to improve the ICU mortality rate of patients with acute myocardial infarction and type II diabetes mellitus

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    BackgroundAnti-Embolism (AE) devices therapy is an additional antithrombotic treatment that is effective in many venous diseases, but the correlations between this medical compression therapy and cardiovascular arterial disease or comorbid diabetes mellitus (DM) are still controversial. In this study we investigated the association between compression therapy and intensive care unit (ICU) mortality in patients with a first acute myocardial infarction (AMI) diagnosis complicated with type II DM.MethodsThis retrospective cohort study analyzed all patients with AMI and type II DM in the Medical Information Mart for Intensive Care-IV database. We extracted the demographics, vital signs, laboratory test results, comorbidities, and scoring system results of patients from the first 24 h after ICU admission. The outcomes of this study were 28-day mortality and ICU mortality. Analyses included Kaplan–Meier survival analysis, Cox proportional-hazards regression, and subgroup analysis.ResultsThe study included 985 eligible patients with AMI and type II DM, of who 293 and 692 were enrolled into the no-AE device therapy and AE device therapy groups, respectively. In the multivariate analysis, compared with no-AE device therapy, AE device therapy was a significant predictor of 28-day mortality (OR = 0.48, 95% CI = 0.24–0.96, P = 0.039) and ICU mortality (OR = 0.50, 95% CI = 0.27–0.90, P = 0.021). In addition to age, gender and coronary artery bypass grafting surgery, there were no significant interactions of AE device therapy and other related risk factors with ICU mortality and 28-day mortality in the subgroup analysis.ConclusionsSimple-AE-device therapy was associated with reduced risks of ICU mortality and 28-day mortality, as well as an improvement in the benefit on in-hospital survival in patients with AMI complicated with type II DM

    Neurophysiological features of STN LFP underlying sleep fragmentation in Parkinson’s disease

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    Background: Sleep fragmentation is a persistent problem throughout the course of Parkinson’s disease (PD). However, the related neurophysiological patterns and the underlying mechanisms remained unclear. Method: We recorded subthalamic nucleus (STN) local field potentials (LFPs) using deep brain stimulation (DBS) with real-time wireless recording capacity from 13 patients with PD undergoing a one-night polysomnography recording, 1 month after DBS surgery before initial programming and when the patients were off-medication. The STN LFP features that characterised different sleep stages, correlated with arousal and sleep fragmentation index, and preceded stage transitions during N2 and REM sleep were analysed. Results: Both beta and low gamma oscillations in non-rapid eye movement (NREM) sleep increased with the severity of sleep disturbance (arousal index (ArI)-betaNREM: r=0.9, p=0.0001, sleep fragmentation index (SFI)-betaNREM: r=0.6, p=0.0301; SFI-gammaNREM: r=0.6, p=0.0324). We next examined the low-to-high power ratio (LHPR), which was the power ratio of theta oscillations to beta and low gamma oscillations, and found it to be an indicator of sleep fragmentation (ArI-LHPRNREM: r=−0.8, p=0.0053; ArI-LHPRREM: r=−0.6, p=0.0373; SFI-LHPRNREM: r=−0.7, p=0.0204; SFI-LHPRREM: r=−0.6, p=0.0428). In addition, long beta bursts (>0.25 s) during NREM stage 2 were found preceding the completion of transition to stages with more cortical activities (towards Wake/N1/REM compared with towards N3 (p<0.01)) and negatively correlated with STN spindles, which were detected in STN LFPs with peak frequency distinguishable from long beta bursts (STN spindle: 11.5 Hz, STN long beta bursts: 23.8 Hz), in occupation during NREM sleep (β=−0.24, p<0.001). Conclusion: Features of STN LFPs help explain neurophysiological mechanisms underlying sleep fragmentations in PD, which can inform new intervention for sleep dysfunction. Trial registration number: NCT02937727

    Periodic Mechanical Stress Induces Extracellular Matrix Expression and Migration of Rat Nucleus Pulposus Cells Through Src-GIT1-ERK1/2 Signaling Pathway

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    Background/Aims: Periodic mechanical stress has been shown to promote extracellular matrix (ECM) synthesis and cell migration of nucleus pulposus (NP) cells, however, the mechanisms need to be fully elucidated. The present study aimed to investigate the signal transduction pathway in the regulation of NP cells under periodic mechanical stress. Methods: Primary rat NP cells were isolated and seeded on glass slides, and then treated in our self-developed periodic stress field culture system. To further explore the mechanisms, data were analyzed by scratch-healing assay, quantitative reverse transcription polymerase chain reaction (RT-qPCR) analysis, western blotting, and co-immunoprecipitation assay. Results: Under periodic mechanical stress, the mRNA expression of ECM collagen 2A1 (Col2A1) and aggrecan, and migration of NP cells were significantly increased (P &#x3c; 0.05 for each), associating with increases in the phosphorylation of Src, GIT1, and ERK1/2 (P &#x3c; 0.05 for each). Pretreatment with the Src inhibitor PP2 reduced periodic mechanical stress-induced ECM synthesis and cell migration of NP cells (P &#x3c; 0.05 for each), while the phosphorylation of GIT1 and ERK1/2 were inhibited. ECM synthesis, cell migration, and phosphorylation of ERK1/2 were inhibited after pretreatment with the small interfering RNA for GIT1 in NP cells under periodic mechanical stress (P &#x3c; 0.05 for each), whereas the phosphorylation of Src was not affected. Pretreatment with the ERK1/2 inhibitor PD98059 reduced periodic mechanical stress-induced ECM synthesis and cell migration of NP cells (P &#x3c; 0.05 for each). Co-immunoprecipitation assay showed that there was a direct interaction between Src and GIT1 and between GIT1 and ERK1/2. Conclusion: In conclusion, periodic mechanical stress induced ECM expression and migration of NP cells via Src-GIT1-ERK1/2 signaling pathway, playing an important role in regulation of NP cells

    PSO-based algorithm for solving lot splitting in unbalanced seru production systems

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    Influence of Stator MMF Harmonics on the Utilization of Reluctance Torque in Six-Phase PMA-SynRM with FSCW

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    Although fractional-slot concentrated winding (FSCW) offers many significant advantages, such as short end-turn windings, high slot filling factor, and low cogging torque, it is frequently limited by excessive stator magnetomotive force (MMF) harmonics which will induce high eddy losses in the permanent magnets (PMs). What is more, in the literature, it can be observed that the reluctance torque of the salient-pole machine with FSCW is usually much lower than that obtained with integral slot winding. To explore the underlying reason why the reluctance torque in a salient machine with FSCW significantly decreases, a new six-phase FSCW with 24 slots and 10 poles, which can significantly reduce the undesirable stator MMF harmonics, is obtained by using the concept of stator shifting. Then, two permanent-magnet-assisted synchronous reluctance machines (PMA-SynRMs) with the proposed winding layout and conventional asymmetric 12-slot/10-pole six-phase winding layout are designed and simulated by the finite-element method (FEM). The reluctance torque, total torque, and d/q-axis inductances with different current phase angles are also compared under different loaded conditions. The results show that a reduction in stator MMF harmonics can indeed lead to a significant enhancement in reluctance torque under heavy loaded conditions, while the dominance will diminish under light loaded conditions

    A genetic mosaic screen identifies genes modulating Notch signaling in Drosophila.

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    Notch signaling is conserved in most multicellular organisms and plays critical roles during animal development. The core components and major signal transduction mechanism of Notch signaling have been extensively studied. However, our understanding of how Notch signaling activity is regulated in diverse developmental processes still remains incomplete. Here, we report a genetic mosaic screen in Drosophila melanogaster that leads to identification of Notch signali ng modulators during wing development. We discovered a group of genes required for the formation of the fly wing margin, a developmental process that is strictly dependent on the balanced Notch signaling activity. These genes encode transcription factors, protein phosphatases, vacuolar ATPases and factors required for RNA transport, stability, and translation. Our data support the view that Notch signaling is controlled through a wide range of molecular processes. These results also provide foundations for further study by showing that Me31B and Wdr62 function as two novel modulators of Notch signaling activity

    Defect Chemistry in Discharge Products of Li-O-2 Batteries

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    10.1002/smtd.201800358SMALL METHODS3

    Interactive Rare-Category-of-Interest Mining from Large Datasets

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    In the era of big data, rare category data examples are often of key importance despite their scarcity, e.g., rare bird audio is usually more valuable than common bird audio. However, existing efforts on rare category mining consider only the statistical characteristics of rare category data examples, while ignoring their ‘true’ interestingness to the user. Moreover, current approaches are unable to support real-time user interactions due to their prohibitive computational costs for answering a single user query.In this paper, we contribute a new model named IRim, which can interactively mine rare category data examples of interest over large datasets. The mining process is carried out by two steps, namely rare category detection (RCD) followed by rare category exploration (RCE). In RCD, by introducing an offline phase and high-level knowledge abstractions, IRim reduces the time complexity of answering a user query from quadratic to logarithmic. In RCE, by proposing a collaborative-reconstruction based approach, we are able to explicitly encode both user preference and rare category characteristics. Extensive experiments on five diverse real-world datasets show that our method achieves the response time in seconds for user interactions, and outperforms state-of-the-art competitors significantly in accuracy and number of queries. As a side contribution, we construct and release two benchmark datasets which to our knowledge are the first public datasets tailored for rare category mining task
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