6,517 research outputs found
ECG Signal Super-resolution by Considering Reconstruction and Cardiac Arrhythmias Classification Loss
With recent advances in deep learning algorithms, computer-assisted
healthcare services have rapidly grown, especially for those that combine with
mobile devices. Such a combination enables wearable and portable services for
continuous measurements and facilitates real-time disease alarm based on
physiological signals, e.g., cardiac arrhythmias (CAs) from electrocardiography
(ECG). However, long-term and continuous monitoring confronts challenges
arising from limitations of batteries, and the transmission bandwidth of
devices. Therefore, identifying an effective way to improve ECG data
transmission and storage efficiency has become an emerging topic. In this
study, we proposed a deep-learning-based ECG signal super-resolution framework
(termed ESRNet) to recover compressed ECG signals by considering the joint
effect of signal reconstruction and CA classification accuracies. In our
experiments, we downsampled the ECG signals from the CPSC 2018 dataset and
subsequently evaluated the super-resolution performance by both reconstruction
errors and classification accuracies. Experimental results showed that the
proposed ESRNet framework can well reconstruct ECG signals from the 10-times
compressed ones. Moreover, approximately half of the CA recognition accuracies
were maintained within the ECG signals recovered by the ESRNet. The promising
results confirm that the proposed ESRNet framework can be suitably used as a
front-end process to reconstruct compressed ECG signals in real-world CA
recognition scenarios
Significant race and gender differences in anterior cruciate ligament tibial footprint location: a 3D-based analysis
BACKGROUND: The aim of the present study was to identify potential race- or gender-specific differences in anterior cruciate ligament (ACL) tibial footprint location from the tibia anatomical coordinate system (tACS) origin, investigate the distances from the tibial footprint to the anterior root of the lateral meniscus (ARLM) and the medial tibial spine (MTS), determine how reliable the ARLM and MTS can be in locating the ACL tibial footprint, and assess the risk of iatrogenic ARLM injuries caused by using reamers with various diameters (7-10Â mm).
PATIENTS AND METHODS: Magnetic resonance images of 91 Chinese and 91 Caucasian subjects were used for the reconstruction of three-dimensional (3D) tibial and ACL tibial footprint models. The anatomical coordinate system was applied to reflect the anatomical locations of scanned samples.
RESULTS: The average anteroposterior (A/P) tibial footprint location was 17.1 ± 2.3 mm and 20.0 ± 3.4 mm in Chinese and Caucasians, respectively (P < .001). The average mediolateral (M/L) tibial footprint location was 34.2 ± 2.4 mm and 37.4 ± 3.6 mm in Chinese and Caucasians, respectively (P < .001). The average difference between men and women was 2 mm in Chinese and 3.1 mm in Caucasians. The safe zone for tibial tunnel reaming to avoid ARLM injury was 2.2 mm and 1.9 mm away from the central tibial footprint in the Chinese and Caucasians, respectively. The probability of damaging the ARLM by using reamers with various diameters ranged from 0% for Chinese males with a 7 mm reamer to 30% in Caucasian females with a 10 mm reamer.
CONCLUSIONS: The significant race- and gender-specific differences in the ACL tibial footprint should be taken in consideration during anatomic ACL reconstruction. The ARLM and MTS are reliable intraoperative landmarks for identifying the tibial ACL footprint. Caucasians and females might be more prone to iatrogenic ARLM injury.
LEVEL OF EVIDENCE: III, cohort study.
TRIAL REGISTRATION: This study has been approved by the ethical research committee of the General Hospital of Southern Theater Command of PLA under the code: [2019] No.10
Heterotypic cell-cell interaction of human stem cells for neural differentiation of hybrid spheroids
Organoids, the condensed 3-D tissues emerged at the early stage of organogenesis, are a promising approach to regenerate functional and vascularized organ mimics [1]. While incorporation of heterotypic cell types such as human mesenchymal stem cells (hMSCs) and human induced pluripotent stem cells (hiPSCs) derived neural progenitors aid neural organ development, the interactions of secreted factors during neurogenesis have not been well understood. The objective of this study is to investigate the impact of the composition and structure of 3-D hybrid spheroids of hiPSCs and hMSCs on dorsal cortical differentiation and the secretion of extracellular matrices and trophic factors in vitro. The hybrid spheroids were formed at different hiPSC:hMSC ratios (100:0, 75:25, 50:50, 25:75, 0:100) using direct mixing or pre-hiPSC aggregation method, which generated dynamic spheroid structure. The cellular organization, proliferation, neural marker expression, the secretion of extracellular matrix proteins and the cytokines were characterized. The incorporation of MSCs upregulated Nestin and β-tubulin III expression (the dorsal cortical identity was shown by Pax6 and TBR1 expression), matrix remodeling proteins and the secretion of transforming growth factor-β1 and prostaglandin E2. This study indicates that the appropriate composition and structure of hiPSC-MSC spheroids promote neural differentiation and trophic factor and matrix secretion due to the heterotypic cell-cell interactions.
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Primordial magnetic field as a common solution of nanohertz gravitational waves and Hubble tension
The origin of interstellar and intergalactic magnetic fields is largely
unknown, and the primordial magnetic fields (PMFs) produced by, e.g., phase
transitions of the early Universe are expected to provide seeds for those
magnetic fields. The PMFs affect the evolution of the Universe at an early
time, resulting in a series of phenomena. In this work, we show that the
PMF-induced turbulence can give rise to nanohertz (nHz) gravitational waves
reported by several pulsar timing arrays, including NANOGrav, PPTA, EPTA, and
CPTA. Using the nHz gravitational wave data, we obtain the constraints on the
characteristic magnetic field strength () and coherent length scale () of PMFs, assuming a generation temperature of
approximately the QCD temperature ( MeV). In addition, the PMFs which
evolve to the recombination era can induce baryon density inhomogeneities, and
then alter the ionization process. This naturally results in an alleviation of
the tension of the Hubble parameter and the matter clumpiness parameter
between early and late-time measurements. Assuming an evolution form of
from the epoch of the production of
PMFs to the epoch of recombination, we find (95\% credible
region).Comment: 7 pages, 4 figure
High serum levels of procalcitonin and soluble TREM-1 correlated with poor prognosis in pulmonary tuberculosis
SummaryObjectivesComparisons of procalcitonin (PCT), C-reactive protein (CRP), and soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) would expand our knowledge of which biomarker is the best predictor for outcomes of patients with pulmonary tuberculosis (PTB).MethodsWe prospectively enrolled 243 PTB patients, in whom PCT, CRP, and sTREM-1 measurement were performed to evaluate their prognostic value for 6-month mortality.ResultsSerum PCT, CRP, and sTREM-1 levels on diagnosis of PTB were significantly higher in nonsurvivors (2.22 ± 6.22 vs. 0.13 ± 0.31 ng/mL, P = 0.043; 42.1 ± 59.4 vs. 12.5 ± 29.1 mg/L, P = 0.004; 332 ± 362 vs. 128 ± 98 pg/mL, P = 0.001, respectively) as compared with 6-month survivors. In multivariate Cox regression analysis, PCT ≧0.5 ng/mL (hazard ratio 4.13, 95% CI, 1.99–8.58) and sTREM-1 ≧129 pg/mL (hazard ratio 3.39, 95% CI, 1.52–7.58) remained independent mortality predictors. Serum PCT and sTREM-1 levels above the cutoffs were also associated with the presence of disseminated tuberculosis.ConclusionsAmong PTB patients, higher PCT, CRP, and sTREM-1 levels are observed in nonsurvivors than in 6-month survivors. Serum levels of PCT and sTREM-1 over the cutoffs are independently associated with a poor outcome. In addition, higher PCT and sTREM-1 levels would raise the clinical suspicion of disseminated tuberculosis
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