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Background Current knowledge on iron's role in rheumatoid arthritis (RA) development is very limited, with studies yielding inconsistent findings. We conducted a two-sample Mendelian randomization study to assess the associations of iron status with the risk of RA. Methods This study leveraged genetic data from a large genome-wide association study (GWAS) of 257,953 individuals to identify single nucleotide polymorphisms (SNPs) associated with iron status. We then analyzed these data in conjunction with summary-level data on RA from the IEU open GWAS project, which included 5,427 RA cases and 479,171 controls. An inverse-variance weighted method with random effects was employed, along with sensitivity analyses, to assess the relationship between iron status and RA risk. Results Genetic predisposition to high ferritin and serum iron status was causally associated with lower odds of RA. Ferritin had an odds ratio (OR) of 0.997 (95% confidence interval [CI]: 0.995-0.997; p = 0.010), indicating that a one-unit increase in ferritin is associated with a 0.3% decrease in the odds of RA. Similarly, serum iron had an OR of 0.997 (95% CI: 0.995-0.999; p = 0.014). However, MR analyses found no significant causal associations between total iron-binding capacity (OR = 1.0, 95% CI: 0.999-1.002; p = 0.592) or transferrin saturation percentage (OR = 0.998, 95% CI: 0.996-1.000; p = 0.080) and risk of developing RA. Conclusions This study suggests that individuals with genes linked to higher iron levels may have a lower risk of developing RA. Our findings indicate that the total amount of iron in the body, rather than how it is distributed, might be more important for RA. This raises the intriguing possibility that iron supplementation could be a preventative strategy, but further research is necessary.
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BACKGROUND: Segmentation of the parotid glands and tumors by MR images is essential for treating parotid gland tumors. However, segmentation of the parotid glands is particularly challenging due to their variable shape and low contrast with surrounding structures. PURPOSE: The lack of large and well-annotated datasets limits the development of deep learning in medical images. As an unsupervised learning method, contrastive learning has seen rapid development in recent years. It can better use unlabeled images and is hopeful to improve parotid gland segmentation. METHODS: We propose Swin MoCo, a momentum contrastive learning network with Swin Transformer as its backbone. The ImageNet supervised model is used as the initial weights of Swin MoCo, thus improving the training effects on small medical image datasets. RESULTS: Swin MoCo trained with transfer learning improves parotid gland segmentation to 89.78% DSC, 85.18% mIoU, 3.60 HD, and 90.08% mAcc. On the Synapse multi-organ computed tomography (CT) dataset, using Swin MoCo as the pre-trained model of Swin-Unet yields 79.66% DSC and 12.73 HD, which outperforms the best result of Swin-Unet on the Synapse dataset. CONCLUSIONS: The above improvements require only 4 h of training on a single NVIDIA Tesla V100, which is computationally cheap. Swin MoCo provides new approaches to improve the performance of tasks on small datasets. The code is publicly available at https://github.com/Zian-Xu/Swin-MoCo.
Subject(s)
Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Parotid Gland , Parotid Gland/diagnostic imaging , Humans , Image Processing, Computer-Assisted/methods , Machine Learning , Deep LearningABSTRACT
The electronic state in terms of charge and spin of metal sites is fundamental to govern the catalytic activity of a photocatalyst. Herein, we show that modulation of the electronic states of Cu sites, without changing the coordination environments, of two metal-organic supramolecular assemblies based on πâ â â π stacking can significantly improve photocatalytic activity. The use of these heterogeneous photocatalysts, without using noble metal cocatalysts, resulted in an increase of the hydrogen production rate from 522 to 3620â µmol h-1 g-1 . A systematical analysis revealed that the charge density and spin density of the metal centers are efficiently modulated via the modulation of the coordination fields around active copper (II) centers by the variation of the non-coordination groups of terminal ligands, leading to the significant enhancement of photocatalytic activity. This work provides an insight into the electronic state of active metal centers for designing high-performance photocatalysts.
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A hierarchical CoP@ZnIn2S4 photocatalyst was prepared via a MOF-templated strategy. Owing to the unique composition and morphology that can facilitate the separation of photoexcited carriers, enhance light absorption and provide high surface area, CoP@ZnIn2S4 exhibited a H2 evolution rate of 0.103 mmol h-1 and remained stable over 24 hours.
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Fabricating heterojunction photocatalysts for H2 production is promising for the development of clean energy. For boosting the photocatalytic activity, modulating the heterojunction interface can facilitate the electron-hole separation and solar energy utilization, but it is highly challenging in synthesis. In this work, by facilely exfoliating the bulk C3N5, ultrathin C3N5 nanosheets (N-CN) with large surface area, improved light absorption, and efficient charge transport were synthesized and further applied to the construction of NH2-UiO-66/N-CN heterojunctions. The optimized NH2-UiO-66/N-CN-2 exhibits high hydrogen evolution rate and cycling stability with Pt as the cocatalyst. Combined with the experimental results, the density functional theory calculation reveals that the high photocatalytic performance is attributed to the promoted photogenerated carrier transfer by the formation of well-contacted and stable Z-scheme heterojunction interface. This contribution renders an insight into the modulation of the heterojunction interface for enhancing the activity of MOF-based photocatalysts.
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A cage-based metal-organic framework (Ni-NKU-101) with biphenyl-3,3',5,5'-tetracarboxylic acid was synthesized via solvothermal method. Ni-NKU-101 contains two types of cages based on trinuclear and octa-nuclear nickel-clusters that are connected with each other by the 4-connected ligands, to form a 3D framework with a new topology. A mixed-metal strategy was used to synthesize isostructural bimetallic MOFs of Mx Ni1-x -NKU-101 (M=Mn, Co, Cu, Zn). The electrocatalytic studies showed that the hydrogen evolution reaction (HER) activity of Cux Ni1-x -NKU-101 is much higher than that of other Mx Ni1-x -NKU-101 catalysts in acidic aqueous solution, owing to the synergistic effect of the bimetallic centers. The optimized Cu0.19 Ni0.81 -NKU-101 has an overpotential of 324â mV at 10â mA cm-2 and a Tafel slope of 131â mV dec-1 . The mechanism of HER activity over these bimetallic MOF-based electrocatalysts are discussed in detail.
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Growing interest in the health benefits of soy isoflavones has led to research in the isolation of individual isoflavone species for further application. Herein, we develop a new strategy to isolate daidzein, genistein, daidzin and genistin in soybean. We investigated the impact of solvents used and the extraction time on the extracted isoflavone contents from soybean. A 30-min extraction with 65% aqueous methanol gave a total isoflavone yield of 345 mg/100 g soybean, the highest value among tested conditions. Further, we proposed a two-stage adsorption/desorption chromatography comprising macroporous resin and aluminium oxide to isolate isoflavone. First, HP-20 resin was used to separate the glucosidic and aglyconic forms of isoflavone, then individual species of isoflavone could be isolated using aluminium oxide by specific retention of 5-hydroxy isoflavone. This process achieved overall high recovery (82-97%) and purity (92-95%) of the four isoflavones, which confirms a high separating efficiency for isoflavones from soybean.
Subject(s)
Aluminum Oxide/chemistry , Glycine max/chemistry , Isoflavones/isolation & purification , Resins, Synthetic/chemistry , Solvents/chemistry , Isoflavones/analysis , Isoflavones/chemistry , Porosity , Resins, PlantABSTRACT
Photocatalytic hydrogen evolution by water splitting is highly important for the application of hydrogen energy and the replacement of fossil fuel by solar energy, which needs the development of efficient catalysts with long-term catalytic stability under light irradiation in aqueous solution. Herein, Zn0.5 Cd0.5 S solid solution was synthesized by a metal-organic framework-templated strategy and then loaded with MoS2 by a hydrothermal method to fabricate a MoS2 /Zn0.5 Cd0.5 S heterojunction for photocatalytic hydrogen evolution. The composition of MoS2 /Zn0.5 Cd0.5 S was fine-tuned to obtain the optimized 5â wt % MoS2 /Zn0.5 Cd0.5 S heterojunction, which showed a superior hydrogen evolution rate of 23.80â mmol h-1 g-1 and steady photocatalytic stability over 25â h. The photocatalytic performance is due to the appropriate composition and the formation of an intimate interface between MoS2 and Zn0.5 Cd0.5 S, which endows the photocatalyst with high light-harvesting ability and effective separation of photogenerated carriers.
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Photocatalytic water splitting taking the advantage of using solar energy directly is one of the most effective strategies for hydrogen evolution. The development of facile methods for synthesizing highly efficient and stable photocatalysts for hydrogen production still remains a great challenge. Herein, a metal-organic framework (MOF)-templated strategy was designed for the synthesis of solid solutions of (Zn0.95Cu0.05)1-xCdxS that exhibit outstanding photocatalytic hydrogen production reaction activity. More importantly, efficient light capturing ability and photogenerated charges separation were accomplished via fine-tuning the composition of the photocatalysts by adjusting the concentrations of doping metals in the template MOFs. Under visible light (λ > 420 nm), an optimized nanocatalyst, (Zn0.95Cu0.05)0.6Cd0.4S, exhibited a higher durability and satisfied photocatalytic hydrogen evolution rate of 4150.1 µmol g-1 h-1 of water splitting.
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The soy isoflavones daidzein (DAI) and genistein (GEN) have beneficial effects on human health. However, their oral bioavailability is hampered by their low aqueous solubility. Our previous study revealed two water-soluble phosphorylated conjugates of isoflavones, daidzein 7-O-phosphate and genistein 7-O-phosphate, generated via biotransformation by Bacillus subtilis BCRC80517 cultivated with isoflavones. In this study, two novel derivatives of isoflavones, daidzein 4'-O-phosphate and genistein 4'-O-phosphate, were identified by HPLC-ESI-MS/MS and 1H, 13C, and 31P NMR, and their biotransformation roadmaps were proposed. Primarily, isoflavone glucosides were deglycosylated and then phosphorylated predominantly into 7-O-phosphate conjugates with traces of 4'-O-phosphate conjugates. Inevitably, trace quantities of glucosides were converted into 6â³-O-succinyl glucosides. GEN was more efficiently phosphorylated than DAI. Nevertheless, the presence of GEN prolonged the time until the exponential phase of cell growth, whereas the other isoflavones showed little effect on cell growth. Our findings provide new insights into the novel microbial phosphorylation of isoflavones involved in xenobiotic metabolism.
Subject(s)
Bacillus subtilis/metabolism , Isoflavones/metabolism , Bacillus subtilis/drug effects , Bacillus subtilis/growth & development , Biotransformation , Chromatography, High Pressure Liquid , Isoflavones/isolation & purification , Isoflavones/pharmacology , Magnetic Resonance Spectroscopy , Phosphorylation , Spectrometry, Mass, Electrospray Ionization , Xenobiotics/metabolismABSTRACT
Cardiovascular diseases are the most popular cause of death in the world recently. For postoperatives, cardiac rehabilitation is still asked to maintain at home (phase II) to improve cardiac function. However, only one third of outpatients do the exercise regularly, reflecting the difficulty for home-based healthcare: lacking of monitoring and motivation. Hence, a cardio-pulmonary rehabilitation system was proposed in this research to improve rehabilitation efficiency for better prognosis. The proposed system was built on mobile phone and receiving electrocardiograph (ECG) signal from a wireless ECG holter via Bluetooth connection. Apart from heart rate (HR) monitor, an ECG derived respiration (EDR) technique is also included to provide respiration rate (RR). Both HR and RR are the most important vital signs during exercise but only used one physiological signal recorder in this system. In clinical test, there were 15 subjects affording Bruce Task (treadmill) to simulate rehabilitation procedure. Correlation between this system and commercial product (Custo-Med) was up to 98% in HR and 81% in RR. Considering the prevention of sudden heart attack, an arrhythmia detection expert system and healthcare server at the backend were also integrated to this system for comprehensive cardio-pulmonary monitoring whenever and wherever doing the exercise.