Real-Time Fracture Aperture Identification Using Mud Loss Data and Solution for LCM Combination

Managing server lost circulation is a major challenge of drilling operation in naturally fractured formations and it causes much nonproductive rig time. When encountered with loss, the fracture aperture intersecting the wellbore is not well-identified in time, which has a significant impact on the decision of drilling operation and the undesired result of loss curing. Therefore, the onset of fracture is identified in a timely manner and evaluated comprehensively to formulate an appropriate strategy over time. However, the mud loss date, which is the primary source of information retrieved from the drilling process, was not properly used in real-time prediction of fracture aperture. This article provides a detailed mathematical study to discuss the mechanism of mud invasion in the near-wellbore region and prediction of fracture aperture. The fracture aperture can be calculated from mud-loss data by solving a cubic equation with input parameters given by the well radius, the overpressure ratio, and the maximum mud-loss volume. It permits the proper selection of loss-circulation material (LCM) with respect to particle size distribution and fiber usage. The case study illustrates the applicability of this methodology with a discussion on LCM particle distribution in different scenarios and the result demonstrates the outcome of inappropriate LCM usage and the advantages of the novel fiber-based LCM treatment.

Cronkhite-Canada综合征1例

Cronkhite-Canada综合征(Cronkhite-Canada’s syndrome, CCS)是临床罕见病,病因及发病机制尚不明确,该病以胃肠道多发息肉及外胚层两大症候群为主,临床表现以腹泻为主,全消化道多发息肉,伴有皮肤色素沉着、毛发脱落、指(趾)甲萎缩脱落等.预后较差,本文报道1例CCS患者并对62篇国内文献进行回顾性分析.

Quasihole Tunneling in Disordered Fractional Quantum Hall Systems

Fractional quantum Hall systems are often described by model wave functions,which are the ground states of pure systems with short-range interaction.A primary example is the Laughlin wave function,which supports Abelian quasiparticles with fractionalized charge.In the presence of disorder,the wave function of the ground state is expected to deviate from the Laughlin form.We study the disorder-driven colla.pse of the quantum Hall state by analyzing the evolution of the ground state and the single-quasihole state.In particular,we demonstrate that the quasihole tunneling amplitude can signal the fractional quantum Hall phase to insulator transition.

Topological Distillation by Principal Component Analysis in Disordered Fractional Quantum Hall States

We study the behavior of two-dimensional electron gas in the fractional quantum Hall(FQH)regime in the presence of disorder potential.The principal component analysis is applied to a set of disordered Laughlin ground state model wave function to enable us to distill the model wave function of the pure Laughlin state.With increasing the disorder strength,the ground state wave function is expected to deviate from the Laughlin state and eventually leave the FQH phase.We investigate the phase transition from the Laughlin state to a topologically trivial state by analyzing the overlap between the random sample wave functions and the distilled ground state wave function.It is proposed that the cross point of the principal component amplitude and its counterpart is the critical disorder strength,which marks the collapse of the FQH regime.

Hepatocellular-cholangiocarcinoma with sarcomatous change:Clinicopathological features and outcomes

Combined hepatocellular-cholangiocarcinoma(c HCC-CCA)is a rare type of cancer,accounting for 0.4%–14.2%of hepato-carcinoma.Hepatic sarcoma is only less than 2%of primary malignant liver tumors.Thus,sarcomatoid c HCC-CCA is extremely rare.To the best of our knowledge,only twenty-six cases had been reported in the literature[1–19].

Clinical proteomics:a driving force for cancer therapeutic target discovery and precision medicine

Precision medicine based on the accurate and comprehensive molecular characterization of tumors has become the most promising therapeutic strategy for cancer.In current clinical practice,patients with cancer normally receive the same treatment as other patients with the same type of cancer.

Functional carbon materials addressing dendrite problems in metal batteries:surface chemistry,multi-dimensional structure engineering,and defects

Metal batteries that directly use active metals as anodes are considered as one of the most promising solutions to achieve the energy upgrade of battery technologies,while their practical application still suffers from dendrite problems.Functional carbon materials(FCMs)have demonstrated their great potential in suppressing metal dendrites benefitting from the multiple merits such as chemical tunability and capability of multi-dimensional structure assembly.Here,we initiate a review to present the recent progress in employing FCMs to deal with dendrite problems.It focuses on the surface chemistry and multi-dimensional carbon material engineering,which systematically overcomes the problems through diverse methods,such as reinforcing desolvation,improving interface compatibility,homogenizing electric field,buffering volume expansion and lattice mismatch.In addition,we also refine the long-standing debate about whether surface defects in FCMs are beneficial to suppress the metal dendrites or not,especially in the non-aqueous electrolyte regime.Finally,the remaining challenges for utilizing FCMs to suppress metal dendrites and the possible solutions are proposed to guide the future development.

Acyl-CoA synthase ACSL4:an essential target in ferroptosis and fatty acid metabolism

Long-chain acyl-coenzyme A(CoA)synthase 4(ACSL4)is an enzyme that esterifies CoA into specific polyunsaturated fatty acids,such as arachidonic acid and adrenic acid.Based on accumulated evidence,the ACSL4-catalyzed biosynthesis of arachidonoyl-CoA contributes to the execution of ferroptosis by triggering phospholipid peroxidation.Ferroptosis is a type of programmed cell death caused by iron-dependent peroxidation of lipids;ACSL4 and glutathione peroxidase 4 positively and negatively regulate ferroptosis,respectively.In addition,ACSL4 is an essential regulator of fatty acid(FA)metabolism.ACSL4 remodels the phospholipid composition of cell membranes,regulates steroidogenesis,and balances eicosanoid biosynthesis.In addition,ACSL4-mediated metabolic reprogramming and antitumor immunity have attracted much attention in cancer biology.Because it facilitates the cross-talk between ferroptosis and FA metabolism,ACSL4 is also a research hotspot in metabolic diseases and ischemia/reperfusion injuries.In this review,we focus on the structure,biological function,and unique role of ASCL4 in various human diseases.Finally,we propose that ACSL4 might be a potential therapeutic target.

FOLR1-induced folate deficiency reduces viral replication via modulating APOBEC3 family expression

Folate receptor alpha(FOLR1)is vital for cells ingesting folate(FA).FA plays an indispensable role in cell pro-liferation and survival.However,it is not clear whether the axis of FOLR1/FA has a similar function in viral replication.In this study,we used vesicular stomatitis virus(VSV)to investigate the relationship between FOLR1-mediated FA deficiency and viral replication,as well as the underlying mechanisms.We discovered that FOLR1 upregulation led to the deficiency of FA in HeLa cells and mice.Meanwhile,VSV replication was notably sup-pressed by FOLR1 overexpression,and this antiviral activity was related to FA deficiency.Mechanistically,FA deficiency mainly upregulated apolipoprotein B mRNA editing enzyme catalytic subunit 3B(APOBEC3B)expression,which suppressed VSV replication in vitro and in vivo.In addition,methotrexate(MTX),an FA metabolism inhibitor,effectively inhibited VSV replication by enhancing the expression of APOBEC3B in vitro and in vivo.Overall,our present study provided a new perspective for the role of FA metabolism in viral infections and highlights the potential of MTX as a broad-spectrum antiviral agent against RNA viruses.

Biomarkers enhance the long-term predictive ability of the KAMIR risk score in Chinese patients with ST-elevation myocardial infarction

Background:The Global Registry of Acute Coronary Events (GRACE) score is recommended by current ST-elevation myocardial infarction (STEMI) guidelines.But it has inherent defects.The present study aimed to investigate the more compatible risk stratification for Chinese patients with STEMI and to determine whether the addition of biomarkers to the Korea Acute Myocardial Infarction Registry (KAMIR) score could enhance its predictive value for long-term outcomes.Methods:A total of 1093 consecutive STEMI patients were included and followed up 48.2 months.Homocysteine,hypersensitive C-reactive protein (hs-CRP),and N-terminal pro-B-type natriuretic peptide (NT-proBNP) were detected.The KAMIR score and the GRACE score were calculated.The performance between the KAMIR and the GRACE was compared.The predictive power of the KAMIR alone and combined with biomarkers were assessed by the receiver-operating characteristic (ROC) curve.Results:The KAMIR demonstrated a better risk stratification and predictive ability than the GRACE (death:AUC = 0.802 vs.0.721,P<0.001;major adverse cardiovascular events (MACE):AUC = 0.683 vs.0.656,P<0.001).It showed that the biomarkers could independently predict death [homocysteine:HR= 1.019 (1.015–1.024),P<0.001;hs-CRP:HR= 1.052 (1.000–1.104),P= 0.018;NT-pro BNP:HR= 1.142 (1.004–1.280),P= 0.021] and MACE [homocysteine:HR= 1.019 (1.015–1.024),P<0.001;hs-CRP:HR= 1.012 (1.003–1.021),P= 0.020;NT-pro BNP:HR= 1.136 (1.104–1.168),P= 0.006].When they were used in combination with the KAMIR,the area under the ROC curve (AUC) significantly increased for death [homocysteine:AUC = 0.802 vs.0.890,Z = 5.982,P<0.001;hs-CRP:AUC = 0.802 vs.0.873,Z= 3.721,P<0.001;NT-pro BNP:AUC= 0.802 vs.0.871,Z = 2.187,P= 0.047;homocysteine,hs-CRP and NT-pro BNP:AUC = 0.802 vs.0.940,Z = 6.177,P<0.001] and MACE [homocysteine:AUC = 0.683 vs.0.771,Z= 6.818,P<0.001;hs-CRP:AUC= 0.683 vs.0.712,Z= 2.022,P= 0.031;NT-pro BNP:AUC= 0.683 vs.0.720,Z= 2.974,P= 0.003;homocysteine,hs-CRP and NT-pro BNP:AUC= 0.683 vs.0.789,Z= 6.900,P<0.001].Conclusion:The KAMIR is better than the GRACE in risk stratification and prognosis prediction in Chinese STEMI patients.A combination of above-mentioned biomarkers can develop a more predominant prediction for long-term outcomes.

Strategies for preventing peritoneal fibrosis in peritoneal dialysis patients： new insights based on peritoneal inflammation and angiogenesis

Peritoneal dialysis （PD） is an established form of renal replacement therapy. Long-term PD leads to morphologic and functional changes to the peritoneal membrane （PM）, which is defined as peritoneal fibrosis, a known cause of loss of peritoneal ultrafiltration capacity. Inflammation and angiogenesis are key events during the pathogenesis of peritoneal fibrosis. This review discusses the pathophysiology of peritoneal fibrosis and recent research progress on key fibrogenic molecular mechanisms in peritoneal inflammation and angiogenesis, including Toll-like receptor ligand-mediated, NOD-like receptor protein 3/interleukin-lp, vascular endothelial growth factor, and angiopoietin-2/Tie2 signaling pathways. Furthermore, novel strategies targeting peritoneal inflammation and angiogenesis to preserve the PM are discussed in depth.