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1Golgi protein-73:A biomarker for assessing cirrhosis and prognosis of liver disease patients显示文摘BACKGROUND Reliable biomarkers of cirrhosis,hepatocellular carcinoma(HCC),or progression of chronic liver diseases are missing.In this context,Golgi protein-73(GP73)also called Golgi phosphoprotein-2,was originally defined as a resident Golgi type II transmembrane protein expressed in epithelial cells.As a result,GP73 expression was found primarily in biliary epithelial cells,with only slight detection in hepatocytes.However,in patients with acute or chronic liver diseases and especially in HCC,the expression of GP73 is significantly up-regulated in hepatocytes.So far,few studies have assessed GP73 as a diagnostic or prognostic marker of liver fibrosis and disease progression.AIM To assess serum GP73 efficacy as a diagnostic marker of cirrhosis and/or HCC or as predictor of liver disease progression.METHODS GP73 serum levels were retrospectively determined by a novel GP73 ELISA(QUANTA Lite®GP73,Inova Diagnostics,Inc.,Research Use Only)in a large cohort of 632 consecutive patients with chronic viral and non-viral liver diseases collected from two tertiary Academic centers in Larissa,Greece(n=366)and Debrecen,Hungary(n=266).Aspartate aminotransferase(AST)/Platelets(PLT)ratio index(APRI)was also calculated at the relevant time points in all patients.Two hundred and three patients had chronic hepatitis B,183 chronic hepatitis C,198 alcoholic liver disease,28 autoimmune cholestatic liver diseases,15 autoimmune hepatitis,and 5 with other liver-related disorders.The duration of follow-up was 50(57)mo[median(interquartile range)].The development of cirrhosis,liver decompensation and/or HCC during follow-up were assessed according to internationally accepted guidelines.In particular,the surveillance for the development of HCC was performed regularly with ultrasound imaging and alpha-fetoprotein(AFP)determination every 6 mo in cirrhotic and every 12 mo in non-cirrhotic patients.RESULTS Increased serum levels of GP73(>20 units)were detected at initial evaluation in 277 out of 632 patients(43.8%).GP73-seropositivity correlated at baseline with the presence of cirrhosis(96.4%vs 51.5%,P<0.001),decompensation of cirrhosis(60.3%vs 35.5%,P<0.001),presence of HCC(18.4%vs 7.9%,P<0.001)and advanced HCC stage(52.9%vs 14.8%,P=0.002).GP73 had higher diagnostic accuracy for the presence of cirrhosis compared to APRI score[Area under the curve(AUC)(95%CI):0.909(0.885-0.934)vs 0.849(0.813-0.886),P=0.003].Combination of GP73 with APRI improved further the accuracy(AUC:0.925)compared to GP73(AUC:0.909,P=0.005)or APRI alone(AUC:0.849,P<0.001).GP73 levels were significantly higher in HCC patients compared to non-HCC[22.5(29.2)vs 16(20.3)units,P<0.001)and positively associated with BCLC stage[stage 0:13.9(10.8);stage A:17.1(16.8);stage B:19.6(22.3);stage C:32.2(30.8);stage D:45.3(86.6)units,P<0.001]and tumor dimensions[very early:13.9(10.8);intermediate:19.6(18.4);advanced:29.1(33.6)units,P=0.004].However,the discriminative ability for HCC diagnosis was relatively low[AUC(95%CI):0.623(0.570-0.675)].Kaplan-Meier analysis showed that the detection of GP73 in patients with compensated cirrhosis at baseline,was prognostic of higher rates of decompensation(P=0.036),HCC development(P=0.08),and liver-related deaths(P<0.001)during follow-up.CONCLUSION GP73 alone appears efficient for detecting cirrhosis and superior to APRI determination.In combination with APRI,its diagnostic performance can be further improved.Most importantly,the simple GP73 measurement proved promising for predicting a worse outcome of patients with both viral and nonviral chronic liver diseases.Nikolaos K Gatselis Tamás Tornai Zakera Shums Kalliopi Zachou Asterios Saitis Stella Gabeta Roger Albesa Gary L Norman Mária Papp George N Dalekos 2020World Journal of Gastroenterology2020,26,34:21
2Resistance to ciprofloxacin by enhancement of antioxidant defenses in biofilm and planktonic Proteusmirubilis显示文摘Aiassa V Barnes AI Albesa I 2010BiochemBiophRes Co2010,393,1:1
3Oxidative stress involved in the antibacterial action of different antibiotics显示文摘ALBESA I BECERRA M C BATTAN P C 0,,02:1
4Lipase of Candida albicans induces activation of NADPH oxidase and L-arginine pathways on resting and activated macrophages显示文摘Paraje MG Correa SG Albesa I 2009Biochem Biophys Res Commun2009,390,2:1
5Resistance to ciprofloxacin by enhancement of antioxidant defenses in biofilm and planktonic Proteus mirabilis显示文摘Virginia Aiassa Ana I. Barnes Inés Albesa 2010Biochemical and Biophysical Research Communications2010,,1:1
6Oxidative and nitrosative stress in Staphylococcus aureus biofilm显示文摘ARCEMIRANDA J E SOTOMAYOR C E ALBESA I 0,,01:1
7Resistance to ciprofloxacin by enhancement of antioxidant defenses in biofilm and planktonic proteus mirabilis显示文摘Aiassa V Barnes AI Albesa I 0,,01:1
8Lipase of Candida albicans induces activation of NADPH oxidase and L-arginine pathways on resting and activated macrophages显示文摘Paraje MG Correa SG Albesa I 2009BiochemBi- ophys Res Commun2009,390,2:1
9Adsorption of CO2/CH4 mixtures in a molecular model of activated carbon through Monte Carlo simulations显示文摘ALBESA A G RAFTI M VICENTE J L 2012Adsorption Science & Technology2012,30,89:1
10Resistance to eipro- floxaein by enhancement of antioxidant defenses in biofilm and planktonie Proteus mirabilis显示文摘Aiassa V Barnes A I Albesa I 2010Bioehem Biophys Res Commun2010,393,:1
11Lipase of Candida al- bieans induces activation of NADPH oxidase and 1-arginine pathways on resting and activated maerophages显示文摘PARAJE M G CORREA S G ALBESA I 2009Bioehem Biophys Res Com- municat2009,390,2:1
12Oxidative stress induced by ciprofloxacin in Staphylococcus aureus显示文摘Becerra M C Albesa I 2002Biochem Biophys Res Commun2002,297,4:1
13Leukotoxlclty of pyoverdin, production of reactive oxygen species, and effect of UV radiation显示文摘Becerra C Albesa I Eraso AJ 2001Biochemical and Biophysical Research Communications2001,285,2:1
14Elevation of alanine amino transferase and aspartate amino transferase produced by pyoverdin, a photolabile pigment of Pseudomonasfluorescens显示文摘Eraso AJ Albesa I 1998Natural Toxins1998,6,2:1
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