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10.1111/liv.14037

http://scihub22266oqcxt.onion/10.1111/liv.14037
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30597709!6767546!30597709
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suck abstract from ncbi

pmid30597709      Liver+Int 2019 ; 39 (7): 1246-1255
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  • Characterization of inflammatory response in hepatorenal syndrome: Relationship with kidney outcome and survival #MMPMID30597709
  • Sole C; Sola E; Huelin P; Carol M; Moreira R; Cereijo U; Mas JM; Graupera I; Pose E; Napoleone L; dePrada G; Juanola A; Fabrellas N; Torres F; Morales-Ruiz M; Farres J; Jimenez W; Gines P
  • Liver Int 2019[Jul]; 39 (7): 1246-1255 PMID30597709show ga
  • BACKGROUND: Several lines of evidence indicate that decompensated cirrhosis is characterized by the presence of systemic inflammation. Hepatorenal syndrome (HRS-AKI) is a unique type of renal failure that occurs at late stages of cirrhosis. However, confirmation of the presence and significance of such inflammatory response in HRS-AKI is lacking. AIM AND METHODS: To characterize the systemic inflammatory response, as estimated by measuring a large number of cytokines, in 161 patients hospitalized for an acute decompensation of cirrhosis: 44 patients without acute kidney injury (AKI), 63 patients with hypovolaemia-induced AKI and 58 patients with HRS-AKI. RESULTS: HRS-AKI was characterized by an altered cytokine profile compared to the other two groups, particularly IL-6, IL-8, TNF-alpha, VCAM-1, fractalkine and MIP-1alpha. The inflammatory response was not related to presence of bacterial infection, concomitant acute-on-chronic liver failure or severity of renal dysfunction. Patients who responded to terlipressin and albumin had only a decrease in TNF-alpha and RANTES after treatment without changes in other cytokines. Interestingly, patients with persistent HRS-AKI had higher levels of IP-10 and VCAM-1 compared to those with resolution of HRS-AKI. VCAM-1 was also an independent predictor of 3-month mortality. A systems biology analysis approach showed that the inflammatory status of HRS-AKI was similar to that of chronic nonhepatic inflammatory conditions, such as lupus erythematosus or inflammatory bowel disease. CONCLUSION: Hepatorenal syndrome is characterized by a marked systemic inflammatory state, reminiscent of that of nonhepatic inflammatory diseases, that correlates with patient outcomes.
  • |Acute Kidney Injury/etiology/*mortality/therapy[MESH]
  • |Acute-On-Chronic Liver Failure/*complications/therapy[MESH]
  • |Aged[MESH]
  • |Albumins/therapeutic use[MESH]
  • |Biomarkers/blood[MESH]
  • |Cytokines/*blood[MESH]
  • |Female[MESH]
  • |Hepatorenal Syndrome/etiology/*mortality/therapy[MESH]
  • |Humans[MESH]
  • |Inflammation/pathology[MESH]
  • |Kidney/physiopathology[MESH]
  • |Liver Cirrhosis/*complications/therapy[MESH]
  • |Liver Transplantation[MESH]
  • |Liver/physiopathology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Prospective Studies[MESH]
  • |Severity of Illness Index[MESH]
  • |Spain[MESH]
  • |Survival Analysis[MESH]
  • |Terlipressin/therapeutic use[MESH]


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