Matches in SemOpenAlex for { <https://semopenalex.org/work/W4385215552> ?p ?o ?g. }
- W4385215552 endingPage "2070" @default.
- W4385215552 startingPage "2070" @default.
- W4385215552 abstract "The liver has a huge impact on the functioning of our body and the preservation of homeostasis. It is exposed to many serious diseases, which may lead to the chronic failure of this organ, which is becoming a global health problem today. Currently, the final form of treatment in patients with end-stage (acute and chronic) organ failure is transplantation. The proper function of transplanted organs depends on many cellular processes and immune and individual factors. An enormous role in the process of acceptance or rejection of a transplanted organ is attributed to, among others, the activation of the complement system. The aim of this study was the evaluation of the concentration of selected biomarkers’ complement system activation (C3a, C5a, and sC5b-9 (terminal complement complex)) in the serum of patients before and after liver transplantation (24 h, two weeks). The study was conducted on a group of 100 patients undergoing liver transplantation. There were no complications during surgery and no transplant rejection in any of the patients. All patients were discharged home 2–3 weeks after the surgery. The levels of all analyzed components of the complement system were measured using the ELISA method. Additionally, the correlations of the basic laboratory parameters—C-reactive protein (CRP), hemoglobin (Hb), total bilirubin, alkaline phosphatase (ALP), alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyl transpeptidase (GGTP), and albumin—with the parameters of the complement system (C3a, C5a, and sC5b-9) were determined. In our study, changes in the concentrations of all examined complement system components before and after liver transplantation were observed, with the lowest values before liver transplantation and the highest concentration two weeks after. The direct increase in components of the complement system (C3a, C5a, and sC5b-9) 24 h after transplantation likely affects liver damage after ischemia-reperfusion injury (IRI), while their increase two weeks after transplantation may contribute to transplant tolerance. Increasingly, attention is being paid to the role of C3a and CRP as biomarkers of damage and failure of various organs. From the point of view of liver transplantation, the most interesting correlation in our own research was found exactly between CRP and C3a, 24 h after the transplantation. This study shows that changes in complement activation biomarkers and the correlation with CRP in blood could be a prognostic signature of liver allograft survival or rejection." @default.
- W4385215552 created "2023-07-25" @default.
- W4385215552 creator A5006118614 @default.
- W4385215552 creator A5012852066 @default.
- W4385215552 creator A5013028311 @default.
- W4385215552 creator A5038425172 @default.
- W4385215552 creator A5041196618 @default.
- W4385215552 creator A5046729469 @default.
- W4385215552 creator A5053049503 @default.
- W4385215552 creator A5058594570 @default.
- W4385215552 creator A5074797757 @default.
- W4385215552 creator A5074911466 @default.
- W4385215552 creator A5077119575 @default.
- W4385215552 creator A5083137669 @default.
- W4385215552 date "2023-07-23" @default.
- W4385215552 modified "2023-10-17" @default.
- W4385215552 title "Biomarkers of the Complement System Activation (C3a, C5a, sC5b-9) in Serum of Patients before and after Liver Transplantation" @default.
- W4385215552 cites W1504886154 @default.
- W4385215552 cites W1602285939 @default.
- W4385215552 cites W1828479613 @default.
- W4385215552 cites W1965211796 @default.
- W4385215552 cites W1967052291 @default.
- W4385215552 cites W1969951594 @default.
- W4385215552 cites W1971467168 @default.
- W4385215552 cites W1972506040 @default.
- W4385215552 cites W1973825764 @default.
- W4385215552 cites W1973917346 @default.
- W4385215552 cites W1974617965 @default.
- W4385215552 cites W1979660545 @default.
- W4385215552 cites W1984743133 @default.
- W4385215552 cites W1986895676 @default.
- W4385215552 cites W1997933460 @default.
- W4385215552 cites W2005900950 @default.
- W4385215552 cites W2008139210 @default.
- W4385215552 cites W2027578103 @default.
- W4385215552 cites W2028703250 @default.
- W4385215552 cites W2032119134 @default.
- W4385215552 cites W2037156953 @default.
- W4385215552 cites W2040135566 @default.
- W4385215552 cites W2044204097 @default.
- W4385215552 cites W2050499780 @default.
- W4385215552 cites W2051124964 @default.
- W4385215552 cites W2051545456 @default.
- W4385215552 cites W2051957939 @default.
- W4385215552 cites W2053576798 @default.
- W4385215552 cites W2053717384 @default.
- W4385215552 cites W2056947937 @default.
- W4385215552 cites W2057194059 @default.
- W4385215552 cites W2059486139 @default.
- W4385215552 cites W2060148591 @default.
- W4385215552 cites W2073752819 @default.
- W4385215552 cites W2073785873 @default.
- W4385215552 cites W2081536518 @default.
- W4385215552 cites W2084722601 @default.
- W4385215552 cites W2086070598 @default.
- W4385215552 cites W2101368282 @default.
- W4385215552 cites W2102941723 @default.
- W4385215552 cites W2106085405 @default.
- W4385215552 cites W2114833349 @default.
- W4385215552 cites W2147416137 @default.
- W4385215552 cites W2150953216 @default.
- W4385215552 cites W2164312004 @default.
- W4385215552 cites W2166266357 @default.
- W4385215552 cites W2170395836 @default.
- W4385215552 cites W2201952665 @default.
- W4385215552 cites W228767759 @default.
- W4385215552 cites W2808143571 @default.
- W4385215552 cites W2937702069 @default.
- W4385215552 cites W2978773858 @default.
- W4385215552 cites W3146964128 @default.
- W4385215552 cites W3199741942 @default.
- W4385215552 cites W4214544393 @default.
- W4385215552 cites W4230795950 @default.
- W4385215552 cites W6635430 @default.
- W4385215552 cites W1964872320 @default.
- W4385215552 doi "https://doi.org/10.3390/biomedicines11072070" @default.
- W4385215552 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37509709" @default.
- W4385215552 hasPublicationYear "2023" @default.
- W4385215552 type Work @default.
- W4385215552 citedByCount "0" @default.
- W4385215552 crossrefType "journal-article" @default.
- W4385215552 hasAuthorship W4385215552A5006118614 @default.
- W4385215552 hasAuthorship W4385215552A5012852066 @default.
- W4385215552 hasAuthorship W4385215552A5013028311 @default.
- W4385215552 hasAuthorship W4385215552A5038425172 @default.
- W4385215552 hasAuthorship W4385215552A5041196618 @default.
- W4385215552 hasAuthorship W4385215552A5046729469 @default.
- W4385215552 hasAuthorship W4385215552A5053049503 @default.
- W4385215552 hasAuthorship W4385215552A5058594570 @default.
- W4385215552 hasAuthorship W4385215552A5074797757 @default.
- W4385215552 hasAuthorship W4385215552A5074911466 @default.
- W4385215552 hasAuthorship W4385215552A5077119575 @default.
- W4385215552 hasAuthorship W4385215552A5083137669 @default.
- W4385215552 hasBestOaLocation W43852155521 @default.
- W4385215552 hasConcept C111684460 @default.
- W4385215552 hasConcept C126322002 @default.
- W4385215552 hasConcept C160160445 @default.
- W4385215552 hasConcept C168444539 @default.