
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title xml:lang="srp">Hepatitis S i parametri inflamacijskog odgovora kod pacijenata sa terminalnom bubrežnom insuficijencijom</dc:title>
  <dc:creator>Lukić,  Ružica, 1976-</dc:creator>
  <dc:description xml:lang="srp">Apstrakt: Hepatitis C virusna infekcija (HCV), jedan od najčešćih uzroka bolesti jetre, česta je komplikacija kod pacijenata sa terminalnom bubrežnom insuficijencijom (eng. end-stage renal disease, ESRD). ESRD se definiše kao smanjena glomerularna filtracija, a takođe je praćena i poremećenom funkcijom imunskog sistema. Galektin-3 je lektin koji povezuje β-galaktozide, uključen u različite biološke procese, uključujući patogenezu hronične bubrežne bolesti. Cilj naše studije je bio da se ispita težina bolesti kod ESRD+ HCV+ pacijenata i analiziraju serumske koncentracije citokina; Anti- HCV antitela; i galektina-3. Takođe, pokušali smo da odredimo potencijalnu korelaciju između nivoa galektina-3 i parametara težine bolesti ALT i AST. Naši rezultati pokazuju smanjene nivoe ALT i AST (p = 0.00), što ukazuje na manje oštećenje jetre kod ESRD+ HCV+ pacijenata u odnosu na HCV+ pacijenate. Povećana koncentracija IL-6 (p = 0.03) implicira hepatoprotektivnu ulogu IL -6 kod ovih pacijenata. Takođe, nivo galektina-3 (r = 0.00) u serumu ESRD+ HCV+ pacijenata veći je nego kod HCV+ pacijenata. Ovu promenu „prati― negativna korelacija između galektina-3 i AST-a i ALT-a (p = 0.029; p = 0.033). Prisustvo povećanih sistemskih vrednosti IL-6 i Gal-3 kod ESRD+ HCV+ pacijenata može biti kompenzatorni mehanizam da se izbegnu ili ograniče tekući proinflamacijski procesi i da se suprimira hronična inflamacija, što ukazuje na nove aspekte HCV infekcije kod pacijenata sa ESRD.</dc:description>
  <dc:description xml:lang="eng">Abstract: Hepatitis C virus infection (HCV), one of the greatest causes of liver disease, is a frequent complication in patients with end-stage renal disease (ESRD) on dialysis. ESRD is defined as decreased glomerular filtration and also accompanied by impaired function of the immune system. Galectin-3 is a β-galactoside-binding lectin, involved in various biological processes including pathogenesis of chronic renal disease. The aim of our study was to estimate disease severity in ESRD HCV+ patients and analyze the serum concentrations of cytokines; anti-HCV antibodies; and galectin-3. Also, we attempted to determine potential correlation between galectin-3 level and parameters of disease severity ALT and AST. Our results showed decreased levels of ALT and AST (p = 0 00), demonstrating less liver destruction in ESRD HCV+ patients in comparison to HCV+ patients. Increased levels of IL-6 (p = 0 03) implicate a hepatoprotective role of IL-6 in these patients. Also, level of galectin-3 (p = 0 00)
in the serum of ESRD HCV+ patients was higher than that of HCV+ patients. This alteration was accompanied with negative correlation between galectin-3 and AST and ALT, respectively (p = 0 029; p = 0 033). The presence of increased systemic levels of IL-6 and Gal-3 in ESRD HCV+ patients may be an attempt to counteract or limit ongoing proinflammatory processes and to downregulate chronic inflammation, suggesting the new aspects of HCV infection in ESRD patients.</dc:description>
  <dc:description xml:lang="srp"></dc:description>
  <dc:contributor>Jovanović,  Ivan P.</dc:contributor>
  <dc:contributor>Arsenijević,  Arsenijević, 1958-</dc:contributor>
  <dc:contributor>Ćupić,  Maja, 1962-</dc:contributor>
  <dc:contributor>Mijailović,  Željko, 1970-</dc:contributor>
  <dc:contributor>Petrović,  Dejan, 1968-</dc:contributor>
  <dc:contributor>Radosavljević,  Gordana, 1976-</dc:contributor>
  <dc:date>2017</dc:date>
  <dc:date>2017</dc:date>
  <dc:date>2017</dc:date>
  <dc:date>2017</dc:date>
  <dc:date>2017</dc:date>
  <dc:date>2017</dc:date>
  <dc:date>2017</dc:date>
  <dc:date>2017</dc:date>
  <dc:type xml:lang="eng">baccalaureate Dissertation</dc:type>
  <dc:format>112 listova</dc:format>
  <dc:format>3750936 bytes</dc:format>
  <dc:identifier>o:800</dc:identifier>
  <dc:identifier>ID=524002197 ; D-3059</dc:identifier>
  <dc:identifier>thesis:5188</dc:identifier>
  <dc:identifier>cobiss:524002197</dc:identifier>
  <dc:identifier>https://phaidrakg.kg.ac.rs/o:800</dc:identifier>
  <dc:source>Thesis:5188</dc:source>
  <dc:source>Cobiss:524002197</dc:source>
  <dc:language>srp</dc:language>
  <dc:rights>CC BY-NC-ND 2.0 AT</dc:rights>
  <dc:rights>http://creativecommons.org/licenses/by-nc-nd/2.0/at/</dc:rights>
</oai_dc:dc>
