About: Functional variants of eNOS and iNOS genes have no relationship to the portal hypertension in patients with liver cirrhosis     Goto   Sponge   NotDistinct   Permalink

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  • Objective. Nitric oxide is an important vasoactive mediator. Changes in NO production, caused by functional variants of both endothelial and inducible NO synthase (eNOS, iNOS), might play a role in portal hypertension. The aim was to study the significance of functional eNOS and iNOS gene variants in cirrhotic patients and their interrelationship to both inflammatory and endothelial activation parameters. Material and methods. One hundred and thirty-two patients with liver cirrhosis (age 36-72 years) and 101 controls were examined for functional variants of eNOS (E298D, 27bpintr4, 786T/C) and iNOS (R221W, S608L) genes. Inflammatory (IL6, IL8, IL10) and vasoactive (sVCAM-1, E-selectin) cytokines were measured using ELISA kits. Results. The frequency of E298D (GG 12%, GT 41%, TT 47%), 28bpintr4 (AA 6%, AB 28%, BB 66%), 786T/C genotypes (CC 17%, CT 45%, TT 38%), as well as R221W (CC 93%, CT 7%, TT 0%), and S608L (CC 65%, CT 32%, TT 3%) genotypes in cirrhotic patients did not differ from the controls (p > 0.05 for all comparisons). No relationship was found between the frequency of these genotypes and the severity of portal hypertension, or either inflammatory or vasoactive cytokines. A positive correlation was found between hepatic venous pressure gradient and cytokine concentration: sVCAM-1, IL6, IL8, IL10. Conclusions. Examined eNOS and iNOS variants have no relationship to pathogenesis of liver cirrhosis. Severity of portal hypertension was associated with the changes in endothelial activation.
  • Objective. Nitric oxide is an important vasoactive mediator. Changes in NO production, caused by functional variants of both endothelial and inducible NO synthase (eNOS, iNOS), might play a role in portal hypertension. The aim was to study the significance of functional eNOS and iNOS gene variants in cirrhotic patients and their interrelationship to both inflammatory and endothelial activation parameters. Material and methods. One hundred and thirty-two patients with liver cirrhosis (age 36-72 years) and 101 controls were examined for functional variants of eNOS (E298D, 27bpintr4, 786T/C) and iNOS (R221W, S608L) genes. Inflammatory (IL6, IL8, IL10) and vasoactive (sVCAM-1, E-selectin) cytokines were measured using ELISA kits. Results. The frequency of E298D (GG 12%, GT 41%, TT 47%), 28bpintr4 (AA 6%, AB 28%, BB 66%), 786T/C genotypes (CC 17%, CT 45%, TT 38%), as well as R221W (CC 93%, CT 7%, TT 0%), and S608L (CC 65%, CT 32%, TT 3%) genotypes in cirrhotic patients did not differ from the controls (p > 0.05 for all comparisons). No relationship was found between the frequency of these genotypes and the severity of portal hypertension, or either inflammatory or vasoactive cytokines. A positive correlation was found between hepatic venous pressure gradient and cytokine concentration: sVCAM-1, IL6, IL8, IL10. Conclusions. Examined eNOS and iNOS variants have no relationship to pathogenesis of liver cirrhosis. Severity of portal hypertension was associated with the changes in endothelial activation. (en)
Title
  • Functional variants of eNOS and iNOS genes have no relationship to the portal hypertension in patients with liver cirrhosis
  • Functional variants of eNOS and iNOS genes have no relationship to the portal hypertension in patients with liver cirrhosis (en)
skos:prefLabel
  • Functional variants of eNOS and iNOS genes have no relationship to the portal hypertension in patients with liver cirrhosis
  • Functional variants of eNOS and iNOS genes have no relationship to the portal hypertension in patients with liver cirrhosis (en)
skos:notation
  • RIV/00216208:11110/13:10192534!RIV14-MZ0-11110___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(NT11247), P(NT12290), S
http://linked.open...iv/cisloPeriodika
  • 5
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 75890
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11110/13:10192534
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • portal hypertension; hemodynamic parameters; eNOS/iNOS functional variants; cirrhosis (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [0506FD6E9E61]
http://linked.open...i/riv/nazevZdroje
  • Scandinavian Journal of Gastroenterology
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 48
http://linked.open...iv/tvurceVysledku
  • Dvořák, Karel
  • Jansa, Pavel
  • Jáchymová, Marie
  • Leníček, Martin
  • Linhart, Aleš
  • Urbánek, Petr
  • Vítek, Libor
  • Brůha, Radan
  • Petrtýl, Jaromír
http://linked.open...ain/vavai/riv/wos
  • 000317933300012
issn
  • 0036-5521
number of pages
http://bibframe.org/vocab/doi
  • 10.3109/00365521.2013.773459
http://localhost/t...ganizacniJednotka
  • 11110
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