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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://repozitorij.uni-lj.si/IzpisGradiva.php?id=159566"><dc:title>Supplementation of vitamin E as an addition to a commercial renal diet does not prolong survival of cats with chronic kidney disease</dc:title><dc:creator>Krofič,	Martina	(Avtor)
	</dc:creator><dc:creator>Tavčar-Kalcher,	Gabrijela	(Avtor)
	</dc:creator><dc:creator>Vovk,	Tomaž	(Avtor)
	</dc:creator><dc:creator>Žegura,	Bojana	(Avtor)
	</dc:creator><dc:creator>Lusa,	Lara	(Avtor)
	</dc:creator><dc:creator>Tozon,	Nataša	(Avtor)
	</dc:creator><dc:creator>Nemec Svete,	Alenka	(Avtor)
	</dc:creator><dc:subject>chronic renal insufficiency</dc:subject><dc:subject>oxidative stress</dc:subject><dc:subject>vitamin E</dc:subject><dc:subject>survival</dc:subject><dc:subject>chronic kidney disease</dc:subject><dc:description>Background The aim of this double-blind, placebo-controlled study was to investigate the effect of vitamin E supplementation as an addition to a commercial renal diet on survival time of cats with different stages of chronic kidney disease (CKD). In addition, we were interested whether vitamin E supplementation affects selected oxidative stress and clinical parameters. Thirty-four cats with CKD and 38 healthy cats were included in the study. Cats with CKD were classified according to the IRIS Guidelines; seven in IRIS stage 1, 15 in IRIS stage 2, five in IRIS stage 3 and seven in IRIS stage 4. Cats with CKD were treated according to IRIS Guidelines. Cats with CKD were randomly assigned to receive vitamin E (100 IU/cat/day) or placebo (mineral oil) for 24 weeks in addition to standard therapy. Plasma malondialdehyde (MDA) and protein carbonyl (PC) concentrations, DNA damage of peripheral lymphocytes and plasma vitamin E concentrations were measured at baseline and four, eight, 16 and 24 weeks thereafter. Routine laboratory analyses and assessment of clinical signs were performed at each visit. 
Results Vitamin E supplementation had no effect on the survival time and did not reduce the severity of clinical signs. Before vitamin E supplementation, no significant differences in vitamin E, MDA and PC concentrations were found between healthy and CKD cats. However, plasma MDA concentration was statistically significantly higher (p = 0.043) in cats with early CKD (IRIS stages 1 and 2) than in cats with advanced CKD (IRIS stages 3 and 4). Additionally, DNA damage was statistically significantly higher in healthy cats (p ≤ 0.001) than in CKD cats. Plasma vitamin E concentrations increased statistically significantly in the vitamin E group compared to the placebo group four (p = 0.013) and eight (p = 0.017) weeks after the start of vitamin E supplementation. During the study and after 24 weeks of vitamin E supplementation, plasma MDA and PC concentrations and DNA damage remained similar to pre- supplementation levels in both the placebo and vitamin E groups. 
Conclusions Vitamin E supplementation as an addition to standard therapy does not prolong survival in feline CKD.</dc:description><dc:date>2024</dc:date><dc:date>2024-07-12 13:00:23</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>159566</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
