Decreased serum antioxidant capacity in patients with Wilson disease is associated with neurological symptoms
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064165%3A_____%2F12%3A11394" target="_blank" >RIV/00064165:_____/12:11394 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11110/12:11394
Result on the web
<a href="http://dx.doi.org/10.1007/s10545-011-9422-5" target="_blank" >http://dx.doi.org/10.1007/s10545-011-9422-5</a>
DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Decreased serum antioxidant capacity in patients with Wilson disease is associated with neurological symptoms
Original language description
Wilson disease (WD) is an inherited disorder of copper disposition caused by an ATP7B transporter gene mutation, leading to copper accumulation in predisposed tissues. In addition to a genetic predisposition, other factors are likely to contribute to itsclinical manifestation. The aim of the study was to assess whether oxidative stress affects the phenotypic manifestation of WD. In 56 patients with WD (29 men; 26 with the hepatic form, 22 with the neurologic form, and eight asymptomatic; mean age 38.5+/- 12 years), total serum antioxidant capacity (TAC) and inflammatory parameters (hs-CRP, IL-1 beta, IL-2, IL-6, IL-10, and TNF-alpha) were analyzed and related to the clinical manifestation, and mutations of the ATP7B gene. The control group for the TAC and inflammatory parameters consisted of 50 age- and gender-matched healthy individuals. WD patients had a significantly lower TAC (p < 0.00001), lower IL-10 levels (p = 0.039), as well as both higher IL-1 beta (p = 0.019) and IL-6 (p =
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CE - Biochemistry
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2012
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Inherited Metabolic Disease
ISSN
0141-8955
e-ISSN
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Volume of the periodical
35
Issue of the periodical within the volume
3
Country of publishing house
NL - THE KINGDOM OF THE NETHERLANDS
Number of pages
8
Pages from-to
541-548
UT code for WoS article
000302492300019
EID of the result in the Scopus database
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