Serum Hepcidin Is Increased in ANCA-Associated Vasculitis and Correlates With Activity Markers

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F18%3A10385026" target="_blank" >RIV/00216208:11110/18:10385026 - isvavai.cz</a>
Alternative codes found
RIV/00064165:_____/18:10385026
Result on the web
<a href="http://www.biomed.cas.cz/physiolres/pdf/67/67_945.pdf" target="_blank" >http://www.biomed.cas.cz/physiolres/pdf/67/67_945.pdf</a>
DOI - Digital Object Identifier
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Result language
angličtina
Original language name
Serum Hepcidin Is Increased in ANCA-Associated Vasculitis and Correlates With Activity Markers
Original language description
Hepcidin is a key regulator of iron metabolism and plays an important role in many pathologies. It is increased by iron administration and by inflammation, while erythropoiesis downregulates its expression. It decreases iron availability and thus contributes to anemia of chronic diseases. The aim of the study was to measure hepcidin as a marker and pathogenetic factor in ANCA-associated vasculitis (AAV). Hepcidin plasma concentration was measured by the immunological method in 59 patients with AAV and compared to patients with non-vasculitic etiology of chronic kidney disease, patients on hemodialysis (HD), with systemic lupus erythematodes (SLE) and to healthy controls and blood donors, and was correlated with the parameters of iron metabolism, inflammation, activity of the process and kidney function. Hepcidin concentration was increased in patients with AAV, SLE and HD and correlated positively with C-reactive protein, serum ferritin and creatinine, and negatively with hemoglobin and serum transferrin. In active form of AAV it correlated with the clinical scoring system (BVAS). Hepcidin can thus be considered as a pathogenetic factor of anemia in AAV and can be used for evaluation of inflammation in AAV and as an additional marker in active forms of the disease.
Czech name
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Czech description
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Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30105 - Physiology (including cytology)

Project
<a href="/en/project/NV15-31662A" target="_blank" >NV15-31662A: Human urinary exosomes - the source of new biomarkers for the diagnosis and follow-up of kidney diseases</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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