Glucocorticoids Reduce Aberrant O-Glycosylation of IgA1 in IgA Nephropathy Patients
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F18%3A00576728" target="_blank" >RIV/61388971:_____/18:00576728 - isvavai.cz</a>
Alternative codes found
RIV/61388971:_____/18:00494330 RIV/00216208:11110/18:10376089 RIV/00216208:11130/18:10376089 RIV/61989592:15110/18:73592333 and 3 more
Result on the web
<a href="https://karger.com/kbr/article/43/2/350/187867/Glucocorticoids-Reduce-Aberrant-O-Glycosylation-of" target="_blank" >https://karger.com/kbr/article/43/2/350/187867/Glucocorticoids-Reduce-Aberrant-O-Glycosylation-of</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1159/000487903" target="_blank" >10.1159/000487903</a>
Alternative languages
Result language
angličtina
Original language name
Glucocorticoids Reduce Aberrant O-Glycosylation of IgA1 in IgA Nephropathy Patients
Original language description
Background/Aims: IgA nephropathy is associated with aberrant O-glycosylation of IgA1, which is recognized by autoantibodies leading to the formation of circulating immune complexes. Some of them, after deposition into kidney mesangium, trigger glomerular injury. In patients with active disease nonresponding to angiotensin-converting enzyme inhibitors or angiotensin II blockers, corticosteroids are recommended. Methods: The relationship between the corticosteroid therapy and serum levels of IgA, aberrantly O-glycosylated IgA1, IgA-containing immune complexes and their mesangioproliferative activity was analyzed in IgA nephropathy patients and disease and healthy controls. Results: Prednisone therapy significantly reduced proteinuria and levels of serum IgA, galactose-deficient IgA1, and IgA-IgG immune complexes in IgA nephropathy patients and thus reduced differences in all of the above parameters between IgAN patients and control groups. A moderate but not significant reduction of mesangioproliferative potential of IgA-IgG immune complexes and IgA sialylation was detected. Conclusion: The prednisone therapy reduces overall aberrancy in IgA1 O-glycosylation in IgA nephropathy patients, but the measurement of IgA1 parameters does not allow us to predict the prednisone therapy outcome in individual patients. (C) 2018 The Author(s) Published by S. Karger AG, Basel.
Czech name
—
Czech description
—
Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
10606 - Microbiology
Result continuities
Project
<a href="/en/project/NV15-33686A" target="_blank" >NV15-33686A: The study of the relation between Epstein-Barr virus infection and development of IgA nephropathy</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Kidney & Blood Pressure Research
ISSN
1420-4096
e-ISSN
1423-0143
Volume of the periodical
43
Issue of the periodical within the volume
2
Country of publishing house
CH - SWITZERLAND
Number of pages
10
Pages from-to
350-359
UT code for WoS article
000434716500005
EID of the result in the Scopus database
2-s2.0-85054692240