Galactose-deficient IgA1 and the corresponding IgG autoantibodies predict IgA nephropathy progression
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu klinické zkoušky, časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
K01 DK106341
NIDDK NIH HHS - United States
R01 DK078244
NIDDK NIH HHS - United States
R01 DK082753
NIDDK NIH HHS - United States
PubMed
30794576
PubMed Central
PMC6386256
DOI
10.1371/journal.pone.0212254
PII: PONE-D-18-32069
Knihovny.cz E-zdroje
- MeSH
- autoprotilátky krev imunologie MeSH
- biologické markery krev MeSH
- dospělí MeSH
- galaktosa krev imunologie MeSH
- IgA nefropatie krev diagnóza imunologie mortalita MeSH
- imunoglobulin A krev imunologie MeSH
- lidé MeSH
- následné studie MeSH
- progrese nemoci MeSH
- prospektivní studie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- autoprotilátky MeSH
- biologické markery MeSH
- galaktosa MeSH
- imunoglobulin A MeSH
BACKGROUND: IgA nephropathy (IgAN), the most common primary glomerulonephritis worldwide, has serious outcomes with end-stage renal disease developing in 30-50% of patients. The diagnosis requires renal biopsy. Due to its inherent risks, non-invasive approaches are needed. METHODS: We evaluated 91 Czech patients with biopsy-proven IgAN who were assessed at time of diagnosis for estimated glomerular filtration rate (eGFR), proteinuria, microscopic hematuria, and hypertension, and then followed prospectively. Serum samples collected at diagnosis were analyzed for galactose-deficient IgA1 (Gd-IgA1) using new native-IgA1 and established neuraminidase-treated-IgA1 tests, Gd-IgA1-specific IgG autoantibodies, discriminant analysis and logistic regression model assessed correlations with renal function and Oxford classification (MEST score). RESULTS: Serum levels of native (P <0.005) and neuraminidase-treated (P <0.005) Gd-IgA1 were associated with the rate of eGFR decline. A higher relative degree of galactose deficiency in native serum IgA1 predicted a faster eGFR decline and poor renal survival (P <0.005). However, Gd-IgA1 has not differentiated patients with low vs. high baseline eGFR. Furthermore, patients with high baseline eGFR that was maintained during follow-up were characterized by low serum levels of Gd-IgA1-specific IgG autoantibodies (P = 0.003). CONCLUSIONS: Including levels of native and neuraminidase-treated Gd-IgA1 and Gd-IgA1-specific autoantibodies at diagnosis may aid in the prognostication of disease progression in Czech patients with IgAN. Future tests will assess utility of these biomarkers in larger patients cohorts from geographically distinct areas.
Institute of Clinical and Experimental Medicine Department of Pathology Prague Czech Republic
Longhua Hospital Shanghai University of Traditional Medicine Shanghai China
Zobrazit více v PubMed
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