Corticosteroids in IgA Nephropathy: A Retrospective Analysis from the VALIGA Study
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25677392
PubMed Central
PMC4552116
DOI
10.1681/asn.2014070697
PII: ASN.2014070697
Knihovny.cz E-zdroje
- Klíčová slova
- IgA nephropathy, immunosuppression, pathology, progression of chronic renal failure, proteinuria, risk factors,
- MeSH
- antihypertenziva terapeutické užití MeSH
- dospělí MeSH
- hodnoty glomerulární filtrace MeSH
- hormony kůry nadledvin terapeutické užití MeSH
- IgA nefropatie farmakoterapie patologie patofyziologie MeSH
- imunosupresiva terapeutické užití MeSH
- kombinovaná farmakoterapie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- následné studie MeSH
- progrese nemoci MeSH
- proteinurie etiologie MeSH
- renin-angiotensin systém MeSH
- retrospektivní studie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antihypertenziva MeSH
- hormony kůry nadledvin MeSH
- imunosupresiva MeSH
Current guidelines suggest treatment with corticosteroids (CS) in IgA nephropathy (IgAN) when proteinuria is persistently ≥1 g/d despite 3-6 months of supportive care and when eGFR is >50 ml/min per 1.73 m(2). Whether the benefits of this treatment extend to patients with an eGFR≤50 ml/min per 1.73 m(2), other levels of proteinuria, or different renal pathologic lesions remains unknown. We retrospectively studied 1147 patients with IgAN from the European Validation Study of the Oxford Classification of IgAN (VALIGA) cohort classified according to the Oxford-MEST classification and medication used, with details of duration but not dosing. Overall, 46% of patients received immunosuppression, of which 98% received CS. Treated individuals presented with greater clinical and pathologic risk factors of progression. They also received more antihypertensive medication, and a greater proportion received renin angiotensin system blockade (RASB) compared with individuals without immunosuppressive therapy. Immunosuppression was associated with a significant reduction in proteinuria, a slower rate of renal function decline, and greater renal survival. Using a propensity score, we matched 184 subjects who received CS and RASB to 184 patients with a similar risk profile of progression who received only RASB. Within this group, CS reduced proteinuria and the rate of renal function decline and increased renal survival. These benefits extended to those with an eGFR≤50 ml/min per 1.73 m(2), and the benefits increased proportionally with the level of proteinuria. Thus, CS reduced the risk of progression regardless of initial eGFR and in direct proportion to the extent of proteinuria in this cohort.
Imperial College Hammersmith Hospital London United Kingdom;
Oxford University Hospitals Oxford United Kingdom;
Regina Margherita Children's Hospital Turin Italy
Sacre Coeur Hospital of Montreal Montreal Quebec Canada;
University Health Network Toronto General Hospital Toronto Canada; and
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Emerging Modes of Treatment of IgA Nephropathy