Predictors of hypogammaglobulinemia in ANCA-associated vasculitis after a rituximab-based induction: a multicentre study
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu multicentrická studie, časopisecké články
PubMed
36562566
DOI
10.1093/rheumatology/keac716
PII: 6958549
Knihovny.cz E-zdroje
- Klíčová slova
- ANCA-associated vasculitis, cyclophosphamide, glucocorticoids, hypogammaglobulinemia, immunoglobulins, immunosuppression, retrospective study, rituximab, severe adverse events, severe infections,
- MeSH
- agamaglobulinemie * chemicky indukované farmakoterapie MeSH
- ANCA-asociované vaskulitidy * farmakoterapie chemicky indukované MeSH
- glukokortikoidy terapeutické užití MeSH
- imunoglobulin G MeSH
- indukce remise MeSH
- lidé MeSH
- prednison terapeutické užití MeSH
- retrospektivní studie MeSH
- rituximab škodlivé účinky MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- Názvy látek
- glukokortikoidy MeSH
- imunoglobulin G MeSH
- prednison MeSH
- rituximab MeSH
OBJECTIVES: Rituximab has become the cornerstone of induction treatment in ANCA-associated vasculitis (AAV). B-cell depletion may increase the risk of hypogammaglobulinemia, potentially leading to severe infections. This study aims to assess factors associated with hypogammaglobulinemia in AAV patients treated with rituximab. METHODS: This retrospective cohort study included AAV patients treated with rituximab induction in 14 European centres. Severe adverse events (SAEs) were defined as episodes requiring hospitalization or intravenous antibiotics, malignancies, or death. Linear and logistic regression were used to identify predictors of IgG levels and of the risk of hypogammaglobulinemia, defined as IgG ≤7 g/l at 6 months. RESULTS: The study included 227 patients. IgG levels at 6 months were lower than baseline (P < 0.001). Patients requiring intravenous antibiotics during the first 6 months had lower IgG levels at 6 months (P = 0.004). Age [β (95% CI): -0.23 (-0.38, -0.08) per 10 years, P = 0.003], oral glucocorticoid dose at induction [β (95% CI): -0.37 (-0.51, -0.24) per sqrt-transformed mg prednisone, P < 0.001] and concomitant use of intravenous glucocorticoid pulses [β (95% CI): -0.88 (-1.73, -0.02), P = 0.044] were associated with IgG levels at 6 months. Hypogammaglobulinemia was identified in 97 (42.7%) patients. In multivariable logistic regression, factors associated with the risk of hypogammaglobulinemia were age [OR (95% CI): 1.46 (1.15, 1.86) per 10 years, P = 0.002] and oral glucocorticoid dose at induction [OR (95% CI): 1.52 (1.23, 1.89) per 10 mg prednisone, P < 0.001]. CONCLUSIONS: In AAV patients treated with rituximab, hypogammaglobulinemia at 6 months after induction is common, and lower IgG levels are associated with serious infections. The risk of hypogammaglobulinemia in these patients increases with age and higher glucocorticoid doses.
Clinical Sciences in Lund Lund University Lund Sweden
Department of Health Medicine and Caring Sciences Linköping University Linköping Sweden
Department of Medicine University of Cambridge Cambridge UK
Department of Nephrology University of Birmingham Birmingham UK
Division of Renal Medicine CLINTEC Karolinska Institutet Stockholm Sweden
Renal Division ASST Santi Paolo e Carlo Università degli Studi di Milano Milano Italy
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