Principles of pediatric lupus nephritis in a prospective contemporary multi-center cohort
Autor: | Scott E. Wenderfer, Rebecca E Sadun, Emily A. Smitherman, Abhijit Dasgupta, Catherine Park, Andrea M. Knight, Beatrice Goilav, Laura B Lewandowski, Ekemini A Ogbu, Brian R. Stotter, Ankana Daga, Daryl M. Okamura, Aimee O. Hersh, Kathleen M Vazzana |
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Rok vydání: | 2021 |
Předmět: |
030203 arthritis & rheumatology
medicine.medical_specialty Pediatrics business.industry Lupus nephritis 030204 cardiovascular system & hematology Kidney medicine.disease Lupus Nephritis Cohort Studies 03 medical and health sciences 0302 clinical medicine Rheumatology Epidemiology Cohort medicine Humans Lupus Erythematosus Systemic Longitudinal Studies Age of Onset Pediatric rheumatology Child business |
Zdroj: | Lupus. 30:1660-1670 |
ISSN: | 1477-0962 0961-2033 |
Popis: | Lupus nephritis (LN) is a life-threatening manifestation of systemic lupus erythematosus (SLE) and is more common in children than adults. The epidemiology and management of childhood-onset SLE (cSLE) have changed over time, prompting the need to reassess expected outcomes. The purpose of this study is to use the Childhood Arthritis and Rheumatology Research Alliance (CARRA) prospective registry to validate historical principles of LN in a contemporary, real-world cohort. After an extensive literature review, six principles of LN in cSLE were identified. The CARRA registry was queried to evaluate these principles in determining the rate of LN in cSLE, median time from cSLE diagnosis to LN, short-term renal outcomes, and frequency of rituximab as an induction therapy. Of the 677 cSLE patients in the CARRA registry, 32% had documented LN. Decline in kidney function was more common in Black cSLE patients than non-Black patients ( p = 0.04). Black race was associated with worse short-term renal outcomes. In short-term follow up, most children with LN had unchanged or improved kidney function, and end stage kidney disease (ESKD) was rare. Ongoing follow-up of cSLE patients in the CARRA registry will be necessary to evaluate long-term outcomes to inform risk, management, and prognosis of LN in cSLE. |
Databáze: | OpenAIRE |
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