Risk factors for mortality in 1528 Brazilian childhood-onset systemic lupus erythematosus patients

Ana P Sakamoto1, Clovis A Silva2, Ana C Pita2

  • 1Pediatric Rheumatology Unit, Universidade Federal de Sao Paulo, Sao Paulo, SP, Brazil.

Lupus
|April 18, 2023
PubMed

Insights

Mortality in childhood-onset systemic lupus erythematosus (cSLE) is low but concerning. Neuropsychiatric lupus (NP-SLE) and chronic kidney disease (CKD) are significant risk factors for death in cSLE patients.

Area of Science:

  • Pediatric Rheumatology
  • Systemic Lupus Erythematosus Research
  • Clinical Epidemiology

Background:

  • Childhood-onset systemic lupus erythematosus (cSLE) is a chronic autoimmune disease with potential for significant morbidity and mortality.
  • Understanding mortality patterns and risk factors in cSLE is crucial for improving patient outcomes and guiding clinical management.

Purpose of the Study:

  • To identify associations between mortality and patient characteristics in cSLE.
  • To evaluate risk factors for mortality in cSLE patients.
  • To determine the primary causes of death in this population.

Main Methods:

  • A multicenter retrospective cohort study involving 1,528 cSLE patients from 27 Brazilian pediatric rheumatology centers.
  • Review of medical records for demographic, clinical, disease activity, damage scores, and treatment data.
  • Univariate and multivariate Cox regression analyses to identify mortality risk factors; Kaplan-Meier plots for survival rates.

Main Results:

  • A total of 63/1,528 (4.1%) patients died. Sepsis (42.8%) and opportunistic infections (11.1%) were leading causes of death.
  • Neuropsychiatric lupus (NP-SLE) (HR=2.56) and chronic kidney disease (CKD) (HR=4.33) were significant risk factors for mortality.
  • Overall 5, 10, and 15-year survival rates were 97%, 95.4%, and 93.8%, respectively.

Conclusions:

  • The mortality rate in cSLE in Brazil is low but warrants attention.
  • NP-SLE and CKD represent major risk factors, highlighting the severity of these manifestations in cSLE-related mortality.
Abstract

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