4.2 Article

Biomarkers for Childhood-Onset Systemic Lupus Erythematosus

Journal

CURRENT RHEUMATOLOGY REPORTS
Volume 17, Issue 1, Pages -

Publisher

SPRINGER
DOI: 10.1007/s11926-014-0471-2

Keywords

Childhood-onset systemic lupus erythematosus; cSLE; SLE; Biomarker; Kidney disease; Urinary biomarkers; Cardiovascular disease; CNS lupus

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Funding

  1. NCATS NIH HHS [UL1 TR000077, UL1 TR001425] Funding Source: Medline
  2. NIDDK NIH HHS [P50 DK096418] Funding Source: Medline

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Childhood-onset systemic lupus erythematosus (cSLE) is a systemic autoimmune disease characterized by the presence of autoantibodies. cSLE often affects multiple organs in the body and is known to have a poorer prognosis than adult-onset disease (Azevedo et al. 2014). Current laboratory tests are clearly insufficient for identifying and monitoring the disease. Recent studies have yielded novel biomarkers for cSLE which can be used for monitoring disease activity and response to treatment. The most encouraging biomarkers will be discussed herein and include cell-bound complement activation products, some genomic profiles, and urinary proteins such as neutrophil gelatinase-associated lipocalin, monocyte chemoattractant protein-1, and others. Previous studies suggested that a combination of the novel biomarkers might help to enhance sensitivity and specificity for early diagnosis, disease monitoring, and prediction of cSLE flares.

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