Urinary CD163 is a marker of active kidney disease in childhood-onset lupus nephritis

Author:

Inthavong Haleigh1ORCID,Vanarsa Kamala1,Castillo Jessica1,Hicks M John23,Mohan Chandra1,Wenderfer Scott E45

Affiliation:

1. Department of Biomedical Engineering, University of Houston

2. Department of Pathology, Texas Children’s Hospital

3. Department of Immunology and Pathology, Baylor College of Medicine

4. Renal Section, Texas Children’s Hospital

5. Department of Pediatrics, Baylor College of Medicine , Houston, TX, USA

Abstract

Abstract Objective The objective of this study was to evaluate the utility of urine CD163 for detecting disease activity in childhood-onset SLE (cSLE) patients. Methods Sixty consecutive pediatric patients fulfilling four or more ACR criteria for SLE and 20 healthy controls were recruited for testing of urinary CD163 using ELISA. SLE disease activity was assessed using the SLEDAI-2K. Results Urine CD163 was significantly higher in patients with active LN than inactive SLE patients and healthy controls, with receiver operating characteristics area under the curve values ranging from 0.93 to 0.96. LN was ascertained by kidney biopsy. Levels of CD163 significantly correlated with the SLEDAI, renal SLEDAI, urinary protein excretion and C3 complement levels. Urine CD163 was also associated with high renal pathology activity index and chronicity index, correlating strongly with interstitial inflammation and interstitial fibrosis based on the examination of concurrent kidney biopsies. Conclusion Urine CD163 emerges as a promising marker for identifying cSLE patients with active kidney disease. Longitudinal studies are warranted to validate the clinical utility of urine CD163 in tracking kidney disease activity in children with lupus.

Funder

NIH

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Reference36 articles.

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3. Lupus nephritis biomarkers;Soliman;Clin Immunol,2017

4. Biomarkers for childhood-onset systemic lupus erythematosus;Abulaban;Curr Rheumatology Rep,2015

5. Adolescent onset of lupus results in more aggressive disease and worse outcomes: results of a nested matched case-control study within LUMINA, a multiethnic US cohort (LUMINA LVII);Tucker;Lupus,2008

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