AI Article Synopsis

  • Lupus nephritis (LN) is a serious complication of systemic lupus erythematosus (SLE), requiring invasive kidney biopsies for diagnosis; researchers are exploring non-invasive urine biomarkers to help in this process.
  • This study focused on urinary galectin-3 binding protein (u-Gal-3BP) levels in 270 subjects, including LN patients and controls, finding elevated levels in LN which correlated with disease activity.
  • The results suggest that u-Gal-3BP could be a useful biomarker for diagnosing and monitoring LN, especially in certain forms of the disease, although other markers like KIM-1 also showed potential for distinguishing LN from other conditions.

Article Abstract

Background: Lupus nephritis (LN) is a major and severe organ involvement in systemic lupus erythematosus (SLE), whose diagnosis and treatment necessitate to perform kidney biopsy, which is an invasive procedure. Non-invasive urine biomarkers are an active area of investigation to support LN diagnosis and management.

Objective: To investigate the role of urinary galectin-3 binding protein (u-Gal-3BP) as a candidate biomarker of renal disease in biopsy proven LN.

Patients And Methods: Levels of u-Gal-3BP were investigated in a cross-sectional fashion by ELISA in 270 subjects: 86 LN patients, 63 active SLE patients with no kidney involvement, 73 SLE patients with inactive disease and 48 age and sex-matched population-based controls (PBC). Moreover, urine samples were analysed separately by ELISA for additional markers of kidney pathology: neutrophil gelatinase-associated lipocalin (NGAL), osteopontin (OPN), kidney injury molecule-1 (KIM-1) and galectin-3 (Gal-3). The concentrations of all studied molecules were normalized to urine creatinine levels. In 10 patients, post-treatment levels of the biomarkers were measured.

Results: Normalized u-Gal-3BP levels were higher in LN patients compared to the other groups (). Comparing different LN classes, u-Gal-3BP levels were higher among patients with proliferative (class III/IV) and membranous (class V) as compared to mesangial (class II) forms (). In proliferative forms, u-Gal-3BP levels correlated with the activity index in renal biopsies (r = 0.42, ). Moreover, in a subset of 10 patients with repeated kidney biopsy and urine sampling before and after induction treatment, a significant decrease of u-Gal-3BP was observed () Among the other markers, KIM-1 was also able to discriminate LN from the other groups, while NGAL, OPN and Gal-3 could not in this cohort.

Conclusion: Given its ability to discriminate LN patients from active non-renal and inactive SLE patients, the observed correlation with the activity index in renal biopsies, and its levels declining following treatment, u-Gal-3BP shows promise as a non-invasive urinary biomarker to help detecting and to monitor renal involvement in SLE patients and should be validated in larger cohorts.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939930PMC
http://dx.doi.org/10.1177/09612033221145534DOI Listing

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