Clinico-pathological associations of serum VCAM-1 and ICAM-1 levels in patients with lupus nephritis

Lupus. 2021 Jun;30(7):1039-1050. doi: 10.1177/09612033211004727. Epub 2021 Mar 26.

Abstract

Objective: We investigated the clinico-pathological associations of serum VCAM-1 and ICAM-1 levels in patients with biopsy-proven Class III/IV±V lupus nephritis (LN).

Methods: Serum VCAM-1 and ICAM-1 levels were determined by ELISAs. Sera from patients with non-renal SLE or non-lupus chronic kidney disease (CKD), and healthy subjects served as controls.

Results: Seropositivity rate for VCAM-1 and ICAM-1 was 93.10% and 37.93% respectively at the time of nephritic flare, and 44.83% and 13.79% respectively at remission, with both showing higher levels during flare (P < 0.05, for both). VCAM-1 level correlated with proteinuria, serum creatinine, and anti-dsDNA antibodies, and inversely correlated with C3. VCAM-1 level also correlated with leukocyte infiltration and fibrinoid necrosis/karyorrhexis scores in active LN kidney biopsies. ICAM-1 level correlated with proteinuria, but not anti-dsDNA or C3, nor histopathological features. VCAM-1 level increased 4.5 months before renal flare, while ICAM-1 increase coincided with flare, and both decreased after treatment. ROC analysis showed that VCAM-1 distinguished active LN from healthy subjects, LN in remission, active non-renal lupus, and CKD (ROC AUC of 0.98, 0.86, 0.93 and 0.90 respectively). VCAM-1 level in combination with either proteinuria or C3 was superior in distinguishing active LN from remission compared to the measurement of individual markers. Serum ICAM-1 level distinguished active LN from healthy subjects and LN patients in remission (ROC AUC of 0.75 and 0.66 respectively), but did not distinguish between renal versus non-renal lupus. ICAM-1 level in combination with markers of endothelial cell activation (syndecan-1, hyaluronan and thrombomodulin) was superior to proteinuria, anti-dsDNA, or C3 in distinguishing active LN from quiescent disease.

Conclusion: Our findings suggest potential utility of serum VCAM-1 and ICAM-1 in clinical management. Monitoring VCAM-1 may facilitate early diagnosis of flare. Combining selected biomarkers may be advantageous in diagnosing active LN. VCAM-1 may have a pathogenic role in renal parenchymal inflammation in active LN.

Keywords: Lupus nephritis; Vascular cell adhesion molecule-1, Intercellular adhesion molecule-1.

MeSH terms

  • Adult
  • Antibodies, Antinuclear / blood
  • Biomarkers / blood
  • Biopsy
  • Case-Control Studies
  • Complement C3 / metabolism
  • Creatinine / blood
  • Early Diagnosis
  • Enzyme-Linked Immunosorbent Assay / methods
  • Female
  • Humans
  • Hyaluronic Acid / blood
  • Intercellular Adhesion Molecule-1 / blood*
  • Kidney / pathology
  • Lupus Nephritis / classification
  • Lupus Nephritis / diagnosis
  • Lupus Nephritis / metabolism*
  • Lupus Nephritis / pathology*
  • Male
  • Middle Aged
  • Proteinuria / complications
  • Proteinuria / diagnosis
  • ROC Curve
  • Syndecan-1 / blood
  • Thrombomodulin / blood
  • Vascular Cell Adhesion Molecule-1 / blood*

Substances

  • Antibodies, Antinuclear
  • Biomarkers
  • C3 protein, human
  • Complement C3
  • SDC1 protein, human
  • Syndecan-1
  • Thrombomodulin
  • Vascular Cell Adhesion Molecule-1
  • anti-dsDNA autoantibody
  • Intercellular Adhesion Molecule-1
  • Hyaluronic Acid
  • Creatinine