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Published on: September 20, 2018
Soluble Vascular Cell Adhesion Molecule-1 Is Associated With Disease Activity in Adult-Onset Minimal Change Disease
Qingyan Zhang1, Miao Zhang1, Cheng Sun1
1Department of Nephrology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Background:
Cell adhesion molecules have been documented to be elevated in numerous immune inflammatory diseases. Minimal change disease (MCD) is an immune disorder. This study aimed to evaluate whether levels of soluble vascular cell adhesion molecule-1 (sVCAM-1) and soluble E-selectin (sE-selectin) reflect disease activity in adult-onset MCD.
Methods:
A sandwich enzyme-linked immunosorbent assay was used to measure the soluble adhesion molecules in 40 patients with nephrotic-range proteinuria and biopsy-proven MCD, obtained at the time of diagnosis and during remission. Thirty-five age- and sex-matched healthy volunteers served as controls.
Results:
Patients with MCD during the active stage showed significantly higher levels of sVCAM-1 and sE-selectin when compared to controls. Moreover, sVCAM-1 had significantly positive correlations with both urine protein and serum cholesterol, and was negatively associated with serum albumin. Multiple analyses showed that serum albumin was an independent predictor of sVCAM-1. The correlations between sE-selectin and other clinical parameters were not statistically significant. At follow-up, these markers systematically decreased as the disease went into remission, but the increase in sVCAM-1 persisted even in patients obtaining complete remission for 6 months.
Conclusions:
Patients with active MCD had increased levels of sVCAM-1 and sE-selectin. The correlation between sVCAM-1 and proteinuria, serum albumin and cholesterol and its decline during remission indicate that sVCAM-1 is associated with disease activity.
Insights
Soluble vascular cell adhesion molecule-1 (sVCAM-1) and E-selectin (sE-selectin) are elevated in active Minimal Change Disease (MCD). sVCAM-1 levels correlate with disease activity, indicating its potential as a biomarker for MCD.
Area of Science:
- Immunology
- Nephrology
- Biomarker Discovery
Background:
- Immune inflammatory diseases are often associated with elevated cell adhesion molecules.
- Minimal Change Disease (MCD) is an immune disorder characterized by nephrotic-range proteinuria.
- The role of soluble adhesion molecules in MCD activity requires further investigation.
Purpose of the Study:
- To investigate the association between soluble vascular cell adhesion molecule-1 (sVCAM-1) and soluble E-selectin (sE-selectin) levels and disease activity in adult-onset Minimal Change Disease (MCD).
- To determine if these soluble adhesion molecules can serve as biomarkers for MCD activity.
Main Methods:
- A sandwich enzyme-linked immunosorbent assay (ELISA) was employed to quantify sVCAM-1 and sE-selectin.
- Levels were measured in 40 adult patients with biopsy-proven MCD at diagnosis and during remission.
- A control group of 35 healthy volunteers was included for comparison.
Main Results:
- Patients with active MCD exhibited significantly higher levels of sVCAM-1 and sE-selectin compared to healthy controls.
- sVCAM-1 showed significant positive correlations with urine protein and serum cholesterol, and a negative correlation with serum albumin.
- Serum albumin was identified as an independent predictor of sVCAM-1 levels. sE-selectin did not show significant correlations with clinical parameters.
- These markers decreased during disease remission, though elevated sVCAM-1 persisted in some patients even after 6 months of complete remission.
Conclusions:
- Elevated levels of sVCAM-1 and sE-selectin are observed in patients with active MCD.
- The strong correlation between sVCAM-1 and clinical indicators of disease activity (proteinuria, serum albumin, cholesterol), along with its decline during remission, suggests its utility as a biomarker for MCD.
- sVCAM-1 may serve as a valuable indicator of disease activity and response to treatment in Minimal Change Disease.
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