Related Experiment Video
Updated: May 4, 2026

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
Urinary MCP-1/creatinine in Henoch-Schönlein purpura and its relationship with nephritis
Yolanda Fuentes1, Ana María Hernández, Pilar García-Roca
1Laboratorio de Investigación en Nefrología, Hospital Infantil de México Federico Gómez, Calle Dr. Márquez 162, Col. Doctores, Deleg. Cuauhtémoc, C. P. 06720, México, D. F., México, fuvy76@hotmail.com.
Background:
Monocyte chemotactic protein-1 (MCP-1) plays a direct role in the infiltration of macrophages and monocytes during the early stages of Henoch-Schönlein purpura (HSP) nephritis. The aim of this study was to compare the urinary MCP-1/creatinine levels in children with and without HSP nephritis and determine if they are associated with the severity of renal lesions.
Methods:
We included 77 patients with HSP and 25 healthy control children. Levels of serum creatinine, urinalysis, and 12-h proteinuria assessments were performed. Urinary MCP-1 levels were determined by ELISA.
Results:
Fifty-seven patients had nephritis (74 %). Urinary MCP-1/creatinine levels were significantly higher in patients with HSP nephritis (median, 653 pg/mg) compared to those with HSP without nephritis (median, 269 pg/mg) or healthy children (191 pg/mg). In addition, higher MCP-1/creatinine levels were observed in HSP patients who had renal biopsy (median, 1,412 pg/mg) in comparison to HSP patients without renal biopsy (median, 302 pg/mg). The urinary MCP-1 cut-off value of 530 pg/mg could be used to distinguish patients who undergo renal biopsy with a sensitivity of 81 % and specificity of 77 %.
Conclusions:
Urinary MCP-1/creatinine levels are elevated in the early stages of severe HSP nephritis and can be used as a biomarker for HSP nephritis.
Insights
Urinary monocyte chemotactic protein-1 (MCP-1) levels are higher in children with Henoch-Schönlein purpura (HSP) nephritis. Elevated MCP-1/creatinine can indicate severe kidney lesions and serve as an early biomarker for HSP nephritis.
Area of Science:
- Pediatric Nephrology
- Immunology
- Biomarker Discovery
Background:
- Monocyte chemotactic protein-1 (MCP-1) is implicated in macrophage and monocyte infiltration during early Henoch-Schönlein purpura (HSP) nephritis.
- Understanding MCP-1's role is crucial for diagnosing and assessing the severity of HSP nephritis in children.
Purpose of the Study:
- To compare urinary MCP-1/creatinine levels in children with and without HSP nephritis.
- To determine if urinary MCP-1/creatinine levels correlate with the severity of renal lesions in HSP.
Main Methods:
- Study included 77 children with HSP and 25 healthy controls.
- Assessed serum creatinine, urinalysis, and 12-h proteinuria.
- Quantified urinary MCP-1 levels using ELISA and calculated MCP-1/creatinine ratios.
Main Results:
- Urinary MCP-1/creatinine levels were significantly elevated in children with HSP nephritis (median, 653 pg/mg) compared to those without nephritis (269 pg/mg) and healthy controls (191 pg/mg).
- Patients with renal biopsies showed higher MCP-1/creatinine levels (1,412 pg/mg) than those without (302 pg/mg).
- A urinary MCP-1 cut-off of 530 pg/mg demonstrated 81% sensitivity and 77% specificity for identifying patients requiring renal biopsy.
Conclusions:
- Urinary MCP-1/creatinine levels are elevated in early-stage severe HSP nephritis.
- Urinary MCP-1/creatinine serves as a potential non-invasive biomarker for identifying severe HSP nephritis and guiding renal biopsy decisions.
Related Concept Videos
Nephrotic Syndrome II : Assessment and Medical Management
Acute Pyelonephritis II: Diagnostic Studies and Management
Renal Corpuscle
Glomerulus: Structure and Function
The glomerulus is a tiny, intricate network of capillaries located at the beginning of the nephron. It's enveloped by the Bowman's capsule and receives its blood supply from an afferent arteriole, which divides into numerous...
Acute Pyelonephritis I: Introduction
Nephrotic Syndrome I : Introduction
Acute Kidney Injury II: Pathophysiology

