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Quantitative Assessment of Human Neutrophil Migration Across a Cultured Bladder Epithelium
Published on: November 7, 2013
Urine macrophage migration inhibitory factor (MIF) in children with urinary tract infection: a possible predictor of
Hasan Otukesh1, Seyed-Mohammad Fereshtehnejad, Rozita Hoseini
1Urology and Nephrology Research Center, Labbafi Nejad Hospital, Tehran, Iran.
Abstract:
Macrophage migration inhibitory factor (MIF) is an important pro-inflammatory cytokine expressed at sites of inflammation. We have assessed this factor (MIF) in urinary tract infections with the aim of determining a non-invasive and sensitive method to differentiate upper and lower renal involvement. Thirty-three pediatric patients with urinary track infection (25 with acute pyelonephritis, eight with acute cystitis) and 40 healthy subjects were recruited for this prospective case-control study. Pyelonephritis was differentiated from cystitis by dimercaptosuccinic acid (DMSA) scan. Urinary MIF concentration was determined using an enzyme-linked immunosorbent assay method. The urine MIF/creatinine (Cr) ratio was significantly higher in pyelonephritis patients than in those with acute cystitis and the control group (P < 0.001). The optimal cut-point of 4.90 pg/micromol Cr for the urine MIF/Cr ratio has the potential to be a biomarker for distinguishing patients with acute pyelonephritis from those with acute cystitis. Determination of the urinary MIF was also useful in selecting the patients at risk of permanent renal damage. Of those patients with pyelonephritis, based on the DMSA scan at the time of infection, scarring on follow-up DMSA scan 9-12 months later occurred in patients with the highest urinary MIF/Cr ratios. We conclude that the urine MIF/Cr ratio is a sensitive test for differentiating acute pyelonephritis from acute cystitis and also for detecting children with acute pyelonephritis who are at a higher risk for permanent renal scars in the future.
Insights
The urine Macrophage Migration Inhibitory Factor (MIF) to creatinine ratio can non-invasively differentiate upper and lower urinary tract infections in children. Higher ratios indicate a greater risk of kidney scarring from pyelonephritis.
Area of Science:
- Pediatric Nephrology
- Immunology
- Biomarker Discovery
Background:
- Macrophage Migration Inhibitory Factor (MIF) is a pro-inflammatory cytokine found at inflammation sites.
- Urinary tract infections (UTIs) require methods to distinguish upper (pyelonephritis) from lower (cystitis) involvement.
- Differentiating UTI types is crucial for timely and appropriate treatment to prevent renal damage.
Purpose of the Study:
- To evaluate urinary MIF concentration as a non-invasive biomarker for differentiating pediatric pyelonephritis from cystitis.
- To assess the utility of the urine MIF/creatinine (Cr) ratio in identifying patients at risk for renal scarring.
- To establish a sensitive diagnostic marker for upper UTIs in children.
Main Methods:
- A prospective case-control study involving 33 pediatric UTI patients and 40 healthy controls.
- Pyelonephritis diagnosis confirmed by dimercaptosuccinic acid (DMSA) scan.
- Urinary MIF concentration measured via enzyme-linked immunosorbent assay (ELISA), with results normalized to creatinine.
Main Results:
- The urine MIF/Cr ratio was significantly elevated in pyelonephritis patients compared to cystitis and control groups (P < 0.001).
- An optimal cut-point of 4.90 pg/micromol Cr for the urine MIF/Cr ratio demonstrated potential for differentiating pyelonephritis from cystitis.
- Higher urine MIF/Cr ratios correlated with the development of renal scars on follow-up DMSA scans in pyelonephritis patients.
Conclusions:
- The urine MIF/Cr ratio serves as a sensitive biomarker for distinguishing acute pyelonephritis from acute cystitis in children.
- This ratio aids in identifying pediatric patients with pyelonephritis who are at higher risk for developing permanent renal scars.
- Urinary MIF assessment offers a valuable, non-invasive tool for pediatric UTI management and prognosis.
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