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Soluble urokinase plasminogen activator receptor suPAR as a marker for inflammation in pediatric inflammatory bowel
Kaija-Leena Kolho1, Elsa Valtonen, Hanne Rintamäki
1Children's Hospital, Helsinki University Central Hospital, University of Helsinki, Helsinki, Finland. kaija-leena.kolho@helsinki.fi
Insights
Soluble urokinase plasminogen activator receptor (suPAR) shows limited value in pediatric inflammatory bowel disease (IBD). While glucocorticoids reduced suPAR levels, it did not correlate with intestinal inflammation or therapeutic response to TNF-α-antagonist.
Area of Science:
- Pediatric Gastroenterology
- Inflammation Biomarkers
- Immunology
Background:
- Early monitoring of therapeutic response in pediatric inflammatory bowel disease (IBD) remains a clinical challenge.
- Conventional blood inflammatory markers like erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) can be low in severe pediatric IBD.
- Soluble urokinase plasminogen activator receptor (suPAR) has emerged as a potential inflammatory marker in adult IBD.
Purpose of the Study:
- To evaluate the performance of suPAR as a biomarker in pediatric IBD.
- To assess the association of suPAR with disease type (Crohn's disease vs. ulcerative colitis) and inflammatory markers.
- To investigate the effect of glucocorticoid and TNF-α-antagonist therapies on suPAR levels in pediatric IBD.
Main Methods:
- Prospective study of pediatric IBD patients initiating glucocorticoid (n=19) or TNF-α-antagonist (n=16) therapy.
- Measurement of suPAR levels at the start of therapy.
- Correlation analysis of suPAR with ESR, CRP, and fecal calprotectin (FC).
Main Results:
- suPAR levels were generally low in pediatric IBD patients, irrespective of disease type.
- Glucocorticoid therapy led to a significant decline in suPAR levels (p < 0.01).
- TNF-α-antagonist therapy did not affect suPAR levels. suPAR did not correlate with ESR, CRP, or FC.
Conclusions:
- suPAR levels in pediatric IBD are low and do not reflect the degree of intestinal inflammation as assessed by FC.
- While glucocorticoids reduce suPAR, this change does not reliably indicate therapeutic response.
- suPAR demonstrates limited utility for assessing systemic inflammatory responses in pediatric IBD patients.
Objective:
In inflammatory bowel disease (IBD), more means to monitor early therapeutic response are needed. In pediatric IBD, blood inflammatory markers erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP) may be low in 10 to 20% of patients with severe disease. Recently, soluble urokinase plasminogen activator receptor (suPAR) was described as a potential blood inflammatory marker in adult IBD.
Methods:
We tested the performance of suPAR by the start of therapy with glucocorticoids (n = 19) or TNF-α-antagonist (n = 16) in pediatric IBD (Crohn's disease n = 19, ulcerative colitis (UC) n = 16).
Results:
The levels of suPAR were low in both patient groups studied. There was no difference in the values regarding the presence of Crohn's disease or ulcerative colitis. Thus, all analyses were performed on the entire sample set. Glucocorticoid therapy, however, resulted in a significant decline in suPAR levels from a median of 3.06 to 2.54 ng/ml (p < 0.01). In contrast, TNF-α-antagonist had no effect. The suPAR levels did not associate with ESR or CRP or fecal calprotectin (FC).
Conclusions:
In pediatric IBD, the suPAR levels in blood are low and do not reflect the level of intestinal inflammation assessed with FC. The introduction of corticoids, however, results in a decline of suPAR levels in blood but not reflect therapeutic response to TNF-α-antagonist. Thus, suPAR is of limited value in assessing systemic inflammatory responses in pediatric IBD.
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