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Serum cytokine inflammatory profile in children with ulcerative colitis during 6-month follow-up
Katarzyna Zdanowicz1, Mateusz Maciejczyk2, Jacek Jamiołkowski3
1Department of Pediatrics, Gastroenterology, Hepatology, Nutrition, Allergology and Pulmonology, Medical University of Bialystok, Waszyngtona 17, 15-274, Bialystok, Poland. katarzyna.zdanowicz@umb.edu.pl.
Insights
Serum biomarkers like IL-17 and eotaxin may help predict ulcerative colitis (UC) course in children. Higher levels at diagnosis indicated better outcomes, but further research is needed.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Biomarker Discovery
Background:
- Inflammation plays a key role in the pathogenesis of ulcerative colitis (UC).
- Identifying reliable biomarkers is crucial for predicting disease course and guiding treatment in pediatric UC.
Purpose of the Study:
- To evaluate serum levels of cytokines, chemokines, and growth factors in children with UC at diagnosis/exacerbation and during follow-up.
- To assess the potential of these biomarkers in predicting disease progression and treatment needs.
Main Methods:
- Multiplex ELISA was used to measure serum biomarker panels in 33 children with UC and 29 healthy controls at three time points (diagnosis/exacerbation, 3 months, 6 months).
- Clinical activity was assessed using the Pediatric Ulcerative Colitis Activity Index (PUCAI).
Main Results:
- Elevated levels of IL-8, IL-17, eotaxin, and G-CSF were observed in UC patients at diagnosis (T0).
- At 3 months (T1), higher IL-17, eotaxin, and FGF levels persisted in the UC group.
- At diagnosis (T0), higher IL-17, eotaxin, and FGF levels were associated with lower disease activity (PUCAI < 10) at 6 months.
Conclusions:
- Serum cytokines and chemokines may reflect disease activity and clinical outcomes in pediatric UC.
- Exploratory findings suggest potential predictive value for biomarkers like IL-17 and eotaxin.
- Further prospective studies with standardized treatment protocols are necessary to confirm the predictive utility of these biomarkers.
Abstract:
The involvement of inflammation in the development of ulcerative colitis (UC) is significant. Therefore, the purpose of our study was to evaluate the serum levels of selected cytokines, chemokines and growth factors in children at the time of diagnosis/exacerbation of UC (T0), as well as 3 (T1) and 6 (T2) months after the introduction or change of treatment, and to assess their usefulness in predicting the course of the disease and the need for treatment intensification. Thirty-three children (study group) with UC, including 25 with new diagnoses of UC (ndUC), and 29 healthy controls (Ctr) were included in the study. Serum cytokine panels were measured at three time points: T0, T1, and T2 using multiplex ELISA method. At T0, significantly higher levels of IL-8, IL-17, eotaxin, and granulocyte colony-stimulating factor (G-CSF) were observed in both the UC and ndUC groups. At T1, higher levels of IL-17, eotaxin, and fibroblast growth factor (FGF) were noted in the study group compared to controls. When the group was stratified according to clinical activity at 6 months, IL-17, eotaxin, and FGF levels at T0 were higher in patients who achieved Pediatric Ulcerative Colitis Activity Index (PUCAI) < 10 compared to those with PUCAI ≥ 10. However, these associations should be interpreted with caution due to the heterogeneity of treatment interventions, which likely influenced the outcomes. Our exploratory analyses indicate that serum cytokines may reflect disease activity and may help in understanding clinical outcomes in pediatric UC, although prospective studies with standardized treatment protocols are needed to confirm their predictive value.
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