Predictive Power of Imaging: Assessing Parenchymal Fibrosis in Pediatric Chronic Pancreatitis
Michelle Saad1,2, Alexander Redman3, Nadeen Abu Ata4,5
1Department of Pediatrics, University of Cincinnati College of Medicine.
Insights
Imaging markers like pancreas volume and T1 signal intensity ratio can identify pancreatic fibrosis in children with chronic pancreatitis (CP). This fibrosis is linked to pancreatic exocrine insufficiency (EPI) and impacts glycemic status.
Area of Science:
- Pediatric Gastroenterology
- Radiology
- Histopathology
Background:
- Chronic pancreatitis (CP) in children is a debilitating condition.
- Assessing pancreatic fibrosis is crucial for understanding disease progression and impact on function.
- Non-invasive imaging markers for fibrosis are needed in pediatric CP.
Purpose of the Study:
- To identify pancreatic parenchymal imaging markers of fibrosis in pediatric CP.
- To describe the pattern of histopathologic fibrosis and its regional variations.
- To examine the association of fibrosis with exocrine pancreatic insufficiency (EPI) and glycemic status.
Main Methods:
- A single-center cross-sectional study included children (0-21 years) undergoing total pancreatectomy islet auto-transplantation (TPIAT).
- Exclusion criteria included prior pancreatic surgeries, missing imaging, or histology.
- Pancreatic parenchymal imaging variables were analyzed against histologic fibrosis scores.
Main Results:
- Reduced pancreas volume and decreased T1 signal intensity ratio (pancreas/spleen) were associated with increased odds of fibrosis.
- A multivariable model using pancreas volume and T1 SIR predicted severe fibrosis with an AUROC of 0.8.
- Histologic fibrosis showed agreement across sampling locations; EPI was linked to higher fibrosis odds.
Conclusions:
- Pancreatic parenchyma imaging can reveal fibrosis in pediatric CP, correlating with pancreatic function.
- A predictive model combining pancreas volume and T1 SIR shows potential for assessing fibrosis in children with CP.
- Fibrosis assessment in pediatric CP offers insights into pancreatic function and disease severity.
Objectives:
The primary aim is to identify pancreatic parenchymal imaging markers of fibrosis in children with chronic pancreatitis (CP). Secondary aims include describing the pattern of histopathologic fibrosis in different pancreatic regions and examining the impact of fibrosis on exocrine pancreatic insufficiency (EPI) and baseline glycemic status.
Methods:
Single-center cross-sectional study that included children aged 0-21 years who underwent total pancreatectomy islet auto-transplantation (TPIAT) before December 2022. Those with prior pancreatic surgeries, missing imaging, or missing histology were excluded.
Results:
Ninety-five patients (56% female, median age 13.3 y) were included. Multiple parenchymal imaging variables were significantly associated with histologic pancreatic fibrosis. A 5 mL decrease in segmented pancreas volume [odds ratio (OR)=1.2, 95% CI: 1.1-1.4, P <0.05] and a 0.1 unit decrease in T1 signal intensity ratio (SIR) pancreas/spleen ( P /s) (OR=1.7, 95% CI: 1.2-2.2, P <0.05) had increased fibrosis odds. A multivariable model with pancreas volume and T1 SIRp/s predicted severe fibrosis with an area under the receiver operating characteristic curve (AUROC) of 0.8 (95% CI:0.7-0.9). Histologic fibrosis scores showed substantial agreement between pancreatic sampling locations (kappa=0.7, 95% CI: 0.6-0.9). EPI by fecal elastase (FE-1) was associated with increased odds of severe fibrosis (OR=11.7, 95% CI: 2.5-54.1, P <0.05) and higher Ammann scores were seen in participants with prediabetes and diabetes [9.0, interquartile range (IQR): 8.0-12.0, P =0.08].
Conclusions:
The pancreatic parenchyma provides insights into pediatric CP through fibrosis assessment, which correlates with pancreatic function. A predictive model using pancreas volume and T1 SIR shows promise for forecasting pancreatic parenchymal fibrosis in children with CP.
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