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Staining Protocols for Human Pancreatic Islets
Published on: May 23, 2012
Changes in pancreatic exocrine function in young at-risk children followed to islet autoimmunity and type 1 diabetes
Megan A S Penno1, Helena Oakey1, Priya Augustine2
1Robinson Research Institute, Adelaide Medical School, University of Adelaide, Adelaide, South Australia, Australia.
Insights
Pancreatic exocrine function declines in children at risk for type 1 diabetes who develop islet autoimmunity. This decline in fecal elastase-1 (FE-1) can precede the onset of islet autoimmunity (IA) and type 1 diabetes (T1D).
Area of Science:
- Pediatrics
- Endocrinology
- Immunology
Background:
- Type 1 diabetes (T1D) development involves islet autoimmunity (IA).
- Pancreatic exocrine function in at-risk children is not well understood in relation to T1D progression.
- The Environmental Determinants of Islet Autoimmunity (ENDIA) study prospectively follows at-risk children.
Purpose of the Study:
- To longitudinally monitor pancreatic exocrine function in children at risk for T1D.
- To assess the relationship between exocrine function and the development of IA and T1D.
- To identify early markers of T1D development.
Main Methods:
- Fecal elastase-1 (FE-1) concentration was measured longitudinally in 85 at-risk children.
- Children were categorized as progressors (developed IA) or non-progressors (remained IA-negative).
- An adjusted linear mixed model compared FE-1 concentrations between groups.
Main Results:
- Baseline FE-1 did not differ between progressors and non-progressors.
- FE-1 concentration decreased over time in progressors compared to non-progressors (P = .02).
- In some progressors, the fall in FE-1 preceded the onset of IA.
Conclusions:
- Pancreatic exocrine function decreases in most young children who progress to IA and T1D.
- Reduced FE-1 may serve as an early indicator of T1D development in at-risk children.
- Longitudinal monitoring of pancreatic exocrine function is valuable in T1D research.
Backgrounds:
We aimed to monitor pancreatic exocrine function longitudinally in relation to the development of islet autoimmunity (IA) and type 1 diabetes (T1D) in at-risk children with a first-degree relative with T1D, who were followed prospectively in the Environmental Determinants of Islet Autoimmunity (ENDIA) study.
Methods:
Fecal elastase-1 (FE-1) concentration was measured longitudinally in 85 ENDIA children from median age 1.0 (IQR 0.7,1.3) year. Twenty-eight of 85 children (progressors) developed persistent islet autoantibodies at median age of 1.5 (IQR 1.1,2.5) years, of whom 11 went on to develop clinical diabetes. The other 57 islet autoantibody-negative children (non-progressors) followed similarly were age and gender-matched with the progressors. An adjusted linear mixed model compared FE-1 concentrations in progressors and non-progressors.
Results:
Baseline FE-1 did not differ between progressors and non-progressors, or by HLA DR type or proband status. FE-1 decreased over time in progressors in comparison to non-progressors (Wald statistic 5.46, P = .02); in some progressors the fall in FE-1 preceded the onset of IA.
Conclusions:
Pancreatic exocrine function decreases in the majority of young at-risk children who progress to IA and T1D.
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