Michelle Saad, Nadeen Abu Ata, Syed Ahmad, Christopher Anton, Appakalai N Balamurugan, John Brunner, Lin Fei, Qin Sun, Maisam Abu-El-Haija, Andrew T Trout
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引用次数: 0
Abstract
Introduction: Total pancreatectomy and islet auto-transplantation (TPIAT) can alleviate symptoms in chronic pancreatitis (CP). We aimed to identify pre-TPIAT imaging markers predicting explanted pancreas health and islet yield.
Methods: We retrospectively analyzed 104 pediatric TPIAT patients, excluding those with pre-surgical diabetes or pancreatic surgeries. Pancreas parenchymal volume was manually segmented and T1 signal intensity ratio pancreas to spleen (T1 SIRp/s) was calculated. An islet biologist assessed fat infiltration, fibrosis, and islet yield. Logarithmic transformation and regression analyses were used for variance stabilization and predictive modeling.
Results: 94 patients (60% female, median age 12.5 years) were included. Univariate analyses revealed that an increase in pancreas volume was associated with less fibrosis (OR=0.88 per 5 mL, 95% CI: 0.77-0.99, p<0.05), higher pellet volume, total islet equivalent (TIE) and total islet count (TIC). For advanced fibrosis, an increase in T1 SIRp/s was linked to decreased odds (OR=0.74 per 0.1 unit, 95% CI: 0.59-0.92, p<0.05), whereas a higher Cambridge score was associated with increased odds (OR=1.34 per 1 unit of Cambridge, 95% CI: 1.01-1.77, p<0.05). A model incorporating segmented pancreas volume and T1 SIRp/s predicted advanced fibrosis with an AUC of 0.75 (95%CI: 0.64-0.87). Additionally, models that included larger pancreas volume and the absence of acute pancreatitis predicted TIC and TIE.
Conclusion: In children with CP, non-invasive cross-sectional imaging focused on the parenchyma can guide the management, as a smaller parenchymal bulk and lower T1 SIRp/s predict advanced fibrosis, while larger pancreas volume and T1 SIRp/s predict larger pellet volumes.
期刊介绍:
Clinical and Translational Gastroenterology (CTG), published on behalf of the American College of Gastroenterology (ACG), is a peer-reviewed open access online journal dedicated to innovative clinical work in the field of gastroenterology and hepatology. CTG hopes to fulfill an unmet need for clinicians and scientists by welcoming novel cohort studies, early-phase clinical trials, qualitative and quantitative epidemiologic research, hypothesis-generating research, studies of novel mechanisms and methodologies including public health interventions, and integration of approaches across organs and disciplines. CTG also welcomes hypothesis-generating small studies, methods papers, and translational research with clear applications to human physiology or disease.
Colon and small bowel
Endoscopy and novel diagnostics
Esophagus
Functional GI disorders
Immunology of the GI tract
Microbiology of the GI tract
Inflammatory bowel disease
Pancreas and biliary tract
Liver
Pathology
Pediatrics
Preventative medicine
Nutrition/obesity
Stomach.