Quantcast

Exocrine pancreatic function in children with Alagille syndrome.

Research paper by Dorota D Gliwicz, Irena I Jankowska, Aldona A Wierzbicka, Anna A Miśkiewicz-Chotnicka, Aleksandra A Lisowska, Jarosław J Walkowiak

Indexed on: 18 Oct '16Published on: 18 Oct '16Published in: Scientific Reports



Abstract

Alagille syndrome (AGS) is often associated with symptoms of maldigestion, such as steatorrhea, hypotrophy and growth retardation. Exocrine pancreatic insufficiency was proposed as the underlying cause. We aimed to assess the exocrine pancreatic function with the use of different methods in AGS patients. Concentrations of fecal elastase-1 (FE1) and fecal lipase (FL) activities were measured in 33 children with AGS. The C-mixed triglyceride breath test (MTBT) in a subgroup comprising 15 patients. In all patients studied, FE1 concentrations and FL activities were normal. Abnormal MTBT results were documented in 4 (26.7%) patients. The FE1 and FL levels in MTBT-positive and MTBT-negative children did not differ. The results of this research do not confirm the presence of exocrine pancreatic dysfunction in AGS patients. Routine screening for exocrine pancreatic insufficiency of this group of patients is not necessary.