Genetic variants in acute, acute recurrent and chronic pancreatitis affect the progression of disease in children

Pancreatology. 2019 Jun;19(4):535-540. doi: 10.1016/j.pan.2019.05.001. Epub 2019 May 7.

Abstract

Background/objectives: Acute pancreatitis (AP) is emerging in pediatrics. A subset of children with AP progresses to acute recurrent pancreatitis (ARP) and chronic pancreatitis (CP). The role of extensive gene testing in the progression has not been investigated previously. We have followed children enrolled in the registry and at our center for progression to ARP and CP after the first attack.

Methods: This study utilizes an extensive gene sequencing panel as a platform to evaluate the role of genetics in first attack AP, and the progression over time, from first attack to ARP and CP in children.

Results: Genes, with corresponding variants were involved in the 3 groups studied: AP, ARP and CP. We have shown that the presence of gene variants from the eight tested genes is enriched in the CP group compared to the AP and ARP groups. The presence of more than one gene was associated with CP (p = 0.01). SPINK1 mutation(s) was significantly associated with faster progression to ARP, (p = 0.04). Having a variant from CFTR, SPINK1 or PRSS1, was associated with the faster progression from AP to CP over time (p < 0.05).

Conclusions: This study shows that genetics have a significant role in progression to ARP and CP from the first attack of pancreatitis.

Keywords: Extensive genetic testing; Pediatric pancreatitis.

MeSH terms

  • Acute Disease
  • Adolescent
  • Child
  • Child, Preschool
  • Cohort Studies
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Disease Progression
  • Female
  • Genetic Testing
  • Genetic Variation
  • Humans
  • Male
  • Pancreatitis / genetics*
  • Pancreatitis, Chronic / genetics*
  • Prospective Studies
  • Recurrence
  • Registries
  • Trypsin / genetics
  • Trypsin Inhibitor, Kazal Pancreatic / genetics

Substances

  • CFTR protein, human
  • SPINK1 protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Trypsin Inhibitor, Kazal Pancreatic
  • PRSS1 protein, human
  • Trypsin