Fucosyltransferase 2 (FUT2) non-secretor status and blood group B are associated with elevated serum lipase activity in asymptomatic subjects, and an increased risk for chronic pancreatitis: a genetic association study

Gut. 2015 Apr;64(4):646-56. doi: 10.1136/gutjnl-2014-306930. Epub 2014 Jul 15.

Abstract

Objective: Serum lipase activities above the threefold upper reference limit indicate acute pancreatitis. We investigated whether high lipase activity-within the reference range and in the absence of pancreatitis-are associated with genetic single nucleotide polymorphisms (SNP), and whether these identified SNPs are also associated with clinical pancreatitis.

Methods: Genome-wide association studies (GWAS) on phenotypes 'serum lipase activity' and 'high serum lipase activity' were conducted including 3966 German volunteers from the population-based Study-of-Health-in-Pomerania (SHIP). Lead SNPs associated on a genome-wide significance level were replicated in two cohorts, 1444 blood donors and 1042 pancreatitis patients.

Results: Initial discovery GWAS detected SNPs within or near genes encoding the ABO blood group specifying transferases A/B (ABO), Fucosyltransferase-2 (FUT2), and Chymotrypsinogen-B2 (CTRB2), to be significantly associated with lipase activity levels in asymptomatic subjects. Replication analyses in blood donors confirmed the association of FUT-2 non-secretor status (OR=1.49; p=0.012) and ABO blood-type-B (OR=2.48; p=7.29×10(-8)) with high lipase activity levels. In pancreatitis patients, significant associations were found for FUT-2 non-secretor status (OR=1.53; p=8.56×10(-4)) and ABO-B (OR=1.69, p=1.0×10(-4)) with chronic pancreatitis, but not with acute pancreatitis. Conversely, carriers of blood group O were less frequently affected by chronic pancreatitis (OR=0.62; p=1.22×10(-05)) and less likely to have high lipase activity levels (OR=0.59; p=8.14×10(-05)).

Conclusions: These are the first results indicating that ABO blood type-B as well as FUT2 non-secretor status are common population-wide risk factors for developing chronic pancreatitis. They also imply that, even within the reference range, elevated lipase activities may indicate subclinical pancreatic injury in asymptomatic subjects.

Keywords: Chronic Pancreatitis; Genetic Polymorphisms; Glycosyltransferases; Linkage Analysis; Pancreatic Enzymes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ABO Blood-Group System / physiology*
  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Fucosyltransferases / physiology*
  • Galactoside 2-alpha-L-fucosyltransferase
  • Genetic Association Studies*
  • Genome-Wide Association Study*
  • Humans
  • Lipase / blood*
  • Male
  • Middle Aged
  • Pancreatitis, Chronic / epidemiology*
  • Pancreatitis, Chronic / genetics*
  • Polymorphism, Single Nucleotide
  • Risk Assessment
  • Young Adult

Substances

  • ABO Blood-Group System
  • Fucosyltransferases
  • Lipase