UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia

Am J Hematol. 2006 May;81(5):377-9. doi: 10.1002/ajh.20574.

Abstract

Enhanced erythrocyte destruction in sickle cell anemia results in chronic hyperbilirubinemia. Only a subset of patients develop cholelithiasis. UGT1A1 promoter polymorphism is associated both with unconjugated bilirubin level and elevated risk for cholelithiasis in such subset. Here, we investigated the role of alpha-thalassemia, yet another genetic factor that modulates hemolysis, in conferring protection from cholelithiasis. We show that, although alpha-thalassemia is associated with modest reduction in hemolysis and unconjugated bilirubin level, UGT1A1 polymorphism outweighs its effect on cholethiogenesis in sickle cell anemia patients.

MeSH terms

  • Adult
  • Anemia, Sickle Cell / blood
  • Anemia, Sickle Cell / complications
  • Anemia, Sickle Cell / genetics*
  • Bilirubin / blood
  • Child
  • Cholelithiasis / blood
  • Cholelithiasis / etiology
  • Cholelithiasis / genetics*
  • Gene Deletion*
  • Globins / genetics
  • Glucuronosyltransferase / genetics*
  • Humans
  • Polymorphism, Genetic*
  • alpha-Thalassemia / blood
  • alpha-Thalassemia / complications
  • alpha-Thalassemia / genetics*

Substances

  • Globins
  • UGT1A1 enzyme
  • Glucuronosyltransferase
  • Bilirubin