Coinheritance of Gilbert syndrome–associated UGT1A1 mutation increases gallstone risk in cystic fibrosis
Hermann E. Wasmuth, Hildegard Keppeler, Ulrike Herrmann, Ramin Schirin‐Sokhan, Michael Barker, Frank Lammert – 23 March 2006 – The prevalence of “black” pigment gallstones is increased in patients with cystic fibrosis (CF). Bile acid malabsorption with augmented bilirubin uptake from the intestine and the development of “hyperbilirubinbilia” have been proposed as key factors in gallstone formation in CF patients.