Differences in presentation and progression between severe FIC1 and BSEP deficiencies.

Pawlikowska, Ludmila Strautnieks, Sandra Jankowska, Irena Czubkowski, Piotr Emerick, Karan Antoniou, Anthony Wanty, Catherine Fischler, Bjorn Jacquemin, Emmanuel Wali, Sami Blanchard, Samra Nielsen, Inge-Merete Bourke, Billy McQuaid, Shirley Lacaille, Florence Byrne, Jane A van Eerde, Albertien M Kolho, Kaija-Leena Klomp, Leo Houwen, Roderick Bacchetti, Peter Lobritto, Steven Hupertz, Vera McClean, Patricia Mieli-Vergani, Giorgina Shneider, Benjamin Nemeth, Antal Sokal, Etienne [UCL] Freimer, Nelson B Knisely, A S Rosenthal, Philip Whitington, Peter F Pawlowska, Joanna Thompson, Richard J Bull, Laura N et al.[show all]

Progressive familial intrahepatic cholestasis (PFIC) with normal serum levels of gamma-glutamyltranspeptidase can result from mutations in ATP8B1 (encoding familial intrahepatic cholestasis 1 [FIC1]) or ABCB11 (encoding bile salt export pump [BSEP]). We evaluated clinical and laboratory features of disease in patients diagnosed with PFIC, who carried mutations in ATP8B1 (FIC1 deficiency) or ABCB11 (BSEP deficiency). Our goal was to identify features that distinguish presentation and course of these two disorders, thus facilitating diagnosis and elucidating the differing consequences of ATP8B1 and ABCB11 mutations. A retrospective multi-center study was conducted, using questionnaires and chart review. Available clinical and biochemical data from 145 PFIC patients with mutations in either ATP8B1 (61 "FIC1 patients") or ABCB11 (84 "BSEP patients") were evaluated. At presentation, serum aminotransferase and bile salt levels were higher in BSEP patients; serum alkaline phosphatase values were higher, and serum albumin values were lower, in FIC1 patients. Elevated white blood cell counts, and giant or multinucleate cells at liver biopsy, were more common in BSEP patients. BSEP patients more often had gallstones and portal hypertension. Diarrhea, pancreatic disease, rickets, pneumonia, abnormal sweat tests, hearing impairment, and poor growth were more common in FIC1 patients. Among BSEP patients, the course of disease was less rapidly progressive in patients bearing the D482G mutation. Severe forms of FIC1 and BSEP deficiency differed. BSEP patients manifested more severe hepatobiliary disease, while FIC1 patients showed greater evidence of extrahepatic disease.