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DOI: 10.1055/s-2003-40138
Genetic cholestasis
Genetische CholestasesyndromePublication History
eingereicht: 11.2.2003
akzeptiert: 14.5.2003
Publication Date:
20 June 2003 (online)
Abbreviations
PFIC = Progressive familial intrahepatic cholestasis
BRIC = benign recurrent intrahepatic cholestasis
BSEP = bile salt export pump
OATP = organic anion transporting polypeptide
MRP = multidrug resistance related protein.
Bile salts are the predominant organic solutes in bile, and their vectorial secretion from liver to bile represents the major driving force for hepatic bile formation. Disturbances of bile salt transport across the basolateral and apical domains of the hepatocyte plasma membrane are important causes of acquired and genetic forms of cholestatic liver disease in humans. Defective bile salt secretion not only leads to progressive liver damage, but also metabolic derangements and malnutrition secondary to reduced intestinal absorption of lipids and fat-soluble vitamins.
References
- 1 Aagenaes O. Hereditary cholestasis with lymphoedema (Aagenaes syndrome, cholestasis- lymphoedema syndrome). New cases and follow-up from infancy to adult age. Scand J Gastroenterol. 1998; 33 335-345
- 2 Bull L N, Carlton V E, Stricker N L, Baharloo S, DeYoung J A, Freimer N B, Magid M S, Kahn E, Markowitz J, DiCarlo F J, McLoughlin L, Boyle J T, Dahms B B, Faught P R, Fitzgerald J F, Piccoli D A, Witzleben C L, O’Connell N C, Setchell K D, Agostini R M Jr, Kocoshis S A, Reyes J, Knisely A S. Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity. Hepatology. 1997; 26 155-164
- 3 Bull L N, Roche E, Song E J, Pedersen J, Knisely A S, Der Hagen C B, Eiklid K, Aagenaes O, Freimer N B. Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q. Am J Hum Genet. 2000; 67 994-999
- 4 Bull L N, van Eijk M J, Pawlikowska L, DeYoung J A, Juijn J A, Liao M, Klomp L W, Lomri N, Berger R, Scharschmidt B F, Knisely A S, Houwen R H, Freimer N B. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis. Nat Genet. 1998; 18 219-224
- 5 Clayton P T, Leonard J V, Lawson A M, Setchell K D, Andersson S, Egestad B, Sjovall J. Familial giant cell hepatitis associated with synthesis of 3 beta, 7 alpha-dihydroxy-and 3 beta,7 alpha, 12 alpha-trihydroxy-5-cholenoic acids. J Clin Invest. 1987; 79 1031-1038
- 6 De Vree J M, Jacquemin E, Sturm E, Cresteil D, Bosma P J, Aten J, Deleuze J F, Desrochers M, Burdelski M, Bernard O, Oude Elferink R P, Hadchouel M. Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis. Proc Natl Acad Sci USA. 1988; 95 282-287
- 7 Deleuze J F, Jacquemin E, Dubuisson C, Cresteil D, Dumont M, Erlinger S, Bernard O, Hadchouel M. Defect of multidrug-resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasis. Hepatology. 1996; 23 904-908
- 8 Jacquemin E, Cresteil D, Manouvrier S, Boute O, Hadchouel M. Heterozygous non-sense mutation of the MDR3 gene in familial intrahepatic cholestasis of pregnancy. Lancet. 1999; 353 210-211
- 9 Jacquemin E, De Vree J M, Cresteil D, Sokal E M, Sturm E, Dumont M, Scheffer G L, Paul M, Burdelski M, Bosma P J, Bernard O, Hadchouel M, Elferink R P. The wide spectrum of multidrug resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood. Gastroenterology. 2001; 120 1448-1458
- 10 Jacquemin E, Hadchouel M. Genetic basis of progressive familial intrahepatic cholestasis. J Hepatol. 1999; 31 377-381
- 11 Jacquemin E, Hermans D, Myara A, Habes D, Debray D, Hadchouel M, Sokal E M, Bernard O. Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis. Hepatology. 1997; 25 519-523
- 12 Jacquemin E, Setchell K D, O’Connell N C, Estrada A, Maggiore G, Schmitz J, Hadchouel M, Bernard O. A new cause of progressive intrahepatic cholestasis: 3 beta-hydroxy-C27- steroid dehydrogenase/isomerase deficiency. J Pediatr. 1994; 125 379-384
- 13 Jansen P L, Strautnieks S S, Jacquemin E, Hadchouel M, Sokal E M, Hooiveld G J, Koning J H, Jager-Krikken A, Kuipers F, Stellaard F, Bijleveld C M, Gouw A, van Goor H, Thompson R J, Muller M. Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis. Gastroenterology. 1999; 117 1370-1379
- 14 Melter M, Rodeck B, Kardorff R, Hoyer P F, Petersen C, Ballauff A, Brodehl J. Progressive familial intrahepatic cholestasis: partial biliary diversion normalizes serum lipids and improves growth in noncirrhotic patients. Am J Gastroenterol. 2000; 95 3522-3528
- 15 Morton D H, Salen G, Batta A K, Shefer S, Tint G S, Belchis D, Shneider B, Puffenberger E, Bull L, Knisely A S. Abnormal hepatic sinusoidal bile acid transport in an Amish kindred is not linked to FIC1 and is improved by ursodiol. Gastroenterology. 2000; 119 188-195
- 16 Palma J, Reyes H, Ribalta J, Hernandez I, Sandoval L, Almuna R, Liepins J, Lira F, Sedano M, Silva O, Toha D, Silva J J. Ursodeoxycholic acid in the treatment of cholestasis of pregnancy: a randomized, double-blind study controlled with placebo. J Hepatol. 1997; 27 1022-1028
- 17 Rosmorduc O, Hermelin B, Poupon R. MDR3 gene defect in adults with symptomatic intrahepatic and gallbladder cholesterol cholelithiasis. Gastroenterology. 2001; 120 1459-1467
- 18 Soubrane O, Gauthier F, Devictor D, Bernard O, Valayer J, Houssin D, Chapuis Y. Orthotopic liver transplantation for Byler disease. Transplantation. 1990; 50 804-806
- 19 Strautnieks S S, Bull L N, Knisely A S, Kocoshis S A, Dahl N, Arnell H, Sokal E, Dahan K, Childs S, Ling V, Tanner M S, Kagalwalla A F, Nemeth A, Pawlowska J, Baker A, Mieli-Vergani G, Freimer N B, Gardiner R M, Thompson R J. A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis. Nat Genet. 1998; 20 233-238
- 20 Thompson R, Jansen P L. Genetic defects in hepatocanalicular transport. Semin Liver Dis. 2000; 20 365-372
Correspondence
Prof. Dr. Peter L. M. Jansen
Division of Gastroenterology and Hepatology, Department of
Medicine, University Hospital
Hanzeplein 1
9717 GZ Groningen
The Netherlands
Email: p.l.m.jansen@int.azg.nl