A new inborn error in bile acid synthesis, manifest in identical infant twins as severe intrahepatic cholestasis, is described involving the delta 4-3-oxosteroid 5 beta-reductase catalyzed conversion of the key intermediates, 7 alpha-hydroxy-4-cholesten-3-one and 7 alpha,12 alpha-dihydroxy-4-cholesten-3-one for chenodeoxycholic and cholic acid synthesis, to the respective 3 alpha-hydroxy-5 beta (H) products. This defect was detected by fast atom bombardment ionization-mass spectrometry from an elevated excretion and predominance of taurine conjugated unsaturated hydroxy-oxo-bile acids. Gas chromatography-mass spectrometry confirmed these to be 7 alpha-hydroxy-3-oxo-4-cholenoic and 7 alpha,12 alpha-dihydroxy-3-oxo-4-cholenoic acids (75-92% of total). Fasting serum bile acid concentrations were greater than 37 mumol/liter; chenodeoxycholic acid was the major bile acid, but significant amounts of allo(5 alpha-H)-bile acids (approximately 30%) were present. Biliary bile acid concentration was less than 2 mumol/liter and consisted of chenodeoxycholic, allo-chenodeoxycholic, and allo-cholic acids. These biochemical findings, which were identical in both infants, indicate a defect in bile acid synthesis involving the conversion of the delta 4-3-oxo-C27 intermediates into the corresponding 3 alpha-hydroxy-5 beta(H)-structures, a reaction that is catalyzed by a delta 4-3-oxosteroid-5 beta reductase enzyme. This defect resulted in markedly reduced primary bile acid synthesis and concomitant accumulation of delta 4-3-oxo-and allo-bile acids. These findings indicate a pathway in bile acid synthesis whereby side chain oxidation can occur despite incomplete alterations to the steroid nucleus, and lend support for an active delta 4-3-oxosteroid 5 alpha-reductase catalyzing the conversion of the delta 4-3-oxosteroid intermediates to the respective 3 alpha-hydroxy-5 alpha(H)-structures.
K D Setchell, F J Suchy, M B Welsh, L Zimmer-Nechemias, J Heubi, W F Balistreri
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Intestinal Bile Acid Transport: Biology, Physiology, and Pathophysiology:
BL Shneider |
Journal of Pediatric Gastroenterology and Nutrition | 2001 |
Genomic organization of a human 5β-reductase and its pseudogene and substrate selectivity of the expressed enzyme
A Charbonneau, VL The |
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression | 2001 |
Identification of unusual 7-oxygenated bile acid sulfates in a patient with Niemann-Pick disease, type C
G Alvelius, O Hjalmarson, WJ Griffiths, I Björkhem, J Sjövall |
Journal of lipid research | 2001 |
Expression cloning of 3beta-hydroxy-delta5-C27-steroid oxidoreductase gene of bile acid synthesis and its mutation in progressive intrahepatic cholestasis
Margrit Schwarz, Angelique C. Wright, Daphne L. Davis, Hisham Nazer, Ingemar Bjorkhem, David W. Russel |
Journal of Clinical Investigation | 2000 |
Bile acids and progesterone metabolites intrahepatic cholestasis of pregnancy
H Reyes, J Sjövall |
Annals of Medicine | 2000 |
The molecular genetics of familial intrahepatic cholestasis
PL Jansen, M Müller |
Gut | 2000 |
The Shwachman Award of the North American Society for Pediatric Gastroenterology and Nutrition, 1999: Presentation
MB Cohen |
Journal of Pediatric Gastroenterology and Nutrition | 2000 |
Nieuwe inzichten in de pathologie van progressieve familiaire intrahepatische cholestase
T Kok, M Müller, PL Jansen, PJ Sauer, F kuipers |
Tijdschrift voor kindergeneeskunde | 2000 |
Chronic cholestatic diseases
R Poupon, O Chazouillères, RE Poupon |
Journal of Hepatology | 2000 |
PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS
E Jacquemin |
Clinics in Liver Disease | 2000 |
Pathologie der Leber und Gallenwege
H Denk, HP Dienes, J Düllmann, HP Fischer, O Klinge, W Lierse, KH zum Büschenfelde, U Pfeifer, KH Preisegger, G Ramadori, A Tannapfel, C Wittekind, U Wulfhekel, H Zhou |
2000 | |
An inborn error of bile acid synthesis (3beta-hydroxy-delta5-C27-steroid dehydrogenase deficiency) presenting as malabsorption leading to rickets
AK Akobeng, PT Clayton, V Miller, M Super, AG Thomas |
Archives of disease in childhood | 1999 |
REGULATION OF BILE ACID BIOSYNTHESIS
ZR Vlahcevic, WM Pandak, RT Stravitz |
Gastroenterology Clinics of North America | 1999 |
INBORN ERRORS OF BILE ACID BIOSYNTHESIS AND TRANSPORT
WF Balistreri |
Gastroenterology Clinics of North America | 1999 |
Genetic basis of progressive familial intrahepatic cholestasis
E Jacquemin, M Hadchouel |
Journal of Hepatology | 1999 |
Profile of Urinary Bile Acids in Infants and Children: Developmental Pattern of Excretion of Unsaturated Ketonic Bile Acids and 7 β-Hydroxylated Bile Acids
A Kimura, R Mahara, T Inoue, Y Nomura, T Murai, T Kurosawa, M Tohma, K Noguchi, A Hoshiyama, T Fujisawa, H Kato |
Pediatric Research | 1999 |
Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease
KD Setchell, M Schwarz, NC O'Connell, EG Lund, DL Davis, R Lathe, HR Thompson, RW Tyson, RJ Sokol, DW Russell |
Journal of Clinical Investigation | 1998 |
Neonatal intrahepatic cholestasis with hepatic siderosis and steatosis
Y Tazawa, F Nishinomiya, D Abukawa, J Aikawa, T Ohura, M Tohma, A Watanabe, T Suzuki, G Takada, T Konno |
Pediatrics International | 1998 |
Diagnosis of the first Japanese patient with 3-oxo-Δ4-steroid 5β-reductase deficiency by use of immunoblot analysis
A Kimura, KH Kondo, KI Okuda, S Higashi, M Suzuki, T Kurosawa, M Tohma, T Inoue, A Nishiyori, M Yoshino, H Kato, T Setoguchi |
European Journal of Pediatrics | 1998 |
Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis
JM de Vree, E Jacquemin, E Sturm, D Cresteil, PJ Bosma, J Aten, JF Deleuze, M Desrochers, M Burdelski, O Bernard, RP Elferink, M Hadchouel |
Proceedings of the National Academy of Sciences | 1998 |
Increased Urinary Excretion of 3-Oxo-Δ4 Bile Acids in Japanese Patients with Idiopathic Neonatal Cholestasis
A Kimura, M Suzuki, M Tohma, T Inoue, F Endo, S Kagimoto, A Matsui, M Kawai, M Hayashi, T Iizuka, H Tajiri, H Kato |
Journal of Pediatric Gastroenterology & Nutrition | 1998 |
Tyrosinemia type Mike disease: A possible manifestation of 3-oxo-Δ-steroid 5β-reductase deficiency
A Kimura, F Endo, S Kagimoto, T Inoue, M Suzuki, T Kurosawa, M Tohma, T Fujisawa, H Kato |
Pediatrics International | 1998 |
Cytotoxic effect of 7?-hydroxy-4-cholesten-3-one on HepG2 cells: Hypothetical role of acetaldehyde-modified ?4-3-ketosteroid-5?-reductase (the 37-kd-liver protein) in the pathogenesis of alcoholic liver injury in the rat
RC Lin, MJ Fillenwarth, X Du |
Hepatology | 1998 |
Urinary 7α-hydroxy-3-oxochol-4-en-24-oic and 3-oxochola-4,6-dien-24-oic acids in infants with cholestasis
A Kimura, M Suzuki, T Murai, T Kurosawa, M Tohma, M Sata, T Inoue, A Hoshiyama, E Nakashima, Y Yamashita, T Fujisawa, H Kato |
Journal of Hepatology | 1998 |
Cholestases intrahépatiques fîbrogènes familiales et anomalies héréditaires du métabolisme hépatocytaire des acides biliaires
E Jacquemin |
Archives de Pédiatrie | 1998 |
METABOLIC LIVER DISEASE IN THE PEDIATRIC PATIENT
DA Kelly, PJ McKiernan |
Clinics in Liver Disease | 1998 |
Diseases of the Liver and Bile Ducts
GY Wu, J Israel |
1998 | |
Diagnosis of the first Japanese patient with 3-oxo-Δ4-steroid 5β-reductase deficiency by use of immunoblot analysis
A Kimura, , , S Higashi, M Suzuki, T Kurosawa, M Tohma, T Inoue, A Nishiyori, M Yoshino, H Kato, T Setoguchi |
European Journal of Pediatrics | 1998 |
Differential Interaction of Bile Acids from Patients with Inborn Errors of Bile Acid Synthesis with Hepatocellular Bile Acid Transporters
B Stieger, J Zhang, B O'Neill, J Sjovall, PJ Meier |
European Journal of Biochemistry | 1997 |
Bile Acid Therapy in Pediatric Hepatobiliary Disease: The Role of Ursodeoxycholic Acid
WF Balistreri |
Journal of Pediatric Gastroenterology & Nutrition | 1997 |
Abnormal Bile Acid Metabolism and Neonatal Hemochromatosis: A Subset with Poor Prognosis
CG Siafakas, MM Jonas, AR Perez-Atayde |
Journal of Pediatric Gastroenterology & Nutrition | 1997 |
Analysis of Bile Acids and Bile Alcohols in Urine by Capillary Column Liquid Chromatography-Mass Spectrometry using Fast Atom Bombardment or Electrospray Ionization and Collision-induced Dissociation
Y Yang, WJ Griffiths, H Nazer, J Sj�vall |
Biomedical Chromatography | 1997 |
Developmental pattern of 3-oxo-delta 4 bile acids in neonatal bile acid metabolism
T Inoue, A Kimura, K Aoki, M Tohma, H Kato |
Archives of disease in childhood. Fetal and neonatal edition | 1997 |
The Optimized Use of Gas Chromatography-Mass Spectrometry and High Performance Liquid Chromatography to Analyse the Serum Bile Acids of Patients with Metabolic Cholestasis and Peroxisomal Disorders
F Courillon, MF Gerhardt, A Myara, F Rocchiccioli, F Trivin |
Clinical Chemistry and Laboratory Medicine | 1997 |
Gene analysis in δ4-3-oxosteroid 5β–reductase deficiency
R Sumazaki, N Nakamura, J Shoda, T Kurosawa, M Tohma |
The Lancet | 1997 |
High-Performance Liquid Chromatographic Determination of Conjugated and Unconjugated 3-Oxo-Δ<sup>4</sup>- and 3-Oxo-Δ<sup>4,6</sup>-Bile Acids in Human Urine
T Yoshimura, T Taniguchi, T Kurosawa, A Kimura, M Tolima |
Journal of Liquid Chromatography & Related Technologies | 1997 |
Advances in Molecular and Cell Biology
KJ Clemetson |
Advances in Molecular and Cell Biology | 1997 |
Profiles of bile acids and progesterone metabolites in the urine and serum of women with intrahepatic cholestasis of pregnancy
LJ Meng, H Reyes, J Palma, I Hernandez, J Ribalta, J Sjövall |
Journal of Hepatology | 1997 |
Determination of fetal bile acids in biological fluids from neonates by gas chromatography-negative ion chemical ionization mass spectrometry
T Murai, R Mahara, T Kurosawa, A Kimura, M Tohma |
Journal of Chromatography B Biomedical Sciences and Applications | 1997 |
Method for combined analysis of profiles of conjugated progesterone metabolites and bile acids in serum and urine of pregnant women
LJ Meng, J Sjövall |
Journal of Chromatography B Biomedical Sciences and Applications | 1997 |
Determination of 3-oxo-Δ4- and 3-oxo-Δ4,6-bile acids and related compounds in biological fluids of infants with cholestasis by gas chromatography–mass spectrometry
M Suzuki, T Murai, T Yoshimura, A Kimura, T Kurosawa, M Tohma |
Journal of Chromatography B: Biomedical Sciences and Applications | 1997 |
High levels of (24S)-24-hydroxycholesterol 3-sulfate, 24-glucuronide in the serum and urine of children with severe cholestatic liver disease
LJ Meng, WJ Griffiths, H Nazer, Y Yang, J Sjövall |
Journal of lipid research | 1997 |
Perinatal bile acid metabolism: analysis of urinary bile acids in pregnant women and newborns
A Kimura, M Suzuki, T Murai, T Inoue, H Kato, D Hori, Y Nomura, T Yoshimura, T Kurosawa, M Tohma |
Journal of lipid research | 1997 |
Disruption of Cholesterol 7α-Hydroxylase Gene in Mice: I. POSTNATAL LETHALITY REVERSED BY BILE ACID AND VITAMIN SUPPLEMENTATION
S Ishibashi, M Schwarz, PK Frykman, J Herz, DW Russell |
The Journal of biological chemistry | 1996 |
Neonatal Hepatobiliary Disorders
JM Andres |
Clinics in Perinatology | 1996 |
Delta 4-3-oxosteroid 5 beta-reductase deficiency: failure of ursodeoxycholic acid treatment and response to chenodeoxycholic acid plus cholic acid
PT Clayton, KA Mills, AW Johnson, A Barabino, MG Marazzi |
Gut | 1996 |
Profile of urinary bile acids in familial intrahepatic cholestasis with Coombs’negative haemolytic anaemia
A Kimura, K Ushijima, M Suzuki, M Tohma, T Inokuchi, H Kato |
Acta Paediatrica | 1995 |
Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease)
E Jacquemin, M Dumont, O Bernard, S Erlinger, M Hadchouel |
European Journal of Pediatrics | 1994 |
Cloning and expression of cDNA of human Delta4-3-oxosteroid 5beta-reductase and substrate specificity of the expressed enzyme
KH KONDO, MH KAI, Y SETOGUCHI, G EGGERTSEN, P SJOBLOM, T SETOGUCHI, KI OKUDA, I BJORKHEM |
European Journal of Biochemistry | 1994 |
Δ4-3-Oxosteroid 5β-reductase deficiency causing neonatal liver failure and hemochromatosis
BL Shneider, KD Setchell, PF Whitington, KA Neilson, FJ Suchy |
The Journal of Pediatrics | 1994 |
A new cause of progressive intrahepatic cholestasis: 3β-Hydroxy-C27-steroid dehydrogenase/isomerase deficiency
E Jacquemin, KD Setchell, NC O'Connell, O Bernard |
The Journal of Pediatrics | 1994 |
Bile acids for babies? Diagnosis and treatment of a new category of metabolic liver disease
FJ Suchy |
Hepatology | 1993 |
Resolution of liver biopsy alterations in three siblings with bile acid treatment of an inborn error of bile acid metabolism (Δ4-3-oxosteroid 5β-reductase deficiency)
YC Daugherty, KD Setchell, JE Heubi, WF Ballstreri |
Hepatology | 1993 |
Derivatization of bile acids with taurine for analysis by fast atom bombardment mass spectrometry with collision-induced fragmentation
J Zhang, WJ Griffiths, T Bergman, J Sjövall |
Journal of lipid research | 1993 |
Oral bile acid treatment and the patient with zellweger syndrome
KD Setchell, P Bragetti, L Zimmer-Nechemias, C Daugherty, MA Pelli, R Vaccaro, G Gentili, E Distrutti, G Dozzini, A Morelli, C Clerici |
Hepatology | 1992 |
Case 3 A New Category of Causes of Intrahepatic Cholestasis
CL Witzleben, DA Piccoli, K Setchell |
Fetal & Pediatric Pathology | 1992 |
Advances in Mass Spectrometry
E Gelpi |
Advances in Mass Spectrometry | 1992 |
Trends in biochemical and biomedical applications of mass spectrometry
E Gelpi |
International Journal of Mass Spectrometry and Ion Processes | 1992 |
Bile acid biosynthesis
DW Russell, KD Setchell |
Biochemistry | 1992 |
Hepatobiliary Diseases
J Prieto, J Rodés, DA Shafritz |
1992 | |
Fetal and neonatal bile acid synthesis and metabolism — Clinical implications
WF Balistreri |
Journal of Inherited Metabolic Disease | 1991 |
Inborn errors of bile acid metabolism
PT Clayton |
Journal of Inherited Metabolic Disease | 1991 |
Charge-remote fragmentation of taurine-conjugated bile acids
WJ Griffiths, B Egestad, J Sjövall |
Rapid Communications in Mass Spectrometry | 1991 |
Δ4-3-Oxosteroid 5β-Reductase. Structure and Function
Y ONISHI, M NOSHIRO, T SHIMOSATO, K OKUDA |
Biological Chemistry Hoppe-Seyler | 1991 |
Bile acids and bile alcohols in a child with hepatic 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase deficiency: effects of chenodeoxycholic acid treatment
H Ichimiya, B Egestad, H Nazer, ES Baginski, PT Clayton, J Sjövall |
Journal of lipid research | 1991 |
Lack of 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase/isomerase in fibroblasts from a child with urinary excretion of 3 beta-hydroxy-delta 5-bile acids. A new inborn error of metabolism
MS Buchmann, EA Kvittingen, H Nazer, T Gunasekaran, PT Clayton, J Sjövall, I Björkhem |
Journal of Clinical Investigation | 1990 |
Di- and trihydroxycholestanoic acidaemia with hepatic failure
H Przyrembel, RJ Wanders, CW Roermund, RB Schutgens, GP Mannaerts, M Casteels |
Journal of Inherited Metabolic Disease | 1990 |
Neonatal cholestasis: An approach for the practicing pediatrician
JE Heubi, CC Daugherty |
Current Problems in Pediatrics | 1990 |
Ultraviolet and light absorption spectrometry
JA Howell, LG Hargis |
Analytical Chemistry | 1990 |
Treatment of chronic liver disease caused by 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase deficiency with chenodeoxycholic acid
H Ichimiya, H Nazer, T Gunasekaran, P Clayton, J Sjovall |
Archives of disease in childhood | 1990 |
Bile acid metabolism in early life: studies of amniotic fluid
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Journal of lipid research | 1990 |
Di- and trihydroxycholestanoic acidaemia with hepatic failure
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Journal of Inherited Metabolic Disease | 1990 |
Ketonic bile acids in urine of infants during the neonatal period
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Journal of lipid research | 1989 |
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