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Citations to this article

Delta 4-3-oxosteroid 5 beta-reductase deficiency described in identical twins with neonatal hepatitis. A new inborn error in bile acid synthesis.
K D Setchell, … , J Heubi, W F Balistreri
K D Setchell, … , J Heubi, W F Balistreri
Published December 1, 1988
Citation Information: J Clin Invest. 1988;82(6):2148-2157. https://doi.org/10.1172/JCI113837.
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Delta 4-3-oxosteroid 5 beta-reductase deficiency described in identical twins with neonatal hepatitis. A new inborn error in bile acid synthesis.

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Abstract

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.

Authors

K D Setchell, F J Suchy, M B Welsh, L Zimmer-Nechemias, J Heubi, W F Balistreri

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T HE E NZYMES , R EGULATION , AND G ENETICSOF B ILE A CID S YNTHESIS
DW Russell
Annual Review of Biochemistry 2003
Nuclear receptors in cholesterol catabolism: molecular biology of the enterohepatic circulation of bile salts and its role in cholesterol homeostasis
RN Redinger
Journal of Laboratory and Clinical Medicine 2003
Lexikon der Syndrome und Fehlbildungen
R Witkowski, O Prokop, E Ullrich, G Thiel
2003
Bile Acid Regulation of Gene Expression: Roles of Nuclear Hormone Receptors
JY Chiang
Endocrine reviews 2002
Mechanisms of Liver Injury Relevant to Pediatric Hepatology
MS Tanner
Critical Reviews in Clinical Laboratory Sciences 2002
Wiley Encyclopedia of Molecular Medicine
WT Morgan
Wiley Encyclopedia of Molecular Medicine 2002
Metabolic Liver Disease
DH Perlmutter
Journal of Pediatric Gastroenterology and Nutrition 2002
Physiological characteristics of allo -cholic acid
ME Mendoza, MJ Monte, MA Serrano, M Pastor-Anglada, B Stieger, PJ Meier, M Medarde, JJ Marin
Journal of lipid research 2002
Intestinal Bile Acid Transport: Biology, Physiology, and Pathophysiology
BL Shneider
Journal of Pediatric Gastroenterology and Nutrition 2001
Lichenification and Enlargement of Hands and Feet: A Sign of Progressive Familial Intrahepatic Cholestasis With Normal γ-Glutamyl-Transpeptidase
BC Ooi, KB Phua, BL Lee, CE Tan, IS Ng, SH Quak
Journal of Pediatric Gastroenterology and Nutrition 2001
The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood
E Jacquemin, JM de Vree, D Cresteil, EM Sokal, E Sturm, M Dumont, GL Scheffer, M Paul, M Burdelski, PJ Bosma, O Bernard, M Hadchouel, RP Elferink
Gastroenterology 2001
ENZYME IMMUNOASSAY FOR CONJUGATED 7α-HYDROXY-3-OXO-4-CHOLENOIC ACID IN HUMAN URINE
T Yoshimura, T Taniguchi, D Kobayashi, T Komiya, T Murai, A Kimura, T Kurosawa, M Tohma
Journal of Immunoassy & Immunochemistry 2001
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 &amp 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
M Nakagawa, KD Setchell
Journal of lipid research 1990
Di- and trihydroxycholestanoic acidaemia with hepatic failure
H Przyrembel, RJ Wanders, CW van Roermund, RB Schutgens, GP Mannaerts, M Casteels
Journal of Inherited Metabolic Disease 1990
Ketonic bile acids in urine of infants during the neonatal period
E Wahlén, B Egestad, B Strandvik, J Sjoóvall
Journal of lipid research 1989
New Comprehensive Biochemistry
S Yamamoto
New Comprehensive Biochemistry 1983
Liver Disorders in Childhood
AP Mowat
Liver Disorders in Childhood 1979

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