Literature DB >> 10203155

Profile of urinary bile acids in infants and children: developmental pattern of excretion of unsaturated ketonic bile acids and 7beta-hydroxylated bile acids.

A Kimura1, R Mahara, T Inoue, Y Nomura, T Murai, T Kurosawa, M Tohma, K Noguchi, A Hoshiyama, T Fujisawa, H Kato.   

Abstract

Unusual bile acids, such as unsaturated ketonic and 7beta-hydroxylated bile acids, have been detected in urine early in life. To elucidate the normal profiles of usual and unusual urinary bile acids in the neonatal and pediatric periods, we measured the concentrations of 28 kinds in urine from normal newborns, infants, and children by gas chromatography-mass spectrometry. The mean total bile acid/Cr ratio in 7-d-old infants was significantly higher than in subjects of other age groups (birth, 2-4 mo, 5-7 mo, 11-12 mo, 2-3 y, 9-14 y, and adult) (p < 0.05). Relatively large amounts of unusual bile acids were detected during infancy, especially during the period up to 1 mo of age. At that time, 1beta,3alpha,7alpha,12alpha-tetrahydroxy-5bet a-cholan-24-oic, 7alpha, 12alpha-dihydroxy-3-oxo-5beta-chol-1-en-24-oic, and 7alpha,12alpha-dihydroxy-3-oxo-4-cholen-24-oic acids were predominant among the unusual urinary bile acids present. Moreover, the levels of 3alpha,7beta,12alpha-trihydroxy-5beta-cholan+ ++-24-oic acid increased significantly after 2-4 mo of age. These results indicate that bile acid synthesis and metabolism in the liver of developing infants are significantly different from that occurring in the liver of adults. Significant amounts of urinary isomerized 7beta-hydroxylated bile acids were detected after late infancy, probably because of changes in the intestinal bacterial flora response to a change in nutrition. We describe, for the first time, evidence of the epimerization of the 7alpha-hydroxyl group of cholic acid, which may be unique to human development.

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Year:  1999        PMID: 10203155     DOI: 10.1203/00006450-199904010-00022

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  12 in total

1.  Prognostic roles of tetrahydroxy bile acids in infantile intrahepatic cholestasis.

Authors:  Chee-Seng Lee; Akihiko Kimura; Jia-Feng Wu; Yen-Hsuan Ni; Hong-Yuan Hsu; Mei-Hwei Chang; Hiroshi Nittono; Huey-Ling Chen
Journal:  J Lipid Res       Date:  2017-01-10       Impact factor: 5.922

Review 2.  Planar bile acids in health and disease.

Authors:  Stephanie J Shiffka; Maureen A Kane; Peter W Swaan
Journal:  Biochim Biophys Acta Biomembr       Date:  2017-09-06       Impact factor: 3.747

3.  Two neonatal cholestasis patients with mutations in the SRD5B1 (AKR1D1) gene: diagnosis and bile acid profiles during chenodeoxycholic acid treatment.

Authors:  Yoshitaka Seki; Tatsuki Mizuochi; Akihiko Kimura; Tomoyuki Takahashi; Akira Ohtake; Shin-Ichi Hayashi; Toshiya Morimura; Yasuharu Ohno; Takayuki Hoshina; Kenji Ihara; Hajime Takei; Hiroshi Nittono; Takao Kurosawa; Keiko Homma; Tomonobu Hasegawa; Toyojiro Matsuishi
Journal:  J Inherit Metab Dis       Date:  2012-11-16       Impact factor: 4.982

4.  Frontal lobe dementia with abnormal cholesterol metabolism and heterozygous mutation in sterol 27-hydroxylase gene (CYP27).

Authors:  S Sugama; A Kimura; W Chen; S Kubota; Y Seyama; N Taira; Y Eto
Journal:  J Inherit Metab Dis       Date:  2001-06       Impact factor: 4.982

5.  Perinatal exposure to UDCA prevents neonatal cholestasis in Cyp2c70-/- mice with human-like bile acids.

Authors:  Hilde D de Vries; Anna Palmiotti; Rumei Li; Milaine V Hovingh; Niels L Mulder; Martijn Koehorst; Vincent W Bloks; Tim van Zutphen; Folkert Kuipers; Jan Freark de Boer
Journal:  Pediatr Res       Date:  2022-09-23       Impact factor: 3.953

6.  Perinatal bile acid metabolism: bile acid analysis of meconium of preterm and full-term infants.

Authors:  Masami Kumagai; Akihiko Kimura; Hajime Takei; Takao Kurosawa; Kumiko Aoki; Takahiro Inokuchi; Toyojiro Matsuishi
Journal:  J Gastroenterol       Date:  2007-11-22       Impact factor: 7.527

Review 7.  Recent advances in the ontogeny of drug disposition.

Authors:  Brian D Chapron; Alenka Chapron; J Steven Leeder
Journal:  Br J Clin Pharmacol       Date:  2021-04-15       Impact factor: 3.716

Review 8.  Infant cholestasis patient with a novel missense mutation in the AKR1D1 gene successfully treated by early adequate supplementation with chenodeoxycholic acid: A case report and review of the literature.

Authors:  Hui-Hui Wang; Fei-Qiu Wen; Dong-Ling Dai; Jian-She Wang; Jing Zhao; Kenneth Dr Setchell; Li-Na Shi; Shao-Ming Zhou; Si-Xi Liu; Qing-Hua Yang
Journal:  World J Gastroenterol       Date:  2018-09-21       Impact factor: 5.742

9.  A combination of mutations in AKR1D1 and SKIV2L in a family with severe infantile liver disease.

Authors:  Neil V Morgan; Jane L Hartley; Kenneth D R Setchell; Michael A Simpson; Rachel Brown; Louise Tee; Sian Kirkham; Shanaz Pasha; Richard C Trembath; Eamonn R Maher; Paul Gissen; Deirdre A Kelly
Journal:  Orphanet J Rare Dis       Date:  2013-05-16       Impact factor: 4.123

10.  Lipidomics of human umbilical cord serum: identification of unique sterol sulfates.

Authors:  Paul L Wood; Heli Siljander; Mikael Knip
Journal:  Future Sci OA       Date:  2017-04-05
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