Literature DB >> 23160874

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

Yoshitaka Seki1, 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.   

Abstract

BACKGROUND AND AIMS: In two Japanese infants with neonatal cholestasis, 3-oxo-Δ(4)-steroid 5β-reductase deficiency was diagnosed based on mutations of the SRD5B1 gene. Unusual bile acids such as elevated 3-oxo-Δ(4) bile acids were detected in their serum and urine by gas chromatography-mass spectrometry. We studied effects of oral chenodeoxycholic acid treatment. PATIENTS AND METHODS: SRD5B1 gene analysis used peripheral lymphocyte genomic DNA. Diagnosis and treatment of these two patients were investigated retrospectively and prospectively investigated.
RESULTS: With respect to SRD5B1, one patient was heterozygous (R266Q, a novel mutation) while the other was a compound heterozygote (G223E/R261C). Chenodeoxycholic acid treatment was effective in improving liver function and decreasing unusual bile acids such as 7α-hydroxy- and 7α,12α-dihydroxy-3-oxo-4-cholen-24-oic acids in serum and urine.
CONCLUSION: Primary bile acid treatment using chenodeoxycholic acid was effective for these patients treated in early infancy before the late stage of chronic cholestatic liver dysfunction.

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Year:  2012        PMID: 23160874     DOI: 10.1007/s10545-012-9526-6

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  24 in total

1.  Molecular genetic and bile acid profiles in two Japanese patients with 3beta-hydroxy-DELTA5-C27-steroid dehydrogenase/isomerase deficiency.

Authors:  Tatsuki Mizuochi; Akihiko Kimura; Isao Ueki; Tomoyuki Takahashi; Takuji Hashimoto; Akira Takao; Yoshitaka Seki; Hajime Takei; Hiroshi Nittono; Takao Kurosawa; Toyojiro Matsuishi
Journal:  Pediatr Res       Date:  2010-09       Impact factor: 3.756

Review 2.  Transcriptional regulation of hepatobiliary transport systems in health and disease: implications for a rationale approach to the treatment of intrahepatic cholestasis.

Authors:  Martin Wagner; Michael Trauner
Journal:  Ann Hepatol       Date:  2005 Apr-Jun       Impact factor: 2.400

3.  3-Oxo-delta 4 bile acids in liver disease.

Authors:  P T Clayton; E Patel; A M Lawson; R A Carruthers; M S Tanner; B Strandvik; B Egestad; J Sjövall
Journal:  Lancet       Date:  1988-06-04       Impact factor: 79.321

4.  Measurement of transport activities of bile acids in human multidrug resistance-associated protein 3 using liquid chromatography-tandem mass spectrometry.

Authors:  Kana Yamaguchi; Tsuyoshi Murai; Hikaru Yabuuchi; Takao Kurosawa
Journal:  Anal Sci       Date:  2010       Impact factor: 2.081

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

Authors:  A Kimura; R Mahara; T Inoue; Y Nomura; T Murai; T Kurosawa; M Tohma; K Noguchi; A Hoshiyama; T Fujisawa; H Kato
Journal:  Pediatr Res       Date:  1999-04       Impact factor: 3.756

Review 6.  Disorders of bile acid synthesis.

Authors:  Peter Theodore Clayton
Journal:  J Inherit Metab Dis       Date:  2011-01-13       Impact factor: 4.982

7.  SRD5B1 gene analysis needed for the accurate diagnosis of primary 3-oxo-Delta4-steroid 5beta-reductase deficiency.

Authors:  Isao Ueki; Akihiko Kimura; Huey-Ling Chen; Tohru Yorifuji; Jun Mori; Susumu Itoh; Kenichi Maruyama; Takashi Ishige; Hajime Takei; Hiroshi Nittono; Takao Kurosawa; Masayoshi Kage; Toyojiro Matsuishi
Journal:  J Gastroenterol Hepatol       Date:  2008-11-03       Impact factor: 4.029

8.  Improved synthesis of 3-keto, 4-ene-3-keto, and 4,6-diene-3-keto bile acids.

Authors:  R A Leppik
Journal:  Steroids       Date:  1983-04       Impact factor: 2.668

9.  Reference values for urinary steroids in Japanese newborn infants: gas chromatography/mass spectrometry in selected ion monitoring.

Authors:  Keiko Homma; Tomonobu Hasegawa; Masami Masumoto; Eiko Takeshita; Kiyoaki Watanabe; Hitoshi Chiba; Takao Kurosawa; Takao Takahashi; Nobutake Matsuo
Journal:  Endocr J       Date:  2003-12       Impact factor: 2.349

10.  Human Delta4-3-oxosteroid 5beta-reductase (AKR1D1) deficiency and steroid metabolism.

Authors:  Mario Palermo; Maria Grazia Marazzi; Beverly A Hughes; Paul M Stewart; Peter T Clayton; Cedric H L Shackleton
Journal:  Steroids       Date:  2007-12-14       Impact factor: 2.668

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  6 in total

1.  [Clinical feature and genetic analysis of a family affected by congenital bile acid synthesis defect type 2: identification of 2 novel mutations in AKR1D1 gene].

Authors:  Ying Cheng; Li Guo; Mei Deng; Yuan-Zong Song
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2017-07

2.  Silencing LRH-1 in colon cancer cell lines impairs proliferation and alters gene expression programs.

Authors:  James R Bayrer; Sridevi Mukkamala; Elena P Sablin; Paul Webb; Robert J Fletterick
Journal:  Proc Natl Acad Sci U S A       Date:  2015-02-09       Impact factor: 11.205

3.  Clinical and genetic features of congenital bile acid synthesis defect with a novel mutation in AKR1D1 gene sequencing: Case reports.

Authors:  Anh-Hoa Nguyen Pham; Kim-Oanh Bui Thi; Mai-Huong Nguyen Thi; Diem-Ngoc Ngo; Nakayuki Naritaka; Hiroshi Nittono; Hisamitsu Hayashi; Trang Thi Dao; Kim-Huong Thi Nguyen; Hoai-Nghia Nguyen; Hoa Giang; Hung-Sang Tang; Tat-Thanh Nguyen; Dinh-Kiet Truong; Minh-Dien Tran
Journal:  Medicine (Baltimore)       Date:  2022-06-24       Impact factor: 1.817

4.  Rate of steroid double-bond reduction catalysed by the human steroid 5β-reductase (AKR1D1) is sensitive to steroid structure: implications for steroid metabolism and bile acid synthesis.

Authors:  Yi Jin; Mo Chen; Trevor M Penning
Journal:  Biochem J       Date:  2014-08-15       Impact factor: 3.857

Review 5.  Role of aldo-keto reductase family 1 (AKR1) enzymes in human steroid metabolism.

Authors:  Tea Lanišnik Rižner; Trevor M Penning
Journal:  Steroids       Date:  2013-11-01       Impact factor: 2.668

Review 6.  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

  6 in total

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