Literature DB >> 14709852

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

Keiko Homma1, Tomonobu Hasegawa, Masami Masumoto, Eiko Takeshita, Kiyoaki Watanabe, Hitoshi Chiba, Takao Kurosawa, Takao Takahashi, Nobutake Matsuo.   

Abstract

Urinary steroid profile analysis using gas chromatography/mass spectrometry (GC/MS) has been reported for the diagnosis of abnormal steroidogenesis in newborn infants with some success. We tried to establish the reference values of 63 urinary steroids in Japanese newborn infant, using GC/MS in selected ion monitoring (SIM) that utilizes two characteristic mass ions for each steroid for definitive identification. We studied 36 healthy full-term newborn infants (1-56 days of age) on spot urine samples to define the reference values (mg/g creatinine, median and 10-90 percentile range) and to investigate the possible difference between daytime and nighttime levels. We also studied 23 healthy adult females (20-24 years of age) on 24-hour-urine for the comparison of the reference values of newborn infants. Fifty metabolites of DHEA, pregnenolone, 17-hydroxypregnenolone, androstenedione, progesterone, 17-hydroxyprogesterone, 21-deoxycortisone, corticosterone, 18-hydroxycorticosterone, aldosterone, 18-hydroxycortisol, 11-deoxycortisol, cortisone, cortisol, and estrogen in each infant were measurable without interference, but 13 metabolites of 11-hydroxyandrostenedione, pregnenolone, 11-deoxycorticosterone, corticosterone, 11-dehydrocorticosterone, 21-deoxycortisol, 11-deoxycortisol and cortisol were unmeasurable in each infant due to the interference of fetal cortex steroids as confirmed by abnormal peak area ratios of two mass ions. All 63 metabolites in each control adult were measurable without interference. 16alpha-, 16beta-, and 15beta-hydroxy metabolites of 3beta-hydroxy-5-en-steroids, and 6beta-, 18-hydroxy and 11-oxo-metabolites of corticosteroids were significantly higher in full-term newborn infants than those in adults as previously reported. Urinary steroids showed little circadian variation in the newborn infants, indicating that spot urine can substitute for 24-hour urine.

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Year:  2003        PMID: 14709852     DOI: 10.1507/endocrj.50.783

Source DB:  PubMed          Journal:  Endocr J        ISSN: 0918-8959            Impact factor:   2.349


  12 in total

1.  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

2.  Close examination of steroidogenesis disorders in a DOC- and progesterone-producing adrenocortical carcinoma.

Authors:  Masakatsu Sone; Hirotaka Shibata; Keiko Homma; Naohisa Tamura; Jun-Ichi Akahira; Satoshi Hamada; Mitsuhiko Yahata; Nobuyuki Fukui; Hiroshi Itoh; Hironobu Sasano; Kazuwa Nakao
Journal:  Endocrine       Date:  2008-11-05       Impact factor: 3.633

3.  Heat-map visualization of gas chromatography-mass spectrometry based quantitative signatures on steroid metabolism.

Authors:  Ju-Yeon Moon; Hyun-Jin Jung; Myeong Hee Moon; Bong Chul Chung; Man Ho Choi
Journal:  J Am Soc Mass Spectrom       Date:  2009-05-05       Impact factor: 3.109

4.  Determination of adrenal steroids by microfluidic chip using micellar electrokinetic chromatography.

Authors:  Shuanglong Shen; Yan Li; Shin-ichi Wakida; Sahori Takeda
Journal:  Environ Monit Assess       Date:  2008-06-13       Impact factor: 2.513

5.  A Case of a Preterm Infant with 21-Hydroxylase Deficiency: Implications of the Biochemical Diagnosis with Urinary Pregnanetriolone by Gas Chromatography/Mass Spectrometry in Selected Ion Monitoring (GCMS-SIM).

Authors:  Takashi Hamajima; Shigeru Ohki; Hiroki Imamine; Haruo Mizuno; Keiko Homma; Tomonobu Hasegawa
Journal:  Clin Pediatr Endocrinol       Date:  2004-07-07

6.  Adrenocortical carcinoma characterized by gynecomastia: A case report.

Authors:  Takako Takeuchi; Yuko Yoto; Akira Ishii; Takeshi Tsugawa; Masaki Yamamoto; Tsukasa Hori; Hotaka Kamasaki; Kazutaka Nogami; Takanori Oda; Akihiro Nui; Sachiko Kimura; Takuya Yamagishi; Keiko Homma; Tomonobu Hasegawa; Maki Fukami; Yoko Watanabe; Hidehiko Sasamoto; Hiroyuki Tsutsumi
Journal:  Clin Pediatr Endocrinol       Date:  2018-01-30

Review 7.  GC/MS in Recent Years Has Defined the Normal and Clinically Disordered Steroidome: Will It Soon Be Surpassed by LC/Tandem MS in This Role?

Authors:  Cedric Shackleton; Oscar J Pozo; Josep Marcos
Journal:  J Endocr Soc       Date:  2018-07-09

8.  MIRAGE syndrome with recurrent pneumonia probably associated with gastroesophageal reflux and achalasia: A case report.

Authors:  Kanako Yoshizaki; Rumi Hachiya; Yutaro Tomobe; Uiko Kaku; Kazuhisa Akiba; Hirohito Shima; Satoshi Narumi; Yukihiro Hasegawa
Journal:  Clin Pediatr Endocrinol       Date:  2019-10-19

9.  Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites.

Authors:  Yuhei Koyama; Keiko Homma; Maki Fukami; Masayuki Miwa; Kazushige Ikeda; Tsutomu Ogata; Mitsuru Murata; Tomonobu Hasegawa
Journal:  Clin Pediatr Endocrinol       Date:  2016-04-28

10.  Pregnanetriolone in paper-borne urine for neonatal screening for 21-hydroxylase deficiency: The place of urine in neonatal screening.

Authors:  José Ramón Alonso-Fernández
Journal:  Mol Genet Metab Rep       Date:  2016-08-18
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