Literature DB >> 19931522

Serum steroid profiling for congenital adrenal hyperplasia using liquid chromatography-tandem mass spectrometry.

Claudia Rossi1, Lisa Calton, Gareth Hammond, Heather A Brown, A Michael Wallace, Paolo Sacchetta, Michael Morris.   

Abstract

BACKGROUND: Diagnosis of Congenital Adrenal Hyperplasia (CAH) is based on the quantification of 17-hydroxyprogesterone (17-OHP), usually by immunoassay. During the neonatal period the specificity of screening for CAH by blood spot 17-OHP immunoassay is low. High false-positive rates result in a relatively high demand for a second-tier serum confirmation test. A robust, specific and selective method for measurement of cortisol, 21-deoxycortisol, 11-deoxycortisol, 4-androstene-3,17-dione (A4) and 17-OHP in serum has been developed. The method involves a simple extraction procedure and a fast analysis using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC/MS/MS).
METHODS: The steroids were extracted from 50microl of serum using methyl-tert-butyl-ether. Analysis was performed on a UPLC tandem quadrupole mass spectrometer system in positive mode electrospray ionization and multiple reaction monitoring acquisition.
RESULTS: The assay was linear over each analyte concentration range with all correlation coefficients (r(2))>0.996. Inter- and intra-day CVs were <or=10% across the analytical range. In addition simultaneous measurement of the full range of steroids on the pathway to cortisol allows confirmation of the affected steroidogenic enzyme.
CONCLUSIONS: A second-tier test for the confirmation of CAH has been developed. The method allows for detection and quantification of 5 steroids related to CAH over the range of the clinical assay with good linearity, sensitivity and precision. Copyright 2009 Elsevier B.V. All rights reserved.

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Year:  2009        PMID: 19931522     DOI: 10.1016/j.cca.2009.11.007

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  16 in total

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Authors:  Alexander J Frey; Qingqing Wang; Christine Busch; Daniel Feldman; Lisa Bottalico; Clementina A Mesaros; Ian A Blair; Anil Vachani; Nathaniel W Snyder
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3.  A Novel Heterozygous Mutation of the CYP17A1 Gene in a Child with a Micropenis and Isolated 17,20-Lyase Deficiency.

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Journal:  Int J Environ Res Public Health       Date:  2022-06-04       Impact factor: 4.614

Review 4.  Biochemical and genetic diagnosis of 21-hydroxylase deficiency.

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5.  Multiplexed analysis of steroid hormones in human serum using novel microflow tile technology and LC-MS/MS.

Authors:  Carolyn J Broccardo; Kevin L Schauer; Wendy M Kohrt; Robert S Schwartz; James P Murphy; Jessica E Prenni
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Review 6.  Steroid assays in paediatric endocrinology.

Authors:  John W Honour
Journal:  J Clin Res Pediatr Endocrinol       Date:  2010-02-01

7.  Sample preparation and liquid chromatography-tandem mass spectrometry for multiple steroids in mammalian and avian circulation.

Authors:  Lee Koren; Ella S M Ng; Kiran K Soma; Katherine E Wynne-Edwards
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8.  Urine steroid metabolomics as a biomarker tool for detecting malignancy in adrenal tumors.

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Journal:  J Clin Endocrinol Metab       Date:  2011-09-14       Impact factor: 5.958

9.  Dried blood spot testing for seven steroids using liquid chromatography-tandem mass spectrometry with reference interval determination in the Korean population.

Authors:  Borahm Kim; Mi Na Lee; Hyung Doo Park; Jong Won Kim; Yun Sil Chang; Won Soon Park; Soo Youn Lee
Journal:  Ann Lab Med       Date:  2015-11       Impact factor: 3.464

Review 10.  Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  Jin-Ho Choi; Gu-Hwan Kim; Han-Wook Yoo
Journal:  Ann Pediatr Endocrinol Metab       Date:  2016-03-31
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