Literature DB >> 32014605

Selective LC-MRM/SIM-MS based profiling of adrenal steroids reveals metabolic signatures of 17α-hydroxylase deficiency.

Chaelin Lee1, Jung Hee Kim2, Sun Joon Moon2, Jaeyoon Shim3, Hugh I Kim4, Man Ho Choi5.   

Abstract

Adrenal steroids are generated in the adrenal cortex and metabolized by various enzymes such as hydroxylases, dehydrogenases, and reductases. Determining the comprehensive metabolic signatures of adrenal steroids can provide insight into their metabolic functions and roles in the pathophysiology of adrenal diseases, including Cushing's syndrome (CS) and congenital adrenal hyperplasia (CAH). To this end, we developed an advanced quantitative profiling method of serum adrenal steroids with liquid chromatography-mass spectrometry (LC-MS) under molecular-specific scan modes. Twenty-seven steroids were separated on a 1.9-μm particle C18 column (50 × 2.1 mm) at a flow rate of 250 μL/min and quantified via triple-quadrupole MS with electrospray ionization. During validation, linearities ( r2) were higher than 0.940 with a limit of quantification of 0.1-5.0 ng/mL, and precision (coefficient of variation) and accuracy (%bias) of 3.7-14.3 % and 96.3-113.1 %, respectively. In contrast with the significantly increased serum levels of mineralocorticoids (P <  0.001), the present LC-MS assay revealed remarkably decreased levels of all glucocorticoids and androgens in a patient diagnosed with 17α-hydroxylase deficiency CAH (P <  0.001) compared to those of age- and sex-matched healthy and CS subjects. In the CAH patient, the metabolic ratios for 17α-hydroxylase were significantly decreased, whereas there was no reduction in the metabolic ratio of 17-hydroxyprogesterone to androstenedione, indicating 17,20-lyase activity. In particular, both pregnenolone and dehydroepiandrosterone sulfates, and their metabolic ratio, were identified as potential biomarkers for 17α-hydroxylase deficiency (all P <  0.001), which were also distinct from those of CS patients. The devised LC-MS assay clearly revealed the metabolic signatures of 17α-hydroxylase deficiency, as a rare phenotype of CAH, compared to both healthy and CS subjects, indicating its utility for screening adrenal diseases.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  17α-Hydroxylase; Adrenal steroids; Congenital adrenal hyperplasia; Mass spectrometry

Mesh:

Substances:

Year:  2020        PMID: 32014605     DOI: 10.1016/j.jsbmb.2020.105615

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  4 in total

1.  Profiling of Steroid Metabolic Pathways in Human Plasma by GC-MS/MS Combined with Microwave-Assisted Derivatization for Diagnosis of Gastric Disorders.

Authors:  Wonwoong Lee; Hyunjung Lee; You Lee Kim; Yong Chan Lee; Bong Chul Chung; Jongki Hong
Journal:  Int J Mol Sci       Date:  2021-02-13       Impact factor: 5.923

2.  Metabolic Subtyping of Adrenal Tumors: Prospective Multi-Center Cohort Study in Korea.

Authors:  Eu Jeong Ku; Chaelin Lee; Jaeyoon Shim; Sihoon Lee; Kyoung-Ah Kim; Sang Wan Kim; Yumie Rhee; Hyo-Jeong Kim; Jung Soo Lim; Choon Hee Chung; Sung Wan Chun; Soon-Jib Yoo; Ohk-Hyun Ryu; Ho Chan Cho; A Ram Hong; Chang Ho Ahn; Jung Hee Kim; Man Ho Choi
Journal:  Endocrinol Metab (Seoul)       Date:  2021-10-21

3.  Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency.

Authors:  Taek Min Kim; Jung Hee Kim; Han Na Jang; Man Ho Choi; Jeong Yeon Cho; Sang Youn Kim
Journal:  Endocrinol Metab (Seoul)       Date:  2022-02-08

Review 4.  Clinical and Technical Aspects in Free Cortisol Measurement.

Authors:  Man Ho Choi
Journal:  Endocrinol Metab (Seoul)       Date:  2022-08-19
  4 in total

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