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Distinct serum steroid profiles between adrenal Cushing syndrome and Cushing disease
BACKGROUND: Differentiating between adrenal Cushing syndrome (adrenal CS) and Cushing disease (CD) can be challenging if there are equivocal or falsely elevated adrenocorticotropic hormone (ACTH) values. We aim to investigate the diagnostic value of serum steroid profiles in differentiating adrenal...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229066/ https://www.ncbi.nlm.nih.gov/pubmed/37260439 http://dx.doi.org/10.3389/fendo.2023.1158573 |
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author | Gao, Chang Ding, Li Zhang, Xiaona Yuan, Menghua Tang, Shaofang Li, Wei Ye, Yuanyuan Liu, Ming He, Qing |
author_facet | Gao, Chang Ding, Li Zhang, Xiaona Yuan, Menghua Tang, Shaofang Li, Wei Ye, Yuanyuan Liu, Ming He, Qing |
author_sort | Gao, Chang |
collection | PubMed |
description | BACKGROUND: Differentiating between adrenal Cushing syndrome (adrenal CS) and Cushing disease (CD) can be challenging if there are equivocal or falsely elevated adrenocorticotropic hormone (ACTH) values. We aim to investigate the diagnostic value of serum steroid profiles in differentiating adrenal CS from CD. METHOD: A total of 11 serum steroids in adrenal CS (n = 13) and CD (n = 15) were analyzed by liquid chromatography with tandem mass spectrometry (LC-MS/MS). Age- and gender-specific steroid ratios were generated by dividing the actual steroid concentration by the upper limit of the relevant reference range. A principal component analysis (PCA) and an orthogonal partial least squares discriminant analysis (OPLS-DA) were performed. RESULTS: The PCA and OPLS-DA analyses showed distinct serum steroid profiles between adrenal CS and CD. Dehydroepiandrosterone sulfate (DHEA-S), dehydroepiandrosterone (DHEA), and androstenedione ratios were identified as biomarkers for discrimination by variable importance in projection (VIP) in combination with t-tests. The sensitivity and specificity of DHEA-S ratios <0.40 were 92.31% (95% CI 64.0%–99.8%) and 93.33% (95% CI 68.1%–99.8%), respectively, in identifying adrenal CS. The sensitivity and specificity of DHEA ratios <0.18 were 100% (95% CI 75.3%–100.0%) and 100% (95% CI 78.2%–100.0%), respectively, in identifying adrenal CS. CONCLUSION: Our data support the clinical use of the DHEA-S and DHEA ratios in the differential diagnosis of adrenal CS and CD, especially when falsely elevated ACTH is suspected. |
format | Online Article Text |
id | pubmed-10229066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102290662023-05-31 Distinct serum steroid profiles between adrenal Cushing syndrome and Cushing disease Gao, Chang Ding, Li Zhang, Xiaona Yuan, Menghua Tang, Shaofang Li, Wei Ye, Yuanyuan Liu, Ming He, Qing Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Differentiating between adrenal Cushing syndrome (adrenal CS) and Cushing disease (CD) can be challenging if there are equivocal or falsely elevated adrenocorticotropic hormone (ACTH) values. We aim to investigate the diagnostic value of serum steroid profiles in differentiating adrenal CS from CD. METHOD: A total of 11 serum steroids in adrenal CS (n = 13) and CD (n = 15) were analyzed by liquid chromatography with tandem mass spectrometry (LC-MS/MS). Age- and gender-specific steroid ratios were generated by dividing the actual steroid concentration by the upper limit of the relevant reference range. A principal component analysis (PCA) and an orthogonal partial least squares discriminant analysis (OPLS-DA) were performed. RESULTS: The PCA and OPLS-DA analyses showed distinct serum steroid profiles between adrenal CS and CD. Dehydroepiandrosterone sulfate (DHEA-S), dehydroepiandrosterone (DHEA), and androstenedione ratios were identified as biomarkers for discrimination by variable importance in projection (VIP) in combination with t-tests. The sensitivity and specificity of DHEA-S ratios <0.40 were 92.31% (95% CI 64.0%–99.8%) and 93.33% (95% CI 68.1%–99.8%), respectively, in identifying adrenal CS. The sensitivity and specificity of DHEA ratios <0.18 were 100% (95% CI 75.3%–100.0%) and 100% (95% CI 78.2%–100.0%), respectively, in identifying adrenal CS. CONCLUSION: Our data support the clinical use of the DHEA-S and DHEA ratios in the differential diagnosis of adrenal CS and CD, especially when falsely elevated ACTH is suspected. Frontiers Media S.A. 2023-05-16 /pmc/articles/PMC10229066/ /pubmed/37260439 http://dx.doi.org/10.3389/fendo.2023.1158573 Text en Copyright © 2023 Gao, Ding, Zhang, Yuan, Tang, Li, Ye, Liu and He https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Gao, Chang Ding, Li Zhang, Xiaona Yuan, Menghua Tang, Shaofang Li, Wei Ye, Yuanyuan Liu, Ming He, Qing Distinct serum steroid profiles between adrenal Cushing syndrome and Cushing disease |
title | Distinct serum steroid profiles between adrenal Cushing syndrome and Cushing disease |
title_full | Distinct serum steroid profiles between adrenal Cushing syndrome and Cushing disease |
title_fullStr | Distinct serum steroid profiles between adrenal Cushing syndrome and Cushing disease |
title_full_unstemmed | Distinct serum steroid profiles between adrenal Cushing syndrome and Cushing disease |
title_short | Distinct serum steroid profiles between adrenal Cushing syndrome and Cushing disease |
title_sort | distinct serum steroid profiles between adrenal cushing syndrome and cushing disease |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229066/ https://www.ncbi.nlm.nih.gov/pubmed/37260439 http://dx.doi.org/10.3389/fendo.2023.1158573 |
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