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Association between posttest dexamethasone and cortisol concentrations in the 1 mg overnight dexamethasone suppression test
It has been suggested that comparison of posttest dexamethasone and cortisol concentrations may improve the evaluation of the dexamethasone suppression test (DST) for Cushing's syndrome. In particular, this would be reasonable if posttest cortisol differs by dexamethasone levels within the rang...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioScientifica
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681321/ https://www.ncbi.nlm.nih.gov/pubmed/23781306 http://dx.doi.org/10.1530/EC-12-0047 |
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author | Åsvold, Bjørn O Grill, Valdemar Thorstensen, Ketil Bjørgaas, Marit R |
author_facet | Åsvold, Bjørn O Grill, Valdemar Thorstensen, Ketil Bjørgaas, Marit R |
author_sort | Åsvold, Bjørn O |
collection | PubMed |
description | It has been suggested that comparison of posttest dexamethasone and cortisol concentrations may improve the evaluation of the dexamethasone suppression test (DST) for Cushing's syndrome. In particular, this would be reasonable if posttest cortisol differs by dexamethasone levels within the range that is usually attained in the DST. Using fractional polynomial regression, we therefore studied the association between posttest 0800 h dexamethasone and cortisol levels in 53 subjects without Cushing's syndrome who were tested with the 1 mg overnight DST. Plasma dexamethasone was associated with plasma cortisol (P<0.001), and the regression line suggested a strong negative association related to dexamethasone levels <5 nmol/l. However, among the 94% of subjects with plasma dexamethasone >5.0 nmol/l, there was no association between dexamethasone and cortisol levels (P=0.55). In conclusion, subjects tested with the 1 mg overnight DST usually attain an 0800 h plasma dexamethasone >5 nmol/l, and plasma cortisol does not differ by plasma dexamethasone in these subjects. This suggests that routine comparison of dexamethasone and cortisol levels may not be a useful approach to improve the performance of the 1 mg DST. However, dexamethasone measurements may identify subjects with inadequately low plasma dexamethasone and may therefore be of value when retesting subjects with possibly false-positive DST results. |
format | Online Article Text |
id | pubmed-3681321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioScientifica |
record_format | MEDLINE/PubMed |
spelling | pubmed-36813212013-06-17 Association between posttest dexamethasone and cortisol concentrations in the 1 mg overnight dexamethasone suppression test Åsvold, Bjørn O Grill, Valdemar Thorstensen, Ketil Bjørgaas, Marit R Endocr Connect Research It has been suggested that comparison of posttest dexamethasone and cortisol concentrations may improve the evaluation of the dexamethasone suppression test (DST) for Cushing's syndrome. In particular, this would be reasonable if posttest cortisol differs by dexamethasone levels within the range that is usually attained in the DST. Using fractional polynomial regression, we therefore studied the association between posttest 0800 h dexamethasone and cortisol levels in 53 subjects without Cushing's syndrome who were tested with the 1 mg overnight DST. Plasma dexamethasone was associated with plasma cortisol (P<0.001), and the regression line suggested a strong negative association related to dexamethasone levels <5 nmol/l. However, among the 94% of subjects with plasma dexamethasone >5.0 nmol/l, there was no association between dexamethasone and cortisol levels (P=0.55). In conclusion, subjects tested with the 1 mg overnight DST usually attain an 0800 h plasma dexamethasone >5 nmol/l, and plasma cortisol does not differ by plasma dexamethasone in these subjects. This suggests that routine comparison of dexamethasone and cortisol levels may not be a useful approach to improve the performance of the 1 mg DST. However, dexamethasone measurements may identify subjects with inadequately low plasma dexamethasone and may therefore be of value when retesting subjects with possibly false-positive DST results. BioScientifica 2012-08-30 /pmc/articles/PMC3681321/ /pubmed/23781306 http://dx.doi.org/10.1530/EC-12-0047 Text en © 2012 The Authors. Published by BioScientifica Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Åsvold, Bjørn O Grill, Valdemar Thorstensen, Ketil Bjørgaas, Marit R Association between posttest dexamethasone and cortisol concentrations in the 1 mg overnight dexamethasone suppression test |
title | Association between posttest dexamethasone and cortisol concentrations in the 1 mg overnight dexamethasone suppression test |
title_full | Association between posttest dexamethasone and cortisol concentrations in the 1 mg overnight dexamethasone suppression test |
title_fullStr | Association between posttest dexamethasone and cortisol concentrations in the 1 mg overnight dexamethasone suppression test |
title_full_unstemmed | Association between posttest dexamethasone and cortisol concentrations in the 1 mg overnight dexamethasone suppression test |
title_short | Association between posttest dexamethasone and cortisol concentrations in the 1 mg overnight dexamethasone suppression test |
title_sort | association between posttest dexamethasone and cortisol concentrations in the 1 mg overnight dexamethasone suppression test |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681321/ https://www.ncbi.nlm.nih.gov/pubmed/23781306 http://dx.doi.org/10.1530/EC-12-0047 |
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