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Steroid concentrations in antepartum and postpartum saliva: normative values in women and correlations with serum

BACKGROUND: Saliva has been advocated as an alternative to serum or plasma for steroid monitoring. Little normative information is available concerning expected concentrations of the major reproductive steroids in saliva during pregnancy and the extended postpartum. METHODS: Matched serum and saliva...

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Autores principales: Hampson, Elizabeth, Phillips, Shauna-Dae, Soares, Claudio N, Steiner, Meir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635986/
https://www.ncbi.nlm.nih.gov/pubmed/23575245
http://dx.doi.org/10.1186/2042-6410-4-7
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author Hampson, Elizabeth
Phillips, Shauna-Dae
Soares, Claudio N
Steiner, Meir
author_facet Hampson, Elizabeth
Phillips, Shauna-Dae
Soares, Claudio N
Steiner, Meir
author_sort Hampson, Elizabeth
collection PubMed
description BACKGROUND: Saliva has been advocated as an alternative to serum or plasma for steroid monitoring. Little normative information is available concerning expected concentrations of the major reproductive steroids in saliva during pregnancy and the extended postpartum. METHODS: Matched serum and saliva specimens controlled for time of day and collected less than 30 minutes apart were obtained in 28 women with normal singleton pregnancies between 32 and 38 weeks of gestation and in 43 women during the first six months postpartum. Concentrations of six steroids (estriol, estradiol, progesterone, testosterone, cortisol, dehydroepiandrosterone) were quantified in saliva by enzyme immunoassay. RESULTS: For most of the steroids examined, concentrations in antepartum saliva showed linear increases near end of gestation, suggesting an increase in the bioavailable hormone component. Observed concentrations were in agreement with the limited data available from previous reports. Modal concentrations of the ovarian steroids were undetectable in postpartum saliva and, when detectable in individual women, approximated early follicular phase values. Only low to moderate correlations between the serum and salivary concentrations were found, suggesting that during the peripartum period saliva provides information that is not redundant to serum. CONCLUSIONS: Low correlations in the late antepartum may be due to differential rates of change in the total and bioavailable fractions of the circulating steroid in the final weeks of the third trimester as a consequence of dynamic changes in carrier proteins such as corticosteroid binding globulin.
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spelling pubmed-36359862013-04-26 Steroid concentrations in antepartum and postpartum saliva: normative values in women and correlations with serum Hampson, Elizabeth Phillips, Shauna-Dae Soares, Claudio N Steiner, Meir Biol Sex Differ Research BACKGROUND: Saliva has been advocated as an alternative to serum or plasma for steroid monitoring. Little normative information is available concerning expected concentrations of the major reproductive steroids in saliva during pregnancy and the extended postpartum. METHODS: Matched serum and saliva specimens controlled for time of day and collected less than 30 minutes apart were obtained in 28 women with normal singleton pregnancies between 32 and 38 weeks of gestation and in 43 women during the first six months postpartum. Concentrations of six steroids (estriol, estradiol, progesterone, testosterone, cortisol, dehydroepiandrosterone) were quantified in saliva by enzyme immunoassay. RESULTS: For most of the steroids examined, concentrations in antepartum saliva showed linear increases near end of gestation, suggesting an increase in the bioavailable hormone component. Observed concentrations were in agreement with the limited data available from previous reports. Modal concentrations of the ovarian steroids were undetectable in postpartum saliva and, when detectable in individual women, approximated early follicular phase values. Only low to moderate correlations between the serum and salivary concentrations were found, suggesting that during the peripartum period saliva provides information that is not redundant to serum. CONCLUSIONS: Low correlations in the late antepartum may be due to differential rates of change in the total and bioavailable fractions of the circulating steroid in the final weeks of the third trimester as a consequence of dynamic changes in carrier proteins such as corticosteroid binding globulin. BioMed Central 2013-04-10 /pmc/articles/PMC3635986/ /pubmed/23575245 http://dx.doi.org/10.1186/2042-6410-4-7 Text en Copyright © 2013 Hampson et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Hampson, Elizabeth
Phillips, Shauna-Dae
Soares, Claudio N
Steiner, Meir
Steroid concentrations in antepartum and postpartum saliva: normative values in women and correlations with serum
title Steroid concentrations in antepartum and postpartum saliva: normative values in women and correlations with serum
title_full Steroid concentrations in antepartum and postpartum saliva: normative values in women and correlations with serum
title_fullStr Steroid concentrations in antepartum and postpartum saliva: normative values in women and correlations with serum
title_full_unstemmed Steroid concentrations in antepartum and postpartum saliva: normative values in women and correlations with serum
title_short Steroid concentrations in antepartum and postpartum saliva: normative values in women and correlations with serum
title_sort steroid concentrations in antepartum and postpartum saliva: normative values in women and correlations with serum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635986/
https://www.ncbi.nlm.nih.gov/pubmed/23575245
http://dx.doi.org/10.1186/2042-6410-4-7
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