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Pregnancy disrupts the accuracy of automated fT4 immunoassays
OBJECTIVE: Thyroid hormone measurements are often performed in pregnant women, as hypo- and hyperthyroidism during pregnancy can severely affect the fetus. Serum free thyroxine (fT4) measurements are well known for their analytical challenges, due to low serum concentrations and the subtle equilibri...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641786/ https://www.ncbi.nlm.nih.gov/pubmed/36219545 http://dx.doi.org/10.1530/ETJ-22-0145 |
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author | Jansen, Heleen I van Herwaarden, Antonius E Huijgen, Henk J Painter, Rebecca C Hillebrand, Jacquelien J Boelen, Anita Heijboer, Annemieke C |
author_facet | Jansen, Heleen I van Herwaarden, Antonius E Huijgen, Henk J Painter, Rebecca C Hillebrand, Jacquelien J Boelen, Anita Heijboer, Annemieke C |
author_sort | Jansen, Heleen I |
collection | PubMed |
description | OBJECTIVE: Thyroid hormone measurements are often performed in pregnant women, as hypo- and hyperthyroidism during pregnancy can severely affect the fetus. Serum free thyroxine (fT4) measurements are well known for their analytical challenges, due to low serum concentrations and the subtle equilibrium between free and bound T4 (to thyroid-binding globulin (TBG), transthyretin and albumin). Pregnant women have high TBG concentrations due to an increase in human chorionic gonadotropin (hCG) and estrogen and lower albumin concentrations which change the equilibrium and may affect the validity of fT4 measurements in their samples. As accurate serum fT4 measurements in pregnant women are important for the long-term health of the fetus, we aimed to evaluate the accuracy of several fT4 immunoassays in the serum of pregnant women. METHODS: FT4 was measured in healthy controls and pregnant women using a candidate-reference method (LC-MS/MS) and five commercially available automated immunoassays (Alinity (Abbott), Atellica (Siemens), Cobas (Roche), Lumipulse (Fujirebio) and UniCel DXI (Beckman Coulter)). Method comparisons (Bland Altman plots and Passing and Bablok analyses) were performed. RESULTS: Serum samples from both healthy controls (n = 30) and pregnant women (n = 30; mean gestational age, 24.8 weeks) were collected. The fT4 immunoassays deviated +7 to +29% more from the LC-MS/MS in serum samples of pregnant women than healthy controls (falsely high). CONCLUSIONS: Our results indicate that immunoassays overestimate fT4 in pregnant women, which might lead to an overestimation of thyroid status. Physicians and laboratory specialists should be aware of this phenomenon to avoid drawing false conclusions about thyroid function in pregnant women. |
format | Online Article Text |
id | pubmed-9641786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-96417862022-11-14 Pregnancy disrupts the accuracy of automated fT4 immunoassays Jansen, Heleen I van Herwaarden, Antonius E Huijgen, Henk J Painter, Rebecca C Hillebrand, Jacquelien J Boelen, Anita Heijboer, Annemieke C Eur Thyroid J Research OBJECTIVE: Thyroid hormone measurements are often performed in pregnant women, as hypo- and hyperthyroidism during pregnancy can severely affect the fetus. Serum free thyroxine (fT4) measurements are well known for their analytical challenges, due to low serum concentrations and the subtle equilibrium between free and bound T4 (to thyroid-binding globulin (TBG), transthyretin and albumin). Pregnant women have high TBG concentrations due to an increase in human chorionic gonadotropin (hCG) and estrogen and lower albumin concentrations which change the equilibrium and may affect the validity of fT4 measurements in their samples. As accurate serum fT4 measurements in pregnant women are important for the long-term health of the fetus, we aimed to evaluate the accuracy of several fT4 immunoassays in the serum of pregnant women. METHODS: FT4 was measured in healthy controls and pregnant women using a candidate-reference method (LC-MS/MS) and five commercially available automated immunoassays (Alinity (Abbott), Atellica (Siemens), Cobas (Roche), Lumipulse (Fujirebio) and UniCel DXI (Beckman Coulter)). Method comparisons (Bland Altman plots and Passing and Bablok analyses) were performed. RESULTS: Serum samples from both healthy controls (n = 30) and pregnant women (n = 30; mean gestational age, 24.8 weeks) were collected. The fT4 immunoassays deviated +7 to +29% more from the LC-MS/MS in serum samples of pregnant women than healthy controls (falsely high). CONCLUSIONS: Our results indicate that immunoassays overestimate fT4 in pregnant women, which might lead to an overestimation of thyroid status. Physicians and laboratory specialists should be aware of this phenomenon to avoid drawing false conclusions about thyroid function in pregnant women. Bioscientifica Ltd 2022-10-11 /pmc/articles/PMC9641786/ /pubmed/36219545 http://dx.doi.org/10.1530/ETJ-22-0145 Text en © The authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Research Jansen, Heleen I van Herwaarden, Antonius E Huijgen, Henk J Painter, Rebecca C Hillebrand, Jacquelien J Boelen, Anita Heijboer, Annemieke C Pregnancy disrupts the accuracy of automated fT4 immunoassays |
title | Pregnancy disrupts the accuracy of automated fT4 immunoassays |
title_full | Pregnancy disrupts the accuracy of automated fT4 immunoassays |
title_fullStr | Pregnancy disrupts the accuracy of automated fT4 immunoassays |
title_full_unstemmed | Pregnancy disrupts the accuracy of automated fT4 immunoassays |
title_short | Pregnancy disrupts the accuracy of automated fT4 immunoassays |
title_sort | pregnancy disrupts the accuracy of automated ft4 immunoassays |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641786/ https://www.ncbi.nlm.nih.gov/pubmed/36219545 http://dx.doi.org/10.1530/ETJ-22-0145 |
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