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Reversible normalisation of serum TSH levels in patients with autoimmune atrophic gastritis who received L-T4 in tablet form after switching to an oral liquid formulation: a case series
BACKGROUND: L-thyroxine (L-T4) malabsorption is a potential concern in patients with autoimmune atrophic gastritis. METHODS: We evaluated five patients with autoimmune gastritis, who showed high serum thyrotropin (TSH) levels (in the hypothyroid range) while in therapy with L-T4 in tablet. All patie...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787146/ https://www.ncbi.nlm.nih.gov/pubmed/26965518 http://dx.doi.org/10.1186/s12876-016-0439-y |
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author | Fallahi, Poupak Ferrari, Silvia Martina Ruffilli, Ilaria Antonelli, Alessando |
author_facet | Fallahi, Poupak Ferrari, Silvia Martina Ruffilli, Ilaria Antonelli, Alessando |
author_sort | Fallahi, Poupak |
collection | PubMed |
description | BACKGROUND: L-thyroxine (L-T4) malabsorption is a potential concern in patients with autoimmune atrophic gastritis. METHODS: We evaluated five patients with autoimmune gastritis, who showed high serum thyrotropin (TSH) levels (in the hypothyroid range) while in therapy with L-T4 in tablet. All patients were switched to receive an oral L-T4 liquid formulation maintaining the same dosage. RESULTS: In all patients who received L-T4 in tablet form after switching to an oral liquid formulation with the same L-T4 dosage, TSH circulating levels were normalized. In four patients who were switched back again to receive L-T4 in tablets, maintaining the dosage, TSH levels worsened again reaching levels in the hypothyroid range. CONCLUSIONS: The fact that the change from tablets to liquid oral formulation normalised serum TSH levels, and that switching back to tablets caused thyrotropin levels to worsen, leads us to believe that absorption of L-T4 is greater with oral liquid formulations in these patients. These results suggest that the L-T4 oral liquid formulation could circumvent the pH alteration resulting from atrophic gastritis. |
format | Online Article Text |
id | pubmed-4787146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47871462016-03-12 Reversible normalisation of serum TSH levels in patients with autoimmune atrophic gastritis who received L-T4 in tablet form after switching to an oral liquid formulation: a case series Fallahi, Poupak Ferrari, Silvia Martina Ruffilli, Ilaria Antonelli, Alessando BMC Gastroenterol Research Article BACKGROUND: L-thyroxine (L-T4) malabsorption is a potential concern in patients with autoimmune atrophic gastritis. METHODS: We evaluated five patients with autoimmune gastritis, who showed high serum thyrotropin (TSH) levels (in the hypothyroid range) while in therapy with L-T4 in tablet. All patients were switched to receive an oral L-T4 liquid formulation maintaining the same dosage. RESULTS: In all patients who received L-T4 in tablet form after switching to an oral liquid formulation with the same L-T4 dosage, TSH circulating levels were normalized. In four patients who were switched back again to receive L-T4 in tablets, maintaining the dosage, TSH levels worsened again reaching levels in the hypothyroid range. CONCLUSIONS: The fact that the change from tablets to liquid oral formulation normalised serum TSH levels, and that switching back to tablets caused thyrotropin levels to worsen, leads us to believe that absorption of L-T4 is greater with oral liquid formulations in these patients. These results suggest that the L-T4 oral liquid formulation could circumvent the pH alteration resulting from atrophic gastritis. BioMed Central 2016-02-24 /pmc/articles/PMC4787146/ /pubmed/26965518 http://dx.doi.org/10.1186/s12876-016-0439-y Text en © Fallahi et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Fallahi, Poupak Ferrari, Silvia Martina Ruffilli, Ilaria Antonelli, Alessando Reversible normalisation of serum TSH levels in patients with autoimmune atrophic gastritis who received L-T4 in tablet form after switching to an oral liquid formulation: a case series |
title | Reversible normalisation of serum TSH levels in patients with autoimmune atrophic gastritis who received L-T4 in tablet form after switching to an oral liquid formulation: a case series |
title_full | Reversible normalisation of serum TSH levels in patients with autoimmune atrophic gastritis who received L-T4 in tablet form after switching to an oral liquid formulation: a case series |
title_fullStr | Reversible normalisation of serum TSH levels in patients with autoimmune atrophic gastritis who received L-T4 in tablet form after switching to an oral liquid formulation: a case series |
title_full_unstemmed | Reversible normalisation of serum TSH levels in patients with autoimmune atrophic gastritis who received L-T4 in tablet form after switching to an oral liquid formulation: a case series |
title_short | Reversible normalisation of serum TSH levels in patients with autoimmune atrophic gastritis who received L-T4 in tablet form after switching to an oral liquid formulation: a case series |
title_sort | reversible normalisation of serum tsh levels in patients with autoimmune atrophic gastritis who received l-t4 in tablet form after switching to an oral liquid formulation: a case series |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787146/ https://www.ncbi.nlm.nih.gov/pubmed/26965518 http://dx.doi.org/10.1186/s12876-016-0439-y |
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