Comparison of pathophysiology in subclinical hyperthyroidism with different etiologies

Subclinical hyperthyroidism (SHyper) is defined as normal levels of free thyroxine (fT4) and free triiodothyronine (fT3) with suppressed levels of TSH. Previous studies have reported the individual pathophysiology of endogenous SHyper patients and athyreotic patients receiving TSH suppression therap...

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Main Authors: Hanna Deguchi-Horiuchi, Mitsuru Ito, Sawako Takahashi, Kazuyoshi Kousaka, Mako Hisakado, Shuji Fukata, Takumi Kudo, Eijun Nishihara, Mitsushige Nishikawa, Akira Miyauchi, Takashi Akamizu
Format: Article
Language:English
Published: The Japan Endocrine Society 2024-04-01
Series:Endocrine Journal
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Online Access:https://www.jstage.jst.go.jp/article/endocrj/71/4/71_EJ23-0497/_html/-char/en
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author Hanna Deguchi-Horiuchi
Mitsuru Ito
Sawako Takahashi
Kazuyoshi Kousaka
Mako Hisakado
Shuji Fukata
Takumi Kudo
Eijun Nishihara
Mitsushige Nishikawa
Akira Miyauchi
Takashi Akamizu
author_facet Hanna Deguchi-Horiuchi
Mitsuru Ito
Sawako Takahashi
Kazuyoshi Kousaka
Mako Hisakado
Shuji Fukata
Takumi Kudo
Eijun Nishihara
Mitsushige Nishikawa
Akira Miyauchi
Takashi Akamizu
author_sort Hanna Deguchi-Horiuchi
collection DOAJ
description Subclinical hyperthyroidism (SHyper) is defined as normal levels of free thyroxine (fT4) and free triiodothyronine (fT3) with suppressed levels of TSH. Previous studies have reported the individual pathophysiology of endogenous SHyper patients and athyreotic patients receiving TSH suppression therapy with levothyroxine; however, apparently no studies have compared the two conditions. Five-hundred-forty untreated endogenous SHyper patients and 1,024 patients receiving TSH suppression therapy who underwent total thyroidectomy for papillary thyroid carcinoma were sampled. Thyroid hormone profiles and peripheral indices related to thyrotoxicosis were investigated in endogenous SHyper patients, athyreotic patients receiving TSH suppression therapy, and healthy participants. Endogenous SHyper patients showed significantly higher thyroid hormone levels (fT4 [p < 0.001] and fT3 [p < 0.001]), and peripheral indices showed a significant tendency towards thyrotoxicosis (strong TSH suppression: alkaline phosphatase [ALP, p < 0.001], creatinine [Cre, p < 0.001], pulse rate [p < 0.05]; and mild TSH suppression: Cre [p < 0.05]) than healthy participants. In contrast, athyreotic patients receiving TSH suppression therapy showed a significant tendency towards thyrotoxicosis than healthy participants only when TSH was strongly suppressed (fT3 [p < 0.001] and Cre [p < 0.001]). Endogenous SHyper patients showed significantly higher fT3 levels (p < 0.001) than athyreotic patients receiving TSH suppression therapy; however, there was a significant tendency towards thyrotoxicosis only when TSH was strongly suppressed (ALP [p < 0.05] and pulse rate [p < 0.05]). The effects of endogenous SHyper and TSH suppression therapy on target organ function are different. Although the serum thyroid hormone profile is similar to that of the thyrotoxic state, athyreotic patients receiving TSH suppression therapy with mildly suppressed serum TSH levels are not thyrotoxic.
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institution Kabale University
issn 1348-4540
language English
publishDate 2024-04-01
publisher The Japan Endocrine Society
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series Endocrine Journal
spelling doaj-art-958caadbb04f475f98c225cd885fafb32025-01-22T06:37:03ZengThe Japan Endocrine SocietyEndocrine Journal1348-45402024-04-0171437338110.1507/endocrj.EJ23-0497endocrjComparison of pathophysiology in subclinical hyperthyroidism with different etiologiesHanna Deguchi-Horiuchi0Mitsuru Ito1Sawako Takahashi2Kazuyoshi Kousaka3Mako Hisakado4Shuji Fukata5Takumi Kudo6Eijun Nishihara7Mitsushige Nishikawa8Akira Miyauchi9Takashi Akamizu10Center for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, JapanSubclinical hyperthyroidism (SHyper) is defined as normal levels of free thyroxine (fT4) and free triiodothyronine (fT3) with suppressed levels of TSH. Previous studies have reported the individual pathophysiology of endogenous SHyper patients and athyreotic patients receiving TSH suppression therapy with levothyroxine; however, apparently no studies have compared the two conditions. Five-hundred-forty untreated endogenous SHyper patients and 1,024 patients receiving TSH suppression therapy who underwent total thyroidectomy for papillary thyroid carcinoma were sampled. Thyroid hormone profiles and peripheral indices related to thyrotoxicosis were investigated in endogenous SHyper patients, athyreotic patients receiving TSH suppression therapy, and healthy participants. Endogenous SHyper patients showed significantly higher thyroid hormone levels (fT4 [p < 0.001] and fT3 [p < 0.001]), and peripheral indices showed a significant tendency towards thyrotoxicosis (strong TSH suppression: alkaline phosphatase [ALP, p < 0.001], creatinine [Cre, p < 0.001], pulse rate [p < 0.05]; and mild TSH suppression: Cre [p < 0.05]) than healthy participants. In contrast, athyreotic patients receiving TSH suppression therapy showed a significant tendency towards thyrotoxicosis than healthy participants only when TSH was strongly suppressed (fT3 [p < 0.001] and Cre [p < 0.001]). Endogenous SHyper patients showed significantly higher fT3 levels (p < 0.001) than athyreotic patients receiving TSH suppression therapy; however, there was a significant tendency towards thyrotoxicosis only when TSH was strongly suppressed (ALP [p < 0.05] and pulse rate [p < 0.05]). The effects of endogenous SHyper and TSH suppression therapy on target organ function are different. Although the serum thyroid hormone profile is similar to that of the thyrotoxic state, athyreotic patients receiving TSH suppression therapy with mildly suppressed serum TSH levels are not thyrotoxic.https://www.jstage.jst.go.jp/article/endocrj/71/4/71_EJ23-0497/_html/-char/ensubclinical hyperthyroidismthyrotoxicosisfree triiodothyronine (ft3)free thyroxine (ft4)thyrotropin (tsh)
spellingShingle Hanna Deguchi-Horiuchi
Mitsuru Ito
Sawako Takahashi
Kazuyoshi Kousaka
Mako Hisakado
Shuji Fukata
Takumi Kudo
Eijun Nishihara
Mitsushige Nishikawa
Akira Miyauchi
Takashi Akamizu
Comparison of pathophysiology in subclinical hyperthyroidism with different etiologies
Endocrine Journal
subclinical hyperthyroidism
thyrotoxicosis
free triiodothyronine (ft3)
free thyroxine (ft4)
thyrotropin (tsh)
title Comparison of pathophysiology in subclinical hyperthyroidism with different etiologies
title_full Comparison of pathophysiology in subclinical hyperthyroidism with different etiologies
title_fullStr Comparison of pathophysiology in subclinical hyperthyroidism with different etiologies
title_full_unstemmed Comparison of pathophysiology in subclinical hyperthyroidism with different etiologies
title_short Comparison of pathophysiology in subclinical hyperthyroidism with different etiologies
title_sort comparison of pathophysiology in subclinical hyperthyroidism with different etiologies
topic subclinical hyperthyroidism
thyrotoxicosis
free triiodothyronine (ft3)
free thyroxine (ft4)
thyrotropin (tsh)
url https://www.jstage.jst.go.jp/article/endocrj/71/4/71_EJ23-0497/_html/-char/en
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