Risk factors for amiodarone-induced thyroid dysfunction in Japan

Background: Amiodarone is associated with a number of significant adverse effects, including elevated transaminase levels, pulmonary fibrosis, arrhythmia, and thyroid dysfunction. Although thyroid dysfunction is considered to be a common and potentially serious adverse effect of amiodarone therapy,...

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Main Authors: Sayoko Kinoshita, Tomohiro Hayashi, Kyoichi Wada, Mikie Yamato, Takeshi Kuwahara, Toshihisa Anzai, Mai Fujimoto, Kouichi Hosomi, Mitsutaka Takada
Format: Article
Language:English
Published: Wiley 2016-12-01
Series:Journal of Arrhythmia
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S188042761630031X
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author Sayoko Kinoshita
Tomohiro Hayashi
Kyoichi Wada
Mikie Yamato
Takeshi Kuwahara
Toshihisa Anzai
Mai Fujimoto
Kouichi Hosomi
Mitsutaka Takada
author_facet Sayoko Kinoshita
Tomohiro Hayashi
Kyoichi Wada
Mikie Yamato
Takeshi Kuwahara
Toshihisa Anzai
Mai Fujimoto
Kouichi Hosomi
Mitsutaka Takada
author_sort Sayoko Kinoshita
collection DOAJ
description Background: Amiodarone is associated with a number of significant adverse effects, including elevated transaminase levels, pulmonary fibrosis, arrhythmia, and thyroid dysfunction. Although thyroid dysfunction is considered to be a common and potentially serious adverse effect of amiodarone therapy, the exact pathogenesis remains unknown because of its complex manifestations. Therefore, the prevalence of, and risk factors for, amiodarone-induced thyroid dysfunction in Japanese patients were investigated in the present study. Methods: A retrospective analysis of patients treated with amiodarone between January 2012 and December 2013 was performed. A total of 317 patients with euthyroidism, or subclinical hyperthyroidism or hypothyroidism, were enrolled in this study. Results: After being treated with amiodarone, 30 (9.5%) and 60 patients (18.9%) developed amiodarone-induced hyperthyroidism and amiodarone-induced hypothyroidism, respectively. Ten (33.3%) patients with amiodarone-induced hyperthyroidism and 40 (66.6%) with amiodarone-induced hypothyroidism were diagnosed within two years of the initiation of amiodarone therapy. Dilated cardiomyopathy (DCM) [Adjusted odds ratio (OR) 3.30 (95% confidence interval (CI): 1.26–8.90)], and cardiac sarcoidosis [Adjusted OR 6.47 (95% CI: 1.60–25.77)] were identified as predictors of amiodarone-induced hyperthyroidism. The baseline free thyroxine (T4) level [Adjusted OR 0.13 (95% CI: 0.03–0.68)], and thyroid-stimulating hormone (TSH) level [Adjusted OR1.47 (95% CI: 1.26–1.74)] were identified as predictors of amiodarone-induced hypothyroidism. Conclusion: DCM and cardiac sarcoidosis were identified as risk factors for amiodarone-induced hyperthyroidism. Risk factors for amiodarone-induced hypothyroidism included higher baseline TSH level and lower baseline free T4 level, suggesting that subclinical hypothyroidism may be a potential risk factor for the development of amiodarone-induced hypothyroidism.
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spelling doaj.art-a76e3ec830474d9b8e224b70e0949ba72022-12-22T03:11:39ZengWileyJournal of Arrhythmia1880-42762016-12-0132647448010.1016/j.joa.2016.03.008Risk factors for amiodarone-induced thyroid dysfunction in JapanSayoko Kinoshita0Tomohiro Hayashi1Kyoichi Wada2Mikie Yamato3Takeshi Kuwahara4Toshihisa Anzai5Mai Fujimoto6Kouichi Hosomi7Mitsutaka Takada8Department of Pharmacy, National Cerebral and Cardiovascular Center, 5-7-1, Fujishiro-dai, Suita, Osaka 565-8565, JapanDepartment of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, 5-7-1, Fujishiro-dai, Suita, Osaka 565-8565, JapanDepartment of Pharmacy, National Cerebral and Cardiovascular Center, 5-7-1, Fujishiro-dai, Suita, Osaka 565-8565, JapanDepartment of Pharmacy, National Cerebral and Cardiovascular Center, 5-7-1, Fujishiro-dai, Suita, Osaka 565-8565, JapanDepartment of Pharmacy, National Cerebral and Cardiovascular Center, 5-7-1, Fujishiro-dai, Suita, Osaka 565-8565, JapanDepartment of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, 5-7-1, Fujishiro-dai, Suita, Osaka 565-8565, JapanDivision of Clinical Drug Informatics, School of Pharmacy, Kinki University, 3-4-1, Kowakae, Higashiosaka, Osaka 577-0818, JapanDivision of Clinical Drug Informatics, School of Pharmacy, Kinki University, 3-4-1, Kowakae, Higashiosaka, Osaka 577-0818, JapanDivision of Clinical Drug Informatics, School of Pharmacy, Kinki University, 3-4-1, Kowakae, Higashiosaka, Osaka 577-0818, JapanBackground: Amiodarone is associated with a number of significant adverse effects, including elevated transaminase levels, pulmonary fibrosis, arrhythmia, and thyroid dysfunction. Although thyroid dysfunction is considered to be a common and potentially serious adverse effect of amiodarone therapy, the exact pathogenesis remains unknown because of its complex manifestations. Therefore, the prevalence of, and risk factors for, amiodarone-induced thyroid dysfunction in Japanese patients were investigated in the present study. Methods: A retrospective analysis of patients treated with amiodarone between January 2012 and December 2013 was performed. A total of 317 patients with euthyroidism, or subclinical hyperthyroidism or hypothyroidism, were enrolled in this study. Results: After being treated with amiodarone, 30 (9.5%) and 60 patients (18.9%) developed amiodarone-induced hyperthyroidism and amiodarone-induced hypothyroidism, respectively. Ten (33.3%) patients with amiodarone-induced hyperthyroidism and 40 (66.6%) with amiodarone-induced hypothyroidism were diagnosed within two years of the initiation of amiodarone therapy. Dilated cardiomyopathy (DCM) [Adjusted odds ratio (OR) 3.30 (95% confidence interval (CI): 1.26–8.90)], and cardiac sarcoidosis [Adjusted OR 6.47 (95% CI: 1.60–25.77)] were identified as predictors of amiodarone-induced hyperthyroidism. The baseline free thyroxine (T4) level [Adjusted OR 0.13 (95% CI: 0.03–0.68)], and thyroid-stimulating hormone (TSH) level [Adjusted OR1.47 (95% CI: 1.26–1.74)] were identified as predictors of amiodarone-induced hypothyroidism. Conclusion: DCM and cardiac sarcoidosis were identified as risk factors for amiodarone-induced hyperthyroidism. Risk factors for amiodarone-induced hypothyroidism included higher baseline TSH level and lower baseline free T4 level, suggesting that subclinical hypothyroidism may be a potential risk factor for the development of amiodarone-induced hypothyroidism.http://www.sciencedirect.com/science/article/pii/S188042761630031XAmiodarone-induced hyperthyroidismAmiodarone-induced hypothyroidismSubclinical hyperthyroidismSubclinical hypothyroidism
spellingShingle Sayoko Kinoshita
Tomohiro Hayashi
Kyoichi Wada
Mikie Yamato
Takeshi Kuwahara
Toshihisa Anzai
Mai Fujimoto
Kouichi Hosomi
Mitsutaka Takada
Risk factors for amiodarone-induced thyroid dysfunction in Japan
Journal of Arrhythmia
Amiodarone-induced hyperthyroidism
Amiodarone-induced hypothyroidism
Subclinical hyperthyroidism
Subclinical hypothyroidism
title Risk factors for amiodarone-induced thyroid dysfunction in Japan
title_full Risk factors for amiodarone-induced thyroid dysfunction in Japan
title_fullStr Risk factors for amiodarone-induced thyroid dysfunction in Japan
title_full_unstemmed Risk factors for amiodarone-induced thyroid dysfunction in Japan
title_short Risk factors for amiodarone-induced thyroid dysfunction in Japan
title_sort risk factors for amiodarone induced thyroid dysfunction in japan
topic Amiodarone-induced hyperthyroidism
Amiodarone-induced hypothyroidism
Subclinical hyperthyroidism
Subclinical hypothyroidism
url http://www.sciencedirect.com/science/article/pii/S188042761630031X
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