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Risk factors for amiodarone-induced thyroid dysfunction in Japan

Abstract 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 t...

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Published in:Journal of arrhythmia 2016-12, Vol.32 (6), p.474-480
Main Authors: Kinoshita, Sayoko, Hayashi, Tomohiro, Wada, Kyoichi, Yamato, Mikie, Kuwahara, Takeshi, Anzai, Toshihisa, Fujimoto, Mai, Hosomi, Kouichi, Takada, Mitsutaka
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container_title Journal of arrhythmia
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creator Kinoshita, Sayoko
Hayashi, Tomohiro
Wada, Kyoichi
Yamato, Mikie
Kuwahara, Takeshi
Anzai, Toshihisa
Fujimoto, Mai
Hosomi, Kouichi
Takada, Mitsutaka
description Abstract 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.
doi_str_mv 10.1016/j.joa.2016.03.008
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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.</description><identifier>ISSN: 1880-4276</identifier><identifier>EISSN: 1883-2148</identifier><identifier>DOI: 10.1016/j.joa.2016.03.008</identifier><identifier>PMID: 27920832</identifier><language>eng</language><publisher>Japan: John Wiley &amp; Sons, Inc</publisher><subject>Amiodarone ; Amiodarone-induced hyperthyroidism ; Amiodarone-induced hypothyroidism ; Antiarrhythmics ; Arrhythmia ; Cardiac arrhythmia ; Cardiomyopathy ; Cardiovascular ; Glycoproteins ; Hospitals ; Hyperthyroidism ; Hypothyroidism ; Iodine ; Medical records ; Medical research ; Medicine, Experimental ; Original ; Regression analysis ; Risk factors ; Subclinical hyperthyroidism ; Subclinical hypothyroidism ; Thyroid gland ; Thyroxine ; Variables</subject><ispartof>Journal of arrhythmia, 2016-12, Vol.32 (6), p.474-480</ispartof><rights>Japanese Heart Rhythm Society</rights><rights>2016 Japanese Heart Rhythm Society</rights><rights>COPYRIGHT 2016 John Wiley &amp; Sons, Inc.</rights><rights>2016. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2016 The Authors 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c7524-1e629ace0ae3311861be3ebeb01195ce0fe2f3b5557050c29cea9fcd5e247b753</citedby><cites>FETCH-LOGICAL-c7524-1e629ace0ae3311861be3ebeb01195ce0fe2f3b5557050c29cea9fcd5e247b753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3074681582/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3074681582?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,11543,25734,27905,27906,36993,36994,44571,46033,46457,53772,53774,74875</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1016%2Fj.joa.2016.03.008$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27920832$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kinoshita, Sayoko</creatorcontrib><creatorcontrib>Hayashi, Tomohiro</creatorcontrib><creatorcontrib>Wada, Kyoichi</creatorcontrib><creatorcontrib>Yamato, Mikie</creatorcontrib><creatorcontrib>Kuwahara, Takeshi</creatorcontrib><creatorcontrib>Anzai, Toshihisa</creatorcontrib><creatorcontrib>Fujimoto, Mai</creatorcontrib><creatorcontrib>Hosomi, Kouichi</creatorcontrib><creatorcontrib>Takada, Mitsutaka</creatorcontrib><title>Risk factors for amiodarone-induced thyroid dysfunction in Japan</title><title>Journal of arrhythmia</title><addtitle>J Arrhythm</addtitle><description>Abstract 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.</description><subject>Amiodarone</subject><subject>Amiodarone-induced hyperthyroidism</subject><subject>Amiodarone-induced hypothyroidism</subject><subject>Antiarrhythmics</subject><subject>Arrhythmia</subject><subject>Cardiac arrhythmia</subject><subject>Cardiomyopathy</subject><subject>Cardiovascular</subject><subject>Glycoproteins</subject><subject>Hospitals</subject><subject>Hyperthyroidism</subject><subject>Hypothyroidism</subject><subject>Iodine</subject><subject>Medical records</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Original</subject><subject>Regression analysis</subject><subject>Risk factors</subject><subject>Subclinical hyperthyroidism</subject><subject>Subclinical hypothyroidism</subject><subject>Thyroid gland</subject><subject>Thyroxine</subject><subject>Variables</subject><issn>1880-4276</issn><issn>1883-2148</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFkk1v1DAQhiMEoqXwA7igSFy4bBh_xE4uiFXFR6tKlfiQuFmOM9k6zdpbOynaf4_TLVsWISEfPBq_89ieebPsJYGCABFv-6L3uqApLIAVANWj7JhUFVtQwqvHdzEsOJXiKHsWYw9QVpyQp9kRlTWFitHj7P0XG6_zTpvRh5h3PuR6bX2rg3e4sK6dDLb5eLUN3rZ5u43d5Mxovcuty8_1Rrvn2ZNODxFf3O8n2fePH76dfl5cXH46O11eLIwsKV8QFLTWBkEjY4RUgjTIsMEGCKnLlO-Qdqwpy1JCCYbWBnXdmbZEymUjS3aSne24rde92gS71mGrvLbqLuHDSukwWjOg0lIktqkYcMnbuqmQUt5IQKh53WiZWO92rM3UrLE16MaghwPo4YmzV2rlb1VJaE0oJMCbe0DwNxPGUa1tNDgM2qGfoiIVF0xIkCJJX_8l7f0UXGqVYiC5qEhZ0QfVSqcPWNf5dK-ZoWopKVDBqZhVxT9UabW4tiZNrLMpf1BAdgUm-BgDdvs_ElCzhVSfnqPVbCEFTCULpZpXfzZnX_HbM0kgdoKf6bbt_4nq_HLJ0iQe2o7JJ7cWgzKDddbo4Rq3GPd9ISpSBerrbN_ZvUQwAEZ-sF8i5eZd</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Kinoshita, Sayoko</creator><creator>Hayashi, Tomohiro</creator><creator>Wada, Kyoichi</creator><creator>Yamato, Mikie</creator><creator>Kuwahara, Takeshi</creator><creator>Anzai, Toshihisa</creator><creator>Fujimoto, Mai</creator><creator>Hosomi, Kouichi</creator><creator>Takada, Mitsutaka</creator><general>John Wiley &amp; 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Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of arrhythmia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Kinoshita, Sayoko</au><au>Hayashi, Tomohiro</au><au>Wada, Kyoichi</au><au>Yamato, Mikie</au><au>Kuwahara, Takeshi</au><au>Anzai, Toshihisa</au><au>Fujimoto, Mai</au><au>Hosomi, Kouichi</au><au>Takada, Mitsutaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk factors for amiodarone-induced thyroid dysfunction in Japan</atitle><jtitle>Journal of arrhythmia</jtitle><addtitle>J Arrhythm</addtitle><date>2016-12</date><risdate>2016</risdate><volume>32</volume><issue>6</issue><spage>474</spage><epage>480</epage><pages>474-480</pages><issn>1880-4276</issn><eissn>1883-2148</eissn><abstract>Abstract 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.</abstract><cop>Japan</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>27920832</pmid><doi>10.1016/j.joa.2016.03.008</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Amiodarone
Amiodarone-induced hyperthyroidism
Amiodarone-induced hypothyroidism
Antiarrhythmics
Arrhythmia
Cardiac arrhythmia
Cardiomyopathy
Cardiovascular
Glycoproteins
Hospitals
Hyperthyroidism
Hypothyroidism
Iodine
Medical records
Medical research
Medicine, Experimental
Original
Regression analysis
Risk factors
Subclinical hyperthyroidism
Subclinical hypothyroidism
Thyroid gland
Thyroxine
Variables
title Risk factors for amiodarone-induced thyroid dysfunction in Japan
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