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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 |
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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 & 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 & 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 & Sons, Inc</general><general>Elsevier</general><general>Wiley</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>201612</creationdate><title>Risk factors for amiodarone-induced thyroid dysfunction in Japan</title><author>Kinoshita, Sayoko ; Hayashi, Tomohiro ; Wada, Kyoichi ; Yamato, Mikie ; Kuwahara, Takeshi ; Anzai, Toshihisa ; Fujimoto, Mai ; Hosomi, Kouichi ; Takada, Mitsutaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c7524-1e629ace0ae3311861be3ebeb01195ce0fe2f3b5557050c29cea9fcd5e247b753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Amiodarone</topic><topic>Amiodarone-induced hyperthyroidism</topic><topic>Amiodarone-induced hypothyroidism</topic><topic>Antiarrhythmics</topic><topic>Arrhythmia</topic><topic>Cardiac arrhythmia</topic><topic>Cardiomyopathy</topic><topic>Cardiovascular</topic><topic>Glycoproteins</topic><topic>Hospitals</topic><topic>Hyperthyroidism</topic><topic>Hypothyroidism</topic><topic>Iodine</topic><topic>Medical records</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Original</topic><topic>Regression analysis</topic><topic>Risk factors</topic><topic>Subclinical hyperthyroidism</topic><topic>Subclinical hypothyroidism</topic><topic>Thyroid gland</topic><topic>Thyroxine</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & 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 & Medical Complete (Alumni)</collection><collection>Health & 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 & 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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