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Effect of eicosapentaenoic acid/docosahexaenoic acid on coronary high-intensity plaques detected with non-contrast T1-weighted imaging (the AQUAMARINE EPA/DHA study): study protocol for a randomized controlled trial

BACKGROUND: Despite the success of HMG-CoA reductase inhibitor (statin) therapy in reducing atherosclerotic cardiovascular events, a residual risk for cardiovascular events in patients with coronary artery disease (CAD) remains. Long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFAs), especially e...

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Autores principales: Nakao, Kazuhiro, Noguchi, Teruo, Asaumi, Yasuhide, Morita, Yoshiaki, Kanaya, Tomoaki, Fujino, Masashi, Hosoda, Hayato, Yoneda, Shuichi, Kawakami, Shoji, Nagai, Toshiyuki, Nishihira, Kensaku, Nakashima, Takahiro, Kumasaka, Reon, Arakawa, Tetsuo, Otsuka, Fumiyuki, Nakanishi, Michio, Kataoka, Yu, Tahara, Yoshio, Goto, Yoichi, Yamamoto, Haruko, Hamasaki, Toshimitsu, Yasuda, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759279/
https://www.ncbi.nlm.nih.gov/pubmed/29310688
http://dx.doi.org/10.1186/s13063-017-2353-1
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author Nakao, Kazuhiro
Noguchi, Teruo
Asaumi, Yasuhide
Morita, Yoshiaki
Kanaya, Tomoaki
Fujino, Masashi
Hosoda, Hayato
Yoneda, Shuichi
Kawakami, Shoji
Nagai, Toshiyuki
Nishihira, Kensaku
Nakashima, Takahiro
Kumasaka, Reon
Arakawa, Tetsuo
Otsuka, Fumiyuki
Nakanishi, Michio
Kataoka, Yu
Tahara, Yoshio
Goto, Yoichi
Yamamoto, Haruko
Hamasaki, Toshimitsu
Yasuda, Satoshi
author_facet Nakao, Kazuhiro
Noguchi, Teruo
Asaumi, Yasuhide
Morita, Yoshiaki
Kanaya, Tomoaki
Fujino, Masashi
Hosoda, Hayato
Yoneda, Shuichi
Kawakami, Shoji
Nagai, Toshiyuki
Nishihira, Kensaku
Nakashima, Takahiro
Kumasaka, Reon
Arakawa, Tetsuo
Otsuka, Fumiyuki
Nakanishi, Michio
Kataoka, Yu
Tahara, Yoshio
Goto, Yoichi
Yamamoto, Haruko
Hamasaki, Toshimitsu
Yasuda, Satoshi
author_sort Nakao, Kazuhiro
collection PubMed
description BACKGROUND: Despite the success of HMG-CoA reductase inhibitor (statin) therapy in reducing atherosclerotic cardiovascular events, a residual risk for cardiovascular events in patients with coronary artery disease (CAD) remains. Long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFAs), especially eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), are promising anti-atherosclerosis agents that might reduce the residual CAD risk. Non-contrast T1-weighted imaging (T1WI) with cardiac magnetic resonance (CMR) less invasively identifies high-risk coronary plaques as high-intensity signals. These high-intensity plaques (HIPs) are quantitatively assessed using the plaque-to-myocardium signal intensity ratio (PMR). Our goal is to assess the effect of EPA/DHA on coronary HIPs detected with T1WI in patients with CAD on statin treatment. METHODS/DESIGN: This prospective, controlled, randomized, open-label study examines the effect of 12 months of EPA/DHA therapy and statin treatment on PMR of HIPs detected with CMR and computed tomography angiography (CTA) in patients with CAD. The primary endpoint is the change in PMR after EPA/DHA treatment. Secondary endpoints include changes in Hounsfield units, plaque volume, vessel area, and plaque area measured using CTA. Subjects are randomly assigned to either of three groups: the 2 g/day EPA/DHA group, the 4 g/day EPA/DHA group, or the no-treatment group. DISCUSSION: This trial will help assess whether EPA/DHA has an anti-atherosclerotic effect using PMR of HIPs detected by CMR. The trial outcomes will provide novel insights into the effect of EPA/DHA on high-risk coronary plaques and may provide new strategies for lowering the residual risk in patients with CAD on statin therapy. TRIAL REGISTRATION: The University Hospital Medical Information Network (UMIN) Clinical Trials Registry, ID: UMIN000015316. Registered on 2 October 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-2353-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-57592792018-01-10 Effect of eicosapentaenoic acid/docosahexaenoic acid on coronary high-intensity plaques detected with non-contrast T1-weighted imaging (the AQUAMARINE EPA/DHA study): study protocol for a randomized controlled trial Nakao, Kazuhiro Noguchi, Teruo Asaumi, Yasuhide Morita, Yoshiaki Kanaya, Tomoaki Fujino, Masashi Hosoda, Hayato Yoneda, Shuichi Kawakami, Shoji Nagai, Toshiyuki Nishihira, Kensaku Nakashima, Takahiro Kumasaka, Reon Arakawa, Tetsuo Otsuka, Fumiyuki Nakanishi, Michio Kataoka, Yu Tahara, Yoshio Goto, Yoichi Yamamoto, Haruko Hamasaki, Toshimitsu Yasuda, Satoshi Trials Study Protocol BACKGROUND: Despite the success of HMG-CoA reductase inhibitor (statin) therapy in reducing atherosclerotic cardiovascular events, a residual risk for cardiovascular events in patients with coronary artery disease (CAD) remains. Long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFAs), especially eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), are promising anti-atherosclerosis agents that might reduce the residual CAD risk. Non-contrast T1-weighted imaging (T1WI) with cardiac magnetic resonance (CMR) less invasively identifies high-risk coronary plaques as high-intensity signals. These high-intensity plaques (HIPs) are quantitatively assessed using the plaque-to-myocardium signal intensity ratio (PMR). Our goal is to assess the effect of EPA/DHA on coronary HIPs detected with T1WI in patients with CAD on statin treatment. METHODS/DESIGN: This prospective, controlled, randomized, open-label study examines the effect of 12 months of EPA/DHA therapy and statin treatment on PMR of HIPs detected with CMR and computed tomography angiography (CTA) in patients with CAD. The primary endpoint is the change in PMR after EPA/DHA treatment. Secondary endpoints include changes in Hounsfield units, plaque volume, vessel area, and plaque area measured using CTA. Subjects are randomly assigned to either of three groups: the 2 g/day EPA/DHA group, the 4 g/day EPA/DHA group, or the no-treatment group. DISCUSSION: This trial will help assess whether EPA/DHA has an anti-atherosclerotic effect using PMR of HIPs detected by CMR. The trial outcomes will provide novel insights into the effect of EPA/DHA on high-risk coronary plaques and may provide new strategies for lowering the residual risk in patients with CAD on statin therapy. TRIAL REGISTRATION: The University Hospital Medical Information Network (UMIN) Clinical Trials Registry, ID: UMIN000015316. Registered on 2 October 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-2353-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-08 /pmc/articles/PMC5759279/ /pubmed/29310688 http://dx.doi.org/10.1186/s13063-017-2353-1 Text en © The Author(s). 2018 Open Access This 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 Study Protocol
Nakao, Kazuhiro
Noguchi, Teruo
Asaumi, Yasuhide
Morita, Yoshiaki
Kanaya, Tomoaki
Fujino, Masashi
Hosoda, Hayato
Yoneda, Shuichi
Kawakami, Shoji
Nagai, Toshiyuki
Nishihira, Kensaku
Nakashima, Takahiro
Kumasaka, Reon
Arakawa, Tetsuo
Otsuka, Fumiyuki
Nakanishi, Michio
Kataoka, Yu
Tahara, Yoshio
Goto, Yoichi
Yamamoto, Haruko
Hamasaki, Toshimitsu
Yasuda, Satoshi
Effect of eicosapentaenoic acid/docosahexaenoic acid on coronary high-intensity plaques detected with non-contrast T1-weighted imaging (the AQUAMARINE EPA/DHA study): study protocol for a randomized controlled trial
title Effect of eicosapentaenoic acid/docosahexaenoic acid on coronary high-intensity plaques detected with non-contrast T1-weighted imaging (the AQUAMARINE EPA/DHA study): study protocol for a randomized controlled trial
title_full Effect of eicosapentaenoic acid/docosahexaenoic acid on coronary high-intensity plaques detected with non-contrast T1-weighted imaging (the AQUAMARINE EPA/DHA study): study protocol for a randomized controlled trial
title_fullStr Effect of eicosapentaenoic acid/docosahexaenoic acid on coronary high-intensity plaques detected with non-contrast T1-weighted imaging (the AQUAMARINE EPA/DHA study): study protocol for a randomized controlled trial
title_full_unstemmed Effect of eicosapentaenoic acid/docosahexaenoic acid on coronary high-intensity plaques detected with non-contrast T1-weighted imaging (the AQUAMARINE EPA/DHA study): study protocol for a randomized controlled trial
title_short Effect of eicosapentaenoic acid/docosahexaenoic acid on coronary high-intensity plaques detected with non-contrast T1-weighted imaging (the AQUAMARINE EPA/DHA study): study protocol for a randomized controlled trial
title_sort effect of eicosapentaenoic acid/docosahexaenoic acid on coronary high-intensity plaques detected with non-contrast t1-weighted imaging (the aquamarine epa/dha study): study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759279/
https://www.ncbi.nlm.nih.gov/pubmed/29310688
http://dx.doi.org/10.1186/s13063-017-2353-1
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