Rationale and design of the EPISTEME trial: efficacy of post-stroke intensive rosuvastatin treatment for aortogenic embolic stroke.
Identifieur interne : 000079 ( Main/Merge ); précédent : 000078; suivant : 000080Rationale and design of the EPISTEME trial: efficacy of post-stroke intensive rosuvastatin treatment for aortogenic embolic stroke.
Auteurs : Yuji Ueno [Japon] ; Kazuo Yamashiro ; Yasutaka Tanaka ; Masao Watanabe ; Yoshiaki Shimada ; Takuma Kuroki ; Nobukazu Miyamoto ; Masao Daimon ; Ryota Tanaka ; Katsumi Miyauchi ; Hiroyuki Daida ; Nobutaka Hattori ; Takao UrabeSource :
- Cardiovascular drugs and therapy / sponsored by the International Society of Cardiovascular Pharmacotherapy [ 1573-7241 ] ; 2014.
Descripteurs français
- KwdFr :
- Accident vasculaire cérébral (anatomopathologie), Accident vasculaire cérébral (traitement médicamenteux), Accident vasculaire cérébral (étiologie), Aorte (anatomopathologie), Embolie (), Encéphalopathie ischémique (anatomopathologie), Encéphalopathie ischémique (traitement médicamenteux), Encéphalopathie ischémique (étiologie), Fluorobenzènes (administration et posologie), Fluorobenzènes (usage thérapeutique), Humains, Hypercholestérolémie (), Hypercholestérolémie (traitement médicamenteux), Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase (administration et posologie), Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase (usage thérapeutique), Plan de recherche, Plaque d'athérosclérose (), Plaque d'athérosclérose (traitement médicamenteux), Pyrimidines (administration et posologie), Pyrimidines (usage thérapeutique), Rosuvastatine de calcium, Sulfonamides (administration et posologie), Sulfonamides (usage thérapeutique), Échocardiographie transoesophagienne, Études prospectives.
- MESH :
- administration et posologie : Fluorobenzènes, Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase, Pyrimidines, Sulfonamides.
- anatomopathologie : Accident vasculaire cérébral, Aorte, Encéphalopathie ischémique.
- traitement médicamenteux : Accident vasculaire cérébral, Encéphalopathie ischémique, Hypercholestérolémie, Plaque d'athérosclérose.
- usage thérapeutique : Fluorobenzènes, Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase, Pyrimidines, Sulfonamides.
- étiologie : Accident vasculaire cérébral, Encéphalopathie ischémique.
- Embolie, Humains, Hypercholestérolémie, Plan de recherche, Plaque d'athérosclérose, Rosuvastatine de calcium, Échocardiographie transoesophagienne, Études prospectives.
English descriptors
- KwdEn :
- Aorta (pathology), Brain Ischemia (drug therapy), Brain Ischemia (etiology), Brain Ischemia (pathology), Echocardiography, Transesophageal, Embolism (complications), Fluorobenzenes (administration & dosage), Fluorobenzenes (therapeutic use), Humans, Hydroxymethylglutaryl-CoA Reductase Inhibitors (administration & dosage), Hydroxymethylglutaryl-CoA Reductase Inhibitors (therapeutic use), Hypercholesterolemia (complications), Hypercholesterolemia (drug therapy), Plaque, Atherosclerotic (complications), Plaque, Atherosclerotic (drug therapy), Prospective Studies, Pyrimidines (administration & dosage), Pyrimidines (therapeutic use), Research Design, Rosuvastatin Calcium, Stroke (drug therapy), Stroke (etiology), Stroke (pathology), Sulfonamides (administration & dosage), Sulfonamides (therapeutic use).
- MESH :
- chemical , administration & dosage : Fluorobenzenes, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Pyrimidines, Sulfonamides.
- complications : Embolism, Hypercholesterolemia, Plaque, Atherosclerotic.
- drug therapy : Brain Ischemia, Hypercholesterolemia, Plaque, Atherosclerotic, Stroke.
- etiology : Brain Ischemia, Stroke.
- pathology : Aorta, Brain Ischemia, Stroke.
- chemical , therapeutic use : Fluorobenzenes, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Pyrimidines, Sulfonamides.
- Echocardiography, Transesophageal, Humans, Prospective Studies, Research Design, Rosuvastatin Calcium.
Abstract
Large atheromatous aortic plaques (AAPs) are associated with stroke recurrence. Rosuvastatin is a potent lipid-lowering agent and suppresses carotid and coronary artery atherosclerosis. It is unclear whether rosuvastatin has anti-atherogenic effects against AAPs in stroke patients. We designed a clinical trial in stroke patients to analyze changes in AAPs after rosuvastatin treatment using repeated transesophageal echocardiography (TEE).
DOI: 10.1007/s10557-013-6493-6
PubMed: 24072337
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pubmed:24072337Le document en format XML
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<author><name sortKey="Ueno, Yuji" sort="Ueno, Yuji" uniqKey="Ueno Y" first="Yuji" last="Ueno">Yuji Ueno</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aorta (pathology)</term>
<term>Brain Ischemia (drug therapy)</term>
<term>Brain Ischemia (etiology)</term>
<term>Brain Ischemia (pathology)</term>
<term>Echocardiography, Transesophageal</term>
<term>Embolism (complications)</term>
<term>Fluorobenzenes (administration & dosage)</term>
<term>Fluorobenzenes (therapeutic use)</term>
<term>Humans</term>
<term>Hydroxymethylglutaryl-CoA Reductase Inhibitors (administration & dosage)</term>
<term>Hydroxymethylglutaryl-CoA Reductase Inhibitors (therapeutic use)</term>
<term>Hypercholesterolemia (complications)</term>
<term>Hypercholesterolemia (drug therapy)</term>
<term>Plaque, Atherosclerotic (complications)</term>
<term>Plaque, Atherosclerotic (drug therapy)</term>
<term>Prospective Studies</term>
<term>Pyrimidines (administration & dosage)</term>
<term>Pyrimidines (therapeutic use)</term>
<term>Research Design</term>
<term>Rosuvastatin Calcium</term>
<term>Stroke (drug therapy)</term>
<term>Stroke (etiology)</term>
<term>Stroke (pathology)</term>
<term>Sulfonamides (administration & dosage)</term>
<term>Sulfonamides (therapeutic use)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Accident vasculaire cérébral (anatomopathologie)</term>
<term>Accident vasculaire cérébral (traitement médicamenteux)</term>
<term>Accident vasculaire cérébral (étiologie)</term>
<term>Aorte (anatomopathologie)</term>
<term>Embolie ()</term>
<term>Encéphalopathie ischémique (anatomopathologie)</term>
<term>Encéphalopathie ischémique (traitement médicamenteux)</term>
<term>Encéphalopathie ischémique (étiologie)</term>
<term>Fluorobenzènes (administration et posologie)</term>
<term>Fluorobenzènes (usage thérapeutique)</term>
<term>Humains</term>
<term>Hypercholestérolémie ()</term>
<term>Hypercholestérolémie (traitement médicamenteux)</term>
<term>Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase (administration et posologie)</term>
<term>Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase (usage thérapeutique)</term>
<term>Plan de recherche</term>
<term>Plaque d'athérosclérose ()</term>
<term>Plaque d'athérosclérose (traitement médicamenteux)</term>
<term>Pyrimidines (administration et posologie)</term>
<term>Pyrimidines (usage thérapeutique)</term>
<term>Rosuvastatine de calcium</term>
<term>Sulfonamides (administration et posologie)</term>
<term>Sulfonamides (usage thérapeutique)</term>
<term>Échocardiographie transoesophagienne</term>
<term>Études prospectives</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en"><term>Fluorobenzenes</term>
<term>Hydroxymethylglutaryl-CoA Reductase Inhibitors</term>
<term>Pyrimidines</term>
<term>Sulfonamides</term>
</keywords>
<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr"><term>Fluorobenzènes</term>
<term>Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase</term>
<term>Pyrimidines</term>
<term>Sulfonamides</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Accident vasculaire cérébral</term>
<term>Aorte</term>
<term>Encéphalopathie ischémique</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Embolism</term>
<term>Hypercholesterolemia</term>
<term>Plaque, Atherosclerotic</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Brain Ischemia</term>
<term>Hypercholesterolemia</term>
<term>Plaque, Atherosclerotic</term>
<term>Stroke</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Brain Ischemia</term>
<term>Stroke</term>
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<term>Brain Ischemia</term>
<term>Stroke</term>
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<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Fluorobenzenes</term>
<term>Hydroxymethylglutaryl-CoA Reductase Inhibitors</term>
<term>Pyrimidines</term>
<term>Sulfonamides</term>
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<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr"><term>Accident vasculaire cérébral</term>
<term>Encéphalopathie ischémique</term>
<term>Hypercholestérolémie</term>
<term>Plaque d'athérosclérose</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Fluorobenzènes</term>
<term>Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase</term>
<term>Pyrimidines</term>
<term>Sulfonamides</term>
</keywords>
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<term>Encéphalopathie ischémique</term>
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<term>Humans</term>
<term>Prospective Studies</term>
<term>Research Design</term>
<term>Rosuvastatin Calcium</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Embolie</term>
<term>Humains</term>
<term>Hypercholestérolémie</term>
<term>Plan de recherche</term>
<term>Plaque d'athérosclérose</term>
<term>Rosuvastatine de calcium</term>
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<term>Études prospectives</term>
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<front><div type="abstract" xml:lang="en">Large atheromatous aortic plaques (AAPs) are associated with stroke recurrence. Rosuvastatin is a potent lipid-lowering agent and suppresses carotid and coronary artery atherosclerosis. It is unclear whether rosuvastatin has anti-atherogenic effects against AAPs in stroke patients. We designed a clinical trial in stroke patients to analyze changes in AAPs after rosuvastatin treatment using repeated transesophageal echocardiography (TEE).</div>
</front>
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