Effects of Fatty Acid Therapy in Addition to Strong Statin on Coronary Plaques in Acute Coronary Syndrome: An Optical Coherence Tomography Study.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
18 08 2020
Historique:
pubmed: 18 8 2020
medline: 10 3 2021
entrez: 18 8 2020
Statut: ppublish

Résumé

BACKGROUND Vascular healing response associated with adjunctive n-3 polyunsaturated fatty acid therapy therapy in patients receiving strong statin therapy remains unclear. The aim of this study was to evaluate the effect of polyunsaturated fatty acid therapy with eicosapentaenoic acid (EPA) or docosahexaenoic acid (DHA) in addition to strong statin therapy on coronary atherosclerotic plaques using optical coherence tomography. METHODS AND RESULTS This prospective multicenter randomized controlled trial included 130 patients with acute coronary syndrome treated with strong statins. They were assigned to either statin only (control group, n=42), statin+high-dose EPA (1800 mg/day) (EPA group, n=40), statin+EPA (930 mg/day)+DHA (750 mg/day) (EPA+DHA group, n=48). Optical coherence tomography was performed at baseline and at the 8-month follow-up. The target for optical coherence tomography analysis was a nonculprit lesion with a lipid plaque. Between baseline and the 8-month follow-up, fibrous cap thickness (FCT) significantly increased in all 3 groups. There were no significant differences in the percent change for minimum FCT between the EPA or EPA+DHA group and the control group. In patients with FCT <120 µm (median value), the percent change for minimum FCT was significantly higher in the EPA or EPA+DHA group compared with the control group. CONCLUSIONS EPA or EPA+DHA therapy in addition to strong statin therapy did not significantly increase FCT in nonculprit plaques compared with strong statin therapy alone, but significantly increased FCT in patients with thinner FCT. Registration URL: https://www.umin.ac.jp/ctr/; Unique identifier: UMIN 000012825.

Identifiants

pubmed: 32805184
doi: 10.1161/JAHA.119.015593
pmc: PMC7660823
doi:

Substances chimiques

Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Docosahexaenoic Acids 25167-62-8
Rosuvastatin Calcium 83MVU38M7Q
Eicosapentaenoic Acid AAN7QOV9EA

Banques de données

UMIN-CTR
['UMIN 000012825']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

e015593

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Auteurs

Yoko Kita (Y)

Department of Cardiovascular Medicine Nara Medical University Kashihara Japan.

Makoto Watanabe (M)

Department of Cardiovascular Medicine Nara Medical University Kashihara Japan.

Daisuke Kamon (D)

Department of Cardiovascular Medicine Nara Medical University Kashihara Japan.

Tomoya Ueda (T)

Department of Cardiovascular Medicine Nara Medical University Kashihara Japan.

Tsunenari Soeda (T)

Department of Cardiovascular Medicine Nara Medical University Kashihara Japan.

Satoshi Okayama (S)

Department of Cardiovascular Medicine Nara Medical University Kashihara Japan.

Kenichi Ishigami (K)

Department of Cardiology Saiseikai Suita Hospital Suita Japan.

Hiroyuki Kawata (H)

Department of Cardiovascular Medicine Nara Prefecture General Medical Center Nara Japan.

Manabu Horii (M)

Department of Cardiovascular Medicine Nara City Hospital Nara Japan.

Fumitaka Inoue (F)

Yamato Kashihara Hospital Kashihara Japan.

Naofumi Doi (N)

Department of Cardiology Nara Prefecture Seiwa Medical Center Nara Japan.

Hiroyuki Okura (H)

Department of Cardiology Gifu University Gradual School of Medicine Gifu Japan.

Shiro Uemura (S)

Division of CardiologyKawasaki Medical School Kurashiki Japan.

Yoshihiko Saito (Y)

Department of Cardiovascular Medicine Nara Medical University Kashihara Japan.

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