Randomized Trial for Evaluation in Secondary Prevention Efficacy of Combination Therapy–Statin and Eicosapentaenoic Acid (RESPECT-EPA)

Author:

Miyauchi Katsumi1ORCID,Iwata Hiroshi1,Nishizaki Yuji1ORCID,Inoue Teruo23,Hirayama Atsushi4,Kimura Kazuo5ORCID,Ozaki Yukio6ORCID,Murohara Toyoaki7ORCID,Ueshima Kenji8,Kuwabara Yoshihiro9,Tanaka-Mizuno Sachiko10ORCID,Yanagisawa Naotake11ORCID,Sato Tosiya12ORCID,Daida Hiroyuki113ORCID,

Affiliation:

1. Department of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan (K.M., H.I., Y.N., H.D.).

2. Japan Red Cross Society, Nasu Red Cross Hospital, Otawara, Tochigi, Japan (T.I.).

3. Dokkyo Medical University, Mibu, Tochigi, Japan (T.I.).

4. Osaka Anti-Tuberculosis Association, Osaka Fukujyuji Hospital, Neyagawa, Osaka, Japan (A.H.).

5. Department of Cardiology, Yokohama City University Medical Center, Kanagawa, Japan (K.K.).

6. Department of Cardiology, Fujita Health University, Toyoake, Aichi, Japan (Y.O.).

7. Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan (T.M.).

8. Medical Examination Center, Uji-Takeda Hospital, Uji, Kyoto, Japan (K.U.).

9. Cancer Control Center, Osaka International Cancer Institute, Osaka, Osaka, Japan (Y.K.).

10. Department of Digital Health and Epidemiology, Graduate School of Medicine, Kyoto University, Kyoto, Kyoto, Japan (S.T.-M.).

11. Medical Technology Innovation Center (N.Y.), Juntendo University, Bunkyo-ku, Tokyo, Japan.

12. Department of Biostatistics, Kyoto University School of Public Health, Kyoto, Kyoto, Japan (T.S.).

13. Faculty of Health Science (H.D.), Juntendo University, Bunkyo-ku, Tokyo, Japan.

Abstract

BACKGROUND: Low plasma levels of eicosapentaenoic acid (EPA) are associated with cardiovascular events. This trial aimed to assess the clinical benefits of icosapent ethyl in patients with coronary artery disease, a low EPA/arachidonic acid (AA) ratio, and statin treatment. METHODS: In this prospective, multicenter, randomized, open-label, blinded end-point study, patients with stable coronary artery disease and a low EPA/AA ratio (<0.4) were randomized to EPA (1800 of icosapent ethyl administered daily) or control group. The primary end point was a composite of cardiovascular death, nonfatal myocardial infarction, nonfatal ischemic stroke, unstable angina pectoris, and coronary revascularization. The secondary composite end points of coronary events included sudden cardiac death, fatal and nonfatal myocardial infarction, unstable angina requiring emergency hospitalization and coronary revascularization, or coronary revascularization. RESULTS: Overall, 3884 patients were enrolled at 95 sites in Japan. Among them, 2506 patients had a low EPA/AA ratio, and 1249 and 1257 patients were randomized to the EPA and control group, respectively. The median EPA/AA ratio was 0.243 (interquartile range, 0.180–0.314) and 0.235 (interquartile range, 0.163–0.310) in the EPA and control group, respectively. Over a median period of 5 years, the primary end point occurred in 112 of 1225 patients (9.1%) and 155 of 1235 patients (12.6%) in the EPA and control group, respectively (hazard ratio, 0.79 [95% CI, 0.62–1.00]; P =0.055). Meanwhile, the secondary composite end point of coronary events in the EPA group was significantly lower (81/1225 [6.6%] versus 120/1235 [9.7%] patients; hazard ratio, 0.73 [95% CI, 0.55–0.97]). Adverse events did not differ between the groups, but the rate of new-onset atrial fibrillation was significantly higher in the EPA group (3.1% versus 1.6%; P =0.017). CONCLUSIONS: Icosapent ethyl treatment resulted in a numerically lower risk of cardiovascular events that did not reach statistical significance in patients with chronic coronary artery disease, a low EPA/AA ratio, and statin treatment. REGISTRATION: URL: https://www.umin.ac.jp/ctr/ ; Unique identifier: UMIN000012069.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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