The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
Stabilizing effect of combined eicosapentaenoic acid and statin therapy on coronary thin-cap fibroatheroma
Abstract
Background The addition of highly purified eicosapentaenoic acid (EPA) to statin therapy prevents cardiovascular events. However, the impact of this treatment on vulnerable plaques remains unclear. The aim of this study was to assess the impact of adding EPA to a standard statin therapy on vulnerable plaques by serial optical coherence tomography (OCT).Methods Forty-nine non-culprit thin-cap fibroatheroma (TCFA) lesions in 30 patients with untreated dyslipidemia were included. Patients were randomly assigned to EPA (1800 mg/day) + statin (23 TCFA, 15 patients) or statin only (26 TCFA, 15 patients) treatment. The statin (rosuvastatin) dose was adjusted to achieve a target low-density lipoprotein (LDL) level of <70 mg/dL. Post-percutaneous intervention and 9-month follow-up OCT were performed to evaluate morphological changes of TCFAs. The EPA/arachidonic acid (EPA/AA) ratio and pentraxin-3 (PTX3) levels were also evaluated.Results Despite similar follow-up LDL levels, the EPA + statin group had higher EPA/AA ratios and lower PTX3 levels than the statin group. OCT analysis showed that the EPA + statin group had a greater increase in fibrous-cap thickness, with a greater decrease in lipid arc and lipid length. Macrophage accumulation was less frequently detected in the EPA + statin group than in the statin group at follow-up. When the patients were categorized according to their follow-up PTX3 tertiles, fibrous-cap thickness showed significant increase, and the incidence of macrophages accumulation decreased with lower PTX3 levels.Conclusion The concomitant use of EPA and rosuvastatin may stabilize vulnerable plaques better than the statin alone, possibly by suppressing arterial inflammation.
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“In addition to beneficial changes to TG‐rich lipoproteins and other plasma lipid markers, some clinical studies with higher‐dose EPA also suggest beneficial effects on markers of oxidation and inflammation, coronary plaque characteristics, and major CV events.16, 25, 26, 29, 31, 32, 33”
From Rationale and design of REDUCE‐IT : Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (2017) · cites this paper as [32]
In the citing paper
“Finally, studies administering higher‐dose EPA suggest additional beneficial effects beyond lipid‐lowering that may be unique to EPA relative to other TG‐lowering therapies, such as beneficial changes in coronary plaque characteristics, which may lead to reductions in major CV events.4, 16, 25, 26, 27, 28, 29, 30, 31, 32, 33”
From Rationale and design of REDUCE‐IT : Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (2017) · cites this paper as [32]
In the citing paper
“EPA has unique lipid and lipoprotein, antiinflammatory, antiplatelet, antithrombotic, and cellular modifying effects, all of which may contribute to benefits in atherosclerotic processes such as reduced development, slowed progression, and increased stabilization of atherosclerotic plaque (19,(54)(55)(56).”
From Effects of Icosapent Ethyl on Total Ischemic Events (2019) · cites this paper as [55]
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“Evaluation using optical coherence tomography and intravascular ultrasound demonstrated that adding on EPA to statin did not change calcified plaque volume; however, it did stabilize the plaques of human coronary arteries [47,48].”
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“…significantly increased FCT by OCT at 9 months compared with rosuvastatin alone (+54.8 μm vs. +23.5 μm, P < 0.001) in 30 patients undergoing PCI 61) , while Kita et al. in 2020 reported that EPA or EPA+docosahexaenoic acid (DHA) therapy in addition to statin therapy did not significantly…”
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“Several studies to date have reported reduction of the plasma PTX3 level with uncombined statin treatment [9, 11, 12] and with combined statin plus EPA treatment [21]; however, there are few reports concerning the effect of addition of EPA to ongoing statin treatment on the”
BackgroundTeo, J. C., Foin, N., Otsuka, F., Bulluck, H., Fam, J. M., Wong, P. E. H., Low, F. H., Leo, H. L., Mari, J. M., Joner, M., et al. (2016) · European Heart Journal - Cardiovascular Imaging · doi:10.1093/ehjci/jew153 · Cited by 13
Wakabayashi, Y., Funayama, H., Ugata, Y., Taniguchi, Y., Hoshino, H., Ako, J., & Momomura, S. (2015) · Journal of Cardiology · doi:10.1016/j.jjcc.2015.01.008 · Cited by 13
Self-citationIrfan, A., Haider, S. H., Nasir, A., Larik, M. O., & Naz, T. (2023) · Current Problems in Cardiology · doi:10.1016/j.cpcardiol.2023.102245 · Cited by 12
Alfaddagh, A., Kapoor, K., Dardari, Z., Bhatt, D. L., Budoff, M. J., Nasir, K., Miller, M. J., Welty, F. K., Miedema, M. D., Shapiro, M. D., et al. (2022) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2022.06.1018 · Cited by 14
Borow, K. M., Mason, R. P., & Vijayaraghavan, K. (2017) · Cardiorenal Medicine · doi:10.1159/000479391 · Cited by 12
Liu, S., Hou, J., Wan, J., Yang, Y., Wang, D., Liang, D., Wang, X., Zhou, P., & Wang, P. (2023) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-023-07511-7 · Cited by 11
“Separate studies have evidenced that concurrent use of EPA and rosuvastatin induced a greater stabilization of vulnerable plaques than standalone statin treatment [16].”
Achieving More Optimal Lipid Control with Non-Statin Lipid Lowering Therapy
Nicholls, S. J., & Nelson, A. J. (2025) · Current Atherosclerosis Reports · doi:10.1007/s11883-025-01280-4 · Cited by 12
Effects of Eicosapentaenoic Acid on Arterial Calcification
Saito, Y., Nakamura, K., & Ito, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155455 · Cited by 11
Bajaj, R., GARCIA-GARCIA, H. M., Courtney, B. K., RAMASAMY, A., TUFARO, V., Erdoğan, E., KHAN, A. H., ALVES, N., Rathod, K. S., Onuma, Y., et al. (2021) · Minerva Cardiology and Angiology · doi:10.23736/s2724-5683.21.05532-0 · Cited by 11
Kim, H., Ahn, J., Kang, D., Lee, J., Choi, Y., Park, S., & Park, D. (2024) · JACC Asia · doi:10.1016/j.jacasi.2024.04.001 · Cited by 10
Doggrell, S. A. (2019) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2019.1609942 · Cited by 11
Omega-3 fatty acids in the treatment of heart failure
Kelling, M., Dimza, M., Bartlett, A., Traktuev, D. O., Duarte, J. D., & Keeley, E. C. (2024) · Current Problems in Cardiology · doi:10.1016/j.cpcardiol.2024.102730 · Cited by 9
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“The number of serial examinations that had sufficient quality to be evaluated was 26, 21, and 24 in CMR and 24, 20, and 23 in CTA.”
Omega-3 Polyunsaturated Fatty Acids in Blood Pressure Control and Essential Hypertension
Colussi, G., Catena, C., Novello, M., & Sechi, L. A. (2016) · InTech eBooks · doi:10.5772/63501 · Cited by 9
“Finally, some studies have shown that omega-3 PUFA intake can enhance the beneficial effects of cardio-protective drugs such as statins and the acetylsalicylic acid [101–104].”
BackgroundRisk of Total Events With Icosapent Ethyl
Granger, C. B., Nelson, A. J., & Pagidipati, N. J. (2019) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2019.03.492 · Cited by 8
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Picard, F. A., & Steg, P. G. (2021) · Current Atherosclerosis Reports · doi:10.1007/s11883-021-00919-2 · Cited by 8
Zhang, C., Xie, Y., Zhou, J., Zhang, C., Xiang, Q., Zhong, Y., Xiao, J., Feng, J., Liao, B., Chen, X., et al. (2025) · Food Science & Nutrition · doi:10.1002/fsn3.70372 · Cited by 8
“…outlined in Table 1 (Sacks et al. 1995; von Schacky et al. 1999; Johansen et al. 1999; Seierstad et al. 2005; Lee et al. 2006; Ishikawa et al. 2010; Nishio et al. 2014; Ahn et al. 2016; Niki et al. 2016; Tani et al. 2017, 2019, 2020; Watanabe et al. 2017; Alfaddagh et al. 2017; Samavat et al.…”
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EPA Versus Mixed EPA/DHA Plus Statin for Coronary Atherosclerosis
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Fujimoto, D., Fuster, V., & Jang, I. (2025) · Nature Cardiovascular Research · doi:10.1038/s44161-025-00664-8 · Cited by 6
“Concurrently, other OCT features of vulnerability, such as the presence and degree of accumulation of macrophages 38,45,50,51 , also undergo changes.”
Kedia, A. W., & Lynch, E. (2015) · Postgraduate Medicine · doi:10.1080/00325481.2015.1100086 · Cited by 6
Optical Coherence Tomography and Virtual-Histology Intravascular Ultrasound
Mintz, G. S. (2015) · Circulation Cardiovascular Imaging · doi:10.1161/circimaging.115.004045 · Cited by 6
Gupta, A., & Alkhalil, M. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12113758 · Cited by 7
“(2014) [79] 30 CAD undergoing PCI 1800:0 Optical coherent tomography 9 months A greater increase in fibrous-cap thickness, with a greater decrease in lipid arc, lipid length and macrophage accumulation was detected in the EPA group”
Naniwa, S., Kawamori, H., Toba, T., Hiromasa, T., Sugizaki, Y., Sasaki, S., Fujii, H., Hamana, T., Osumi, Y., Yamamoto, T., et al. (2025) · EuroIntervention · doi:10.4244/eij-d-24-00971 · Cited by 5
Self-citationPatti, G., Grisafi, L., Azzolina, D., Cumitini, L., D’Amario, D., & Mennuni, M. G. (2025) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2025.120433 · Cited by 5
Metadata
- Authors
- Nishio, R., Shinke, T., Otake, H., Nakagawa, M., Nagoshi, R., Inoue, T., Kozuki, A., Hariki, H., Osue, T., Taniguchi, Y., Iwasaki, M., Hiranuma, N., Konishi, A., Kinutani, H., Shite, J., & Hirata, K.-I.
- Affiliations
- Kobe University (JP)
- ORCID
- Venue
- Atherosclerosis
- Publisher
- Elsevier BV
- Published
- 2014-05
- Volume
- 234
- Issue
- 1
- Pages
- 114-119
- ISSN
- 0021-9150 (ISSN-L)
- OpenAlex
- W2048776656
- Cited by
- 133
- References
- 29
- Citations by year
- 2026: 2 · 2025: 10 · 2024: 9 · 2023: 16 · 2022: 20 · 2021: 14 · 2020: 14 · 2019: 13 · 2018: 3 · 2017: 9 · 2016: 11 · 2015: 10 · 2014: 2
- FWCI
- 9.94
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Atherosclerosis (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Fatty Acid Research and Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Coronary Interventions and Diagnostics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipoproteins and Cardiovascular Health
- Keywords
- eicosapentaenoic acid, statin therapy, rosuvastatin, thin-cap fibroatheroma, coronary artery disease, pentraxin 3, fibrous cap thickness, lipid arc, macrophage accumulation, arterial inflammation, dyslipidemia, percutaneous coronary intervention
- MeSH terms
- Coronary Artery Disease, Drug Therapy, Combination, Female, Humans, Male, Middle Aged, Eicosapentaenoic Acid, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Tomography, Optical Coherence, Plaque, Atherosclerotic
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