Register Log In Login with facebook

Low-dose statin plaque formation stopped by Omega-3 – RCT Dec 2017

Effect of Eicosapentaenoic and Docosahexaenoic Acids Added to Statin Therapy on Coronary Artery Plaque in Patients With Coronary Artery Disease: A Randomized Clinical Trial.

J Am Heart Assoc. 2017 Dec 15;6(12). pii: e006981. doi: 10.1161/JAHA.117.006981.
Alfaddagh A1, Elajami TK1, Ashfaque H1, Saleh M1, Bistrian BR1, Welty FK2.
1 Division of Cardiology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
2 Division of Cardiology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA fwelty at bidmc.harvard.edu.


 Download the PDF from VitaminDWiki

Also: Significantly less pain in Omega-3 group


Although statins reduce cardiovascular events, residual risk remains. Therefore, additional modalities are needed to reduce risk. We evaluated the effect of eicosapentaenoic acid and docosahexaenoic acid in pharmacologic doses added to statin treatment on coronary artery plaque volume.

A total of 285 subjects with stable coronary artery disease on statins were randomized to omega-3 ethyl-ester (1.86 g of eicosapentaenoic acid and 1.5 g of docosahexaenoic acid daily) or no omega-3 (control) for 30 months. Coronary plaque volume was assessed by coronary computed tomographic angiography. Mean (SD) age was 63.0 (7.7) years; mean low-density lipoprotein cholesterol ≤80 mg/dL. In the intention-to-treat analysis, our primary endpoint, noncalcified plaque volume, was not different between groups (P=0.14) but approached significance in the per protocol analysis (P=0.07). When stratified by age in the intention-to-treat analysis, younger omega-3 subjects had significantly less progression of the primary endpoint, noncalcified plaque (P=0.013), and fibrous, calcified and total plaque. In plaque subtype analysis, controls had significant progression of fibrous plaque compared to no change in the omega-3 ethyl-ester group (median % change [interquartile range], 5.0% [-5.7, 20.0] versus -0.1% [-12.3, 14.5], respectively; P=0.018). Among those on low-intensity statins, omega-3 ethyl-ester subjects had attenuation of fibrous plaque progression compared to controls (median % change [interquartile range], 0.3% [-12.8, 9.0] versus 4.8% [-5.1, 19.0], respectively; P=0.032). In contrast, those on high-intensity statins had no difference in plaque change in either treatment arm.

High-dose eicosapentaenoic acid and docosahexaenoic acid provided additional benefit to statins in preventing progression of fibrous coronary plaque in subjects adherent to therapy with well-controlled low-density lipoprotein cholesterol levels. The benefit on low-intensity statin, but not high-intensity statin, suggests that statin intensity affects plaque volume.

CLINICAL TRIAL REGISTRATION: url: http://www.ClinicalTrials.gov. Unique identifier: NCT01624727.

PMID: 29246960 DOI: 10.1161/JAHA.117.006981

Created by admin. Last Modification: Sunday January 7, 2018 23:37:29 UTC by admin. (Version 2)

Attached files

ID Name Comment Uploaded Size Downloads
8974 Statin Omega-3 pain.jpg admin 20 Dec, 2017 14:52 19.78 Kb 24
8973 Statin Omega-3.pdf PDF 2017 admin 20 Dec, 2017 14:51 851.31 Kb 42
See any problem with this page? Report it to the webmaster.