Key result
REDUCE-IT biomarker changes link to ~12% lower ASCVD risk versus STRENGTH comparator effects.
Why the study?
The REDUCE-IT and STRENGTH trials showed contrasting results for high-dose purified omega-3 fatty acids in preventing ASCVD, and whether differences in the effects of active and comparator oils on lipid traits and C-reactive protein explain this discrepancy was tested.
Can differences in the effects of active and comparator oils on lipid traits and C-reactive protein explain the contrasting ASCVD outcomes between the REDUCE-IT and STRENGTH trials?
Cohort (n=106,088)
Can differences in the effects of active and comparator oils on lipid traits and C-reactive protein explain the contrasting ASCVD outcomes between the REDUCE-IT and STRENGTH trials?
Differences in the effects of comparator oils (mineral vs. corn oil) on lipids and CRP partly explain the contrasting cardiovascular outcomes of REDUCE-IT and STRENGTH, though an additional 13% risk reduction in REDUCE-IT remains unexplained by these biomarkers.
Comparator oil effects on lipids and CRP may partly explain REDUCE-IT vs STRENGTH divergence; leaves open residual mechanisms requiring prospective confirmation.
AIMS: We tested the hypothesis that the contrasting results for the effect of high-dose, purified omega-3 fatty acids on the prevention of atherosclerotic cardiovascular disease (ASCVD) in two randomized trials, Reduction of Cardiovascular Events with Icosapent Ethyl-Intervention Trial (REDUCE-IT) vs. Long-Term Outcomes Study to Assess Statin Residual Risk with Epanova in High Cardiovascular Risk Patients with Hypertriglyceridaemia (STRENGTH), can be explained by differences in the effect of active and comparator oils on lipid traits and C-reactive protein. METHODS AND RESULTS: In the Copenhagen General Population Study (CGPS) with 106 088 individuals, to mimic trial designs we analysed those who met key inclusion criteria in REDUCE-IT (n = 5684; ASCVD = 852) and STRENGTH (n = 6862; ASCVD = 697). Atherosclerotic cardiovascular disease incidence was followed for the median durations of REDUCE-IT and STRENGTH (4.9 and 3.5 years), respectively. When combining changes in plasma triglycerides, low-density lipoprotein cholesterol, and C-reactive protein observed in the active oil groups of the original studies, estimated hazard ratios for ASCVD in the CGPS were 0.96 [95% confidence interval 0.93-0.99] mimicking REDUCE-IT and 0.94 (0.91-0.98) mimicking STRENGTH. In the comparator oil groups, corresponding hazard ratios were 1.07 (1.04-1.10) and 0.99 (0.98-0.99). Combining these results, the active oil vs. comparator oil hazard ratio was 0.88 (0.84-0.93) in the CGPS mimicking REDUCE-IT compared to 0.75 (0.68-0.83) in the REDUCE-IT. The corresponding hazard ratio was 0.96 (0.93-0.99) in the CGPS mimicking STRENGTH compared to 0.99 (0.90-1.09) in STRENGTH. CONCLUSION: The contrasting results of REDUCE-IT vs. STRENGTH can partly be explained by a difference in the effect of comparator oils (mineral vs. corn), but not of active oils [eicosapentaenoic acid (EPA) vs. EPA + docosahexaenoic acid], on lipid traits and C-reactive protein. The unexplained additional 13% risk reduction in REDUCE-IT likely is through other effects of EPA or mineral oil.
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Doi et al. (2021) conducted a cohort in Atherosclerotic cardiovascular disease (ASCVD) prevention in high-risk hypertriglyceridaemia (n=106,088). Modelled changes in plasma triglycerides, LDL cholesterol, and C-reactive protein from active omega-3 fatty acid oils (EPA vs. EPA + DHA) vs. Modelled changes in lipid traits and C-reactive protein from comparator oils (mineral oil vs. corn oil) was evaluated on Atherosclerotic cardiovascular disease (ASCVD) incidence (HR 0.88, 95% CI 0.84-0.93). Active vs comparator oil lipid/CRP changes yielded an estimated ASCVD HR of 0.88 (95% CI 0.84-0.93) mimicking REDUCE-IT and 0.96 (95% CI 0.93-0.99) mimicking STRENGTH.
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