Affiliation:
1. Department of Nutritional Sciences, Penn State University, University Park, PA
2. Health Diagnostic Laboratory, Inc, Richmond, VA
3. Department of Animal Science, Penn State University, University Park, PA
Abstract
Background
The erythrocyte membrane content of eicosapentaenoic acid (
EPA
) and docosahexaenoic acid (
DHA
), which constitutes the omega‐3 index (O3I), predicts cardiovascular disease mortality. The amount of
EPA
+
DHA
needed to achieve a target O3I is poorly defined, as are the determinants of the O3I response to a change in
EPA
+
DHA
intake. The objective of this study was to develop a predictive model of the O3I response to
EPA
+
DHA
supplementation in healthy adults, specifically identifying factors that determine the response.
Methods and Results
A randomized, placebo‐controlled, double‐blind, parallel‐group study was conducted in 115 healthy men and women. One of 5 doses (0, 300, 600, 900, 1800 mg) of
EPA
+
DHA
was given daily as placebo or fish oil supplements for ≈5 months. The O3I was measured at baseline and at the end of the study. There were no significant differences in the clinical characteristics between the groups at baseline. The O3I increased in a dose‐dependent manner (
P
<0.0001), with the dose of
EPA
+
DHA
alone accounting for 68% (quadratic,
P
<0.0001) of the variability in the O3I response. Dose adjusted per unit body weight (g/kg) accounted for 70% (linear,
P
<0.0001). Additional factors that improved prediction of treatment response were baseline O3I, age, sex, and physical activity. Collectively, these explained 78% of the response variability (
P
<0.0001).
Conclusions
Our findings validate the O3I as a biomarker of
EPA
+
DHA
consumption and identify additional factors, particularly body weight, that can be used to tailor
EPA
+
DHA
recommendations to achieve a target O3I.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
Cited by
182 articles.
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