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Supplement: n–3 Fatty Acids: Recommendations for Therapeutics and Prevention |
1 From the Laboratory of Membrane Biochemistry and Biophysics and the National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD
2 Presented at the symposium "n–3 Fatty Acids: Recommendations for Therapeutics and Prevention," held at the Institute of Human Nutrition, Columbia University, New York, NY, 21 May 2005. 3 This article reflects solely the scientific opinions of the authors and is not to be considered as a statement from any agency of the US federal government. 4 Supported by the Intramural Research Program of the National Institute on Alcohol Abuse and Alcoholism and by a gift from John M Davis, MD. 5 Address reprint requests to JR Hibbeln, Senior Clinical Investigator, LMBB, National Institute on Alcohol Abuse and Alcoholism, NIH, 31 Center Drive 1B58 MSC2088, Bethesda, MD 20892-2088. E-mail:jhibbeln{at}mail.nih.gov.
ABSTRACT
Background: The worldwide diversity of dietary intakes of n–6 and n–3 fatty acids influences tissue compositions of n–3 long-chain fatty acids (LCFAs: eicosapentaenoic, docosapentaenoic, and docosahexaenoic acids) and risks of cardiovascular and mental illnesses.
Objective: We aimed to estimate healthy dietary allowances for n–3 LCFAs that would meet the nutrient requirements of 97–98% of the population.
Design: Deficiency in n–3 LCFAs was defined as attributable risk from 13 morbidity and mortality outcomes, including all causes, coronary heart disease, stroke, cardiovascular disease, homicide, bipolar disorder, and major and postpartum depressions. Dietary availability of n–3 LCFAs from commodities for 38 countries and tissue composition data were correlated by best fit to each illness in deficiency risk models.
Results: The potential attributable burden of disease ranged from 20.8% (all-cause mortality in men) to 99.9% (bipolar disorder). n–3 LCFA intake for Japan (0.37% of energy, or 750 mg/d) met criteria for uniformly protecting >98% of the populations worldwide. n–3 LCFA intakes needed to meet a tissue target representative of Japan (60% n–3 in LCFA) ranged from 278 mg/d (Philippines, with intakes of 0.8% of energy as linoleate, 0.08% of energy as 
-linolenate, and 0.06% of energy as arachidonic acid) to 3667 mg/d (United States, with 8.91% of energy as linoleate, 1.06% of energy as - linolenate, and 0.08% of energy as arachidonic acid).
Conclusions: With caveats inherent for ecologic, nutrient disappearance analyses, a healthy dietary allowance for n–3 LCFAs for current US diets was estimated at 3.5 g/d for a 2000-kcal diet. This allowance for n–3 LCFAs can likely be reduced to one-tenth of that amount by consuming fewer n–6 fats.
Key Words: n–3 Fatty acids • Dietary Reference Intake • Adequate Intake • Recommended Dietary Allowance • docosahexaenoic acid • eicosapentaenoic acid • arachidonic acid • linoleic acid • dose-response study • omega-3 fatty acids
INTRODUCTION
The charge of this conference was to consider factors relevant to estimating healthy intakes of the n–3 long-chain fatty acids (LCFAs) with special consideration of the role of the 18-carbon fatty acids -linolenate (-LNA) and linoleate (LA), which are precursors for the n–3 LCFAs and the n–6 LCFAs [predominantly arachidonic acid (AA)], respectively. n–3 LCFAs are 20- and 22-carbon fatty acids, operationally defined here as the sum of eicosapentaenoic acid (20:5n–3, or EPA), docosapentaenoic acid (22:5n–3, or DPA), and docosahexaenoic acid (226:n–3, or DHA). In recent years, n–3 LCFAs have been specifically recommended for the secondary prevention of cardiovascular disease (1) and are the focus of considerable attention for the prevention and treatment of disorders with an inflammatory component, including type 2 diabetes, irritable bowel syndrome, macular degeneration, rheumatoid arthritis, asthma, several cancers, and psychiatric disorders (2-8). These illnesses represent significant burdens of disease around the world.
The process of determining a recommendation is too complex to be considered here, but 3 criteria served as useful endpoints in estimating healthy intakes: the percentage of the population protected, the reduction in chronic disease, and the consideration of tissue compositions. For example, a Recommended Dietary Allowance functions as a subgroup of the Dietary Reference Intake and is defined as the "average daily nutrient intake level sufficient to meet the nutrient requirement of nearly all (97–98%) healthy individuals in a particular life stage and sex group" (9, 10). In the past, the idea of a "nutrient requirement" was linked to the concept of "essentiality," and dietary allowances were developed with the goal of preventing signs or symptoms of deficiency. In the relatively new guidelines for Dietary Reference Intakes, the Institute of Medicine requires that "reduction in the risk of chronic degenerative disease [be] included in the formulation of the recommendation rather than just the absence of signs of deficiency" (9, 10). To meet the definition for reducing chronic diseases, the nutrient requirement for n–3 LCFAs was characterized as decreasing the risk of morbidity and mortality for n–3 LCFA-related chronic illnesses rather than simply preventing scaly dermatitis or skin atrophy, as is the case for LA.
This analysis focuses on cardiovascular disease mortality and the prevalence of mental illness in our estimation of healthy dietary intakes of n–3 LCFAs for 3 reasons. First, recent reviews of evidence-based medicine link deficient intakes of n–3 LCFAs with increased risk of cardiovascular disease and stroke (2-8), and a compelling, but still emerging body of data indicates efficacy in psychiatric illnesses. Second, comparable data are available regarding current human diversity of both apparent dietary intakes (11) and risks of morbidity and mortality for use in international ecologic analyses. Mortality data were available from a single source, World Health Organization age-adjusted surveillance data (12), and for each psychiatric illness, morbidity or mortality data were available from prior publications by one of the authors (JRH) (13-16). Third, mechanistic links between n–3 LCFA deficiencies and increased risks of illness are biologically plausible (13, 14).
Dose-response deficiency models were constructed for our analysis by using ecologic data from 38 countries with a target of identifying a representative population with a reduction of 98% in all risks potentially attributable to deficient intakes of n–3 LCFAs. However, tissue compositions of n–3 LCFAs are closer determinants of risk than are unadjusted dietary intakes. World diversity of tissue LCFA composition predicts world diversity of cardiovascular mortality (17). Concurrent intakes of -LNA, the precursor for n–3 LCFAs, and of the n–6 fatty acids LA and AA were considered, because these essential fatty acids all influence tissue proportions of n–3 fatty acids in LCFAs (18-21).
MATERIALS AND METHODS
Ecologic dose-response models
Commodities data for the domestic supply of foods available for human consumption, or disappearance data, expressed as metric tons · capita–1 · d–1, were available for 1995 for 38 countries from the statistical services of the Food and Agriculture Organization (FAO-STAT) of the World Health Organization (11). FAO-STAT categories included poultry meats, pig meats, eggs, bovine meats, goat and mutton, crustaceans, demersal fish, freshwater fish, marine fish, pelagic fish, mollusks, coconut oil, cottonseed oil, groundnut, maize germ oil, olive oil, palm oil, palm kernel oil, rape or mustard oil, rice bran oil, sesame oil, soybean oil, and sunflower oil. These food categories were chosen because the aggregate of meat, eggs, and seafood has been shown to account for 97% of all n–3 LCFA dietary intake, and seed oils are the dominant sources of LA and -LNA (22, 23).
The essential fatty acid compositions of foods representative of each commodities category (Table 1
) were estimated from the US Department of Agriculture food-composition database version 17 (24), except for several commodities with reported n–3 LCFA composition values for specific foods that better represented the world diversity of food composition (25-27). Disappearance data for each food category were then converted to gross availability, or "available intake," for each essential fatty acid in each commodity category by using our estimated food source composition values (eg, mg n–3 LCFA/100 g food source). The disappearance of the total milligram quantities of each fatty acid was summed from all commodities and then converted to energy (9 kcal/g). The contribution of each fatty acid was expressed as a percentage of energy available from disappearance of total calories from all commodities to adjust for differences between disappearance and actual consumption. In Table 1, estimations for pig, bovine, goat and mutton, and poultry were calculated by using weighted averages of shown food samples to derive the fatty acid composition of meat with equal parts untrimmed cuts and lean-portion-only cuts. Poultry meats were the average of 4 poultry samples. Pig meats were the average of pork loin without fat from 2 sources and composite pork with fat (weighted twice). n–3 LCFAs for bovine meats were estimated as the average of 6 lean samples and 1 US Department of Agriculture sample including fat (weighted 6 times). Goat and mutton was the average of lamb food samples plus the average of goat food samples divided by 2. Freshwater fish was the average of freshwater bass (weighted twice) and rainbow trout. Demersal fish was the average of flatfish and halibut. Pelagic fish was the average of tuna, salmon, cod, and pollock. Marine fish (other) was an average of the derived values for mollusks, crustaceans, pelagic, demersal, and freshwater fish. These estimations assumed uniform discrepancies between nutrients available for dietary intake and actual ingestion for all foods, ie. the waste of meat or fat calories due to spoilage, trimming, discarding, or other causes was similar for seed oils, seafood, and other foods.
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Statistical analysis
Twelve independent comparisons of available dietary n–3 LCFA percentages of energy with disease outcomes across countries were assessed for best linear and nonlinear relation by using iterative curve fitting regression analyses with SIGMA PLOT (version 8.0; SPSS Inc, Chicago, IL). Linear, exponential decay, power, and logarithmic models were each examined with positive and negative slopes. Data were examined for normality of distribution and residuals. In addition to the 12 models of dietary available intake with risk, a correlation comparing lower percentages of n–3 fatty acids in tissue LCFAs to greater cardiovascular mortality was generated from previously published data (19, 29) by using the following relation (17):
 | (1) |
Estimation of morbidity and mortality attributable to deficiencies of n–3 LCFAs
The asymptote for each dose-response curve was operationally defined as the available intake of n–3 LCFAs (as a percent of energy) associated with no further decreased risk of illness. To avoid extrapolation beyond the available data, the asymptote also operationally defined the y value occurring at the intersection of the dose-response curve and the highest subpopulation mean available intake of n–3 LCFAs. In most cases, this corresponded to Icelandic concentrations of 0.43% of energy as n–3 LCFAs, except for the major depression model, for which the furthest point was 0.374% of energy (Japan). The area below the operationally defined asymptote was regarded as the baseline rate of disease that persisted regardless of further increases in intake of n–3 LCFAs. Integral calculus was used to calculate all areas under the curves (Maths Helper Plus; Teachers' Choice Software, Goodna Queensland, Australia). Morbidity or mortality attributable to n–3 LCFA deficiency was defined as the area above the baseline rate of illness, but below the fitted curve, between available intakes of zero and maximal available intakes of n–3 LCFAs and also expressed as a percentage of potentially attributable disease burden.
The efficacy of 3 possible healthy allowances of n–3 LCFAs (0.08% of energy or 180 mg/d, 0.22% of energy or 500 mg/d, and 0.34% of energy or 750 mg/d) was assessed by using integral calculus to determine the areas between the curve and the asymptote, with each of the possible Recommended Dietary Allowances as right boundaries in 3 different scenarios (illustrated in Figure 2 by areas 
, ß, and ). These boundary values defined the percentage of the population potentially protected from each disease outcome for each choice. Four factors (dietary availabilities of LA, -LNA, AA, and EPA + DPA + DHA as a percent of energy) were used as input functions to estimate the percentage of n–3 LCFA in tissues by using a formula empirically derived from human and animal data with modified constants (19, 29). The dietary percentage of energy of n–3 LCFAs needed to maintain n–3 LCFAs in tissue comparable with concentrations in Japan was calculated for 13 countries representing the worldwide diversity of LA in diets (which ranged from <0.89% of energy to nearly 9% of energy). Conversion of required amounts from % of energy to mg n–3 LCFA/d was based on a 2000-kcal/d diet.
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Major sources of n–3 LCFAs were fish and seafood, whereas seed oils, eggs, poultry, and pig meat contained the greatest amount of n–6 fatty acids (Table 1
). Greater n–3 LCFA availability was inversely related with disease rates in all 12 risk models (Table 2 and Figure 1). Three-factor negative exponential equations provided the best fit for all models, except for major depression, which was a linear fit. These correlations were significant for reduced mortality from stroke for men (r = –0.59, P < 0.002), stroke for women (r = –0.57, P < 0.004), CHD for women (r = –0.45, P < 0.04), cardiovascular disease for men (r = –0.60, P < 0.002), cardiovascular disease for women (r = –0.65, P < 0.001), all causes for men (r = –0.53, P < 0.008), and all causes for women (r = –0.57, P < 0.004), and for reduced morbidity from postpartum depression (r = –0.78, P < 0.001), bipolar disorder (r = –0.86, P < 0.002), and homicide mortality (r = –0.78, P < 0.001). Additionally, there was a trend for major depression (r = –0.69, P < 0.15) and CHD for men (r = –0.38, P < 0.1). Greater n–3 LCFAs in tissue correlated with a lower risk of cardiovascular mortality in a linear regression as previously published (r2 = –0.97, P < 0.001) (17).
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). Rates of illness in Iceland and Greenland were uniformly lower than the projected regression curves, which indicated that further protection was likely to occur with greater n–3 LCFA intake (Figure 1 and Figure 2). Evaluation of the 3 possible choices for healthy allowances indicated that available intake at 0.08% of energy prevented enough attributable disease to protect nearly all healthy individuals in only 2 conditions (stroke mortality for men and for women). Available intake at 0.22% of energy did not protect nearly all healthy individuals for CHD mortality for men and for women, total mortality for men and for women, major depression, or bipolar disorder. Available intake at 0.34% of energy was sufficient to reduce risk for 
98% of the mortality and morbidity in all illness models (Table 3). This level of available intake corresponded with intakes common in Japan. Results of the CHD risk model with tissue composition in Figure 2 also indicate that a tissue composition of 60% of n–3 fatty acids in LCFA, a value common in Japan (30-33), may protect 98.6% of the worldwide risk of cardiovascular mortality potentially attributable to n–3 LCFA deficiency.
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). In general, as concurrent LA availability increased, the estimated requirement for n–3 LCFA intake increased, although intake of -LNA and AA also played a role. In recognizing that dietary intakes in Mediterranean countries result in a substantial decrease in risk of cardiovascular disease, dietary data are also presented reflecting a tissue goal of 50% n–3 LCFAs, which is nearer to that in Mediterranean countries (Table 4). For Americans consuming a 2000-kcal/d diet, 2178 mg/d (0.98% of energy) may achieve 50% n–3 in tissue LCFA, whereas 3667 mg/d appears necessary to reach a goal of 60% n–3 in LCFA. Lowering LA intake can likely decrease an individual's need for n–3 LCFAs by one-tenth.
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There was a convergence from 13 dose-response models of n–3 LCFA intake and disease risk on the basis of commodities data for percent of energy as n–3 LCFAs (available dietary intakes) and plasma phospholipid n–3 LCFA composition. These models indicated that the diets and tissue compositions common in Japan meet the nutrient requirements of nearly all the healthy population. Deficiency was defined here as the increased risk of illness attributable to insufficient n–3 LCFA intake. In 12 of 13 independent dose-response models, three-factor negative exponential regression equations provided the best fit between lower available intakes of n–3 LCFAs and greater morbidity and mortality. These models allowed calculation of intakes sufficient to protect 98% of the population from risks of deficiency. Thus, healthy available intakes corresponded with tissue compositions of 
60% n–3 fatty acids in LCFA (and 40% n–6 fatty acids in LCFA), which has been shown to be associated with low cardiovascular mortality in the Japanese population (30-33).
Japan is a modern industrialized society with a large population and well-documented rates of illnesses and nutrient intakes. Low rates of cardiovascular disease have been consistently reported in Japan, despite high rates of smoking and high blood pressure (34, 35). Thus, we had reasonable confidence in targeting Japanese n–3 LCFA composition as a reliable endpoint. However, because dietary intakes of n–3 LCFAs are not the sole determinants of tissue n–3 LCFAs, we also considered background intakes of 18-carbon n–3 and n–6 fatty acids and of AA when estimating the dietary intakes of n–3 LCFAs needed to achieve tissue compositions of 60% n–3 LCFAs. We note that the burden of potentially attributable risk for bipolar disorder appears to be unrealistically high (99.9%; see Table 3) on the basis of the regression equation generated from data in an original publication (16). Subsequently, additional data reporting a low annual prevalence rate of bipolar disorder in Japan (0.1%) were published (36). Inclusion of these new data did virtually nothing to alter the regression equation or the percentage of potentially attributable disease, which gives greater confidence in this finding. Nonetheless, bipolar disorder is likely due to a multitude of factors, and it is unlikely that 99.9% of bipolar illness is attributable to n–3 LCFA deficiency. To our knowledge, rates of bipolar disorder in Iceland and among Inuits have not been published.
Current recommendations for n–3 LCFA intake are not specified by the Institute of Medicine (10), but have been estimated at 130–260 mg/d (37). Other recommendations range from 200 mg/d in the Netherlands (37) to the American Heart Association's recommendation of 1 g/d for persons with documented CHD (1). According to the analysis presented here, these recommendations are inadequate to meet the criteria of a Recommended Dietary Allowance for US and world populations. One exception is the International Society for the Study of Fatty Acids and Lipids recommendation of 500 mg/d, which also includes an adequate intake of LA at 2% of energy and a healthy intake of -LNA of 0.7% of energy. With the use of an empirical formula (19), this combination translates into a tissue composition of 53% n–3 fatty acids in LCFAs (29, 38). Concurrent dietary intakes of LA, -LNA, AA, EPA, and DHA should be considered in predicting final tissue proportions of n–3 fatty acids in LCFAs (19). Thus, a healthy dietary allowance for n–3 LCFA intake must be made dependent on concurrent intakes of LA, -LNA, and AA. A healthy dietary allowance of 3.5 g EPA + DHA/d, which is based on the current per capita background available intake of n–6 fatty acids and -LNA in the United States, could be reduced to one-tenth of that amount if the intake of n–6 fatty acids, in particular LA, can be lowered to <2% of energy.
A related biomarker of n–3 intake and predicted risk is the omega-3 index (red blood cell EPA + DHA as a percentage of total red blood cell lipids) proposed by Harris and von Schacky (39), for which values >8% are associated with greater decreases in cardiovascular disease risk. This target was based on trials conducted primarily in the United States and does not reflect the worldwide diversity of n–3 and n–6 intakes. In fact, n–6 intake was not considered. For comparison, 60% n–3 fatty acids in LCFAs in tissue is associated with an omega-3 index of 12–15%, as seen in Japan. The biomarker target and the target proposed here may seem excessive in comparison with current US dietary habits and other recommendations. However, this allowance can also be regarded as conservative because morbidity and mortality rates for nearly all diseases are even lower for Iceland and Greenland, populations with greater intakes of n–3 LCFAs than in Japan. These countries fell below the dose-response curves generated by the regression analyses, which indicates that greater protection was achieved than was predicted (see Figures 1 and 2).
The approach to determining healthy dietary allowances for n–3 LCFAs described here has several unique aspects. To our knowledge, this is the first attempt to set an allowance for n–3 LCFAs that adheres to criteria of meeting the nutrient requirements of nearly all the healthy population. n–3 LCFA deficiency was defined as an increased risk of chronic diseases for which substantial efficacy data exist and for which these nutrients reduce pathophysiologic mechanisms. This ecologic approach took advantage of uniform disappearance data estimating dietary available intakes, compared with direct survey data, which were not available or uniform for every country. The worldwide diversity of available intake of essential fatty acids was also compared with the worldwide diversity of disease burdens to estimate dose-response relations. One additional strength is that both the total n–3 and n–6 dietary availability and resulting tissue profiles from different countries were taken into consideration when determining possible allowances.
There are several obvious weaknesses inherent in comparing countries in these cross-sectional ecologic analyses. These include the lack of adjustment for potential confounding variables; variations in actual compositions of foods; waste that makes food disappearance not equal to intake; differences in diagnostic classifications, especially for psychiatric disorders; and differences in qualities of data collection. The assumption of a uniform composition of meats, eggs, and other food sources across countries is likely confounded by diverse amounts of n–3 LCFAs available to domestic animals; for example, soybean- and corn-fed animals are likely to have very different fatty acid proportions than do grass-fed animals. Thus, the data are not adjusted for country-specific differences in the nutrient compositions of foods. Although intakes are normally expressed specifically for each of 16 life-stage categories, the data necessary to make such inferences were not available in this analysis. The prevalence rates of major depression and CHD were not significantly associated with the disappearance data and thus their contribution should be considered cautiously. Estimation of a healthy intake would preferably have been done with outcome data from large-scale longitudinal intervention trials that each used multiple dose comparisons; assessed several disease outcomes, including cardiovascular and psychiatric morbidity; and monitored tissue proportions of LCFAs. Because of cost considerations, relatively few large-scale longitudinal intervention trials have been conducted, let alone as comparisons of multiple doses; thus, this information is not readily available.
It seems likely that a combination of EPA and DHA reflecting nature may be optimally used in dietary supplementation to meet n–3 LCFA intake goals. A major source of dietary n–3 LCFA in our calculations was seafood containing both EPA and DHA in an average ratio of 1:2.3, as calculated from data presented here. High intakes of n–3 LCFAs may be associated with an increased risk of hemorrhagic stroke (31), but this risk may be offset by a decrease in thrombotic stroke and overall stoke mortality. A review of the literature on mental health outcomes shows supplementation with a combination of both EPA and DHA likely to be more effective than use of either alone (40-45). Reports of 50% reductions in depressive symptoms and 37% reductions in felony-level violence (46) in interventional trials are consistent with the large potentially attributable burdens of disease reported in Table 3. However, effect sizes in interventional trials are difficult to compare with these ecologic data, which reflect prenatal and lifetime dietary exposures. In contrast, most intervention trials have, understandably, been conducted over comparatively short periods of time.
This work focuses directly on estimates of the 20- and 22-carbon varieties of n–3 and n–6 essential fatty acids available in membranes, because these are the precursors for the eicosanoids that mediate inflammatory and thrombotic tissue responses (17, 47, 48). The biological availability and activity of n–6 LCFAs, in particular AA, are inversely related to n–3 fatty acids in tissue LCFAs. Greater compositions of EPA, DPA, and DHA in membranes competitively lower the availability of AA for the production of eicosanoids (17, 47, 48). The prevention of the formation of n–6 eicosanoids derived from AA with medications, including cox-2 inhibitors, ibuprofen, acetaminophen, and aspirin, constitutes a substantial proportion of pharmaceutical industry activity. The available tissue composition of AA can be lowered by reducing dietary intakes of the 18-carbon precursor, LA. Conversely, it has been known since the early 1960s that greater dietary intakes of LA increase tissue concentrations of AA, while reducing tissue concentrations of EPA and DHA (20, 49-51). Greater direct intake of preformed EPA and DHA most directly influences greater tissue compositions in comparison with conversion from -LNA to EPA and DHA, which is poor in humans (21). Thus, recommendations for essential fatty acid intakes focusing only on the 18-carbon fatty acids are subject to substantial variance in tissue proportions of n–3 and n–6 fatty acids in LCFAs. It is likely that the success and failure of different clinical trials using similar doses of n–3 LCFAs were influenced by differing background intakes of the n–6 fatty acids LA and AA. For example, in the case of the Lyon Diet Heart Study (52), the positive outcomes attributed to -LNA may be related, in part, to a lower n–6 fatty acid intake, which would enhance conversion of -LNA to n–3 LCFAs (49, 53). Although LA has been associated with positive health outcomes, including reduced risk of ischemic stroke (54), we are aware of no intervention trials in which LA was actively increased in humans and cardiovascular or psychiatric disease outcomes were measured.
In contrast with considering n–3 fatty acids as a pharmaceutical treatment, Crawford, Cordain, Simolopous, and others (55-57) have advanced the concept of population-wide deficiencies of n–3 LCFAs in modern societies that rely on industrialized agriculture. Those authors cited, in part, that diets during the 4–5 million years of hominid evolution were likely abundant in seafood and other sources of n–3 LCFAs but had sparingly little contribution of calories from n–6-rich seed oils. In stark contrast, at the turn of the recent millennium, a single food source, soybean oil, appears to deliver 20% of all calories in the median US diet, with 9% of all calories from linoleic acid alone (58). To our knowledge, inadequate information is available to determine whether it is safe or unsafe to consume 9% of all calories as LA, a precursor to the proinflammatory arachidonic acid. One ecologic study indicated that greater intakes of LA from 1960 to 1999 in each of 5 countries predicted a 100-fold greater risk of homicide mortality (59). The increases in world LA consumption over the past century may be considered a very large uncontrolled experiment that may have contributed to increased societal burdens of aggression, depression, and cardiovascular mortality. Conversely, actively lowering LA intake must be carefully considered because of the large potential effects on agricultural economies. Alternative soybean variants or other sources of seed oils could be used to reduce LA intakes to levels currently seen in countries such as the Philippines, resulting in up to one-tenth lower estimated allowances for n–3 LCFAs as a percentage of energy. The limited worldwide fisheries and aquaculture production would be more likely to be able to meet world needs. Because LA constitutes such a large percent of calories in the US diet, it seems prudent to conduct large-scale intervention trials to determine whether lowering intakes can reduce cardiovascular risk and psychiatric morbidity. Increasing tissue concentrations of n–3 LCFAs on a population level may result in a substantial decrease in health care costs by reducing the illnesses that account for the largest burden of disease worldwide.
ACKNOWLEDGMENTS
Although the term highly unsaturated fatty acids (HUFAs) is preferred by the authors, LCFAs was used for stylistic commonality for this conference. JRH, LRGN, TLB, JAR, and WEML each contributed to the writing of the article, the data analysis, and the interpretation. JRH originated the conceptual framework of the article. LRGN and JAR performed most of the calculations. None of the authors had a personal or financial conflict of interest.
REFERENCES
This article has been cited by other articles:
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  J. Whelan Dietary Stearidonic Acid Is a Long Chain (n-3) Polyunsaturated Fatty Acid with Potential Health Benefits J. Nutr., January 1, 2009; 139(1): 5 - 10. [Abstract] [Full Text] [PDF]
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C. T. Damsgaard, H. Frokiaer, A. D. Andersen, and L. Lauritzen Fish Oil in Combination with High or Low Intakes of Linoleic Acid Lowers Plasma Triacylglycerols but Does Not Affect Other Cardiovascular Risk Markers in Healthy Men J. Nutr., June 1, 2008; 138(6): 1061 - 1066. [Abstract] [Full Text] [PDF]
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