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Front. Nutr., 12 November 2019
Sec. Clinical Nutrition

Oily Fish and Omega-3s Across the Life Stages: A Focus on Intakes and Future Directions

  • Nutritional Insight Limited, London, United Kingdom

Background: There is a tendency to report oily fish intakes for adults collectively. This means that certain population groups tend to be overlooked. The purpose of the present article is to derive and evaluate oily fish and omega-3 intakes across the lifespan.

Methods: A secondary analysis of the UK National Diet and Nutrition Survey (years 2008–2016) was undertaken. Data from n = 2,949 participants ≥4 years was analyzed. Alongside this, data was extracted from surveys published within the last 5-years reporting omega-3 intakes.

Results: Overall, only a quarter (25.2%) of the UK population are oily fish consumers. Amongst those eating oily fish only 7.3% of children, 12.8% of teenagers, and 15.6% of young adults (20–29 years) met oily fish recommendations. Mean intakes of oily fish ranged between 3.4 and 19.1 g/day. Females aged 30–39 and 60–69 years had significantly lower daily oily fish intakes than males (P = 0.05 and P = 0.049) although their intakes were higher than men in their fifties (P = 0.048). Between 2008 and 2016 oily fish intakes have remained relatively stable although a significant decline was seen amongst those aged 50–59 years (P = 0.048). Survey data (n = 10 publications) showed that EPA and DHA intakes were consistently lower than guidelines, with children, teenagers, females, and pregnant women having some of the largest dietary gaps.

Conclusions: Younger generations, women of childbearing age and pregnant mothers appear to be at particular risk of oily fish and omega-3 shortfalls. Declining EPA and DHA profiles of farmed fish and plant-based food movements are only likely to exacerbate already inadequate intakes. Urgent public health campaigns are needed to improve UK intakes, which should include a combined approach of dietary and supplemental sources.


Oily fish is a valuable source of energy, protein, fat and long-chain omega-3 polyunsaturated fatty acids, mainly taking the form of Eicosapentaenoic Acid (EPA) and Docosahexaenoic acid (DHA), which play a valuable role in disease prevention and health promotion (1, 2). Within the diet oily fish is an important provider of EPA and DHA which is attributed to the fact that microalgae rich in EPA and DHA is the main food of many fish (3, 4). However, there is a generic tendency to under consume oily fish which means that meat (particularly poultry) and eggs are some of the main dietary contributors (5, 6).

Omega-3 fatty acids (n-3 FAs) have been a focal point of interest to scientists for many years (7). Alpha-linoleic acid (ALA) is an “essential fatty acid” as it cannot be produced by the human body or higher organisms and is converted into other longer n-3 FAs including eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) (8). n-3 FAs are a heterogeneous group of fatty acids which have a double bond located between the third and fourth carbon atoms from the methyl end (7). As the human body does not produce longer n-3 FAs efficiently it is necessary to obtain suitable amounts through dietary sources (9).

As shown in Figure 1 the n-3 FA alpha-linoleic acid (ALA) is the only real “essential” FA as it is required to yield EPA and DHA which, in turn, produce anti-inflammatory eicosanoids (8). Linoleic acid (LA) is the essential omega-6 fatty acid (n-6 FA), which yields arachidonic acid (ARA) and produces eicosanoids that can exacerbate inflammation (8). Unfortunately, many factors can affect the conversion of ALA to DHA. This process tends to be more effective in infants and young women compared with young men with the inefficient conversion further emphasizing the importance of obtaining preformed DHA from dietary and supplementary sources (10). It has been proposed that higher rates of conversion to DHA amongst women may be due to their higher requirements during pregnancy and lactation (11).


Figure 1. Metabolic pathways of omega-6 and 3 fatty acids.

Previous information suggests that human beings once evolved on diets with a balanced 1:1 ratio of n-6 to n-3 FAs (12). Unfortunately, in modern Westernized diets this once balanced ratio appears to have shifted up to 15/1-17/1 (12). Modern diets now provide around 80 to 90% of polyunsaturated fatty acids as n-6 LA and are lacking in n-3 FAs—creating an unnatural balance of LA to α-linoleic acid, EPA and DHA (13). Rising soybean oil intakes during the Twentieth century are thought to be one driver behind rising n-6 LA intakes and reduced EPA and DHA tissue concentrations (14).

Oily fish and their associated n-3 content have been linked to an array of health benefits. Increased n-3 FA intakes elevate EPA and DHA levels in blood lipids, modifying the structure of cell membranes and membrane proteins which have extended roles in cell signaling and gene expression (15). DHA plays a key role in brain and eye development while EPA and DHA together alter cell and tissue receptiveness in a manner that provides optimal conditions for development, growth and the preservation of health (15). Unfortunately n-3 status is generally poor—a large global survey of n-3 profiles showed that Europe has very low blood levels (<4%) of EPA+DHA in erythrocytes, increasing chronic disease risk (16).

n-3 dietary guidelines between countries are also not fully aligned (Table 1). Mostly, two kinds of dietary reference values are derived for n-3 FAs, the Adequate Intake as established by the European Food Safety Authority (17), and the acceptable macronutrient distribution range, set by Food and Agriculture Organization/World Health Organization (18). Other guidance has also been compiled by the World Association of Perinatal Medicine Dietary Guidelines Working Group (19). Regarding fish guidance in the UK advice to eat two weekly (140 g) portions of fish, of which one should be oily has been set in place since 2004 (20).


Table 1. n-3 FA recommendations.

Data from the United Kingdom (UK) National Diet and Nutrition Survey Rolling Programme (NDNS-RP) has shown few changes in oily fish intakes over the last 9 years (between 2008/09 and 2016/17) (21). The percentage of children aged 11–18 years consuming oily fish did increase by 10 percentage points between 2008/09 and 2016/17 although mean intakes remained well beneath recommended levels across all age groups (21). Whilst this survey provides valuable data for children aged 11 to 18 years and adults aged 19 to 64 years, intakes for other key life stages is not formally reported.

This article undertakes a secondary analysis of the UK NDNS-RP delving deeper into this dataset and evaluating patterns of oily fish consumption across the life span, including early adulthood and across mid-life. A separate literature search was undertaken to derive habitual omega-3 intakes across these population groups. This novel approach will add to the evidence-base providing new insights on oily fish and n-3 FA intakes across the life course.


Survey Design

The NDNS-RP is a cross-sectional survey conducted annually since 2008 in the United Kingdom and designed to assess the diet, nutrient intake and status of the general UK population who are aged 1.5 years and older (22). The survey is conducted across all four countries of the UK and is designed to provide a representative UK population (22). Each year since 2008 the survey aimed to recruited 1,000 people per year comprised of 500 adults aged ≥19 years and 500 children aged 1.5 to 18 years (22).

The NDNS-RP adopts a stratified two-stage clustered design using post-code addresses as the Primary Sampling Units (PSUs) (22). This helps to ensure that the included sample is representative of UK population. Households are then randomly sampled within PSUs with one adult (19≥ years) and one child (1.5–18 years) being invited to participate in the survey (22). Children were asked to take part within some households to ensure that an adequate number of children is included in order to perform various comparisons (22). The present analysis uses data collected from the stage 1 interviewer visit—from the face-to-face computer assisted personal interview and 4-day food diary (22).

Secondary Analysis

In the UK, public health guidance recommends that a healthy and balanced diet should contain two portions of fish each week of which one should be oily (i.e., herring, mackerel, pilchards, sardines, sprats, trout) (23). A portion is defined as around 140 grams when cooked (23). This guidance reflects the previously reported Scientific Advisory Committee on Nutrition (SACN) recommendations for fish and oily fish (20). Given this guidance in the present publication this was calculated to be equivalent to a daily average minimum of 40 grams of total fish, of which 20 grams should be from oily fish.

In the present analysis and NDNS-RP oily fish consumers included: “Any oily fish or roe such as herrings, kippers, mackerel, sprats, eels, salmon, tuna (not canned), sardines, trout (baked, fried, grilled) and any homemade recipes using oily fish” along with “any type of oily fish purchased/retail product including canned in oil/brine/tomato, pickled, sushi, ready meals, taramasalata, pate and paste” (24). Using this data mean average daily intakes of oily fish were calculated (oily fish + composite dishes). Including composite dishes provides a more realistic estimate as dishes with multiple food components are disaggregated into their separate ingredients (25).

The percentage of overall oily fish consumers in the UK was calculated along with the percentage with mean average daily intakes above the recommendation (≥20 g of oily fish/day). Mean daily intakes were calculated among the total UK population, and among those reporting any intake of oily fish. Similar approaches have been adopted and used in previously reported literature (26).

To assess patterns of oily fish consumption data from the UK Data Service (27) was coded and collated for key life stages including: childhood: 4–11 years, the teenage years: 12–19 years, adulthood: 20–29 years (early adulthood) and 30–39 years, mid-life: 40–49 years, 50–59 years, advancing age: 60–69 years, and ≥70 years. The analysis was also stratified by sex. In this section the analysis was exclusive to oily fish consumers. Thus, when collating the data zeros were excluded (non-oily fish consumers).


Survey weights provided by NDNS-RP were used in all descriptive and trend analyses to account for participant non-selection and non-response. The NDNS datasets for years 1–4, 5–6, and 7–8 were combined for analysis of years 1–8. Data was filtered to include only participants who were aged 4 years and older. Weights were recalculated after merging the datasets because there were more participants per year in years 1–4 than in years 5–6 and years 7–8. Calculations were performed as follows:

i The weight variable in each data set was divided by the sum of the weights in the respective dataset.

ii Weights were multiplied by the total (combined) sum of the three weights.

iii Weights were multiplied by ½ for Years 1–4, by ¼ for years 5 and 6, and by ¼ for year 7 and 8.

Statistical Analysis

Statistical analysis was performed using Rv3.5.2. Data was weighed so that the results are representative of the UK population. The use of survey weights means that only percentages, 95% confidence intervals (CIs), are presented rather than raw frequencies. Weighed frequencies were also reported. Oily fish intake was described using the mean and 95% CIs. Categorical variables were summarized using counts and percentages Two-sample t-test was used to compare the average consumption of oily fish intake across males and females.

Degrees of freedom were corrected to take into account the complex survey design. Hypothesis testing was performed at percentage margin of error. Design corrected linear regression was used to assess whether there was a statistically significant linear trend in the mean consumption of oily fish intake across the following four time periods: years 1–2, 3–4, 5–6, and 7–8.

Only oily fish consumers were included in the linear trend analysis and data was adjusted for gender. The analysis was performed for all oily fish consumers and separately for each age group. Data was taken to be statistically significant if the p-value was ≤ 0.05.

Habitual n-3 FA Intakes

A separate National Center for Biotechnology Information (NCBI) search (PubMed) was conducted to extract relevant English-language surveys published between January 2014 and March 2019.

Medical Subject Headings (MeSH) were used to filter publications. The search terms “Fatty acids”, “Omega 3” and “surveys” were used to filter publications. For inclusion studies needed to report data on habitual n-3 intakes. The fatty acids of interest were EPA and DHA so intakes needed to report on these. Articles were excluded if they were published before 2004, focused on omega-6 or 9 fatty acids, circulating/tissue n-3 status or aspects of health rather than dietary intakes.

Data extracted from each article included: (1) Author and country of research, (2) subjects (number of participants), (3) life-stage (age), (4) design and methods, (5) habitual intakes, and (6) main findings.


Oily Fish Intakes

The full NDNS-RP data included dietary data for 12,097 UK individuals. Data was filtered to include participants who were ≥4 years leaving a total of 11,715 participants. Of these, total fish consumers represented 62.2% (weighed n = 7,284, = 95% CI 60.8, 63.5%) of the UK population who were 4 years or older. Oily fish consumers represented 25.2% (n = 2,949, 95% CI 23.9%, 26.5%) of the UK population ≥4 years.

As shown in Table 2 only a quarter (25.2%) of the entire population were “oily fish consumers.” The percentage of oily fish consumers was higher with age with the exception of those aged 40–49 years (30.3% were oily fish consumers). In childhood (4–11 years) only 12.7% consumed oily fish during the survey period. Higher intakes were observed with advancing aged with 38% of those aged ≥60 years eating some oily fish. However, oily fish consumption does not necessarily mean that recommendations are being met. Amongst those consuming fish only a quarter-−25.5% consumed ≥20 g/day of oily fish and aligned with dietary recommendations. Only 7.3, 12.8, and 15.6% of children, teenagers and those in early adulthood (20–29 years) met oily fish recommendations, respectively. Achievement of oily fish benchmarks peaked at age 60–69 years with 40.6% meeting dietary targets. When data collated oily fish consumers and non-consumers the overall percentage meeting recommendations declined to 15.9%.


Table 2. Oily fish consumption in the UK (percentage of consumers/those meeting recommendations).

Except for UK adults in their forties oily fish intakes increased proportionately with age up to 69 years and became lower when adults reached their seventies (Table 3). Mean oily fish intakes were just 12.1 g/day—substantially lower than the ≥20 g/d benchmark used to indicate when recommendations were being met. Males aged 30–39 years consumed significantly more oily fish compared with females of this age (15.4 vs. 11 g/day P ≤ 0.05). Males aged 60–69 years also ate more oily fish than similarly aged women (21.8 vs. 16.6 g/day P = 0.049). Interestingly, in mid-life (age 50–59 years) women consumed more oily fish than men of this age (17.4 vs. 12.7 g/day P = 0.048).


Table 3. Average daily consumption of oily fish across the UK population.

Results showed that there were no statistically significant linear trends in the mean consumption of oily fish (g/day) across the four NDNS-RP periods (P > 0.05) (Table 4). No statistically significant linear trend was observed within any of the age groups except for the 50–59 years age group which showed a statistically significant decreasing linear trend across the four periods (P < 0.05).


Table 4. Mean oily fish consumption (g/day) by year.

Habitual n-3 FA Intakes

The NCBI search identified 251 publications. After the exclusion of irrelevant papers (n = 179), those focusing on health (n = 43), intervention studies (n = 11), those where omega-3 intakes were not reported (n = 6) or studies focusing on athletic populations (n = 2) this left ten key surveys for general review. The procedure of qualifying papers is shown in Figure 2. Of these, seven studies were conducted in the USA or Canada, one in New Zealand and two in Europe (Table 5).


Figure 2. Flow diagram for database search results.


Table 5. Surveys and key studies reporting data on habitual omega-3 intakes.

The US NHANES (National Health and Nutrition Examination Survey) is presently one of the largest sources of information helping to ascertain intakes of EPA and DHA in the developed world. Six of the surveys identified used data from the NHANES dataset (28, 29, 31, 33, 36, 37). An updated assessment using data from years 2003 to 2014 showed that young children and adolescents had some of the lowest n-3 FA intakes compared to adults and seniors, whilst women tended to eat less fish and have lower n-3 FA intakes than males (28).

An earlier evaluation of the NHANES dataset (2003–2008) similarly found that n-3 FA intakes were highest in males but lowest in children and females, including those of childbearing age (33). In terms of dietary sources, fish was the largest dietary contributor (71.2%) of n-3 FAs and only 6.2 percent reported n-3 FA supplement use (33). Other work analyzing the same U.S. dataset (2003–2008) showed that amongst adults mean EPA and DHA intakes (23 and 63 mg/day, respectively) from food sources were substantially lower than recommendations, indicating a need for supplementation strategies (37).

Several NHANES surveys have focused on EPA and DHA intakes during the childbearing years, pregnancy and lactation periods (28, 29, 31). n-3 FA intakes do not appear to differ between pregnant and non-pregnant females. Thompson et al. found that pregnant women consumed less n-3 rich fish and intakes were “sustained” via supplements (28). Other research using NHANES data from cycles 2001–2002 to 2013–2014 reported slight increases in n-3 intakes over the 14-year span although most recent EPA and DHA intakes were 26.8 and 62.2 mg/day, and 95% of the population failed to meet n-3 benchmarks (250 mg/day) (29). Similarly, Nordgren et al. using NHANES 2003–2012 cycles found mean EPA + DHA intakes to be just 80 mg, with no evidence of change during pregnancy (31). This suggests a clear need for n-FA acid intakes to be increased given consistent levels of under consumption.

Other work has looked at n-3 FA intakes during pregnancy in New Zealand and Canada. In the New Zealand study women consuming omega-3 supplements (19.6%) were 16.5 times more likely to align with dietary recommendations for DHA (32). In Canada, a cross-sectional survey of women of high socioeconomic status showed that only 66.7% met the DHA 200 mg/d recommendation indicating that ongoing education about the importance of oily fish and n-3 FA supplementation is needed (30).

One survey using NHANES data (2003–2008) collated n-3 intakes during the early years of life. Amongst children aged 12–60 months mean EPA and DHA intakes were 6.03 and 20.47 mg/day with younger children (12–24 months) have lower average intakes than older children (49–60 months) (36). Low prevalence of fish intakes were one explanation provided for such poor omega-3 intakes (36). Forsyth et al. also conducted an evaluation of DHA intakes in infants and young children (6–36 months) and estimated that mean daily dietary intake of DHA would be around 48.9 mg/day in developing countries (35).

In the UK the NDNS-RP does not presently collate data on n-3 FA intakes. However, a publication written by British authors' collated data from 53 studies on EPA and DHA intakes across 17 different European countries (34). It was concluded that EPA and/or DHA intakes were only as recommended in 26% of the countries studies implying that intakes are inadequate across many parts of Europe (34).


Guidelines for oily fish intakes have been developed to promote adequate intakes of EPA and DHA in children and adults whilst taking on board toxicological considerations (20). There is a growing body of science that oily fish, fish-oil products and their constituent n-3 FAs can have extended health benefits throughout life including with respect to: fetal development, neuronal, retinal, and immune function (9).

Unfortunately, the present paper shows that oily fish is under consumed across the lifespan—a trend that is even more apparent amongst children, teenagers and young adults. Females also have a tendency toward lower oily fish intakes, as evidenced by the present analysis and others (33, 37). The explanations behind this are likely to be multi-factorial. Reported barriers to oily fish consumption have included its expense and poor satisfaction with its quality and sensory properties (3840).

From the surveys identified EPA and DHA intakes were continually below dietary guidelines with young people, females, and pregnant mothers appearing to have some of the lowest intakes (2932, 34, 36, 37). Shortfalls become more apparent in pregnancy when guidelines have incremental changes widening the gap between intakes and recommendations (28, 29). Unfortunately, in the UK n-3 FA data is not reported as part of the NDNS-RP and the addition would be of value. Should this be undertaken it would be advised that nutritional “compositional data” should be updated first. A recent publication reports that the EPA and DHA content of farmed salmon has halved due to altered fish production methods and the replacement of marine-based fish feeds with sustainable alternatives (41). Subsequently, it is tenable that EPA and DHA intakes are even lower than values reported in this review.

Confusions and misconceptions could be further hampering intakes. From surveys identified it was consistently seen that oily fish/n-3 FA intakes were no different between pregnant and non-pregnant women. As observed by Thompson et al. oily fish intakes even declined in pregnancy (28). This uncertainty may be due to concerns about potential contaminants such as methylmercury or lack of confidence about buying and preparing seafood (42). Ongoing trepidations about sustainability and ethics of fish consumption (43) could also potentially drive future oily fish intakes down further. Healthcare professionals can play a key role in helping to clear up confusions, particularly amongst women who are pregnant and caregivers of young children (42).

In terms of perceptions, a study of 340 family physicians showed that 51 percent believed their blood n-3 FA status to be “desirable” but only 5 percent had an omega-3 index ≥8 percent indicating discrepancies between perceived and actual n-3 FA status (44). Similarly, a cross-sectional study of German and U.S adults showed that more than half were aware that n-3 FAs were beneficial for heart and brain health and could provide examples of foods sources but this “knowledge” did not correlate with n-3 FA status (45). Amongst young adults (18–25 years) research shows that EPA and DHA abbreviations were recognized by 51 and 66%, respectively, but it was not assessed whether this knowledge led to better omega-3 profiles (46).

n-3 FAs appear to be particularly important at key phases of the life-cycle. In pregnancy, supplementation with brain specific fatty acids (two Equazen Mumomega capsules daily with each capsule providing 300 mg DHA, 42 mg EPA, 150 mg n-6 evening primrose oil and 15 mg GLA vs. oleic acid placebo) has been found to augment new-born infants' brain size (47). In particular, males born to mothers taking omega-3 capsules had larger brain volumes, total gray matter, corpus callosum and cortical volumes indicating differential sex sensitivity of fetal brain to pregnancy fatty acid profiles (47).

Observational evidence has shown that low EPA/DHA levels may be connected with rising prevalence rates of development disorders in childhood such as ADHD and dyslexia (48). Amongst those with ADHD one study found that children receiving Omega-3/6 fatty acids—Equazen—delivering 558 mg EPA, 174 mg DHA, and 60 mg Gamma Linolenic Acid (GLA) in a respective ratio of 9:3:1 over a 12-month duration did not require such a high dose of methylphenidate to manage and reduce their ADHD symptoms (0.8 mg/kg/day vs. 1.0 mg/kg/day) (49). Other research has also shown that similar n-3 FA Equazen supplement improved reading ability, namely “phonologic decoding time” and “visual analysis” in mainstream children and particularly those with attention problems (50). Given this, increased awareness of the importance of n-3 FAs is needed amongst healthcare and educational professionals.

Overall, the results of this publication demonstrate that policies are needed to improve oily fish consumption and integrate supplementation strategies alongside this. The latter becomes particularly important during life stages such as pregnancy, childhood and adolescence. Should a UK analysis of n-3 intakes be conducted it seems likely that the “real picture” could be more foreboding if updated food compositional data was to be used.

Limitation and Future Directions

There are a number of limitations that may be associated with the methods adopted in the present publication. Firstly, the UK NDNS-RP only collects dietary data over a 4-day period using dietary records. It is therefore possible that some participants who were fish consumers may have simply reported during a period of 4 days when they consumed no oily fish.

Equally, when collating data on EPA and DHA there was heterogeneity between study methods e.g., dietary recalls vs. food frequency questionnaires that makes comparisons more cumbersome (34). Of these methods it has been reported elsewhere that food frequency questionnaires appear to derive suitable estimates of n-3 FA intakes (51). These methods now need to be applied to extended populations and used alongside or in replacement of 4-day food diaries to enable a more accurate estimate of long-term of n-3 intakes. Nutritional biomarkers should also ideally be used to better reflect an individual's “normal” intakes.

When extrapolating data from n-3 FA intake surveys a range of metrics were applied to represent the intake data. Some used the mean (arithmetic or geometric), others the median and different age cut-offs applied when calculating these. EPA and DHA data was also not always reported per 100 grams, with some reporting this as per 1,000 kcal (28). This makes direct comparisons difficult. Bearing this in mind there is a need to harmonize methodologies and the way in which data is presented.


The present publication has identified that UK oily fish intakes are suboptimal across the lifespan. Some of the lowest intakes were amongst children, teenagers and adults which poses a cause for concern. This appears to be coupled with inadequate global EPA and DHA intakes. Unfortunately, declining EPA and DHA profiles of farmed fish and the movement toward plant-based diets is only likely to exacerbate this already concerning situation. Urgent public health strategies are needed to promote lipid health which should also include suitable supplementation strategies.

Data Availability Statement

Publicly available datasets were analyzed in this study. This data can be found here:

Author Contributions

The author confirms being the sole contributor of this work and has approved it for publication.


The authors' time for writing this article was funded by the company Equazen, makers of evidence-based brain health supplements (see The views expressed are those of the author alone and Equazen had no role in writing the review.

Conflict of Interest

ED is the Director of Nutritional Insight, a writing consultancy.

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


The assistance of A. Kamel, Clinical Pharmacy Department, Faculty of Pharmacy, Cairo University for his input into the statistical analysis is gratefully acknowledged.


1. Gil A, Gil F. Fish, a Mediterranean source of n-3 PUFA: benefits do not justify limiting consumption. Br J Nutr. (2015) 113(Suppl. 2):S58–67. doi: 10.1017/S0007114514003742

CrossRef Full Text | Google Scholar

2. Calder PC, Yaqoob P. Omega-3 polyunsaturated fatty acids and human health outcomes. Biofactors. (2009) 35:266–72. doi: 10.1002/biof.42

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Fialkow J. Omega-3 fatty acid formulations in cardiovascular disease: dietary supplements are not substitutes for prescription products. Am J Cardiovasc Drugs. (2016) 16:229–39. doi: 10.1007/s40256-016-0170-7

CrossRef Full Text | Google Scholar

4. Monroig O, Tocher DR, Navarro JC. Biosynthesis of polyunsaturated fatty acids in marine invertebrates: recent advances in molecular mechanisms. Mar Drugs. (2013) 11:3998–4018. doi: 10.3390/md11103998

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Mori TA. Marine OMEGA-3 fatty acids in the prevention of cardiovascular disease. Fitoterapia. (2017) 123:51–8. doi: 10.1016/j.fitote.2017.09.015

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Ian Givens D, Gibbs RA. Current intakes of EPA and DHA in European populations and the potential of animal-derived foods to increase them. Proc Nutr Soc. (2008) 67:273–80. doi: 10.1017/S0029665108007167

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Cholewski M, Tomczykowa M, Tomczyk M. A comprehensive review of chemistry, sources and bioavailability of omega-3 fatty acids. Nutrients. (2018) 10:E1662. doi: 10.3390/nu10111662

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Saini RK, Keum YS. Omega-3 and omega-6 polyunsaturated fatty acids: Dietary sources, metabolism, and significance - A review. Life Sci. (2018) 203:255–67. doi: 10.1016/j.lfs.2018.04.049

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Swanson D, Block R, Mousa SA. Omega-3 fatty acids EPA and DHA: health benefits throughout life. Adv Nutr. (2012) 3:1–7. doi: 10.3945/an.111.000893

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Calder PC. Docosahexaenoic acid. Ann Nutr Metab. (2016) 69(Suppl. 1):7–21. doi: 10.1159/000448262

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Carnielli VP, Simonato M, Verlato G, Luijendijk I, De Curtis M, Sauer PJ, et al. Synthesis of long-chain polyunsaturated fatty acids in preterm newborns fed formula with long-chain polyunsaturated fatty acids. Am J Clin Nutr. (2007) 86:1323–30. doi: 10.1093/ajcn/86.5.1323

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Simopoulos AP. The importance of the ratio of omega-6/omega-3 essential fatty acids. Biomed Pharmacother. (2002) 56:365–79. doi: 10.1016/S0753-3322(02)00253-6

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Innis SM. Omega-3 fatty acid biochemistry: perspectives from human nutrition. Mil Med. (2014) 179(11 Suppl):82–7. doi: 10.7205/MILMED-D-14-00147

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Blasbalg TL, Hibbeln JR, Ramsden CE, Majchrzak SF, Rawlings RR. Changes in consumption of omega-3 and omega-6 fatty acids in the United States during the 20th century. Am J Clin Nutr. (2011) 93:950–62. doi: 10.3945/ajcn.110.006643

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Calder PC. Very long-chain n-3 fatty acids and human health: fact, fiction and the future. Proc Nutr Soc. (2018) 77:52–72. doi: 10.1017/S0029665117003950

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Stark KD, Van Elswyk ME, Higgins MR, Weatherford CA, Salem N Jr. Global survey of the omega-3 fatty acids, docosahexaenoic acid and eicosapentaenoic acid in the blood stream of healthy adults. Prog Lipid Res. (2016) 63:132–52. doi: 10.1016/j.plipres.2016.05.001

PubMed Abstract | CrossRef Full Text | Google Scholar

17. EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA). European Food Safety Authority NDA Panel Scientific opinion on dietary reference values for fats, including saturated fatty acids, polyunsaturated fatty acids, monounsaturated fatty acids, trans fatty acids, and cholesterol. EFSA J. (2010) 8:1461. doi: 10.2903/j.efsa.2010.1507

CrossRef Full Text | Google Scholar

18. FAO/WHO. Expert Consultation on Fats and Fatty Acids in Human Nutrition. Fats and Fatty Acids in Human Nutrition: Report of an Expert Consultation. Geneva: Food and Agriculture Organization of the United Nations (2010).

Google Scholar

19. Koletzko B, Lien E, Agostoni C, Böhles H, Campoy C, Cetin I, et al. The roles of long-chain polyunsaturated fatty acids in pregnancy, lactation and infancy: review of current knowledge and consensus recommendations. J Perinat Med. (2008) 36:5–14. doi: 10.1515/JPM.2008.001

PubMed Abstract | CrossRef Full Text | Google Scholar

20. SACN. Advice on Fish Consumption: Benefits & Risks. London: CoT/TSO (2004).

Google Scholar

21. PHE. NDNS: Time Trend and Income Analyses for Years 1 to 9. London: PHE (2019).

Google Scholar

22. PHE. National Diet and Nutrition Survey Years 7 and 8 (2014/15-2015/16) User Guide for UK Data. London: PHE (2018).

Google Scholar

23. NHS. Fish and Shellfish. London: NHS (2018).

Google Scholar

24. PHE. Appendix R Main and Subsidiary Food Groups and Disaggregation Categories. London: PHE (2018).

Google Scholar

25. Fitt E, Mak TN, Stephen AM, Prynne C, Roberts C, Swan G, et al. Disaggregating composite food codes in the UK National Diet and Nutrition Survey food composition databank. Eur J Clin Nutr. (2010) 64(Suppl. 3):S32–6. doi: 10.1038/ejcn.2010.207

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Kranz S, Jones NRV, Monsivais P. Intake levels of fish in the UK paediatric population. Nutrients. (2017) 9:E392. doi: 10.3390/nu9040392

PubMed Abstract | CrossRef Full Text | Google Scholar

27. MRC. Elsie Widdowson Laboratory, NatCen Social Research. National Diet and Nutrition Survey Years 1-8, 2008/09-2015/16. [data collection], 12th Edn. UK Data Service (2019). SN: 6533. Available online at:

Google Scholar

28. Thompson M, Hein N, Hanson C, Smith LM, Anderson-Berry A, Richter CK, et al. Omega-3 fatty acid intake by age, gender, and pregnancy status in the United States: National Health and Nutrition Examination Survey 2003(-)2014. Nutrients. (2019) 11:E177. doi: 10.3390/nu11010177

CrossRef Full Text | Google Scholar

29. Zhang Z, Fulgoni VL, Kris-Etherton PM, Mitmesser SH. Dietary intakes of EPA and DHA omega-3 fatty acids among US childbearing-age and pregnant women: an analysis of NHANES 2001-2014. Nutrients. (2018) 10:E416. doi: 10.3390/nu10040416

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Bishop NA, Leblanc CP. Dietary intake of DHA and EPA in a group of pregnant women in the moncton area. Can J Diet Pract Res. (2017) 78:59–65. doi: 10.3148/cjdpr-2016-033

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Nordgren TM, Lyden E, Anderson-Berry A, Hanson C. Omega-3 fatty acid intake of pregnant women and women of childbearing age in the United States: potential for deficiency? Nutrients. (2017) 9:E197. doi: 10.3390/nu9030197

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Eickstaedt M, Beck KL, Conlon CA. New Zealand women have suboptimal intakes of long chain omega-3 polyunsaturated fatty acids during pregnancy-a cross sectional study. N Z Med J. (2017) 130:37–45.

PubMed Abstract | Google Scholar

33. Richter CK, Bowen KJ, Mozaffarian D, Kris-Etherton PM, Skulas-Ray AC. Total long-chain n-3 fatty acid intake and food sources in the United States compared to recommended intakes: NHANES 2003-2008. Lipids. (2017) 52:917–27. doi: 10.1007/s11745-017-4297-3

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Sioen I, van Lieshout L, Eilander A, Fleith M, Lohner S, Szommer A, et al. Systematic review on N-3 and N-6 polyunsaturated fatty acid intake in european countries in light of the current recommendations - focus on specific population groups. Ann Nutr Metab. (2017) 70:39–50. doi: 10.1159/000456723

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Forsyth S, Gautier S, Salem N Jr. Estimated dietary intakes of arachidonic acid and docosahexaenoic acid in infants and young children living in developing Countries. Ann Nutr Metab. (2016) 69:64–74. doi: 10.1159/000448526

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Keim SA, Branum AM. Dietary intake of polyunsaturated fatty acids and fish among US children 12-60 months of age. Matern Child Nutr. (2015) 11:987–98. doi: 10.1111/mcn.12077

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Papanikolaou Y, Brooks J, Reider C, Fulgoni VL III. U.S. adults are not meeting recommended levels for fish and omega-3 fatty acid intake: results of an analysis using observational data from NHANES 2003-2008. Nutr J. (2014) 13:31. doi: 10.1186/1475-2891-13-64

CrossRef Full Text | Google Scholar

38. Dijkstra SC, Neter JE, van Stralen MM, Knol DL, Brouwer IA, Huisman M, et al. The role of perceived barriers in explaining socio-economic status differences in adherence to the fruit, vegetable and fish guidelines in older adults: a mediation study. Public Health Nutr. (2015) 18:797–808. doi: 10.1017/S1368980014001487

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Trondsen T, Scholderer J, Lund E, Eggen AE. Perceived barriers to consumption of fish among Norwegian women. Appetite. (2003) 41:301–14. doi: 10.1016/S0195-6663(03)00108-9

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Carlucci D, Nocella G, De Devitiis B, Viscecchia R, Bimbo F, Nardone G. Consumer purchasing behaviour towards fish and seafood products. Patterns and insights from a sample of international studies. Appetite. (2015) 84:212–27. doi: 10.1016/j.appet.2014.10.008

PubMed Abstract | CrossRef Full Text | Google Scholar

41. de Roos B, Sneddon AA, Sprague M, Horgan GW, Brouwer IA. The potential impact of compositional changes in farmed fish on its health-giving properties: is it time to reconsider current dietary recommendations? Public Health Nutr. (2017) 20:2042–9. doi: 10.1017/S1368980017000696

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Quam J, Casavale K. Five strategies for encouraging seafood consumption: what health professionals need to know. Home Healthc Now. (2017) 35:391–3. doi: 10.1097/NHH.0000000000000568

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Verbeke W, Vanhonacker F, Sioen I, Van Camp J, De Henauw S. Perceived importance of sustainability and ethics related to fish: a consumer behavior perspective. Ambio. (2007) 36:580–5. doi: 10.1579/0044-7447(2007)36[580:PIOSAE]2.0.CO;2

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Matusheski NV, Marshall K, Hartunian-Sowa S, McBurney MI. US family physicians overestimate personal omega-3 fatty acid biomarker status: associations with fatty fish and omega-3 supplement intake. Curr Dev Nutr. (2018) 2:nzx007. doi: 10.3945/cdn.117.002188

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Thuppal SV, von Schacky C, Harris WS, Sherif KD, Denby N, Steinbaum SR, et al. Discrepancy between knowledge and perceptions of dietary omega-3 fatty acid intake compared with the omega-3 index. Nutrients. (2017) 9:E930. doi: 10.3390/nu9090930

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Roke K, Rattner J, Brauer P, Mutch DM. Awareness of omega-3 fatty acids and possible health effects among young adults. Can J Diet Pract Res. (2018) 79:106–12. doi: 10.3148/cjdpr-2018-005

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Ogundipe E, Tusor N, Wang Y, Johnson MR, Edwards AD, Crawford MA. Randomized controlled trial of brain specific fatty acid supplementation in pregnant women increases brain volumes on MRI scans of their newborn infants. Prostaglandins Leukot Essent Fatty Acids. (2018) 138:6–13. doi: 10.1016/j.plefa.2018.09.001

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Schuchardt JP, Huss M, Stauss-Grabo M, Hahn A. Significance of long-chain polyunsaturated fatty acids (PUFAs) for the development and behaviour of children. Eur J Pediatric. (2010) 169:149–64. doi: 10.1007/s00431-009-1035-8

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Barragan E, Breuer D, Dopfner M. Efficacy and safety of omega-3/6 fatty acids, methylphenidate, and a combined treatment in children with ADHD. J Atten Disord. (2017) 21:433–41. doi: 10.1177/1087054713518239

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Johnson M, Fransson G, Östlund S, Areskoug B, Gillberg C. Omega 3/6 fatty acids for reading in children: a randomized, double-blind, placebo-controlled trial in 9-year-old mainstream schoolchildren in Sweden. J Child Psychol Psychiatry. (2017) 58:83–93. doi: 10.1111/jcpp.12614

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Overby NC, Serra-Majem L, Andersen LF. Dietary assessment methods on n-3 fatty acid intake: a systematic review. Br J Nutr. (2009) 102(Suppl. 1):S56–63. doi: 10.1017/S000711450999314X

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: oily fish, omega-3 fatty acids, dietary intakes, supplementation, health

Citation: Derbyshire E (2019) Oily Fish and Omega-3s Across the Life Stages: A Focus on Intakes and Future Directions. Front. Nutr. 6:165. doi: 10.3389/fnut.2019.00165

Received: 24 May 2019; Accepted: 04 October 2019;
Published: 12 November 2019.

Edited by:

Alessio Molfino, Sapienza University of Rome, Italy

Reviewed by:

Annette Lucy West, University of Southampton, United Kingdom
Caroline Elizabeth Childs, University of Southampton, United Kingdom

Copyright © 2019 Derbyshire. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Emma Derbyshire,

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.