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Dietary intake of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in children – a workshop report

Published online by Cambridge University Press:  26 February 2010

Berthold Koletzko*
Affiliation:
Division of Metabolic Diseases and Nutrition, Dr von Hauner Children's Hospital, University of Munich Medical Centre, Lindwurmstrasse 4, D-80337Munich, Germany
Ricardo Uauy
Affiliation:
Public Health Nutrition, London School of Hygiene and Tropical Medicine, London, UK Institute of Nutrition and Food Technology (INTA), University of Chile, Santiago, Chile
Andreu Palou
Affiliation:
Laboratory of Molecular Biology, Nutrition and Biotechnology, Universitat de les Illes Balears, Palma de Mallorca, Spain CIBER Fisiopatología de la Obesidad y Nutrición (CB06/03) (Instituto de Salud Carlos III), Palma de Mallorca, Spain
Frans Kok
Affiliation:
Division of Human Nutrition, Wageningen University, Wageningen, The Netherlands
Gerard Hornstra
Affiliation:
Nutrition and Toxicology Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands
Ans Eilander
Affiliation:
Unilever Food and Health Research Institute, Unilever R&D, Vlaardingen, The Netherlands
Diego Moretti
Affiliation:
Unilever Food and Health Research Institute, Unilever R&D, Vlaardingen, The Netherlands
Saskia Osendarp
Affiliation:
Unilever Food and Health Research Institute, Unilever R&D, Vlaardingen, The Netherlands
Peter Zock
Affiliation:
Unilever Food and Health Research Institute, Unilever R&D, Vlaardingen, The Netherlands
Sheila Innis
Affiliation:
Department of Paediatrics, University of British Columbia, Vancouver, BC, Canada
*
*Corresponding author: Professor Berthold Koletzko, fax +49 89 5160 7742, email [email protected]
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Abstract

There is controversy whether children should have a dietary supply of preformed long-chain polyunsaturated n-3 fatty acids EPA and DHA. The aims of the workshop were to review evidence for a possible benefit of a preformed EPA and/or DHA supply, of data required to set desirable intakes for children aged 2–12 years, and of research priorities. The authors concluded that EPA and DHA intakes per kg body weight may often be low in 2- to 12-year-old children, relative to intakes per kg body weight of breast-fed infants and adult intakes, but reliable data are scarce. Little information is available that increasing dietary intakes of EPA or DHA in children has benefits to physical or mental function or other health endpoints. Studies addressing EPA and DHA intakes and tissue status among groups of children with different dietary habits, and measures of relevant development and health endpoints, are needed for developing potential advice on desirable intakes of EPA and/or DHA in children. At this time it appears prudent to advise that dietary intakes in childhood are consistent with future eating patterns supporting adult health, such as prevention of metabolic disorders and CVD, supporting immune function, and reproductive health. In conclusion, the available information relating dietary EPA and DHA intakes in children aged 2–12 years to growth, development and health is insufficient to derive dietary intake recommendations for EPA and DHA. Adequately designed studies addressing dietary intakes, measures of status and relevant functional or health effects across this age group are needed.

Type
Full Papers
Copyright
Copyright © The Authors 2010

Several national and international organisations have provided guidance on desirable dietary intakes of the long-chain PUFA DHA and EPA from fish for adults and for infants (Table 1). For adults, these recommendations are based mainly on primary and secondary prevention of CVD, ranging from one to two portions of fatty fish per week or about 500 mg EPA and DHA per d(Reference Mozaffarian and Rimm1, Reference Kris-Etherton and Innis2). For pregnant and lactating women, the advice of an average daily intake of at least 200 mg DHA is based on optimal pregnancy outcomes(Reference Szajewska, Horvath and Koletzko3Reference Makrides, Duley and Olsen5), and on possible beneficial effects on fetal and infant development(Reference Koletzko, Cetin and Brenna6, Reference Koletzko, Lien and Agostoni7). For infants (0–2 years of age), in 1994, the FAO/WHO(8) recommended 20 mg DHA per kg body weight per d for optimal growth and development. However, there are no agreed recommendations for the advisable dietary intake of EPA and/or DHA for children above 2 years of age.

Table 1 Recommendations for daily intake of DHA and EPA in adults and infants

BW, body weight; CNERNA-CNRS, Centre Nationale d'Etudes et de Recommendations sur la Nutrition et l'Alimentation & Centre National de la Recherche Scientifique; AA, arachidonic acid.

* Supported by Perinatal Lipid Nutrition Project, Early Nutrition Programming Project, Child Health Foundation, Diabetic Pregnancy Study Group, European Association of Perinatal Medicine, European Society for Clinical Nutrition and Metabolism, European Society for Paediatric Gastroenterology, Hepatology and Nutrition, International Federation of Placenta Associations, and International Society for the Study of Fatty Acids and Lipids.

A workshop was organised in July 2007 to review and discuss the available evidence on dietary intakes of EPA and DHA and their potential physiological relevance to growth and health in children, and to evaluate whether there are sufficient scientific data for issuing evidence-based guidelines on EPA and DHA intake in 2- to 12-year-old children. The present paper summarises the outcomes of the discussions held at the workshop on current knowledge of dietary intakes among children 2–12 years of age and published literature regarding the potential importance of EPA and DHA at this stage of the life cycle.

EPA and DHA intakes in children

The richest food sources of both EPA and DHA are fatty fish, with smaller amounts in lean fish and other seafood(Reference Innis and Elias9, Reference Meyer, Mann and Lewis10). The distributions of dietary EPA and DHA intakes within populations are generally skewed with lower median than mean intakes, explained by a substantial number of individuals eating no or very little fish(Reference Meyer, Mann and Lewis10Reference Welch, Lund and Amiano12). However, information of dietary intakes of EPA and DHA, particularly among children, is limited. This has several reasons, including the limitations of dietary intake methodology, collecting accurate information on dietary intakes from children, and the completeness of fatty acid data on foods listed in databases. For example, the fat and fatty acid composition of fish varies widely, meaning that specific information on the types of fish and seafood consumed is essential; eggs can be an important source of fatty acids and are often hidden in other foods such as cakes and puddings, but depending on the recall method their intake may be missed. Moreover, children frequently consume food outside of the home, and without the parents' knowledge.

The rather limited available information on dietary intake in children suggests that EPA and DHA intake tends to be lower than in adults(13). Similarly, the intake of children may also be lower per kg body weight than in infants who are breast-fed or fed infant formulas containing DHA(Reference Koletzko, Lien and Agostoni7, Reference Koletzko, Rodriguez-Palmero and Demmelmair14). Children's current dietary intake of EPA and DHA may also be lower than some decades ago(Reference Ailhaud, Massiera and Weill15). Whether current intakes of EPA and DHA among children are adequate for optimal functional and health outcomes requires information on dietary intakes of children following different diets together with measures of functional endpoints sensitive to potential biological effects of these fatty acids. It is conceivable that EPA and/or DHA intakes might contribute to health promotion and chronic disease prevention, but reliable and comparable data on dietary intake of n-3 fatty acids and on biochemical markers of status in different populations of children are scarce. The available data do not allow us to conclude that changing intakes of EPA and/or DHA can affect physical or mental development or yield specific functional benefits.

The effects of EPA and DHA on biological function, health and prevention of disease

Historically, recommended intake levels for nutrients have been defined to prevent signs of deficiency in the general population. In recent years, however, nutritional recommendations and guidelines are being progressively formulated based on evidence linking specific nutrients at given intakes to disease prevention and optimal performance and health(16). An example is the Acceptable Macronutrient Distribution Range used by the Institute of Medicine(17), which represents the range of energy intakes from the different macronutrient intakes that, when consumed as part of a diet providing an appropriate amount of energy to maintain ideal body weight, are associated with low risk of chronic disease.

Individuals that have low EPA and/or DHA intakes but eat plentiful sources of α-linolenic acid, such as vegans and vegetarians, do have a lower EPA and DHA status than omnivores, but are not known to develop signs of deficiency(Reference Davis and Kris-Etherton18). Higher intake levels of EPA and DHA have been associated with a range of possible physiological and health benefits in humans(Reference Akabas and Deckelbaum19), such as the improvement in neurological functions in infancy(Reference Cheatham, Colombo and Carlson20), the primary and secondary prevention of CVD and the metabolic syndrome in adults(Reference Mozaffarian and Rimm1, Reference Carpentier, Portois and Malaisse21), modulation of immune response(Reference Sijben and Calder22) and improved pregnancy outcomes(Reference Szajewska, Horvath and Koletzko3Reference Makrides, Duley and Olsen5). The evidence for beneficial effects of EPA and DHA intakes on health outcomes in children is limited and will be summarised here.

The importance of attaining optimal brain and retina DHA for visual and neurological development and function is considered critical in the perinatal period(Reference Eilander, Hundscheid and Osendarp23). Beyond infancy, evidence linking DHA intake or blood levels of DHA with neurological benefits is limited to children following restricted diets with very low dietary intakes of EPA and DHA, such as children with phenylketonuria(Reference Beblo, Reinhardt and Muntau24Reference Agostoni, Massetto and Biasucci26). These studies show that increasing DHA status with fish oil supplements is consistent with improvements in speed of information processing in the central nervous system as assessed by latencies of visual evoked potentials(Reference Beblo, Reinhardt and Muntau24), as well as significant improvements of coordination and fine motor skills(Reference Beblo, Reinhardt and Demmelmair25). These findings indicate that a continuous dietary supply of preformed DHA and/or EPA may be essential for achieving optimal neural function even in children who have a high intake of the precursor α-linolenic acid with restricted diets due to phenylketonuria(Reference Agostoni, Verduci and Massetto27). This conclusion may be relevant for healthy children as well, since children with early treated phenylketonuria are generally healthy and have no detectable alterations of energy and fatty acid metabolism.

EPA and DHA in combination with n-6 fatty acids have also been reported to improve behaviour in children with neurodevelopmental disorders such as attention-deficit hyperactivity disorder and dyspraxia in some(Reference Stevens, Zhang and Peck28Reference Richardson and Montgomery30) but not all(Reference Hirayama, Hamazaki and Terasawa31, Reference Voigt, Llorente and Jensen32) studies. A recent systematic review of these studies concluded that there is insufficient evidence to identify any effect of nutrition, diet and dietary change on learning, education or performance of school-aged children from the developed world(Reference Ells, Hillier and Summerbell33). Further research of high quality, representative of all populations, undertaken for longer durations and using universal standardised measures of educational attainment is needed(Reference Ells, Hillier and Summerbell33) and should evaluate the potential relative roles of EPA and DHA, respectively, in children with neurodevelopmental disorders.

High intakes of EPA and/or DHA may beneficially modulate the immune system by decreasing the synthesis of pro-inflammatory arachidonic acid-derived eicosanoids(Reference Calder34) and by shifting the balance of T helper 1 (Th1), T helper 2 (Th2) and T regulatory cells(Reference Krauss-Etschmann, Hartl and Rzehak35). Evidence for beneficial effects on asthma in children is not established, but some studies suggested that for certain subgroups of respondent children, symptoms of asthma may be alleviated with DHA/EPA supplementation(Reference Nagakura, Matsuda and Shichijyo36). It is unclear to what extent these and other observations using high dosages of EPA and DHA supplements relate to possible effects with lower intakes achieved with foods.

A regular intake of fatty fish is widely advised to adult populations for the prevention of CVD, and a large part of associated beneficial effects is thought to be mediated by the supply of EPA and DHA with fatty fish(Reference Mozaffarian and Rimm1). Potential beneficial effects of EPA and DHA intakes in children on their future risk of developing CVD have not been documented. However, food preferences and eating habits that are established in childhood appear to show a certain degree of tracking into adulthood(Reference Parsons, Manor and Power37, Reference Lanigan, Turnbull and Singhal38). Therefore, it seems desirable to accustom children to dietary patterns that are likely to promote health in adulthood.

Approaches to develop possible advice on dietary intakes of EPA and DHA

Advice on dietary nutrient intake values for children is based on a variety of different methodological approaches, including consideration of deficiency states, usual intake levels, factorial approaches to calculate needs for maintenance and growth, effects on physiological function and health(Reference Prentice, Branca and Decsi39) and extrapolation from reference values established for other age groups such as adults or infants(Reference Atkinson and Koletzko40). The authors of the present paper conclude that the current lack of reliable data on the relationship between EPA and DHA intake or status and functional and health outcomes in 2- to 12-year-old children does not allow determination of physiological requirements or nutrient intake levels using classical approaches to derive dietary recommendations. Extrapolating n-3 fatty acid intake levels, including those for EPA and DHA, for children from existing reference values for either adults or infants (Table 1) seems inappropriate, not only because there is still considerable uncertainty regarding nutrient intake levels for DHA and/or EPA in both adults and infants, but also because extrapolation based for example on body mass or energy expenditure is expected to inadequately reflect age-specific physiological requirements, such as continuing neurological development and lean tissue growth, that determine dietary nutrient needs(Reference Atkinson and Koletzko40). Thus, at present the available evidence is insufficient to formulate quantitative nutrient intake values for EPA and DHA in children. However, it seems reasonable that dietary advice for children should be consistent with advice for the adult population, such as regular intake of one to two fatty fish meals per week providing DHA and EPA associated with the risk reduction of CVD. If such a habit can be established early in life and be maintained, it may also support a desirable long-chain n-3 fatty acid supply among females of child-bearing age to support optimal pregnancy outcomes. There is no reason why children in a family setting should be excluded from the consumption of at least one to two meals of fatty fish per week, which is recommended for the adult population(Reference Kris-Etherton and Innis2).

Present and future research

The possible relationships between intake and effects of DHA and/or EPA need to be studied in detail. Presently, the research project ‘Nutrition and Mental Health’ funded by the European Commission's 7th Framework Research Programme will try to establish whether there is a relationship between the level of dietary DHA supply and neurological functions in children. Further studies should also include evaluating effects of the intake of α-linolenic acid, as well as factors affecting its endogenous conversion to EPA and DHA, such as the concomitant intake of linoleic acid(Reference Blank, Neumann and Makrides41) and the role of genetic polymorphisms of the desaturating enzymes Δ-6 and Δ-5 desaturases(Reference Schaeffer, Gohlke and Muller42).

Relevant public health outcomes that are likely to be linked to lifelong intakes of EPA and DHA include the risk of (future) CVD and the metabolic syndrome, optimal mental development and behaviour, and immune response.

Dietary studies should be carefully conducted and analysed, with a specific and standardised methodology, considering the substantial challenges in assessing individual intakes of EPA and DHA in children. Since assessment methods for dietary intake are imprecise, age-specific information on fatty acid status based on biological markers are also required. Cross-sectional analyses from prospective birth and childhood cohort studies are likely to provide valuable insights that can contribute to designing intervention trials. Age-specific effects of different fatty acid intakes and dosages on relevant endpoints should be assessed in controlled intervention studies. The data obtained should aim at establishing the effect of different doses of individual fatty acids, and of different combinations and ratios of PUFA, on well-defined and quantifiable outcomes. Such outcomes may include:

  1. (1) Markers of cardiovascular risk and the metabolic syndrome;

  2. (2) Measures of neural function, cognition and behaviour;

  3. (3) Markers of inflammatory response, immune function and their related diseases, such as allergy or autoimmune disease.

Studies in children aiming at evaluating these and other outcomes must respect the limitations determined by the ethical rules for research with children(Reference Ungar, Joffe and Kodish43, Reference Knudson44).

Although recent risk analyses tend to support the safety and overall benefit of increased fish consumption(Reference Cohen, Bellinger and Connor45, Reference Sioen, De and Verbeke46), potential adverse effects of recommending increased dietary intakes of EPA and DHA from fish oil concentrates or fatty fish, such as the risk of adverse effects of contamination with environmental pollutants(Reference Oken, Radesky and Wright47, Reference Halldorsson, Meltzer and Thorsdottir48), should be taken into account.

Conclusions

A better understanding of the functional roles of EPA and DHA in children is required in order to determine adequate dietary intakes. Currently there is a lack of sufficient evidence to link levels of dietary intake of DHA and/or EPA to improved physical, mental or other functional benefits in children. Therefore, quantitative dietary intake recommendations for children cannot be established at this time.

Food-based dietary guidelines that apply to adults for enhancing health and preventing chronic diseases such as CVD will usually apply to the whole population, including children, unless there are specific arguments for alternative guidelines or recommendations. There is no reason why children should be excluded from the advice to consume at least one to two meals of fatty fish per week as recommended for adults. Establishing a quantitative dietary intake recommendation for EPA and DHA for children aged 2–12 years will require a research programme focusing on well-defined, public health-relevant and age-specific outcomes in this specific age group.

Acknowledgements

All authors reviewed and discussed the available evidence on dietary intakes of EPA and DHA and agreed on the conclusions at the workshop held in July 2007. B. K., A. E., D. M. and S. I. wrote the first draft of the manuscript. All authors reviewed and contributed to the revision of the manuscript.

S. O., D. M., A. E. and P. Z. are employees of Unilever. Unilever markets foods, among which products rich in n-3 fatty acids. Unilever Food and Health Research Institute organised and funded the workshop attended by all authors.

Research by B. K. on functional effects of EPA and DHA has been carried out with partial financial support from the Commission of the European Communities, within the 7th Framework Programme, contract no. FP7-212652. This paper does not necessarily reflect the views of the Commission and in no way anticipates future policy in this area.

B. K. and S. I. are recipients of Freedom-to-Discover Awards of the Bristol-Myers-Squibb Foundation (New York, NY, USA).

R. U. was President of the International Union of Nutrition Sciences (IUNS), he does not receive personal income from Unilever, his research funding comes from the Wellcome Trust and the Chilean Council for Scientific and Technological Development; he declares no conflicting interests relative to the content of this paper.

References

1Mozaffarian, D & Rimm, EB (2006) Fish intake, contaminants, and human health: evaluating the risks and the benefits. JAMA 296, 18851899.CrossRefGoogle ScholarPubMed
2Kris-Etherton, PM & Innis, S (2007) Position of the American Dietetic Association and Dietitians of Canada: dietary fatty acids. J Am Diet Assoc 107, 15991611.Google ScholarPubMed
3Szajewska, H, Horvath, A & Koletzko, B (2006) Effect of n-3 long-chain polyunsaturated fatty acid supplementation of women with low-risk pregnancies on pregnancy outcomes and growth measures at birth: a meta-analysis of randomized controlled trials. Am J Clin Nutr 83, 13371344.CrossRefGoogle ScholarPubMed
4Horvath, A, Koletzko, B & Szajewska, H (2007) Effect of supplementation of women in high-risk pregnancies with long-chain polyunsaturated fatty acids on pregnancy outcomes and growth measures at birth: a meta-analysis of randomized controlled trials. Br J Nutr 98, 253259.Google Scholar
5Makrides, M, Duley, L & Olsen, SF (2006) Marine oil, and other prostaglandin precursor, supplementation for pregnancy uncomplicated by pre-eclampsia or intrauterine growth restriction. The Cochrane Database of Systematic Reviews 2006, issue 3, CD003402. http://www.mrw.interscience.wiley.com/cochrane/clsysrev/articles/CD003402/frame.html.Google Scholar
6Koletzko, B, Cetin, I & Brenna, JT (2007) Dietary fat intakes for pregnant and lactating women. Br J Nutr 98, 873877.Google Scholar
7Koletzko, B, Lien, E, Agostoni, C, et al. (2008) The roles of long-chain polyunsaturated fatty acids in pregnancy, lactation and infancy: review of current knowledge and consensus recommendations. J Perinat Med 36, 514.CrossRefGoogle ScholarPubMed
8Food and Agriculture Organization & World Health Organization (1994) Fats and Oils in Human Nutrition. FAO Food and Nutrition Paper no. 57. Rome: FAO.Google Scholar
9Innis, SM & Elias, SL (2003) Intakes of essential n-6 and n-3 polyunsaturated fatty acids among pregnant Canadian women. Am J Clin Nutr 77, 473478.Google Scholar
10Meyer, BJ, Mann, NJ, Lewis, JL, et al. (2003) Dietary intakes and food sources of omega-6 and omega-3 polyunsaturated fatty acids. Lipids 38, 391398.CrossRefGoogle ScholarPubMed
11Astorg, P, Arnault, N, Czernichow, S, et al. (2004) Dietary intakes and food sources of n-6 and n-3 PUFA in French adult men and women. Lipids 39, 527535.Google Scholar
12Welch, AA, Lund, E, Amiano, P, et al. (2002) Variability of fish consumption within the 10 European countries participating in the European Investigation into Cancer and Nutrition (EPIC) study. Public Health Nutr 5, 12731285.Google Scholar
13United States Department of Agriculture Agricultural Research Service (2007) Nutrient Intakes from Food: Mean Amounts Consumed per Individual, One Day, 2003–2004. http://www.ars.usda.gov/SP2UserFiles/Place/12355000/pdf/0506/Table_2_NIF_05.pdf.Google Scholar
14Koletzko, B, Rodriguez-Palmero, M, Demmelmair, H, et al. (2001) Physiological aspects of human milk lipids. Early Hum Dev 65, Suppl., S3S18.CrossRefGoogle ScholarPubMed
15Ailhaud, G, Massiera, F, Weill, P, et al. (2006) Temporal changes in dietary fats: role of n-6 polyunsaturated fatty acids in excessive adipose tissue development and relationship to obesity. Prog Lipid Res 45, 203236.CrossRefGoogle ScholarPubMed
16World Health Organization & Food and Agriculture Organization (2004) Vitamin and Mineral Requirements in Human Nutrition. Joint FAO/WHO Expert Consultation on Human Vitamin and Mineral Requirements. Geneva: WHO/FAO.Google Scholar
17Institute of Medicine (2005) Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients). Washington, DC: The National Academies Press.Google Scholar
18Davis, BC & Kris-Etherton, PM (2003) Achieving optimal essential fatty acid status in vegetarians: current knowledge and practical implications. Am J Clin Nutr 78, 640S646S.CrossRefGoogle ScholarPubMed
19Akabas, SR & Deckelbaum, RJ (2006) Summary of a workshop on n-3 fatty acids: current status of recommendations and future directions. Am J Clin Nutr 83, 1536S1538S.Google Scholar
20Cheatham, CL, Colombo, J & Carlson, SE (2006) n-3 Fatty acids and cognitive and visual acuity development: methodologic and conceptual considerations. Am J Clin Nutr 83, 1458S1466S.Google Scholar
21Carpentier, YA, Portois, L & Malaisse, WJ (2006) n-3 Fatty acids and the metabolic syndrome. Am J Clin Nutr 83, 1499S1504S.CrossRefGoogle ScholarPubMed
22Sijben, JWC & Calder, PC (2007) Differential immunomodulation with long-chain n-3 PUFA in health and chronic disease. Proc Nutr Soc 66, 237259.Google Scholar
23Eilander, A, Hundscheid, DC, Osendarp, SJ, et al. (2007) Effects of n-3 long chain polyunsaturated fatty acid supplementation on visual and cognitive development throughout childhood: a review of human studies. Prostaglandins Leukot Essent Fatty Acids 76, 189203.CrossRefGoogle ScholarPubMed
24Beblo, S, Reinhardt, H, Muntau, AC, et al. (2001) Fish oil supplementation improves visual evoked potentials in children with phenylketonuria. Neurology 57, 14881491.CrossRefGoogle ScholarPubMed
25Beblo, S, Reinhardt, H, Demmelmair, H, et al. (2007) Effect of fish oil supplementation on fatty acid status, coordination, and fine motor skills in children with phenylketonuria. J Pediatr 150, 479484.Google Scholar
26Agostoni, C, Massetto, N, Biasucci, G, et al. (2000) Effects of long-chain polyunsaturated fatty acid supplementation on fatty acid status and visual function in treated children with hyperphenylalaninemia. J Pediatr 137, 504509.CrossRefGoogle ScholarPubMed
27Agostoni, C, Verduci, E, Massetto, N, et al. (2003) Long term effects of long chain polyunsaturated fats in hyperphenylalaninemic children. Arch Dis Child 88, 582583.Google Scholar
28Stevens, L, Zhang, W, Peck, L, et al. (2003) EFA supplementation in children with inattention, hyperactivity, and other disruptive behaviors. Lipids 38, 10071021.Google Scholar
29Richardson, AJ & Puri, BK (2002) A randomized double-blind, placebo-controlled study of the effects of supplementation with highly unsaturated fatty acids on ADHD-related symptoms in children with specific learning difficulties. Prog Neuropsychopharmacol Biol Psychiatry 26, 233239.CrossRefGoogle ScholarPubMed
30Richardson, AJ & Montgomery, P (2005) The Oxford–Durham study: a randomized, controlled trial of dietary supplementation with fatty acids in children with developmental coordination disorder. Pediatrics 115, 13601366.CrossRefGoogle ScholarPubMed
31Hirayama, S, Hamazaki, T & Terasawa, K (2004) Effect of docosahexaenoic acid-containing food administration on symptoms of attention-deficit/hyperactivity disorder – a placebo-controlled double-blind study. Eur J Clin Nutr 58, 467473.Google Scholar
32Voigt, RG, Llorente, AM, Jensen, CL, et al. (2001) A randomized, double-blind, placebo-controlled trial of docosahexaenoic acid supplementation in children with attention-deficit/hyperactivity disorder. J Pediatr 139, 189196.Google Scholar
33Ells, LJ, Hillier, FC & Summerbell, CD (2007) A Systematic Review of the Effect of Nutrition, Diet and Dietary Change on Learning, Education and Performance of Children of Relevance to UK Schools. Middlesbrough, UK: University of Teesside, School of Health & Social Care, Centre for Food, Physical Activity and Obesity Research.Google Scholar
34Calder, PC (2006) n-3 Polyunsaturated fatty acids, inflammation, and inflammatory diseases. Am J Clin Nutr 83, 1505S1519S.Google Scholar
35Krauss-Etschmann, S, Hartl, D, Rzehak, P, et al. (2008) Decreased cord blood IL-4, IL-13, and CCR4 and increased TGF-β levels after fish oil supplementation of pregnant women. J Allergy Clin Immunol 121, 464470.CrossRefGoogle ScholarPubMed
36Nagakura, T, Matsuda, S, Shichijyo, K, et al. (2000) Dietary supplementation with fish oil rich in omega-3 polyunsaturated fatty acids in children with bronchial asthma. Eur Respir J 16, 861865.Google Scholar
37Parsons, TJ, Manor, O & Power, C (2006) Physical activity and change in body mass index from adolescence to mid-adulthood in the 1958 British cohort. Int J Epidemiol 35, 197204.Google Scholar
38Lanigan, J, Turnbull, B & Singhal, A (2007) Toddler diets in the UK: deficiencies and imbalances. 2. Relationship of toddler diet to later health. J Fam Health Care 17, 197200.Google ScholarPubMed
39Prentice, A, Branca, F, Decsi, T, et al. (2004) Energy and nutrient dietary reference values for children in Europe: methodological approaches and current nutritional recommendations. Br J Nutr 92, Suppl. 2, S83S146.Google Scholar
40Atkinson, SA & Koletzko, B (2007) Determining life-stage groups and extrapolating nutrient intake values (NIVs). Food Nutr Bull 28, S61S76.Google Scholar
41Blank, C, Neumann, MA, Makrides, M, et al. (2002) Optimizing DHA levels in piglets by lowering the linoleic acid to α-linolenic acid ratio. J Lipid Res 43, 15371543.Google Scholar
42Schaeffer, L, Gohlke, H, Muller, M, et al. (2006) Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids. Hum Mol Genet 15, 17451756.Google Scholar
43Ungar, D, Joffe, S & Kodish, E (2006) Children are not small adults: documentation of assent for research involving children. J Pediatr 149, S31S33.Google Scholar
44Knudson, PL (2002) Research with children. Arch Med Res 33, 203204.CrossRefGoogle ScholarPubMed
45Cohen, JT, Bellinger, DC, Connor, WE, et al. (2005) A quantitative risk–benefit analysis of changes in population fish consumption. Am J Prev Med 29, 325334.Google Scholar
46Sioen, I, De, HS, Verbeke, W, et al. (2008) Fish consumption is a safe solution to increase the intake of long-chain n-3 fatty acids. Public Health Nutr 11, 11071116.Google Scholar
47Oken, E, Radesky, JS, Wright, RO, et al. (2008) Maternal fish intake during pregnancy, blood mercury levels, and child cognition at age 3 years in a US cohort. Am J Epidemiol 167, 11711181.Google Scholar
48Halldorsson, TI, Meltzer, HM, Thorsdottir, I, et al. (2007) Is high consumption of fatty fish during pregnancy a risk factor for fetal growth retardation? A study of 44 824 Danish pregnant women. Am J Epidemiol 166, 687696.Google Scholar
49Agence Française de Sécurité Sanitaire des Aliments, Centre Nationale d'Etudes et de Recommendations sur la Nutrition et l'Alimentation & Centre National de la Recherche Scientifique (2001) Apports Nutritionnels Conseilles pour la Population Française (Dietary Advice for the French Population), 3rd ed.Paris: Editions Tec & Doc.Google Scholar
50Health Council of The Netherlands (2001) Dietary Reference Intakes: Energy, Proteins, Fats, and Digestible Carbohydrates, publication no. 2001/19. The Hague: Health Council of The Netherlands.Google Scholar
51Rajala, M (2001) Nutrition and diet for healthy lifestyles in Europe: science and policy implications. Public Health Nutr 4, 339340.Google ScholarPubMed
52World Health Organization (2003) Diet, Nutrition and the Prevention of Chronic Diseases. Joint WHO/FAO Expert Consultation. WHO Technical Report Series no. 916. Geneva: WHO.Google Scholar
53UK Scientific Advisory Committee on Nutrition (2004) Advice on Fish Consumption: Benefits and Risks. London: The Stationery Office.Google Scholar
54Cunnane, SC, Drevon, CA, Harris, B, et al. (2004) Recommendations for Intake of Polyunsaturated Fatty Acids in Healthy Adults. Tiverton, UK: International Society for the Study of Fatty Acids and Lipids.Google Scholar
55Brasseur, D, Delzenne, N, Henderickx, H, et al. (2004) Recommandations et Allégations Concernant les Acides Gras Oméga-3 (Recommendations and Claims Concerning Omega-3 Fatty Acids). Brussels: Conseil Supérieur d'Hygiène.Google Scholar
56Deutsche Gesellschaft für Ernährung (German Nutrition Society) (2005) Nutrition Report 2004. Bonn: DGE.Google Scholar
Figure 0

Table 1 Recommendations for daily intake of DHA and EPA in adults and infants