Advertising Disclaimer
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Helland, I. B.
Right arrow Articles by Drevon, C. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Helland, I. B.
Right arrow Articles by Drevon, C. A.
Related Collections
Right arrow Nutrition & Metabolism
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

PEDIATRICS Vol. 111 No. 1 January 2003, pp. e39-e44


ELECTRONIC ARTICLE

Maternal Supplementation With Very-Long-Chain n-3 Fatty Acids During Pregnancy and Lactation Augments Children’s IQ at 4 Years of Age

Ingrid B. Helland, MD*,{ddagger}, Lars Smith, PhD§, Kristin Saarem, PhD||, Ola D. Saugstad, MD, PhD{ddagger}, Christian A. Drevon, MD, PhD*

* Institute for Nutrition Research
{ddagger} Department of Pediatric Research
§ Institute of Psychology, University of Oslo, Oslo, Norway
|| Peter Möller, avd Orkla, ASA, Oslo, Norway

-->
    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
Objectives. Docosahexaenoic acid (DHA; 22:6 n-3) and arachidonic acid (AA; 20:4 n-6) are important for development of the central nervous system in mammals. There is a growth spurt in the human brain during the last trimester of pregnancy and the first postnatal months, with a large increase in the cerebral content of AA and DHA. The fetus and the newborn infant depend on maternal supply of DHA and AA. Our hypothesis was that maternal intake of DHA during pregnancy and lactation is marginal and that high intake of this fatty acid would benefit the child. We examined the effect of supplementing pregnant and lactating women with very-long-chain n-3 polyunsaturated fatty acids (PUFAs; cod liver oil) on mental development of the children, compared with maternal supplementation with long-chain n-6 PUFAs (corn oil).

Methods. The study was randomized and double-blinded. Pregnant women were recruited in week 18 of pregnancy to take 10 mL of cod liver oil or corn oil until 3 months after delivery. The cod liver oil contained 1183 mg/10 mL DHA, 803 mg/10 mL eicosapentaenoic acid (20:5 n-3), and a total of 2494 mg/10 mL {sum} n-3 PUFAs. The corn oil contained 4747 mg/10 mL linoleic acid (18:2 n-6) and 92 mg/10 mL {alpha}-linolenic acid (18:3 n-3). The amount of fat-soluble vitamins was identical in the 2 oils (117 µg/mL vitamin A, 1 µg/mL vitamin D, and 1.4 mg/mL dl-{alpha}-tocopherol). A total of 590 pregnant women were recruited to the study, and 341 mothers took part in the study until giving birth. All infants of these women were scheduled for assessment of cognitive function at 6 and 9 months of age, and 262 complied with the request. As part of the protocol, 135 subjects from this population were invited for intelligence testing with the Kaufman Assessment Battery for Children (K-ABC) at 4 years of age. Of the 135 invited children, 90 came for assessment. Six children did not complete the examination. The K-ABC is a measure of intelligence and achievement designed for children aged 2.5 years through 12.5 years. This multisubtest battery comprises 4 scales: Sequential Processing, Simultaneous Processing, Achievement (not used in the present study), and Nonverbal Abilities. The Sequential Processing and Simultaneous Processing scales are hypothesized to reflect the child’s style of problem solving and information processing. Scores from these 2 scales are combined to form a Mental Processing Composite, which serves as the measure of intelligence in the K-ABC.

Results. We received dietary information from 76 infants (41 in the cod liver oil group and 35 in the corn oil group), documenting that all of them were breastfed at 3 months of age. Children who were born to mothers who had taken cod liver oil (n = 48) during pregnancy and lactation scored higher on the Mental Processing Composite of the K-ABC at 4 years of age as compared with children whose mothers had taken corn oil (n = 36; 106.4 [7.4] vs 102.3 [11.3]). The Mental Processing Composite score correlated significantly with head circumference at birth (r = 0.23), but no relation was found with birth weight or gestational length. The children’s mental processing scores at 4 years of age correlated significantly with maternal intake of DHA and eicosapentaenoic acid during pregnancy. In a multiple regression model, maternal intake of DHA during pregnancy was the only variable of statistical significance for the children’s mental processing scores at 4 years of age.

Conclusion. Maternal intake of very-long-chain n-3 PUFAs during pregnancy and lactation may be favorable for later mental development of children.

Key Words: dietary supplements • n-3 fatty acids • docosahexaenoic acid • arachidonic acid • pregnancy • breastfeeding • intelligence test • K-ABC

Abbreviations: DHA, docosahexaenoic acid • AA, arachidonic acid • PUFA, polyunsaturated fatty acid • K-ABC, Kaufman Assessment Battery for Children • EPA, eicosapentaenoic acid


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
Docosahexaenoic acid (DHA; 22:6 n-3) and arachidonic acid (AA; 20:4 n-6) are important for development of the central nervous system in mammals.1,2 There is a growth spurt in the human brain during the last trimester of pregnancy and the first postnatal months, with a large increase in the cerebral content of AA and DHA. The capacity for elongation and desaturation of {alpha}-linolenic acid (18:3 n-3) to DHA is inadequate in the fetus and the newborn.36 Maternal very-long-chain polyunsaturated fatty acid (PUFA) status during pregnancy is critical for the very-long-chain PUFA status in the newborn,7 and newborn infants depend on dietary supply of these fatty acids.8,9 In contrast to most formulas, breast milk contains DHA and AA, but the concentrations of these very-long-chain PUFAs are variable, depending on the mother’s diet.1012

Several studies have shown a positive correlation between breastfeeding and cognitive development.1317 Lucas et al13,15 indicated that breast milk includes biological factors that may be beneficial for mental development in preterm infants. This may be attributable to AA and DHA in the breast milk. However, studies on the effect of adding preformed very-long-chain n-3 and n-6 PUFAs to infant formulas have been inconclusive, because some studies of visual acuity, problem solving, and general neurologic development found enhanced performance,6,1822 whereas others showed no effect in term infants.2326 In 1 study, infants who received formula with DHA and without AA scored lower than infants in the breast milk or control formula groups on language assessments at 14 months of age.27 Similar studies have been performed on infants who were born prematurely. Premature infants are probably more vulnerable to DHA deficiency than are term infants, because they do not receive the third-trimester intrauterine supply of DHA. They have small tissue stores, the metabolic transformation via elongation and desaturation of fatty acids is insufficient, and the intake of DHA from infant formulas is small.4,5 Supplementation with DHA to premature infants may increase early maturation of visual function and information processing.2830

In the present study, we tested the hypothesis that maternal intake of very-long-chain n-3 PUFAs is marginal and that the fetus and the newborn infant will benefit from increasing the mother’s intake during pregnancy and lactation. Pregnant women were supplemented with very-long-chain n-3 PUFAs (cod liver oil) or n-6 long-chain PUFAs (corn oil) from 18 weeks of pregnancy, and the children were examined at 4 years of age with an intelligence test.


    METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
Study Design
Pregnant women were enrolled between December 1994 and October 1996 at Rikshospitalet University Hospital and Baerum Central Hospital in the Oslo, Norway, area. Inclusion and exclusion criteria are listed in Table 1. The participating infants were followed up in the present study after examination of the effect of supplementing mothers with very-long-chain n-3 PUFAs on birth weight, gestational length, and infant development during first year of life.31 A total of 341 mothers took part in the study until giving birth. All infants of these women were scheduled for assessment of cognitive function at 6 and 9 months of age, and 262 complied with the request. As part of the protocol, 135 subjects from this population were invited for intelligence testing with the Kaufman Assessment Battery for Children (K-ABC) at 4 years of age.32 Of the 135 invited children, 90 came for assessment. Six children did not complete the examination.


View this table:
[in this window]
[in a new window]
 
TABLE 1. Inclusion and Exclusion Criteria

 
The mothers randomly received either 10 mL/d cod liver oil or 10 mL/d corn oil from 18 weeks of pregnancy until 3 months after delivery. Peter Möller (Oslo, Norway) supplied both oils. The cod liver oil contained 1183 mg/10 mL DHA, 803 mg/10 mL eicosapentaenoic acid (EPA; 20:5 n-3), and a total of 2494 mg/10 mL {sum} n-3 PUFAs. The corn oil contained 4747 mg/10 mL linoleic acid (18:2 n-6) and 92 mg/10 mL {alpha}-linolenic acid.31 The amount of fat-soluble vitamins was identical in the 2 oils (117 µg/mL vitamin A, 1 µg/mL vitamin D, and 1.4 mg/mL dl-{alpha}-tocopherol). Norwegian guidelines for infant nutrition recommend that all infants receive 5 mL of cod liver oil daily from 4 weeks of age.

The study was double-blinded, and a computer program conducted the randomization. The participating women received written information and consented to enroll in the study, which was approved by the regional ethics committee. Information about the mothers was collected from pregnancy records and from food frequency questionnaires. Characteristics of the infants were collected from birth records and information given by the mothers via questionnaires.

Blood and Milk Samples
Blood samples were collected from the umbilical cords and from the infants by venipuncture at the age of 4 weeks and 3 months. Milk samples were collected at 4 weeks and 3 months after delivery. The samples were taken from a morning feed (never the first one), 3 to 5 minutes after the infant started suckling. The samples were collected the day before they were provided to the hospital and kept in a home refrigerator until the next day when they were frozen at -70°C under nitrogen. Before storage, the samples were sonicated, and ethylenediaminetetraacetic acid and butylated hydroxytoluene were added to a final concentration of 1.85 mg/mL and 75 µg/mL, respectively. The content of fatty acids in plasma and breast milk was determined by gas liquid chromatography.12,33

Dietary Evaluation
All participating mothers filled out a self-administered food frequency questionnaire when they entered the study (week 18) and at week 35 of pregnancy. The questionnaire has been validated repeatedly, demonstrating that the questionnaire may be used for estimation of dietary intake of very-long-chain n-3 fatty acids.3436 The mothers were asked to continue their habitual diet during the study period.

When the infants were 3 months old, the mothers answered a questionnaire covering the infants’ usual diet. This included questions about breastfeeding and supplements with cod liver oil given to the infants.

Assessment of Intelligence
The K-ABC is a measure of intelligence and achievement designed for children aged 2.5 years through 12.5 years.32 This multisubtest battery comprises 4 scales: Sequential Processing, Simultaneous Processing, Achievement (not used in the present study), and Nonverbal Abilities. The Sequential Processing and Simultaneous Processing scales are hypothesized to reflect the child’s style of problem solving and information processing. Scores from these 2 scales are combined to form a Mental Processing Composite, which serves as the measure of intelligence in the K-ABC. The Nonverbal Scale is not an independent scale. It is composed of the subtests from the Sequential Processing and Simultaneous Processing scales that do not require words. The examiner may convey instructions through gestures, and the child may respond with movements. The Sequential Processing and Simultaneous Processing scales were designed to reduce the effects of verbal processing and of gender and ethnic bias. The Sequential Processing scale was designed to measure children’s ability to solve problems that require the arrangement of stimuli in sequential or serial order, whereas the Simultaneous Processing scale was designed to measure children’s ability to solve spatial, analogic, or organizational problems that require processing of many stimuli at once. Raw scores are transformed into standard scores with mean = 100 and standard deviation = 15. Internal consistency reliability for the Mental Processing Composite is, on the average, 0.91 for preschool children.32 The Mental Processing Composite has an average standard error of measurement of 4.6 points for preschool children.32 Because the K-ABC does not have a Norwegian standardization, the raw scores were converted to standard scores according to the US norms.

Statistics
Data are presented as means (standard deviations). Student t test was used to examine differences between different groups for continuous variables. For categorical values, the {chi}2 test was used. Correlation coefficients were calculated using the Pearson test. Multiple regression analyses were also conducted. P values <=.05 were considered significant. SPSS for Macintosh 6.1.1. (SPSS Inc, Chicago, IL) was used for calculations.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
Study Population
Birth data of the study population and characteristics of their parents are described in Table 2. The study population did not differ from the population not tested with K-ABC on gestational length, birth weight, birth length, head circumference, placental weight, maternal age, maternal body mass index, maternal or paternal education, or parity.


View this table:
[in this window]
[in a new window]
 
TABLE 2. Birth Data and Characteristics of the Parents of Children Assessed With K-ABC (Mean [SD])

 
We received dietary information from 76 infants (41 in the cod liver oil group and 35 in the corn oil group), documenting that all of them were breastfed at 3 months of age. The breast milk of mothers who received cod liver oil contained more DHA (approximately 270%) and less AA (88%) than breast milk of mothers who received corn oil (Table 3). At 3 months of age, 35 infants (19 in the cod liver oil group and 16 in the corn oil group) received cod liver oil.


View this table:
[in this window]
[in a new window]
 
TABLE 3. Fatty Acids in Breast Milk (wt%) 4 Weeks and 3 Months After Delivery (Mean [SD])

 
Fatty Acid Patterns in Umbilical and Plasma Phospholipids
The concentrations of {Sigma}n-3, EPA, DHA, and the ratio {Sigma}n-3/{Sigma}n-6 in plasma phospholipids were significantly higher in the cod liver oil group as compared with the corn oil group, whereas the concentrations of AA and Osbond acid (22:5 n-6) were higher in the corn oil group (Table 4).


View this table:
[in this window]
[in a new window]
 
TABLE 4. Fatty Acids (µg/mL) in Umbilical Plasma Phospholipids and in Infant Plasma Phospholipids at 4 Weeks and 3 Months of Age (Mean [SD])

 
Maternal Dietary Intake
There were no differences between the cod liver oil group and the corn oil group in maternal nutrient intake at the start of the study (18 weeks of pregnancy; data not shown). After 35 weeks of pregnancy, there were significant differences between the 2 groups for intake of linoleic acid, AA, EPA, and DHA (Table 5), reflecting the intake of different supplements.


View this table:
[in this window]
[in a new window]
 
TABLE 5. Daily Intake of Energy and Nutrients as Evaluated by a Food Frequency Questionnaire in Week 35 of Pregnancy (Mean [SD])

 
Cognitive Tests
Children in the cod liver oil group had significantly higher scores than the children in the corn oil group on the Mental Processing Composite of the K-ABC test at 4 years of age (106.4 [7.4] vs 102.3 [11.3]; P = .049; Fig 1). There was a clear tendency to higher scores for the Sequential Processing scale, Simultaneous Processing scale, and Nonverbal scale among children who were born to mothers who were given cod liver oil (Fig 1), but these differences were not statistically significant. No differences were observed between children who received cod liver oil or not (Table 6). The Mental Processing Composite score correlated significantly with head circumference at birth (r = 0.23; P = .04), but no relation was found with birth weight or gestational length.



View larger version (32K):
[in this window]
[in a new window]
 
Fig. 1. Scores on the K-ABC for children whose mothers had taken cod liver oil (n = 48) or corn oil (n = 36) during pregnancy and lactation. Values for the different subtests are shown. MPCOMP, Mental Processing Composite; SEQPROC, Sequential Processing; SIMPROC, Simultaneous Processing; NONVERB, Nonverbal Abilities.

 

View this table:
[in this window]
[in a new window]
 
TABLE 6. Mental Composite Scores for Infants Receiving Cod Liver Oil or Not When Mothers Received Supplements of Cod Liver Oil or Corn Oil (Mean [SD])

 
No correlation was observed between very-long-chain n-3 PUFAs in umbilical plasma phospholipids and intelligence scores, but Mead acid (20:3 n-9) and Osbond acid correlated negatively with intelligence sores (Mead acid: Simultaneous Processing, r = -0.24, P = .04; Nonverbal Scale, r = -0.25, P = .03; Osbond acid: Mental Processing Composite, r = -0.29, P = .01; Sequential Processing, r = -0.31, P = .008, Nonverbal Scale, r = -0.25, P = .03). Moreover, intelligence scores at 4 years of age correlated with plasma phospholipid concentrations of docosapentaenoic acid n-3 (22:5 n-3; Mental Processing Composite, r = 0.23, P = .03) and DHA (Mental Processing Composite, r = 0.28, P = .01; Sequential Processing, r = 0.22, P = .05; Simultaneous Processing, r = 0.25, P = .03) at 4 weeks of age. Mental processing skills of the children correlated significantly with maternal intake of EPA (Mental Processing Composite, r = 0.27, P = .02; Simultaneous Processing, r = 0.25, P = .04) and DHA (Mental Processing Composite, r = 0.26, P = .03; Simultaneous Processing, r = 0.24, P = .04) during pregnancy.

In a regression model (backward stepwise) with Mental Processing Composite as dependent variable and maternal intake of DHA, gestational length, head circumference, maternal age, parity, parental education, maternal smoking, and cod liver oil intake of the infant as independent variables, maternal intake of DHA was the only variable with statistical significance (r2 = 0.07; P = .03) unilaterally evaluated.


    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
This is the first study to examine the long-term effects on children of maternal supplementation with very-long-chain n-3 PUFAs during pregnancy and lactation. Our present study shows that 4-year-old children have higher mental processing scores when the mothers are supplemented with very-long-chain n-3 PUFAs (from cod liver oil) during pregnancy and lactation, as compared with children of mothers who are supplemented with long-chain n-6 PUFAs (from corn oil).

The maternal intake of DHA during pregnancy seems to be important for mental development measured at 4 years of age. Higher maternal intake of DHA results in higher maternal plasma levels and thereby increased transfer of DHA to the fetus.31,37 In an observational study, it was recently reported that stereoacuity at age 3.5 years was enhanced among full-term infants whose mothers had a DHA-rich diet during pregnancy.38 Breastfeeding was also associated with enhanced stereopsis, compared with children who had not been breastfed.38 In our study, at least 76 infants were breastfed at 3 months of age, thereby receiving AA as well as DHA via their mothers’ milk. However, the infants of cod liver oil-supplemented mothers received approximately 2.7-fold more DHA than infants of corn oil-supplemented mothers postnatal. Approximately half of all of the infants in both groups received cod liver at 3 months of age. However, we did not observe any effect of cod liver oil supplementation to breastfed infants on later mental development.

The difference of 4.1 points in the scores on the Mental Processing Composite of the K-ABC between the 2 groups may have limited significance on individual basis but may be of epidemiologic importance. Didactic procedures increasing IQ with 4 points among school children, with no harmful side effects, would immediately be implemented in schools.

We also observed a significant correlation between head circumference and mental processing skills. Severely reduced blood flow to the fetus associated with growth retardation may be followed by impairment of intellectual development and partial neurodevelopment delay.39 Reduced supply of DHA and AA may explain some of the neurologic impairment. Children who are born small for gestational age have smaller head circumference than children who are born appropriate for gestational age, even at 13 months of age.40 They also score lower on the Bayley Mental Scale of Infant Development. At school age, children who were born small for gestational age seem to show learning deficits.41,42 Our study is the first to show such a correlation between head circumference at birth and mental processing skills in healthy term infants. Head circumference at 6 months of age has previously been shown to correlate with IQ at 3 years of age.43

We furthermore observed a relation between intelligence scores at 4 years of age and concentrations of docosapentaenoic acid n-3 and DHA in plasma phospholipids at 4 weeks of age but not at birth or at 3 months of age. It is possible that the small number of individuals in our groups makes it difficult to find significant correlations at different time points, but it is tempting to assume that DHA may be important for mental development at least during childhood. We will follow up our study population to the age of 7 years to evaluate whether cod liver oil supplementation to pregnant and lactating women will influence long-term mental skills among children.

At birth, Osbond and Mead acid correlated negatively with intelligence scores, and these fatty acids have been proposed to be markers of DHA depletion.44 High levels of these fatty acids might also represent nonoptimal ligands for transcription factors, substrates for enzymatic activities, or structural components in the central nervous system.45


    CONCLUSION
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
This study indicates that maternal supplementation with very-long-chain n-3 PUFAs during pregnancy and lactation improves the intelligence of children at 4 years of age. Perhaps adequate supply of very-long-chain PUFA during pregnancy is just as important as in the neonatal period.46

Whether supplementation during pregnancy or during lactation (or both) is of more importance remains to be elucidated. We still do not know whether cod liver oil supplements are important for formula-fed infants. Neither do we know whether length of the breastfeeding period beyond 3 months may be important.


    ACKNOWLEDGMENTS
 
Grant support for this work was provided by Peter Møller, avd. Orkla ASA, Eckbos Legater, and Aktieselskabet Freia Chocoladefabriks Medicinske Fond.

We thank Anne-Margrethe Larsen, a master of science student, for administering the mental testing; university lecturer Kari Solvoll for performing dietary analyses; Asbjørg Flo for performing the fatty acid analyses; Kathrine Frey Frøslie for helping with the statistical analyses; and Tove Myhre and Marion Fierro for helping with practical procedures. We also thank the staff at Kvinneklinikken, Rikshospitalet University Hospital, and Baerum Central Hospital for participating in recruiting women and sampling umbilical blood, and Louise Tunge and her colleagues for taking blood samples from the infants.


    FOOTNOTES
 
Received for publication Mar 11, 2002; Accepted Aug 27, 2002.

Address correspondence to Ingrid B. Helland, MD, Department of Pediatrics, Rikshospitalet University Hospital, N-0032 Oslo, Norway. Email: ingrid.helland{at}rikshospitalet.no


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
1. Crawford MA, Hassam AG, Williams G. Essential fatty acids and fetal brain growth. Lancet.1976; 1 :452 –453[CrossRef][Web of Science][Medline]

2. Neuringer M, Connor WE, Van Petten C, Barstad L. Dietary omega-3 fatty acid deficiency and visual loss in infant rhesus monkeys. J Clin Invest.1984; 73 :272 –276

3. Clandinin MT, Chappell JE, Leong S, Heim T, Swyer PR, Chance GW.Intrauterine fatty acid accretion rates in human brain: implications for fatty acid requirements. Early Hum Dev.1980; 4 :121 –129[CrossRef][Web of Science][Medline]

4. Carlson SE, Rhodes PG, Ferguson MG. Docosahexaenoic acid status of preterm infants at birth and following feeding with human milk or formula. Am J Clin Nutr.1986; 44 :798 –804[Abstract/Free Full Text]

5. Hoffman DR, Uauy R. Essentiality of dietary omega 3 fatty acids for premature infants: plasma and red blood cell fatty acid composition. Lipids.1992; 27 :886 –895[Web of Science][Medline]

6. Makrides M, Neumann M, Simmer K, Pater J, Gibson R. Are long-chain polyunsaturated fatty acids essential nutrients in infancy? Lancet.1995; 345 :1463 –1468[CrossRef][Web of Science][Medline]

7. Al MD, Hornstra G, van der Schouw YT, Bulstra-Ramakers MT, Huisjes HJ. Biochemical EFA status of mothers and their neonates after normal pregnancy. Early Hum Dev.1990; 24 :239 –248[CrossRef][Web of Science][Medline]

8. Farquharson J, Cockburn F, Patrick WA, Jamieson EC, Logan RW. Infant cerebral cortex phospholipid fatty-acid composition and diet. Lancet.1992; 340 :810 –813[CrossRef][Web of Science][Medline]

9. Makrides M, Neumann MA, Byard RW, Simmer K, Gibson RA. Fatty acid composition of brain, retina, and erythrocytes in breast- and formula-fed infants. Am J Clin Nutr.1994; 60 :189 –194[Abstract/Free Full Text]

10. Innis SM, Kuhnlein HV. Long-chain n-3 fatty acids in breast milk of Inuit women consuming traditional foods. Early Hum Dev.1988; 18 :185 –189[CrossRef][Web of Science][Medline]

11. Harris WS, Connor WE, Lindsey S. Will dietary omega-3 fatty acids change the composition of human milk? Am J Clin Nutr.1984; 40 :780 –785[Abstract/Free Full Text]

12. Helland IB, Saarem K, Saugstad OD, Drevon CA. Fatty acid composition in maternal milk and plasma during supplementation with cod liver oil. Eur J Clin Nutr.1998; 52 :839 –845[CrossRef][Web of Science][Medline]

13. Lucas A, Morley R, Cole TJ, Lister G, Leeson-Payne C. Breast milk and subsequent intelligence quotient in children born preterm. Lancet.1992; 339 :261 –264[CrossRef][Web of Science][Medline]

14. Rogan WJ, Gladen BC. Breast-feeding and cognitive development. Early Hum Dev.1993; 31 :181 –193[CrossRef][Web of Science][Medline]

15. Lucas A, Morley R, Cole TJ, Gore SM. A randomised multicentre study of human milk versus formula and later development in preterm infants. Arch Dis Child Fetal Neonatal Ed.1994; 70 :F141 –F146[Abstract/Free Full Text]

16. Anderson JW, Johnstone BM, Remley DT. Breast-feeding and cognitive development: a meta-analysis. Am J Clin Nutr.1999; 70 :525 –535[Abstract/Free Full Text]

17. Angelsen NK, Vik T, Jacobsen G, Bakketeig LS. Breast feeding and cognitive development at age 1 and 5 years. Arch Dis Child.2001; 85 :183 –188[Abstract/Free Full Text]

18. Agostoni C, Trojan S, Bellu R, Riva E, Giovannini M. Neurodevelopmental quotient of healthy term infants at 4 months and feeding practice: the role of long-chain polyunsaturated fatty acids. Pediatr Res.1995; 38 :262 –266[Web of Science][Medline]

19. Carlson SE, Ford AJ, Werkman SH, Peeples JM, Koo WW. Visual acuity and fatty acid status of term infants fed human milk and formulas with and without docosahexaenoate and arachidonate from egg yolk lecithin. Pediatr Res.1996; 39 :882 –888[Web of Science][Medline]

20. Willatts P, Forsyth JS, DiModugno MK, Varma S, Colvin M. Effect of long-chain polyunsaturated fatty acids in infant formula on problem solving at 10 months of age. Lancet.1998; 352 :688 –691[CrossRef][Web of Science][Medline]

21. Birch EE, Hoffman DR, Uauy R, Birch DG, Prestidge C. Visual acuity and the essentiality of docosahexaenoic acid and arachidonic acid in the diet of term infants. Pediatr Res.1998; 44 :201 –209[Web of Science][Medline]

22. Birch EE, Garfield S, Hoffman DR, Uauy R, Birch DG. A randomized controlled trial of early dietary supply of long-chain polyunsaturated fatty acids and mental development in term infants. Dev Med Child Neurol.2000; 42 :174 –181[CrossRef][Web of Science][Medline]

23. Horby Jorgensen M, Holmer G, Lund P, Hernell O, Michaelsen KF. Effect of formula supplemented with docosahexaenoic acid and gamma-linolenic acid on fatty acid status and visual acuity in term infants. J Pediatr Gastroenterol Nutr.1998; 26 :412 –421[CrossRef][Web of Science][Medline]

24. Lucas A, Stafford M, Morley R, et al. Efficacy and safety of long-chain polyunsaturated fatty acid supplementation of infant-formula milk: a randomised trial. Lancet.1999; 354 :1948 –1954[CrossRef][Web of Science][Medline]

25. Makrides M, Neumann MA, Simmer K, Gibson RA. A critical appraisal of the role of dietary long-chain polyunsaturated fatty acids on neural indices of term infants: a randomized, controlled trial. Pediatrics.2000; 105 :32 –38[Abstract/Free Full Text]

26. Auestad N, Halter R, Hall RT, et al. Growth and development in term infants fed long-chain polyunsaturated fatty acids: a double-masked, randomized, parallel, prospective, multivariate study. Pediatrics.2001; 108 :372 –381[Abstract/Free Full Text]

27. Scott DT, Janowsky JS, Carroll RE, Taylor JA, Auestad N, Montalto MB. Formula supplementation with long-chain polyunsaturated fatty acids: are there developmental benefits? Pediatrics.1998; 102(5) . Available at: www.pediatrics.org/cgi/content/full/102/5/e59

28. Uauy RD, Birch DG, Birch EE, Tyson JE, Hoffman DR. Effect of dietary omega-3 fatty acids on retinal function of very-low-birth-weight neonates. Pediatr Res.1990; 28 :485 –492[Web of Science][Medline]

29. Carlson SE, Werkman SH, Rhodes PG, Tolley EA. Visual-acuity development in healthy preterm infants: effect of marine-oil supplementation. Am J Clin Nutr.1993; 58 :35 –42[Abstract/Free Full Text]

30. O’Connor DL, Hall R, Adamkin D, et al. Growth and development in preterm infants fed long-chain polyunsaturated fatty acids: a prospective, randomized controlled trial. Pediatrics.2001; 108 :359 –371[Abstract/Free Full Text]

31. Helland IB, Saugstad OD, Smith L, et al. Similar effects on infants of n-3 and n-6 fatty acids supplementation to pregnant and lactating women. Pediatrics.2001; 108(5) . Available at: www.pediatrics.org/cgi/content/full/108/5/e82

32. Kaufman AS, Kaufman NL. Kaufman Assessment Battery for Children. Circle Pines, MN: American Guidance Service; 1983

33. Clark RM, Roche ME. Gas chromatographic procedure for measuring total lipid in breast milk. J Pediatr Gastroenterol Nutr.1990; 10 :271 –272[CrossRef][Web of Science][Medline]

34. Nes M, Frost Andersen L, Solvoll K, et al. Accuracy of a quantitative food frequency questionnaire applied in elderly Norwegian women. Eur J Clin Nutr.1992; 46 :809 –821[Web of Science][Medline]

35. Solvoll K, Lund-Larsen K, Søyland E, Sandstad B, Drevon CA. A quantitative food frequency questionnaire evaluated in a group of dermatologic outpatients. Scand J Nutr.1993; 37 :150 –155

36. Andersen LF, Solvoll K, Drevon CA. Very-long-chain n-3 fatty acids as biomarkers for intake of fish and n-3 fatty acid concentrates. Am J Clin Nutr.1996; 64 :305 –311[Abstract/Free Full Text]

37. Connor WE, Lowensohn R, Hatcher L. Increased docosahexaenoic acid levels in human newborn infants by administration of sardines and fish oil during pregnancy. Lipids.1996; 31(suppl) :S183 –S187

38. Williams C, Birch EE, Emmett PM, Northstone K. Stereoacuity at age 3.5 y in children born full-term is associated with prenatal and postnatal dietary factors: a report from a population-based cohort study. Am J Clin Nutr.2001; 73 :316 –322[Abstract/Free Full Text]

39. Wienerroither H, Steiner H, Tomaselli J, Lobendanz M, Thun-Hohenstein L. Intrauterine blood flow and long-term intellectual, neurologic, and social development. Obstet Gynecol.2001; 97 :449 –453[CrossRef][Web of Science][Medline]

40. Markestad T, Vik T, Ahlsten G, et al. Small-for-gestational-age (SGA) infants born at term: growth and development during the first year of life. Acta Obstet Gynecol Scand Suppl.1997; 165 :93 –101[Medline]

41. Low JA, Handley-Derry MH, Burke SO, et al. Association of intrauterine fetal growth retardation and learning deficits at age 9 to 11 years. Am J Obstet Gynecol.1992; 167 :1499 –1505[Web of Science][Medline]

42. Larroque B, Bertrais S, Czernichow P, Leger J. School difficulties in 20-year-olds who were born small for gestational age at term in a regional cohort study. Pediatrics.2001; 108 :111 –115[Abstract/Free Full Text]

43. Sells CJ, Robinson NM, Brown Z, Knopp RH. Long-term developmental follow-up of infants of diabetic mothers. J Pediatr.1994; 125 :S9 –S17[CrossRef][Web of Science][Medline]

44. Hornstra G, Al MD, van Houwelingen AC, Foreman-van Drongelen MM. Essential fatty acids in pregnancy and early human development. Eur J Obstet Gynecol Reprod Biol.1995; 61 :57 –62[CrossRef][Web of Science][Medline]

45. Drevon CA. Omega-3 Fatty Acids. Metabolism and Biological Effects. Basel, Switzerland: Birkhäuser; 1993

46. Forsyth JS, Carlson SE. Long-chain polyunsaturated fatty acids in infant nutrition: effects on infant development. Curr Opin Clin Nutr Metab Care.2001; 4 :123 –126[CrossRef][Web of Science][Medline]


PEDIATRICS (ISSN 1098-4275). ©2003 by the American Academy of Pediatrics

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
Am. J. Clin. Nutr.Home page
R. W Friesen and S. M Innis
Linoleic acid is associated with lower long-chain n-6 and n-3 fatty acids in red blood cell lipids of Canadian pregnant women
Am. J. Clinical Nutrition, January 1, 2010; 91(1): 23 - 31.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
R. W. Friesen and S. M. Innis
Dietary Arachidonic Acid to EPA and DHA Balance Is Increased among Canadian Pregnant Women with Low Fish Intake
J. Nutr., December 1, 2009; 139(12): 2344 - 2350.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
S. E Carlson
Early determinants of development: a lipid perspective
Am. J. Clinical Nutrition, May 1, 2009; 89(5): 1523S - 1529S.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
S. E Carlson
Docosahexaenoic acid supplementation in pregnancy and lactation
Am. J. Clinical Nutrition, February 1, 2009; 89(2): 678S - 684S.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
S. H Zeisel
Is maternal diet supplementation beneficial? Optimal development of infant depends on mother's diet
Am. J. Clinical Nutrition, February 1, 2009; 89(2): 685S - 687S.
[Abstract] [Full Text] [PDF]


Home page
Postgrad. Med. J.Home page
B M Yashodhara, S Umakanth, J M Pappachan, S K Bhat, R Kamath, and B H Choo
Omega-3 fatty acids: a comprehensive review of their role in health and disease
Postgrad. Med. J., February 1, 2009; 85(1000): 84 - 90.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
C. Agostoni, G. V. Zuccotti, G. Radaelli, R. Besana, A. Podesta, A. Sterpa, A. Rottoli, E. Riva, and M. Giovannini
Docosahexaenoic acid supplementation and time at achievement of gross motor milestones in healthy infants: a randomized, prospective, double-blind, placebo-controlled trial
Am. J. Clinical Nutrition, January 1, 2009; 89(1): 64 - 70.
[Abstract] [Full Text] [PDF]


Home page
Schizophr BullHome page
A. S. Brown and E. S. Susser
Prenatal Nutritional Deficiency and Risk of Adult Schizophrenia
Schizophr Bull, November 1, 2008; 34(6): 1054 - 1063.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
L. Xie and S. M. Innis
Genetic Variants of the FADS1 FADS2 Gene Cluster Are Associated with Altered (n-6) and (n-3) Essential Fatty Acids in Plasma and Erythrocyte Phospholipids in Women during Pregnancy and in Breast Milk during Lactation
J. Nutr., November 1, 2008; 138(11): 2222 - 2228.
[Abstract] [Full Text] [PDF]


Home page
Am J EpidemiolHome page
T. I. Halldorsson, I. Thorsdottir, H. M. Meltzer, F. Nielsen, and S. F. Olsen
Linking Exposure to Polychlorinated Biphenyls With Fatty Fish Consumption and Reduced Fetal Growth Among Danish Pregnant Women: A Cause for Concern?
Am. J. Epidemiol., October 15, 2008; 168(8): 958 - 965.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
J. A. Armitage, S. Gupta, C. Wood, R. I. Jensen, A.-M. Samuelsson, W. Fuller, M. J. Shattock, L. Poston, and P. D. Taylor
Maternal dietary supplementation with saturated, but not monounsaturated or polyunsaturated fatty acids, leads to tissue-specific inhibition of offspring Na+,K+-ATPase
J. Physiol., October 15, 2008; 586(20): 5013 - 5022.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
E. Oken, M. L. Osterdal, M. W Gillman, V. K Knudsen, T. I Halldorsson, M. Strom, D. C Bellinger, M. Hadders-Algra, K. F. Michaelsen, and S. F Olsen
Associations of maternal fish intake during pregnancy and breastfeeding duration with attainment of developmental milestones in early childhood: a study from the Danish National Birth Cohort
Am. J. Clinical Nutrition, September 1, 2008; 88(3): 789 - 796.
[Abstract] [Full Text] [PDF]


Home page
Am J EpidemiolHome page
E. Oken, J. S. Radesky, R. O. Wright, D. C. Bellinger, C. J. Amarasiriwardena, K. P. Kleinman, H. Hu, and M. W. Gillman
Maternal Fish Intake during Pregnancy, Blood Mercury Levels, and Child Cognition at Age 3 Years in a US Cohort
Am. J. Epidemiol., May 15, 2008; 167(10): 1171 - 1181.
[Abstract] [Full Text] [PDF]


Home page
AMERICAN JOURNAL OF LIFESTYLE MEDICINEHome page
H. A. Ricciotti
State of the Art Reviews: Nutrition and Lifestyle for a Healthy Pregnancy
American Journal of Lifestyle Medicine, April 1, 2008; 2(2): 151 - 158.
[Abstract] [PDF]


Home page
Am. J. Clin. Nutr.Home page
S. M Innis and R. W Friesen
Essential n-3 fatty acids in pregnant women and early visual acuity maturation in term infants
Am. J. Clinical Nutrition, March 1, 2008; 87(3): 548 - 557.
[Abstract] [Full Text] [PDF]


Home page
Arch. Dis. Child. Fetal Neonatal Ed.Home page
C King and M Fewtrell
Fishing for brain power?
Arch. Dis. Child. Fetal Neonatal Ed., January 1, 2008; 93(1): F4 - F6.
[Full Text] [PDF]


Home page
Arch. Dis. Child. Fetal Neonatal Ed.Home page
J A Dunstan, K Simmer, G Dixon, and S L Prescott
Cognitive assessment of children at age 21/2 years after maternal fish oil supplementation in pregnancy: a randomised controlled trial
Arch. Dis. Child. Fetal Neonatal Ed., January 1, 2008; 93(1): F45 - F50.
[Abstract] [Full Text] [PDF]


Home page
cfpHome page
G. Dubnov-Raz, Y. Finkelstein, and G. Koren
{omega}-3 fatty acid supplementation during pregnancy: For mother, baby, or neither?
Can Fam Physician, May 1, 2007; 53(5): 817 - 818.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
S. Krauss-Etschmann, R. Shadid, C. Campoy, E. Hoster, H. Demmelmair, M. Jimenez, A. Gil, M. Rivero, B. Veszpremi, T. Decsi, et al.
Effects of fish-oil and folate supplementation of pregnant women on maternal and fetal plasma concentrations of docosahexaenoic acid and eicosapentaenoic acid: a European randomized multicenter trial
Am. J. Clinical Nutrition, May 1, 2007; 85(5): 1392 - 1400.
[Abstract] [Full Text] [PDF]


Home page
NeoReviewsHome page
M. Makrides and R. A. Gibson
Marine Oil Supplements for Pregnant Women: Good for Mum, Good for Baby?
NeoReviews, April 1, 2007; 8(4): e152 - e158.
[Abstract] [Full Text] [PDF]


Home page
JAMAHome page
D. Mozaffarian and E. B. Rimm
Fish intake, contaminants, and human health: evaluating the risks and the benefits.
JAMA, October 18, 2006; 296(15): 1885 - 1899.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
H. Szajewska, A. Horvath, and B. Koletzko
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. Clinical Nutrition, June 1, 2006; 83(6): 1337 - 1344.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
P. Coti Bertrand, J. R. O'Kusky, and S. M. Innis
Maternal Dietary (n-3) Fatty Acid Deficiency Alters Neurogenesis in the Embryonic Rat Brain
J. Nutr., June 1, 2006; 136(6): 1570 - 1575.
[Abstract] [Full Text] [PDF]


Home page
J Pediatr PsycholHome page
S. L. Hart, L. M. Boylan, S. R. Carroll, Y. A. Musick, C. Kuratko, B. G. Border, and R. M. Lampe
Brief Report: Newborn Behavior Differs with Decosahexaenoic Acid Levels in Breast Milk
J. Pediatr. Psychol., March 1, 2006; 31(2): 221 - 226.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
J. C McCann and B. N Ames
Is docosahexaenoic acid, an n-3 long-chain polyunsaturated fatty acid, required for development of normal brain function? An overview of evidence from cognitive and behavioral tests in humans and animals
Am. J. Clinical Nutrition, August 1, 2005; 82(2): 281 - 295.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
J. Zhang, J. R. Hebert, and M. F. Muldoon
Dietary Fat Intake Is Associated with Psychosocial and Cognitive Functioning of School-Aged Children in the United States
J. Nutr., August 1, 2005; 135(8): 1967 - 1973.
[Abstract] [Full Text] [PDF]


Home page
Toxicol SciHome page
G. Latini, M. Massaro, and C. De Felice
Prenatal Exposure to Phthalates and Intrauterine Inflammation: A Unifying Hypothesis
Toxicol. Sci., May 1, 2005; 85(1): 743 - 743.
[Full Text] [PDF]


Home page
J. Nutr.Home page
F. A. J. Muskiet, M. R. Fokkema, A. Schaafsma, E. R. Boersma, and M. A. Crawford
Is Docosahexaenoic Acid (DHA) Essential? Lessons from DHA Status Regulation, Our Ancient Diet, Epidemiology and Randomized Controlled Trials
J. Nutr., January 1, 2004; 134(1): 183 - 186.
[Full Text] [PDF]


Home page
J. Cell Sci.Home page
G. M. Lesa, M. Palfreyman, D. H. Hall, M. T. Clandinin, C. Rudolph, E. M. Jorgensen, and G. Schiavo
Long chain polyunsaturated fatty acids are required for efficient neurotransmission in C. elegans
J. Cell Sci., December 15, 2003; 116(24): 4965 - 4975.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Helland, I. B.
Right arrow Articles by Drevon, C. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Helland, I. B.
Right arrow Articles by Drevon, C. A.
Related Collections
Right arrow Nutrition & Metabolism
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?