A fishy recommendation: omega-3 fatty acidintake in pregnancy
Department of Obstetrics and Gynecology, Faculty of Medicine, University of Alberta, Edmonton, Alberta, CanadaCorrespondence: Dr SJ Genuis, University of Alberta, 2935-66 Street, Edmonton, Alberta, Canada T6K 4C1. Email sgenuis@ualberta.ca
Please cite this paper as: Genuis S. A fishy recommendation: omega-3 fatty acid intake in pregnancy. BJOG 2008;115:1–4.
offspring for diabetes,16 asthma,17 adverse bone health,18and multiple sclerosis19 illustrate the truism that the human
With recent concern about aquatic contamination from
being requires specific nutrients during gestation to carry out
potential teratogens including heavy metals, dioxins, pharma-
the molecular processes within cells and tissues, processes
ceutical residues, polychlorinated biphenyls (PCBs), and syn-
which on the macroscale influence both maternal physiology
thetic estrogens,1–6 some public health agencies throughout
and fetal development. Considerable attention has recently
the world have recommended limiting gestational fish con-
focused on the role of EFAs in maternal and fetal metabolism.
sumption to minimise fetal harm associated with toxicantexposure.7 Conversely, a well-publicised research paper inLancet concluded that adequate seafood consumption in
pregnancy correlates with improved child development andthat ‘advice to limit seafood consumption could actually be
EFAs refer to lipids that cannot be synthesised within the
detrimental’.8 This commentary will consider the issue of
body and must be ingested to meet metabolic demands.
maternal fish consumption in the context of recent medical
The two families of essential lipids—omega-3 fatty acids
literature on nutrition and essential fatty acids (EFAs).
(v3FAs) and omega-6 fatty acids (v6FAs)—are required for
With discussion of intricate laparoscopic techniques,
physiological functions including oxygen transport, energy
avant-garde reproductive interventions, complex microsur-
storage, cell membrane function, and regulation of inflam-
gery, and epigenetic therapies, many medical practitioners
mation and cell proliferation.20,21 In pregnancy, EFAs are
find the practice of dietary or nutritional therapy to be dull,
required for early development of the fetal-placental unit;22
alternative, and perhaps simplistic medicine. Exploration of
docosahexaenoic acid (DHA), a type of v3FA commonly
the aetiological factors contributing to the global escalation in
derived from seafood, is vital for maternal homeostasis, as
chronic disease,9 however, has revealed that some contempo-
well as fetal brain and retinal development throughout the
rary ill health results from nutritional compromise.10 Further-
more, recent research demonstrates that certain obstetric and
Various studies have demonstrated that EFA deficiency as
paediatric afflictions might effectively be prevented by pro-
well as unbalanced consumption of v3FAs and v6FAs may
vision during pregnancy of the nutrients required for optimal
be significant to health outcomes.26 With an overall 80%
decline in v3FA intake in the past century,6,27 combined with
The correlation between deficient folate and neural tube
a noteworthy increase in v6FA intake, epidemiological
defects11 (NTDs) previously prompted widespread pericon-
research suggests that EFA malnutrition may be a determinant
ceptional supplementation and recent concerns about poten-
of several chronic and degenerative disease states.20,26 Various
tial fetal sequelae (including cleft palate)12 of maternal biotin
recent papers and meta-analyses report an increased risk of
deficiency13 as well as considerable risk for NTDs with low
a variety of condition such as heart disease,28 rheumatoid
maternal vitamin B12 status14 have fuelled intensified re-
arthritis,29 breast cancer,30 hypertension,31 osteoporosis,32
search on the link between gestational nutrient requirements
and neurological33 and psychiatric disease34 in association
and maternal and fetal outcome. Correlations including
with inadequate v3FA consumption. Maternal and fetal
those of maternal selenium levels with pre-eclampsia15 and
research has also begun to evaluate the consequences of
maternal vitamin D status with subsequent risk in the
ª 2008 The Author Journal compilation ª RCOG 2008 BJOG An International Journal of Obstetrics and Gynaecology
behaviour,51 and less risk of metabolic disorders such as type
I diabetes in the developing offspring.52 In review, there isabundant evidence in the medical literature that links ade-
It has been hypothesised that sufficient gestational v3FA
quate gestational fatty acid status with maternal and fetal
intake may diminish the likelihood of preterm labour by
the downregulation of prostaglandin formation.35 Juxtaposedwith recent evidence that inadequate consumption of v3FAs
significantly increases the likelihood of early labour,36 an epi-
demiological study has reported a marked rise in pretermbirth among white American women from 1981 to 1998.37
To secure safe and appropriate v3FA gestational intake, two
Furthermore, a prospective cohort study demonstrated that
principles merit consideration. Marine sources of v3FAs
women who avoided seafood had a 7.1% incidence of preterm
contain required DHA, while plant foods generally do not;
birth compared with a 1.9% risk for those eating fish once
conversion from plant source v3FAs to DHA is possible
weekly.38 In addition, maternal consumption of cod liver oil
but requires energy and enzymatic availability. As v3FAs
and increased v3FA:v6FA intake ratio have been associated
and v6FAs use the same enzymes, dietary intake ratio of
with longer gestations and higher birthweights,35,39,40 except
these lipids can determine enzymatic availability. Accord-
in women with high pre-existing levels of v3FAs.35 Whether
ingly, while some pregnant women produce sufficient DHA
the results from these interesting studies should change our
through biochemical conversion from plant source v3FAs,
clinical practice remains uncertain.
direct DHA from fish intake secures provision of this required
Hypertension complicates about 6% of pregnancies in the
developed world. A cross-sectional case–control study found
As a result of multiple potential teratogens contaminating
that pregnant women with low levels of v3FAs were 7.6 times
seafood sources,1–6 however, some authors warn about risks
more likely to have pre-eclampsia than those with high levels
associated with gestational seafood intake. With potentially
of this EFA41 and that a 46% risk reduction for pre-eclampsia
long induction times from toxicant exposure to ultimate
could be achieved by a moderate increase in the proportion of
outcomes53 [as in the diethylstilbestrol (DES) tragedy], with
v3FAs consumed.41 While meta-analytical reviews confirm
insufficient research on the long-term impact of many
a dose-dependent relationship between v3FAs intake and
contemporary aquatic contaminants (acting in isolation or
blood pressure outside pregnancy,30,41 recent evidence sug-
synergistically with other pollutants), and with pronounced
gests that blood pressure control later in life may also be
vulnerability of the fetus to seemingly minuscule levels of
affected negatively by inadequate maternal and neonatal
toxicants,53 debate continues as to whether risks from EFA
intake of v3FAs.42 While many studies show significant
insufficiency outweigh the risks of harm from seafood toxi-
benefit in relation to hypertension, a controlled trial of
cants. In response, some have suggested that supplementation
supplementation in selected high-risk pregnancies found
with fish oil rather than seafood consumption might be a pre-
that additional v3FA intake was associated with reduced
ferred approach to providing required DHA. Recent research,
recurrence risk for preterm delivery but had no impact on
however, has challenged this approach.
recurrence risks for intrauterine growth restriction or preg-
Most work examining fish oil use in pregnancy demon-
strates benefit; a few recent studies, however, fail to confirm
The demonstrated correlation between lower gestational
benefit and some outcomes appear to suggest harm.54,55 A
seafood consumption and higher rates of postpartum depres-
major confounder in current work, however, is that oil pre-
sion44 suggests that individual v3FA indices may also be
pared from fish liver (the major organ of detoxification) is
a determinant of postpartum mood status.45,46 Possibly asso-
often contaminated with the same toxicants including heavy
ciated with the limited seafood intake in North America, the
metals23 found in source fish. Accordingly, consumers of reg-
incidence of postpartum depression is in the range of 12%
ular fish oil consume toxicants that may affect physiological
compared with about 2% in Japan where fish consumption is
processes and influence metabolic outcomes. Methyl mer-
high44 (although major cultural differences in the way the two
cury, for example, is a common aquatic contaminant and
societies are organised may also be important). Furthermore,
can induce hypertension in animals56—this may account for
low DHA in breast milk and maternal red cells, resulting from
adverse outcomes, such as gestational hypertension in con-
low gestational intake of EFAs,47 are commonly found in
sumers of regular fish oil.55 Furthermore, some toxicants can
impair or modify absorption, utilisation, and metabolism of
Maternal v3FA status also appears to correlate with fetal
nutrients potentially resulting in adverse sequelae.
outcome. Ensuring a sufficiency of v3FAs for women during
To address the toxicity concern, however, gestational EFA
pregnancy and lactation has been correlated with enhanced
requirements can be secured with avoidance of toxic exposure
cognitive and behavioural functioning,48–50 improved sleep
by replacing gestational seafood intake with regular ingestion
ª 2008 The Author Journal compilation ª RCOG 2008 BJOG An International Journal of Obstetrics and Gynaecology
of plant source v3FAs and supplementation with purified fish
7 US Department of Health and Human Services UEPA. What you need
oil.57,58 Through distillation and subsequent toxicological
to know about mercury in fish and shellfish. EPA and FDA advice forwomen who might become pregnant, women who are pregnant,
testing, purified fish oil preparations are available. As well
nursing mothers, and young children. 2004 [www.cfsan.fda.gov/;dms/
as obviating patient hazard, toxicant confounding in research
admehg3.html]. Accessed 9 March 2007.
can be precluded by use of purified preparations.
8 Hibbeln JR, Davis JM, Steer C, Emmett P, Rogers I, William C, et al.
Maternal seafood consumption in pregnancy and neurodevelopmentaloutcomes in childhood (ALSPAC study): an observational cohort study. Lancet 2007;369:578–85.
9 Horton R. The neglected epidemic of chronic disease. Lancet 2005;
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10 Genuis SJ. Nutritional transition: a determinant of global health.
nutrient and dietary transitions with health sequelae makes it
J Epidemiol Community Health 2005;59:615–17.
evident that nutritional status is a major determinant of
11 Czeizel AE, Dudas I. Prevention of the first occurrence of neural-tube
health and wellbeing throughout life, including intrauterine
defects by periconceptional vitamin supplementation. N Engl J Med1992;327:1832–5.
development. Regardless of beneficial outcomes in research or
12 University of Arkansas for Medical S. UAMS Leads Search for Answers
epidemiological study, however, medical history has repeat-
on Cleft Palate, Other Biotin-related Birth Defects. 2006 [www.uams.
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edu/newsbureau/2003/January/biotinbirthdefects.htm]. Accessed 3
findings into clinical practice is generally a slow process.59 It
often takes a generation—corresponding to the time required
13 Mock DM, Quirk JG, Mock NI. Marginal biotin deficiency during nor-
mal pregnancy. Am J Clin Nutr 2002;75:295–9.
for new trainees untainted by status quo ideas and biases to
14 Ray JG, Wyatt PR, Thompson MD, Vermeulen MJ, Meier C, Wong PY,
achieve positions of influence—before innovative clinical pat-
et al. Vitamin B12 and the risk of neural tube defects in a folic-acid-
terns emerge. While concerns about gestational folate defi-
fortified population. Epidemiology 2007;18:362–6.
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15 Rayman MP, Bode P, Redman CW. Low selenium status is associ-
decades before routine supplementation was widespread.
ated with the occurrence of the pregnancy disease preeclampsia inwomen from the United Kingdom. Am J Obstet Gynecol 2003;189:
Research confirms the need for essential v3FAs in preg-
nancy, and population analyses suggest that deficiency is
16 Fronczak CM, Baron AE, Chase HP, Ross C, Brady HL, Hoffman M, et al.
common. Accordingly, it is important that providers of
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maternity care be familiar with principles of clinical nutrition
and possess the necessary tools to assess and manage concerns
17 Camargo CA Jr, Rifas-Shiman SL, Litonjua AA, Rich-Edward JW, Weiss
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Rabbit anti-CD163 Cat. No. and Size: 503-3964 : 1 ml rabbit monoclonal antibody purified by protein A/G in PBS/1% BSA buffer pH 7.6 with less than 0.1% sodium azide. 503-3961 : 7.0 ml pre-diluted rabbit monoclonal antibody purified by protein A/G in TBS/1% BSA buffer pH 7.6 with less than 0.1% sodium azide. Intended Use: For research use only. Not for use in
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