PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of canfamphysLink to Publisher's site
 
Can Fam Physician. 2010 October; 56(10): 1001–1002.
PMCID: PMC2954077

Language: English | French

Fish consumption in pregnancy and fetal risks of methylmercury toxicity

Gideon Koren, MD FRCPC FACMT and John R. Bend, PhD

ABSTRACT

QUESTION Because I practise in a rural area with a large number of lakes, I have patients planning pregnancy who consume relatively large amounts of fish harvested by their families. What should be my advice to them?

ANSWER A recent Motherisk study has shown that fairly commonly these women’s mercury levels exceed the threshold level for cognitive effects. Women should not consume excessive amounts of seafood in pregnancy (ie, no more than 2 weekly average size servings). Hair mercury level above 0.3 μg/g indicates a potentially excessive body burden.

RÉSUMÉ

QUESTION Je pratique la médecine dans une région rurale où se trouvent beaucoup de lacs, et plusieurs de mes patientes qui planifient une grossesse consomment d’assez grandes quantités de poissons pêchés par les membres de leur famille. Quels conseils devrais-je leur donner?

RÉPONSE Une récente étude par Motherisk révèle qu’il est assez fréquent de trouver chez ces femmes des taux de mercure qui dépassent le seuil recommandé pour éviter des effets cognitifs. Les femmes ne devraient pas consommer des quantités excessives de poissons durant la grossesse (c.-à-d. pas plus de 2 portions moyennes par semaine). Un taux de mercure capillaire de plus de 0,3 μg/g indique une charge corporelle potentiellement excessive.

Fish and other forms of seafood are important components of healthy diets.1 Fish consumption is particularly advantageous for pregnant women because it contains relatively high concentrations of ω-3 polyunsaturated fatty acids not commonly found in other foods, as well as proteins that are essential for the developing fetal brain.24 The predominant drawback of fish consumption for expectant mothers is that some species of fish contain organic mercury at concentrations sufficient for high consumption to cause adverse developmental effects to the unborn child.5,6 Methylmercury, the form of environmental mercury most detrimental to humans, is produced from inorganic mercury by the action of anaerobic organisms that live in aquatic environments.7 Because fish have limited ability to eliminate this contaminant, methylmercury bioaccumulates at highest concentrations in muscle of large and old predatory fish.8

Key studies

The best evidence for methylmercury toxicity in the fetus comes from well-publicized incidents in Minamata, Japan,913 and Iraq.1417 Using data collected after the Iraqi disaster, Clarkson and colleagues defined threshold toxicologic levels associated with severe adverse effects to the fetus as low as 10 μg/g in maternal hair.18 We recently performed a systematic review of all relevant research on humans and the effects of prenatal mercury exposure through fish consumption on neurodevelopment after fetal exposure, and have defined a lowest observable adverse effect level of hair mercury concentrations for adverse effects on child neurodevelopment resulting from fetal exposure.19

Maternal mercury content in hair was chosen as the biomarker for the extent (dose) of exposure to methylmercury because these values were reported by most studies, reflect longer exposure periods than do maternal whole blood values, and represent a less invasive method of sampling for concerned women who are planning to become pregnant. Overall, 48 articles met the inclusion criteria for our systematic review.19 Of the 48 articles, 30 were of longitudinal and 18 were of cross-sectional design. Of the 30 longitudinal articles, 11 involved work done in the original Seychelles Child Development Nutrition Study conducted in the Seychelles. Eight articles were of studies conducted in the main Faroe Islands study and 2 were from the second Faroe Islands longitudinal study. Another 2 articles described a longitudinal study conducted in the United States. Finally, 2 of the included articles were of studies conducted in New Zealand and 2 were of studies done in Poland.

All 48 of the included studies evaluated the risk of prenatal methylmercury exposure on neurodevelopment. Of the 18 cross-sectional studies, 12 articles reported on adverse dose-dependent effects. Of the 9 longitudinal studies analyzed, 5 studies found a detectable effect of methylmercury on brain function of the children.

From a comprehensive review of the data, it was apparent that neurodevelopmental abnormalities occurred in children after a range of gestational exposures from maternal consumption of highly contaminated fish: maternal hair 0.3 to 12.7 μg/g, cord blood 0.75 to 25.7 μg/L, maternal blood 3.8 μg/L.19

Data from the National Health and Nutrition Examination Survey conducted in the United States between 1999 and 2000 show that consuming fish 1 to 2 times a month corresponds to a geometric mean total mercury concentration of 0.20 μg/g in hair and 1.05 μg/L in blood for women of reproductive age. Consumption of fish 3 or more times a month corresponds to a geometric mean mercury content of 0.38 μg/g in hair and 1.94 μg/L in blood. Avoiding fish consumption corresponded to a mean total mercury content of 0.11 μg/g in hair and 0.51 μg/L in blood.

The threshold of 0.3 μg/g of mercury in maternal hair was selected by us from all of the studies analyzed because in the cross-sectional studies there were different adverse neuropsychologic end points detected when maternal hair mercury levels exceeded 0.3 μg/g.

Relevance of this threshold to Canada

Subsequently, we studied hair mercury concentrations among women of reproductive age in relation to fish intake in Ontario.20 Three groups of women were studied: women who had called the Motherisk Program for information on the reproductive safety of consuming fish during pregnancy (n = 22), a group of Japanese men and women residing in Toronto who consumed much larger than average amounts of fish (n = 23), and a group of Canadian women of reproductive age not seeking advice (n = 20). Mercury concentrations in hair samples were measured using inductively coupled plasma mass spectrometry. Seafood consumption habits were recorded for each participant. Based on the types of fish consumed and consumption frequencies, the estimated monthly intake of mercury was calculated. Hair mercury concentrations were correlated to both the number of monthly seafood servings and the estimated ingested mercury dose.

There were significant correlations between fish servings and hair mercury (Spearman r = 0.73, P < .0001) and between amounts of consumed mercury and hair mercury concentrations (Spearman r = 0.81, P < .0001). Nearly two-thirds of the Motherisk callers, all of the Japanese women, and 15% of the Canadian women of reproductive age had hair mercury above 0.3 μg/g, which was shown by us to be the lowest observable adverse effect level in the large systematic review of all perinatal studies.19

Conclusion

Because of very wide variability, general recommendations for a safe number of fish servings might not be sufficient to protect the fetus. Analysis of hair mercury might be warranted before pregnancy in selected groups of women who consume more than 12 oz of fish per week, as dietary modification can decrease body burden and ensure fetal safety.

Notes

MOTHERISK

Motherisk questions are prepared by the Motherisk Team at the Hospital for Sick Children in Toronto, Ont. Dr Koren is Director of the Motherisk Program. Dr Bend is a toxicologist at the University of Western Ontario in London. Dr Koren is supported by the Research Leadership for Better Pharmacotherapy during Pregnancy and Lactation. He holds the Ivey Chair in Molecular Toxicology in the Department of Medicine at the University of Western Ontario.

Do you have questions about the effects of drugs, chemicals, radiation, or infections in women who are pregnant or breastfeeding? We invite you to submit them to the Motherisk Program by fax at 416 813–7562; they will be addressed in future Motherisk Updates.

Published Motherisk Updates are available on the Canadian Family Physician website (www.cfp.ca) and also on the Motherisk website (www.motherisk.org).

Footnotes

This article is eligible for Mainpro-M1 credits. To earn credits, go to www.cfp.ca and click on the Mainpro link.

Competing interests

None declared

References

1. Mozaffarian D, Rimm EB. Fish intake, contaminants, and human health: evaluating the risks and the benefits. JAMA. 2006;296(15):1885–99. Erratum in: JAMA 2007;297 (6):590. [PubMed]
2. Makrides M, Neumann M, Simmer K, Pater J, Gibson R. Are long-chain polyunsaturated fatty acids essential nutrients in infancy? Lancet. 1995;345(8963):1463–8. [PubMed]
3. Innis SM. Fatty acids and early human development. Early Hum Dev. 2007;83(12):761–6. Epub 2007 Oct 24. [PubMed]
4. Hadders-Algra M. Prenatal long-chain polyunsaturated fatty acid status: the importance of a balanced intake of docosahexaenoic acid and arachidonic acid. J Perinat Med. 2008;36(2):101–9. [PubMed]
5. Dovydaitis T. Fish consumption during pregnancy: an overview of the risks and benefits. J Midwifery Womens Health. 2008;53(4):325–30. [PubMed]
6. Costa LG. Contaminants in fish: risk-benefit considerations. Arh Htg Rada Toksikol. 2007;58(3):367–74. [PubMed]
7. Clarkson TW, Magos L. The toxicology of mercury and its chemical compounds. Crit Rev Toxicol. 2006;36(8):609–62. [PubMed]
8. Dórea JG. Persistent, bioaccumulative and toxic substances in fish: human health considerations. Sci Total Environ. 2008;400(1–3):93–114. Epub 2008 Jul 23. [PubMed]
9. Harada M. Congenital Minamata disease: intrauterine methylmercury poisoning. Teratology. 1978;18(2):285–8. [PubMed]
10. Yorifuji T, Tsuda T, Takao S, Suzuki E, Harada M. Total mercury content in hair and neurologic signs: historic data from Minamata. Epidemiology. 2009;20(2):188–193. [PubMed]
11. Harada M. Minamata disease: methylmercury poisoning in Japan caused by environmental pollution. Crit Rev Toxicol. 1995;25(1):1–24. [PubMed]
12. Ekino S, Susa M, Ninomiya T, Imamura K, Kitamura T. Minamata disease revisited: an update on the acute and chronic manifestations of methyl mercury poisoning. J Neurol Sci. 2007;262(1–2):131–44. Epub 2007 Aug 2. [PubMed]
13. Harada M, Akagi H, Tsuda T, Kizaki T, Ohno H. Methylmercury level in umbilical cords from patients with congenital Minamata disease. Sci Total Environ. 1999;234(1–3):59–62. [PubMed]
14. Amin-Zaki L, Elhassani S, Majeed MA, Clarkson TW, Doherty RA, Greenwood M. Intra-uterine methylmercury poisoning in Iraq. Pediatrics. 1974;54(5):587–95. [PubMed]
15. Greenwood MR. Methylmercury poisoning in Iraq. An epidemiological study of the 1971–1972 outbreak. J Appl Toxicol. 1985;5(3):148–59. [PubMed]
16. Bakir F, Damluji SF, Amin-Zaki L, Murtadha M, Khalidi A, al-Rawi NY, et al. Methylmercury poisoning in Iraq. Science. 1973;181(96):230–41. [PubMed]
17. Rustam H, Hamdi T. Methyl mercury poisoning in Iraq. A neurological study. Brain. 1974;97(3):500–10. [PubMed]
18. Clarkson TW, Magos L, Myers GJ. The toxicology of mercury—current exposures and clinical manifestations. N Engl J Med. 2003;349(18):1731–7. [PubMed]
19. Schoeman K, Bend JR, Hill J, Nash K, Koren G. Defining a lowest observable adverse effect hair concentrations of mercury for neurodevelopmental effects of prenatal methylmercury exposure through maternal fish consumption: a systematic review. Ther Drug Monit. 2009;31(6):670–82. [PubMed]
20. Schoeman K, Tanaka T, Bend JR, Koren G. Hair mercury levels of women of reproductive age in Ontario, Canada: implications to fetal safety and fish consumption. J Pediatr. 2010;157(1):127–31. Epub 2010 Mar 24. [PubMed]

Articles from Canadian Family Physician are provided here courtesy of College of Family Physicians of Canada