A 20-year retrospective analysis of methylmercury in fish involving over 38,000
individuals in Canada did not find any identifiable health problems related to mercury.5
No negative health effects from eating contaminated fish have been established; no
clinical cases of methylmercury poisoning from fish have been found in Canada or Sweden.6
Two important scientific studies that are currently under way aim to address the effect
of mercury in the food chain; these are the Seychelles study and the Faroe Islands study.
Of the two studies, the double-blind study in the Seychelles has by far the best design
and has the potential to yield the most valid scientific data.
The Seychelles study. Controversy exists concerning the fetal risk associated
with exposure to low-dose methylmercury from maternal fish consumption.7
Previous studies of the effects of acute prenatal mercury exposure identified delays in
achieving developmental milestones among exposed children. This led to public health
concerns that prenatal low-dose exposure from fish consumption could also adversely affect
the fetus.
The extensive Seychelles Child Development Study that began in 1986 is examining the
association between fetal methylmercury exposure from a maternal diet high in fish and
subsequent child development. The study is double blind and uses maternal hair mercury as
the index of fetal exposure. No definite effects have been detected through 29 months of
age in the main study.8 Toddlers who had prenatal exposure to methylmercury are
achieving the developmental milestones of walking and talking at normal ages.9
The authors do say that more detailed studies in older children are needed to determine if
there are adverse effects in fish-eating populations.
The Faroe Islands study. Human milk as a source of methylmercury exposure in infants
has been studied by Grandjean and others.10 In a community in the Faroe
Islands, high maternal consumption of pilot whale meat and blubber and other seafood had
the potential to cause a considerable transfer of neurotoxicants during breast-feeding.
The researchers followed 583 children from a birth cohort. Three developmental milestones
that are usually reached between 5 and 12 months of age, i.e., sitting, crawling and
standing, were examined. It was found that infants who reached the milestone criteria
early had significantly higher mercury concentrations in the hair at 12 months of age.
This association is contrary to what would be expected from possible neurotoxic effects of
mercury. The authors point out that early milestone development is clearly associated with
breast-feeding, which suggests that, if methylmercury exposure from human milk had any
adverse effect on milestone development in these infants, the effect was compensated by
the advantages associated with breast-feeding.
Thus, although a number of studies have looked at methylmercury in human breast milk,
no strong evidence of toxicity has been reported. Dose-response relationships are not
clearly established for developmental neurotoxicity under conditions of chronic exposure
(exposure for 365 days or more) to methylmercury; shorter periods of time such as the
duration of breast-feeding are even more challenging. In light of these findings it is
difficult to understand the recent change in the guidelines from Health Canada.
Mercury release is associated with the removal of an oxide layer from the surface of
the amalgam alloy. Only inorganic and ionic forms of mercury are released from amalgam
restorations. Release of mercury from restorations is time-dependent and proportional to
the surface area of the restorations.16 Mackert and Berglund17 have reported
that the rate of unstimulated mercury release from amalgam averages 0.4 µg per amalgam
surface per day; higher rates occur during the eating of some foods and during
tooth-brushing. (A number of reports have assumed that meals and snacks affect mercury
release to a degree similar to gum-chewing and tooth-brushing. This is, however, an
erroneous assumption, which leads to serious overestimations in calculating release of
mercury from restorations.18,19) If we assume that the stimulated condition
occurs during a period of 4 hours and that it is three times higher than the unstimulated
rate, it can be calculated that the 4-hour stimulated release during the day would be:
0.4 µg Hg/day ÷ 24 hours x 20 = 0.334 µg Hg/day.
Many researchers studying the release of mercury from amalgam have made use of a Jerome
401 instrument for sampling mercury in air. It takes the instrument 40 seconds to aspirate
500 mL of air; this amount of air (500 mL) is typical for an ordinary inhalation into the
lungs, but the lungs inhale that much air in just 2.5 seconds. The mercury vapour taken in
by the instrument in 40 seconds compared with the 2.5 seconds needed by the lungs produces
a mercury-in-air value (40 ÷ 2.5) that is 16 times too high. Mackert and Berglund17
point out that several publications misinterpret mercury in air by a factor of 16; when
used to make further calculations, these incorrect values compound inaccuracy.
WHO standards for occupational exposure to inorganic mercury are currently 50 µg/m3 in
air and 50 µg/g creatinine in urine.20 The mean total mercury level in urine
for 1,073 male subjects with a mean of 8.2 amalgam restorations has been reported as 3.1
µg/L.21
WHO's maximum acceptable daily intake (ADI) for mercury is 40 µg/day. An individual
can be exposed to 44 µg/day of organic mercury in food, of which about 90% is absorbed,22
and still keep within the limit of 40 µg/day:
An individual can be exposed to 262 µg/day of inorganic mercury from amalgam fillings
with only 15.25% absorption and be within the same limit of 40 µg/day:
Assuming a combined stimulated and unstimulated release of 0.535 µg/day per amalgam
surface, this 262 µg/day of mercury vapour and ionic mercury given off from amalgam
fillings would be equivalent to the mercury released from 490 amalgam surfaces. How many
patients do you know who have 490 amalgam surfaces?
A woman weighing 54 kg under the old Health Canada maximum exposure limit of 0.47
µg/kg/day would be permitted to be exposed to 25.38 µg/day Hg. Assuming no mercury being
contributed from food, this 54-kg woman would have to have 47 amalgam surfaces (assuming
an average mercury release per surface of 0.534 µg/day) to reach the maximum level of
mercury permitted. With the new lower Health Canada maximum exposure limit, the number of
amalgam surfaces would be reduced to 20, again assuming no mercury intake from other
sources such as food; this would be equal to an absorption of 1.6 µgHg/day. In other
words, with the new Canadian exposure limit of 0.2 µg/Hg/kg/day, a 54-kg woman would be
permitted to be exposed to:
The resultant absorbed dose differs greatly with the form of mercury. If all of the
mercury is food-related, then the absorbed dose would be 90% of 10.8, i.e., 9.7 µg.
Alternatively, if the mercury is all contributed from dental amalgam fillings, then the
absorbed dose would be
Thus, the uptake of food-related organic mercury is six times higher than the uptake of
mercury from amalgam; moreover, food-related mercury is significantly more toxic. The
constantly repeated statement that most mercury is derived from amalgam fillings is
puzzling.
Recent announcements in Canada and the United Kingdom raise the question, Should
governments be developing limits and issuing precautionary advice for exposure to mercury
from food or dental amalgam in the absence of new, definitive scientific data? Do such
announcements themselves create unease and stress that can affect the health of the
population? The public should not be misled about the difference between exposure to
mercury and the absorbed dose of mercury, or about the different chemical forms in which
it exists. When the public see an item reported in the media they assume that it is true.
If governments change position statements or guidelines regarding health and safety, the
public assume that the situation has become worse. That assumption holds even if, as in
the case of the British government and dental amalgam, the new guidelines are introduced
with the qualifying statement that there is no evidence on the health risk.
According to some people who view dental amalgam as causing a variety of health
problems, no level of mercury is acceptable in the human body. The concept that an actual
tolerance may exists for low levels of mercury in the human body can, however, be
rationalized. The prevalence of naturally occurring mercury in the Earth's crust, coupled
with the relative ease with which it can be chemically modified, transported and exchanged
among land, aquatic and air environments, suggests that living organisms have been in
contact with mercury and mercury compounds throughout the long evolution of biological
systems leading up to human development.26,27 Given the epidemiological
evidence we have, it seems likely that humans may have evolved with a threshold level for
mercury below which there is no response or observable adverse health effects.
Dr. Derek W. Jones is professor of biomaterials at Dalhousie
University, Halifax.
Reprint requests to: Dr. D.W. Jones, Dalhousie University, Department
of Applied Oral Sciences, 5981 University Ave., Halifax, NS B3H 3J5.
1. Amdur MO, Doull J, Klassen CD. Cassaret and Doull's Toxicology: The basic science of
poisons. New York: Pergamon Press; 1991. p. 650.
2. Lakowicz JR, Anderson CJ. Permeability of lipid biolayers to methylmercuric
chloride: quantification by fluorescence quenching of a carbazole-labeled phospholipid.
Chem Biol Inter 1980; 30:309-23.
3. Grieb TM, Driscoll CT, Gloss SP, and others. Factors affecting mercury accumulation
in fish in the Upper Michigan Peninsula. Environ Toxicol Chem 1990; 9:919-30.
4. Fitzgerald W. Fate and transport of mercury in the environment: global aspects.
Paper presented at 12th International Neurotoxicology Conference; 1994 Oct 30-Nov 2; Hot
Springs, Arkansas.
5. Wheatley B, Paradis S. Balancing human exposure, risk and reality: questions raised
by the Canadian Aboriginal Methylmercury Program. Neurotoxicology 1996; 17:241-50.
6. Clarkson T. Human exposure to methylmercury from fish: studies of fish eating
populations. Paper presented at 12th International Neurotoxicology Conference; 1994 Oct
30-Nov 2; Hot Springs, Arkansas.
7. Axtell CD, Myers GJ, Davidson PW, Choi AL, Cernichiari E, Sloane-Reeves J, and
others. Semiparametric modeling of age at achieving developmental milestones after
prenatal exposure to methylmercury in the Seychelles Child Development Study. Environ
Health Perspect 1998; 106:559-63.
8. Myers GJ, Davidson PW, Cox C, Shamlaye CF, Tanner MA, Marsh DO, and others. Summary
of the Seychelles Child Development Study on the relationship of fetal methylmercury
exposure to neurodevelopment. Neurotoxicology 1995; 16:711-6.
9. Myers GJ, Davidson PW, Shamlaye CF, Axtell CD, Cernichiari E, Choissy D, and others.
Effects of prenatal methylmercury exposure from a high fish diet on developmental
milestones in the Seychelles Child Development Study. Neurotoxicology 1997; 18:819-29.
10. Grandjean P, Weihe P, White RF. Milestone development in infants exposed to
methylmercury from human milk. Neurotoxicology 1995; 16:27-33.
11. Oskarsson A, Schultz A, Skerfving S, Hallen IP, Ohlin B, Lagerkvist BJ. Total and
inorganic mercury in breast milk in relation to fish consumption and amalgam in lactating
women. Arch Environ Health 1996; 51:234-41.
12. Smith JC, Allen PV, Von Burg R. Hair methylmercury levels in U.S. women. Arch
Environ Health 1997; 52:476-80.
13. Drexler H, Schaller KH. The mercury concentration in breast milk resulting from
amalgam fillings and dietary habits. Environ Res 1998; 77:124-9.
14. Chang SB, Siew C, Gruninger SE. Factors affecting blood mercury concentrations in
practicing dentists. J Dent Res 1992; 71:66-74.
15. Mjor IA, Pakhomov GN. Dental amalgam and alternative direct restorative materials,
WHO, Division of Noncommunicable Diseases, Geneva; 1997.
16. Berglund A, Pohl L, Olsson S, Bergman M. Determination of the rate of release of
intra-oral mercury vapour from amalgam. J Dent Res 1988; 67:1235-42.
17. Mackert JR Jr, Berglund A. Mercury from dental amalgam fillings: absorbed dose and
the potential for adverse health effects. Crit Rev Oral Biol Med 1997; 8:410-36.
18. Berglund A. Estimation by a 24-hour study of the dose of intra-oral mercury vapour
inhaled after release from dental amalgam. J Dent Res 1990; 69:1646-51.
19. Berglund A, Molin M. Mercury vapour release from dental amalgam in patients with
symptoms allegedly caused by amalgam fillings. Eur J Oral Sci 1996; 104:56-63.
20. World Health Organization. Inorganic mercury. Environmental health criteria 118.
International Program on Chemical Safety. Geneva; 1991.
21. Derouen T, Martin M, Woods J, Townes B, Leroux B, and others. Casa Pia study of the
health effects of dental amalgam. J Dent Res 1998; 77(Spec Iss B - Abst 2594):956.
22. World Health Organization. Methylmercury. Environmental health criteria 101.
International Program on Chemical Safety. Geneva; 1990.
23. Bate, R. editor. What risk?, Oxford: Butterworth-Heinmann; 1997.
24. Anger WK, Johnson BL. Chemicals affecting behaviour. In: O'Donoghue J, editor.
Neurotoxicity of industrial and commercial chemicals. Vol. I. Boca Raton (FL): CRC Press;
1985. p. 51-148.
25. Kingman A, Albertini T, Brown LJ. Mercury concentrations in urine and whole blood
associated with amalgam exposure in a US military population. J Dent Res 1998; 77:461-71.
26. Clarkson T. Mercury. In: Nriagu JO, editor. Changing metal cycles and human health.
Berlin: Springer-Verlag; 1984. p. 285-309.
27. Nriagu JO, editor. The biogeochemistry of mercury in the environment. New York:
Elsevier- North Holland Biomedical Press; 1979.