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MERCURY 308<br />

2. HEALTH EFFECTS<br />

most recent NOAEL of 6.8 ppm <strong>for</strong> the Seychelles cohort at 66 months of age strongly supports the findings<br />

at earlier ages, <strong>and</strong> that the benefits of eating fish outweigh the small risk of adverse effects from an<br />

increased exposure to methylmercury <strong>for</strong> this exposure pathway.<br />

The differences in these studies highlight the importance of interpreting epidemiology results <strong>and</strong>, indeed, all<br />

study results on mercury toxicity within a fairly comprehensive context of the numerous factors that might<br />

affect the toxicokinetics <strong>and</strong> the amount absorbed (e.g., <strong>for</strong>m of mercury, route of exposure, age, diet of<br />

population exposed, health status, other potential sources of exposure to mercury, dose duration, constancy<br />

of dose amount over time, etc.)<br />

A route of exposure unique to children is breast milk. Both organic <strong>and</strong> inorganic mercury can move into<br />

breast milk from a nursing woman’s body, <strong>and</strong> children will readily absorb this mercury. Oskarsson et al.<br />

(1996) assessed the total <strong>and</strong> inorganic mercury content in breast milk <strong>and</strong> blood in relation to fish<br />

consumption <strong>and</strong> amalgam fillings (an exposure source <strong>for</strong> older children). Total mercury concentrations<br />

were evaluated in breast milk, blood, <strong>and</strong> hair samples collected 6 weeks after delivery from 30 lactating<br />

Swedish women. In breast milk, about half of the total mercury was inorganic <strong>and</strong> half was methylmercury,<br />

whereas in blood only 26% was inorganic <strong>and</strong> 74% was methylmercury. That is because, unlike the<br />

placental barrier, which is crossed more easily by methylmercury than by inorganic mercury, inorganic<br />

mercury moves more easily into breast milk. Some researchers think that a carrier mediated process is<br />

involved (Sundberg et al 1998).<br />

For the Swedish population in the study, Oskarsson et al. (1996) reports that there was an efficient transfer of<br />

inorganic mercury from blood to breast milk <strong>and</strong> that mercury from amalgam fillings was probably the main<br />

source of mercury in breast milk, while methylmercury levels in blood did not appear to be efficiently<br />

transferred to breast milk . Exposure of the infant to mercury in breast milk was calculated to range up to<br />

0.3 µg/kg/day of which approximately one-half was inorganic mercury. This exposure corresponds to<br />

approximately one-half the tolerable daily intake of total mercury <strong>for</strong> adults recommended by the World<br />

Health organization. The authors concluded that ef<strong>for</strong>ts should be made to decrease total mercury burden in<br />

women of reproductive age Oskarsson et al. (1996).<br />

The metabolism of mercury is relatively straight<strong>for</strong>ward compared, <strong>for</strong> example, to pesticides or some<br />

organic solvents. No in<strong>for</strong>mation was identified to indicate that metabolic pathways are different <strong>for</strong><br />

children <strong>and</strong> adults, or that children have unique metabolites. Once absorbed, metallic <strong>and</strong> inorganic

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