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MERCURY 245<br />

2. HEALTH EFFECTS<br />

In addressing the potential influence of concurrent PCB exposure on the Faroe results, the Confounders <strong>and</strong><br />

Variables (Epidemiology) panel indicated that with respect to four of the prenatal outcomes (related<br />

primarily to verbal <strong>and</strong> memory per<strong>for</strong>mance), when PCBs were included in the model, only one of these<br />

outcomes is specifically related to mercury exposure. Concerning this matter, the panel wrote that “... the<br />

most likely explanation is that both (mercury <strong>and</strong> PCBs)... affect these three outcomes, but their relative<br />

contributions cannot be determined given their concurrence in this population.” The Neurobehavioral<br />

Endpoints Panel also looked at this issue, <strong>and</strong> noted that “PCB exposure might act as an effect modifier,<br />

increasing the susceptibility to MeHg”; however, this panel further indicated that it did not believe that the<br />

effects seen in the Faroe Isl<strong>and</strong>s were due to uncontrolled confounding by PCBs. A third panel that<br />

addressed the issue of concurrent PCB exposures, the Statistics/Design Panel, noted that only 3 of 208 PCB<br />

congeners were measured in the Faroe study, <strong>and</strong> stated that it “seems likely that mercury was measured<br />

more accurately than the biologically relevant PCB exposure. Consequently even if the neurological effects<br />

seen in this study were caused entirely by PCBs, it is possible that mercury would still be more highly<br />

correlated with these effects than PCBs.” The Statistics/Design Panel also said that “the best method to deal<br />

with this problem would be to study a population where exposure to PCBs is not an issue.” This statement<br />

points directly to the Seychelles study as the study most appropriate <strong>for</strong> MRL derivation.<br />

Another issue raised at Raleigh workshop concerned the taking of hair samples <strong>for</strong> determining pre-natal<br />

exposure. In the Seychelles, hair samples were collected 6 months post-partum, <strong>and</strong> segments<br />

corresponding to pregnancy were selected <strong>for</strong> analysis. In the case of the Faroese, hair samples were taken<br />

at the scalp. Regarding that, the Confounders <strong>and</strong> Variables (Epidemiology) panel stated that “Given the<br />

time it takes the Hg to be excreted into the hair, we can assume that samples collected at parturition do not<br />

cover the last 6 weeks of gestation, during which critically important neuronal proliferation <strong>and</strong><br />

differentiation is taking place.”<br />

Regarding the Seychelles <strong>and</strong> Faroe studies, the Neurobehavioral Endpoints Panel found “no specific<br />

neurobehavioral signature injury from MeHg” in the data from either study (Seychelles or Faroe). The<br />

same panel also noted that episodic exposure in the Faroese (1–2 fish meals/week <strong>and</strong>

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