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Health Risks of Ionizing Radiation: - Clark University

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Appendix B 184<br />

cities and 2,729 settlements in Russia and Belarus<br />

and found an ERR <strong>of</strong> 23/Gy (8.6-82). The dose-response<br />

relationship in this study appeared linear and<br />

a significant risk was observed in the lowest dose<br />

group (< 0.1 Gy, mean thyroid dose <strong>of</strong> 0.05 Gy).<br />

Ivanov et al. (2003) studied adolescents and adults<br />

(aged 15-69 at the time <strong>of</strong> the accident) in the Bryansk<br />

district <strong>of</strong> Russia. There was no evidence <strong>of</strong> increased<br />

thyroid cancer risk in the total cohort, which<br />

is consistent with other studies. However, the subcohort<br />

aged 15-29 at the time <strong>of</strong> the accident showed a<br />

significant ERR <strong>of</strong> 8.65/Gy (0.81-11.47).<br />

These risk estimates left a possible confounding<br />

issue unaccounted for- a relatively low intake<br />

<strong>of</strong> natural iodine in the diet <strong>of</strong> children near Chernobyl<br />

may have increased their thyroid cancer risk<br />

by increasing the amount <strong>of</strong> radioiodine sequestered<br />

by the thyroid. This possibility was addressed in<br />

another study <strong>of</strong> Bryansk children (ages 6-18) by<br />

Shakhtarin et al. (2003). These researchers found<br />

that dietary iodine did play a role in radiation-induced<br />

cancer risk so that although the overall ERR<br />

was 18.1/Gy (11.3-26.9), the ERR in areas with sufficient<br />

dietary iodine was 13/Gy (-11-71.2). Another<br />

important consideration in interpreting these studies<br />

is the fact that follow-up was for a small number <strong>of</strong><br />

years after exposure. Since background cancer risk<br />

is low in children, relative risk estimates based on<br />

childhood cancer incidence may overestimate lifetime<br />

risks.<br />

Medical exposures<br />

Iodine-131 has been used at low doses to diagnose<br />

thyroid disease and at high doses to treat hyperthyroidism<br />

by killing <strong>of</strong>f part <strong>of</strong> the thyroid. Results <strong>of</strong><br />

an ongoing cohort follow-up in Sweden have been<br />

published a few times (Holm et al. 1988, Hall et al.<br />

1996, Dickman et al. 2003). The study participants<br />

had received average doses <strong>of</strong> ~1 Gy <strong>of</strong> 131I between<br />

1951 and 1962. Holm et al. found an SIR <strong>of</strong><br />

1.27 (0.94-1.67) and a positive dose-response relationship<br />

that was not quantified. Hall et al. confirmed<br />

the elevated SIR (1.35, 1.05-1.71) and quantified<br />

the dose-response relationship for patients<br />

younger than 20 (ERR 0.25/Gy, 0-2.7). Dickman et<br />

al. did not report either an elevated SIR or a significant<br />

dose-response relationship (although the data<br />

suggest a positive dose-response), but note the fact<br />

that only 300 subjects in their study were under the<br />

age <strong>of</strong> 10, the period <strong>of</strong> highest observed sensitivity<br />

in other studies. Another study <strong>of</strong> diagnostic 131I,<br />

again with an average dose <strong>of</strong> ~1 Gy, was carried<br />

out in Germany (Hahn et al. 2001). This study found<br />

no increase in risk (RR 0.86, 0.14-5.13) but, as in<br />

the case <strong>of</strong> the Swedish cohort, was largely limited<br />

to adults.<br />

<strong>Radiation</strong> treatment for hyperthyroidism involves<br />

131I doses in the tens or hundreds <strong>of</strong> Gy.<br />

A cohort <strong>of</strong> Swedish patients showed an elevated<br />

SMR (1.95, 1.01-3.41)) and a nonsignificant doseresponse<br />

pattern with thyroid cancer mortality (Hall<br />

et al. 1992). A UK study found an SIR <strong>of</strong> 3.25 (1.69-<br />

6.25) and an SMR <strong>of</strong> 2.78 (1.16-6.67) (Franklyn<br />

et al. 1999). A U.S. study found an SMR <strong>of</strong> 3.94<br />

(2.52-5.86) and noted a marginally significant doseresponse<br />

relationship (Ron et al. 1998). Although<br />

these three studies generally agree with each other in<br />

terms <strong>of</strong> the magnitude <strong>of</strong> mortality risk that hyperthyroid<br />

patients face with 131I treatment, they <strong>of</strong>fer<br />

little insight on the question <strong>of</strong> low doses to healthy<br />

people because the thyroid was severely damaged<br />

and there was an underlying thyroid disease in all <strong>of</strong><br />

the study subjects.<br />

B.4 Non-cancer Thyroid Disease<br />

Non-cancer effects <strong>of</strong> radiation have been observed<br />

in the exposed populations described above, although<br />

they haven’t been examined with the same<br />

quantitative detail as cancer. The atomic bomb survivors<br />

have shown an excess <strong>of</strong> thyroid disease, a<br />

general category that includes hypothyroidism, thyroiditis,<br />

goiter and thyrotoxicosis. It has been estimated<br />

that 16% <strong>of</strong> the thyroid disease in the Adult<br />

<strong>Health</strong> Study can be attributed to a-bomb radiation<br />

exposures (Wong et al. 1993). A significant dose-response<br />

relationship was observed in this study with<br />

an ERR <strong>of</strong> 0.30/Gy (0.16-0.47); this was attributed<br />

to the effects <strong>of</strong> exposure at younger ages. Hypothyroidism<br />

was also specifically analyzed in this cohort<br />

by Nagataki et al. (1994), who found a concave<br />

dose-response curve with a maximum incidence <strong>of</strong><br />

hypothyroidism (OR ~2.5) occurring with a dose <strong>of</strong><br />

~0.7 Sv. Below 0.5 Sv the dose-response relationship<br />

was linear with an apparent ERR <strong>of</strong> ~3/Sv.<br />

Autoimmune thyroid disease is a condition<br />

where the immune system attacks the thyroid. Evi-

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