Jt. Babbitt et al., Hematopoietic neoplasia in C57BL/6 mice exposed to split-dose ionizing radiation and circularly polarized 60 Hz magnetic fields, CARCINOGENE, 21(7), 2000, pp. 1379-1389
This study assessed the effect of chronic exposure to a 60 Hz circularly po
larized magnetic field on the occurrence of ionizing radiation-induced lymp
homa and other hematopoietic neoplasia in mice. Female C57BL/6 mice receive
d lifetime exposure to either a magnetic field flux density of 1.42 mT for
18 h/day, or an ambient magnetic field of 0.13 mu T Beginning- on the first
day of magnetic field exposure, 1710 mice were treated with one of three l
evels of split-dose Cobalt-60 gamma-radiation (cumulative 3.0, 4.0 or 5.1 C
y), The remaining 570 mice received sham irradiation treatment, Sections fr
om 10 lymphoid tissues were evaluated histopathologically for hematopoietic
neoplasia, The primary statistical analysis used the Poly3 method to compa
re lymphoma incidences in magnetic field (MF)-exposed and control mice. Sec
ondary analyses used the Cox proportional hazards model to analyze incidenc
e rates for mortality and development of specific types of neoplasia, The m
ortality incidence rate was increased by ionizing radiation treatment, and
all neoplasms were observed sooner in irradiated mice. However, the lifetim
e incidence of hematopoietic neoplasia was similar in all experimental grou
ps, including those that were not exposed to ionizing radiation. Chronic ex
posure to MFs did not affect the mortality incidence rates and did not chan
ge the relative incidences of hematopoietic neoplasia in mice that received
the same ionizing radiation treatment, with the exception of a marginally
significant reduced relative risk of 0.97 (P = 0.05) for lymphoblastic lymp
homa in mice exposed to a magnetic field and treated with 5.1 Cy, Lymphomas
and histiocytic sarcomas were first observed similar to 50 days sooner in
mice that were exposed to magnetic fields but not ionizing radiation, altho
ugh this comparison was not statistically significant and the incidence of
hematopoietic neoplasia in these mice was not different from that of mice i
n the 0 T/0 Gy group.