
Studies in a Unique Arsenic-exposed Area of Chile
Our new ecologic evidence from Northern Chile suggests that
arsenic exposure in childhood or in utero could cause up to a 10-fold
increase in adverse health effects in the lungs in young adults. This may be
the first time that early-life exposure to a common environmental agent has
been linked to high risks of adverse health effects in adult humans. Importantly,
these data are preliminary and need to be confirmed. The highly unique arsenic
exposure scenario in Northern Chile offers a
rare opportunity to do this. Because almost everyone in Northern
Chile obtains their water from large municipal sources, and past
arsenic levels in all of these sources are well documented, arsenic
carcinogenicity can be studied using exposure data that are much more accurate
than anywhere else in the world. In addition, a very distinct 14-year period of
high exposure in this area, with low exposure before and after, has created a
population where tens of thousands of people were exposed to high arsenic
levels only in utero or as young children offering a unique opportunity
to study the long-term impacts of an early-life carcinogen with excellent data
on past exposure. We propose a case-control study of 675 cases of lung and
bladder cancer obtained over a three-year period using a rapid case
ascertainment system involving all local pathologists. Controls will be
obtained from the Chile
electoral register containing 94% of the Chilean population. Dose-response
relationships and other aspects of susceptibility will also be investigated.
For example, we have found evidence that people producing high levels of
monomethylated arsenic (MMA) have 2-5 times higher cancer risks than others,
perhaps due to the highly toxic trivalent form (MMA3). Biological samples will
be collected on all subjects and susceptibility related to metabolism, diet,
genetics, and other factors will be investigated. Millions of people in the US are exposed
to drinking water arsenic. But, current US arsenic regulations do not
incorporate information on potentially susceptible subgroups despite the fact
that cancer risks in these groups could be exceedingly high. The information
gained from this project may help to determine if some groups, such as
children, those who metabolize arsenic poorly, or those with poor nutrition,
may need special consideration in regulatory standard setting. Information on
MMA3, diet, and the future genetic and proteomic studies we will plan could add
further insight into the co-factors and mechanisms of environmental
carcinogenesis.
Chile Research Teams
Antofagasta
Team:
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Jacqueline Elizabeth
Calle Cotapos
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Liliana Matilde Pérez Rodríguez
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Patricio Javier
Quintremán Lara
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Roxana Loreto Parra Lara
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Arica Team:
Under construction.
Iquique
Team:
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Johanna Acevedo Romo
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Yasna Oyarzun Aguilar
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Glenn Rojas Parra
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University
of California, Berkeley ~ School of Public Health ~ 50 University Hall MC7360
~ Berkeley, CA 94720-7360
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Telephone:
510/843-1736
E-mail: asrg@berkeley.edu
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