Publication Date:
2017
abstract:
Human exposure to mercury is still a major public health concern. In this context, children
have a higher susceptibility to adverse neurological mercury effects, compared to adults with similar
exposures. Moreover, there exists a marked variability of personal response to detrimental mercury
action, in particular among population groups with significant mercury exposure. New scientific
evidence on genetic backgrounds has raised the issue of whether candidate susceptibility genes can
make certain individuals more or less vulnerable to mercury toxicity. In this review, the aim is to
evaluate a new genetic dimension and its involvement in mercury risk assessment, focusing on the
important role played by relevant polymorphisms, located in attractive gene targets for mercury
toxicity. Existing original articles on epidemiologic research which report a direct link between the
genetic basis of personal vulnerability and different mercury repercussions on human health will be
reviewed. Based on this evidence, a careful evaluation of the significant markers of susceptibility will
be suggested, in order to obtain a powerful positive "feedback" to improve the quality of life. Large
consortia of studies with clear phenotypic assessments will help clarify the "window of susceptibility"
in the human health risks due to mercury exposure.
Iris type:
01.01 Articolo in rivista
Keywords:
mercury; toxicokinetics; human health; risk assessment; children exposure; environmental genetics; DNA variants; biomarkers of susceptibility
List of contributors:
Andreoli, Virginia; Sprovieri, Francesca
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