Ten years
ago, 2 events occurred that have transformed biomedical research. In 2001, the
draft sequence of the human genome was announced. One year later, the Institute
of Medicine released “Unequal Treatment,” the first comprehensive report on
racial and ethnic health care disparities in the United States.1 Although the
report downplayed the contribution of genetics to disparities, enthusiasm about
the human genome spread rapidly to disparities research, creating a new field
focused on translating knowledge of human genetic variation into reductions in
disparities in health and health care.2 This Viewpoint examines the potential
contribution of 2 pathways in this field—the identification of genetic
variation as a cause of disparities and the reduction of clinical uncertainty
and statistical discrimination. The terms race and ethnicity are used to mean
socially determined, generally self-reported, categories…
Source:
Genomics and Health Care Disparities: The Role of Statistical
Discrimination. Armstrong K. JAMA. 2012 Nov 8:1-2.
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