Genomics and Health Care Disparities: The Role of Statistical Discrimination
Ten years ago, two events occurred that have transformed biomedical research. In 2001, the draft sequence of the human genome was announced and a year later, the Institute of Medicine released "Unequal Treatment," the first comprehensive report on racial and ethnic health care disparities...
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Veröffentlicht in: | JAMA : the journal of the American Medical Association 2012-11, Vol.308 (19), p.1979-1980 |
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Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Ten years ago, two events occurred that have transformed biomedical research. In 2001, the draft sequence of the human genome was announced and a year later, the Institute of Medicine released "Unequal Treatment," the first comprehensive report on racial and ethnic health care disparities in the US. 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. Here, Armstrong examines the potential contribution of two 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. |
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ISSN: | 0098-7484 1538-3598 |
DOI: | 10.1001/2012.jama.10820 |