Format

Send to

Choose Destination
BMC Med Genomics. 2017 Jan 9;10(1):3. doi: 10.1186/s12920-016-0240-3.

Health and genetic ancestry testing: time to bridge the gap.

Author information

1
Department of Sociology, Bath Spa University, Newton Park, Bath, BA2 9BN, UK. a.smart@bathspa.ac.uk.
2
Department of Anthropology, University of Texas at Austin, 2201 Speedway, Stop C3200, Austin, TX, 78712-1723, USA.
3
Department of Sociology, Lancaster University, Bowland North, Bailrigg, LA1 4YN, UK.

Abstract

BACKGROUND:

It is becoming increasingly difficult to keep information about genetic ancestry separate from information about health, and consumers of genetic ancestry tests are becoming more aware of the potential health risks associated with particular ancestral lineages. Because some of the proposed associations have received little attention from oversight agencies and professional genetic associations, scientific developments are currently outpacing governance regimes for consumer genetic testing.

MAIN TEXT:

We highlight the recent and unremarked upon emergence of biomedical studies linking markers of genetic ancestry to disease risks, and show that this body of scientific research is becoming part of public discourse connecting ancestry and health. For instance, data on genome-wide ancestry informative markers are being used to assess health risks, and we document over 100 biomedical research articles that propose associations between mitochondrial DNA and Y chromosome markers of genetic ancestry and a wide variety of disease risks. Taking as an example an association between coronary heart disease and British men belonging to Y chromosome haplogroup I, we show how this science was translated into mainstream and online media, and how it circulates among consumers of genetic tests for ancestry. We find wide variations in how the science is interpreted, which suggests the potential for confusion or misunderstanding.

CONCLUSION:

We recommend that stakeholders involved in creating and using estimates of genetic ancestry reconsider their policies for communicating with each other and with the public about the health implications of ancestry information.

KEYWORDS:

Direct-to-consumer genetic tests; Disease/Health risk; Genetic ancestry; Public understanding; Regulation; Social implications

PMID:
28069037
PMCID:
PMC5223458
DOI:
10.1186/s12920-016-0240-3
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for BioMed Central Icon for PubMed Central
Loading ...
Support Center