In clinical research, scientists often invoke race, ethnicity and ancestry to better understand underlying factors that contribute to disease, even when the connection is not quite clear. This approach is prevalent in clinical genetics, a field of study that harnesses genetic testing to understand aspects of a patient’s personal health. But while race- or ancestry-based information can play an important role in health research — such as ensuring a particular clinical study represents diverse populations — its use in science can be misguided, said Alice Popejoy, PhD, a postdoctoral scholar who studies the intersection of public health and genetics. Including race, ethnicity or ancestry in a scientific study can produce misleading results that present sociocultural factors, such as race, as a biological cause of certain diseases — when, in fact, environmental factors or actual biology, such as genetic mutations, may underlie the disease.
To better understand the use of race, ethnicity and ancestry in clinical genetics, Popejoy and her mentors Carlos Bustamante, PhD, professor of biomedical data science and of genetics, and Kelly Ormond, MS, professor of genetics, led a team of scientists to conduct a nationwide survey asking clinical genetics professionals and researchers about the importance of race, ethnicity and ancestry in their work, including questions about how they define the terms and use the concepts as variables in their research or clinical practice.
The study was published June 2 in the American Journal of Human Genetics.
In a conversation with science writer Hanae Armitage, Popejoy discussed the role of race, ethnicity and ancestry in research.
1. What is the difference between race, ethnicity and ancestry?
Popejoy: There really aren’t universal definitions of race, ethnicity and ancestry, which is likely part of the reason there’s so much confusion about what they mean and how they overlap, especially in science. Race, for instance, is more often used in a sociopolitical context — as a construct that’s broadly tied to societal hierarchies of power.
Often with ethnicity, people tend to use the term in a more cultural or community-based context. Sometimes people will use race and ethnicity interchangeably, as some may feel more comfortable saying ethnicity because race can invoke discomfort related to racism. Ancestry is an interesting one, because people have really personal opinions about what ancestry means to them. For some, the term ancestry might invoke feelings about culture or heritage, and may even have spiritual undertones. But when I talk about ancestry, it’s in terms of genetics, and it’s derived from genomic analyses. We’re talking about the fact that we all inherit pieces of DNA, little bits of genetic material, from our parents who inherited it from their parents, and so on.
2. Is there a role for race, ethnicity and ancestry in science, and if so, what is it?
Popejoy: That’s one of the most common questions I get asked in my field. If race and ethnicity are social or cultural constructs, why include them in our research at all, when genetic ancestry seems so much more scientific? And the answer is that unfortunately, in a society plagued by systemic and institutionalized racism, sociocultural identity has a very real impact on health, as not everyone has equal access to nutrition, education and health care. So, race is not biological, but it does have real biological effects in an unequal society.
In the case of ancestry, it’s a little more ambiguous; we’re still trying to figure out the most accurate and useful applications of genetic ancestry in research and medicine. In genomics, ancestry is often used to account for clusters of individuals in a sample population who are more closely related to one another, and their shared genomic background could impact the results of a genetic-association study. In clinical genetics, a person’s ancestral background is also important for tracking the representation of groups from different genetic ancestries in population databases; adequate representation of these groups ensures the results of a genetic test are interpreted appropriately. Let’s say you get a genetic test, the results come back and the doctor says, “I’m sorry. We see a genetic variant of unknown or uncertain significance, and we don’t know how to interpret this for you.” One of the reasons they might not be able to interpret that variant is that it’s never been seen in any of the databases, meaning the patient may be of a certain ancestral background that is not well represented. We don’t know whether it’s missing from the database because it’s really rare and likely to be causing the patient’s condition, or if it is somewhat common and benign, or not disease-causing, in that person’s ancestral population, but the population has not been adequately sampled, as most of the genetic research that’s been done has been in people of European ancestry.
