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Studies probe value, impact of direct-to-consumer genetic testing

Illustration of a person examining a strand of DNA. Icon via Gan Khoon Lay, The Noun ProjectANN ARBOR—Despite being on the market for nearly a decade, direct-to-consumer genetic testing continues to be controversial among experts and raises concerns with health care providers and regulatory agencies.

A new NIH-funded "Impact of Personal Genomics (PGen) Study" addresses these concerns by empirically measuring the perceptions and tracking the behaviors of individuals who have received direct-to-consumer genetic testing from two separate companies.

J. Scott Roberts, associate professor of health behavior and health education at the University of Michigan School of Public Health, serves as a co-principal investigator on the large-scale collaborative study, which involves researchers from a number of institutions.

The research already has generated numerous new scientific reports that shed light on who seeks testing and why, and how they respond to the results that they receive. The latest report, "Personal Genomic Testing for Cancer Risk: Results From the Q:1 Impact of Personal Genomics Study," appears in the Journal of Clinical Oncology.

It examines how customers respond to common cancer risk information (not Mendelian cancer risks like BRCA1/2). In this analysis, researchers specifically looked at personal genomic testing for cancer risk, and found that 12-24 percent of individuals received elevated cancer risk estimates for prostate, breast and colon cancer.

Despite learning they were at increased risk for these common cancers, most customers did not report changing their diet, exercise, supplement use, advanced care planning or cancer screening in comparison to the customers who learned they were at average or lower risk. The one exception is men who received elevated prostate cancer risk estimates as some of these men changed their vitamin and supplement use more than those at average or reduced risk.

This counterintuitive finding may have resulted, the researchers say, because the increased cancer risks reported to the customers were very modest, and because the kind of individual who purchases DTC genetic testing may already have been very proactive about their health and using other available screening tests for cancer.

"These results suggest that people are not overreacting to very modest cancer risks in DTC genetic testing. This is consistent with some of our other findings showing that early adopters of DTC genetic testing understand the limited predictive impact of DTC results and do not overreact either emotionally or in terms of generating additional and unnecessary medical expenses," said co-principal investigator Dr. Robert Green of Brigham and Women's Hospital, the Broad Institute and Harvard Medical School.

The PGen Study cohort is a group of more than 1,600 consumers who purchased personal genomic tests prior to the imposition of FDA restrictions in 2013 from 23andMe and Pathway Genomics (Pathway has since changed their business model and no longer provides DTC testing). In addition to sharing their actual test results with investigators, participants completed surveys before receiving their results and again two weeks and six months after receiving their results. The surveys also presented mock results to determine if consumers could accurately interpret them.

"As far as many of the speculated risks and harms around direct-to-consumer genomic testing, we have not uncovered evidence that they are either common or severe," Roberts said. "Although we have found some areas where informed consent for testing and communication of results could be improved, our data suggest most consumers find their results as potentially useful in informing future health decisions and advance planning."

Green said that the PGen Study has provided "a goldmine of data on consumer expectations, how consumers interpret, recall and experience their results, how their results impact their state of mind, what actions they take after testing, and how all of these factors change over time."

This research was supported by the NIH National Human Genome Research Institute, American Cancer Society, a Canadian Institutes of Health Research Doctoral Foreign Study Award and other NIH grants.

 

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