[Home]
[Full version]
Toward the ethical treatment of whole genome research participants
Mar 25 ,General Science
Recent technological developments have made it possible for scientists to sequence an entire human genome, but these advances may be a mixed blessing. While much has been made of the benefits of whole-genome sequencing, from improved disease diagnosis to rational drug design, the impacts on the privacy and autonomy of individual participants has received much less scrutiny. In a new essay published in the open-access journal PLoS Biology, Timothy Caulfield and his colleagues argue that the ability to sequence a person's entire genome has created a whole new set of moral challenges that standard research ethics guidelines were not designed to solve.
Several aspects of whole-genome sequencing challenge existing research ethics norms. Some of the most pressing ethical issues arising from whole genome research include the vast amount of data produced, the uncertainly regarding future research uses of the data, implications of the data for family members, and the technological ability (and expectations) to publicly release the data. To date, very little effort has been put into providing new ethical standards to address these unique challenges.
With an eye toward remedying this oversight, Caulfield et al. offer a consensus statement aimed at providing "ethically rigorous and practical guidance for investigators and research ethics boards." The consensus statement, a product of a workshop involving an interdisciplinary panel of eminent bioethicists, lawyers, and researchers, tackles the central issues facing whole-genome research: informed consent, the right to withdraw from research, the return of results, and the public release of data. In each case, the authors argue, the public dissemination of collected data presents challenges to the standard methods researchers use to protect participants' privacy and autonomy. In whole-genome research, participants quickly lose control over access to their personal information, and they run the risk of "genetic profiling." Protecting participants in whole genome research studies requires updating informed consent to include information about future use, the limited ability to withdraw information, disclosure of research results, and the potentially wide distribution of personal data.
Central to Caulfield et al.'s recommendations is the use of "robust governance and oversight mechanisms." Review boards must play a much larger role in genomic research than it has in other areas, the authors argue, "in part because the unique challenges associated with the research make it impractical to satisfy the norms, tools, and processes usually utilized to respect autonomy." Even if controversial events are rare, responding to these concerns is essential, they maintain, because "history has told us that they do occur and can have a devastating impact on public trust and the research environment."
Fully acknowledging that many related policy issues also warrant attention--including commercialization and patenting, for example--Caulfield et al. urge immediate action on whole genome research ethics guidance, while the ethical, legal, and social implications of this rapidly evolving field continue.
Citation: Caulfield T, McGuire AL, Cho M, Buchanan JA, Burgess MM, et al. (2008) Research ethics recommendations for whole-genome research: Consensus statement. PLoS Biol 6(3): e73. doi:10.1371/journal.pbio.0060073
Source: Public Library of Science
Related stories:
Managing incidental findings in human subjects research
Article offers first major consensus recommendations for IFs
An incidental finding (IF) is a finding concerning an individual research participant that has potential health or reproductive importance, is discovered in the course of conducting research, but is beyond the aims of the study. IFs are an increasingly common byproduct of research using powerful technologies that generate "extra" data. Because IFs can potentially save lives but also cause alarm, the decision on whether or not to disclose them to research participants has been a major dilemma. Little guidance currently exists on how to approach this problem. A two-year project supported by the National Human Genome Research Institute at NIH has now published the first major recommendations for how to anticipate and manage IFs in genetic, genomic, and imaging research, suggesting broader application to other research domains. This project, led by Prof. Susan Wolf at the University of Minnesota's Consortium on Law and Values in Health, Environment & the Life Sciences, involved a multidisciplinary group of leading experts from the U.S. and Canada. The project has published a 17-article symposium including the consensus paper, which appears in the Summer '08 issue of the
Journal of Law, Medicine & Ethics.
Researchers urge ethics guidelines for human-genome research
A global team of legal, scientific and ethics experts have put forward eight key recommendations to establish much needed guidelines for conducting human-genome sequencing research.
NIH awards $11.5M for science education
Eleven projects exploring different aspects of science will share nearly $11.5 million from the U.S. National Institutions of Health.
Understanding Algae As An Alternative Fuel Source: Will The Real Algae X Please Stand Up
The recent creation of AXI, LLC is an alliance between Allied Minds, Inc. a seed investment company and the University of Washington. The alliance came about because of Professor Rose Ann Cattolico PhD, an algae-to-fuel expert. Professor Cattolico has been on the faculty and conducting algae research since 1975. Her research includes, chloroplast genome architecture and gene function in non-chlorophy b containing algae and functional genetic diversity within stramenopile population. Professor Cattolico has discovered a unique patented technology, she calls Algae X.
Parsing the genome of a deadly brain tumor
The most comprehensive to-date genomic analysis of a cancer – the deadly brain tumor glioblastoma multiforme – shows previously unrecognized changes in genes and provides an overall view of the missteps in the pathways that govern the growth and behavior of cells, said members of The Cancer Genome Atlas Research Network in a report that appears online today in the journal
Nature.
Thumbs up -- a tiny ancestral remnant lends developmental edge to humans
Subtle genetic changes that confer an evolutionary advantage upon a species, such as the dexterity characteristic of the human hand, while difficult to detect and even harder to reproduce in a model system, have nevertheless generated keen interest amongst evolutionary biologists. In findings published online in the September 5 edition of the journal
Science, researchers from the U.S. Department of Energy's Lawrence Berkeley National Laboratory and their collaborators, have uncovered a specifically human 13-nucelotide change concealed in the vast three-billion-letter landscape of the human genome.
Researchers map first plant-parasitic nematode genome sequence
(PhysOrg.com) -- There are numerous plant-parasitic nematodes in the world, but only a handful are responsible for the largest part of an estimated $157 billion in agricultural damage globally every year. Nematodes are small worms that burrow into plant roots and feed off living cells.
Gene enhancer in evolution of human opposable thumb
Scientists have discovered a gene enhancer, known as HACNS1, that may have contributed to the evolution of the uniquely opposable human thumb, and possibly also modifications in the ankle or foot that allow humans to walk on two legs, according to a paper published in
Science on Sept. 5, 2008.
[Home]
[Full version]