NIH SEEKS INPUT ON PROPOSED REPOSITORY FOR GENETIC INFORMATION

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U.S. Department of Health and Human Services 
NATIONAL INSTITUTES OF HEALTH 
NIH News 
NIH Office of the Director (OD)  
http://www.nih.gov/icd/od/

FOR IMMEDIATE RELEASE: Wednesday, August 30, 2006  

CONTACT: Bonnie Flock (flockb@xxxxxxxxxx), NIH Press Office,
301-496-5787  

NIH SEEKS INPUT ON PROPOSED REPOSITORY FOR GENETIC INFORMATION

The National Institutes of Health (NIH) is seeking public input on a
proposed new policy designed to facilitate the research community's
access to data resulting from NIH-funded, genome-wide association
studies. NIH has published a Request for Information in the Federal
Register today and will be accepting public comments until October 31.

Genome-wide association studies (GWAS) rely on the newly available
research tools and technologies to rapidly and cost-effectively analyze
genetic differences between people with specific illnesses, such as
diabetes or heart disease, compared to healthy individuals. The
differences may point to genetic risk factors for the development or
progression of disease. Several NIH institutes recently launched, or are
planning, GWAS initiatives with the expectation that the results will
accelerate the development of better diagnostic tools and the design of
new, safe and highly effective treatments.

"I predict that comprehensive, genomics-based health care will become
the norm, with individualized preventive medicine and early detection of
illnesses," said NIH Director Elias A. Zerhouni, M.D. "The NIH policies
that give researchers rapid access to these findings will be an
important step along that path."

As numerous GWAS programs get underway, NIH seeks to harmonize the
policies by which the results will be made available to researchers. The
proposed GWAS Policy calls-on NIH-funded GWAS investigators to quickly
submit genetic data (genotypes) along with relevant health information
(phenotypes) about individuals to a centralized NIH data repository.
Data will be submitted in a form that protects the privacy and
confidentiality of research participants. The data will be made freely
available to all approved researchers to accelerate their studies.

The draft policy also proposes terms and conditions for investigators to
access GWAS data for research purposes. Data will be released in a
manner that preserves the privacy and confidentiality of research
participants.

NIH encourages patenting of intellectual property that addresses public
need, such as creating new treatments that can be brought to the clinic,
but seeks to prevent premature or inappropriate patents that impede
future research. Because publication credit is critical to academic
promotion, the proposed NIH policy also defines a grace period during
which GWAS data will be available for access, but principal
investigators submitting the data would be the only ones allowed to
publish analyses in scientific journals. The policy also asks that
recipients of GWAS data acknowledge the submitting investigator in any
published works.

"The NIH believes that the various and complex interests related to the
submission of, and access to, GWAS data must be discussed with the
public," said Elizabeth G. Nabel, M.D., director of National Heart,
Lung, and Blood Institute and head of the NIH-wide team developing the
policies. "Wide and rapid access to GWAS data may have implications for
participants in studies, their families and communities, investigators,
institutions and industry."

Some of the issues on which public consultation will be solicited
include:

-- Participant privacy concerns

-- Potential risks and benefits for individual participants

-- Professional recognition for the labor of investigators

-- Intellectual property rights

-- The development of a centralized NIH data repository 

The NIH is soliciting comments on the proposed policy through:
http://grants.nih.gov/grants/gwas/index.htm. Comments can also be
submitted to gwas@xxxxxxxx A town hall meeting is also planned for early
December 2006. 
 
The Office of the Director, the central office at NIH, is responsible
for setting policy for NIH, which includes 27 Institutes and Centers.
This involves planning, managing, and coordinating the programs and
activities of all NIH components. The Office of the Director also
includes program offices which are responsible for stimulating specific
areas of research throughout NIH. Additional information is available at
http://www.nih.gov/icd/od/. 

The National Institutes of Health (NIH) -- "The Nation's Medical
Research Agency" -- includes 27 Institutes and Centers and is a
component of the U.S. Department of Health and Human Services. It is the
primary federal agency for conducting and supporting basic, clinical and
translational medical research, and it investigates the causes,
treatments, and cures for both common and rare diseases. For more
information about NIH and its programs, visit www.nih.gov.
  
##
 
This NIH News Release is available online at:
http://www.nih.gov/news/pr/aug2006/od-30.htm.

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