by Jennifer Kowalewski
In five years, the
Appalachian Rural Health Institute’s (AHRI) Diabetes/Endocrine
Diseases Biorepository could have blood samples from more than 5,000
persons — samples that will be used to further endocrine disease
research in Southeastern Ohio and nationwide.
“The Diseases
Biorepository will be one of the first biorepositories for diabetes
and other endocrine diseases that has specific clinical information
associated with it,” says Frank Schwartz, M.D., director of
the ARHI Diabetes/Endocrine Center and an OU-COM associate professor
of endocrinology.
“A major portion of
the biorepository’s blood samples will be from a specific group of
Appalachian people. The biorepository will allow the long-term
storage of blood samples from individuals with different endocrine
diseases at various stages. These samples will be available for Ohio
University scientists and others to study.”
“It is the only
biorepository that I know of that is dedicated to diabetes/
endocrine disease research in the state of Ohio,” says Dawn Ford,
Ph.D., biorepository coordinator. One other in Ohio is dedicated
to tissue sample research, says Ford.
Tuesday, Nov. 8, as
part of ARHI’s monthly Diabetes Research Seminar series, Schwartz
will give an update on the biorepository’s progress. Schwartz’s
presentation will take place at 11:30 a.m. in Grosvenor West 111.
The biorepository
itself consists of two ultra-low temperature freezers with a
dedicated computer and bar-coding machines. After arrival, DNA, RNA
and plasma components will be separated from the blood samples.
These components are then divided into sub-samples. The freezers are
for long-term storage of the separated blood samples; the computer
maintains a specimen/
records database; and the bar-coding machines apply bar codes to the
stored blood sub-samples.
These blood
components will be refrigerated at -80° Celsius to keep them from
degrading and remain in storage until needed. When researchers need
samples, their requests must be approved before they receive them,
Ford says.
Patients of
University Medical Associates (UMA) may donate blood to help build
up the biorepository. Donors will be asked to give a family disease
history.
“I will pick up the
blood samples donated through UMA,” says Ford. “The medical records
of donors will be electronically transferred to the repository’s
database. I won’t know who the donors are, as all personal identity
information is encrypted.”
If necessary, donors
can be identified by UMA. Ford is the only person who can request
that a sample be identified.
By having a plethora
of samples on hand from different patient donors,
the biorepository will save
researchers time by making it easier to find suitable subjects for
their studies.
Researchers also will have a larger sample base from which to
choose. And in five or 10 years, researchers will be able to look at
diseases at various stages of development. Through observing how a
disease matures in the body, researchers will be better equipped to
fight them.
“One of the big
things is being able to link samples with clinical information,”
Ford says. “We will have information, such as the age of the person
or what they were presenting when they went to the clinic. We also
will look at patients over a period of time. We will know how their
blood chemistry changed.”
“There will be a
three-step approval process for researchers who want to access
samples from the biorepository,” says Ford. First, researchers must
go to biorepository advisory board to have their research proposals
reviewed and approved. Second, they must obtain approval from the
University’s Institutional Review Board. Last, they also must attain
approval from UMA.
“Right now we are
working on (blood) separation protocols,” says Ford. “Possibly by
Thanksgiving or early December we might be able to begin to collect
samples.”
Until then Ford will
continue working out protocols and quality control/quality assurance
measures. Ford began at the biorepository in July.
Eventually the
repository’s samples will head to Athens-based researchers or
researchers across the country to help study endocrine diseases. Out
of these collaborative efforts, it is hoped, new discoveries will be
made to combat these diseases.
“Diabetes and
endocrine diseases are genetically linked, and patients who have
these conditions want to know what causes them and what can be done
to protect other family members,” says Schwartz. “Although there may
not likely be immediate benefits to donors, they know that they will
be helping to further research into these diseases.”
There are, says
Schwartz, animal models of many of these diseases, and it’s hoped
that the biorepository will facilitate the building of human disease
models that could be correlated with animal ones. This, he says,
“will facilitate collaboration between clinical and basic science
researchers at Ohio for a true ‘bench to bedside’” scheme of medical
care.
“If this is
successful, it will increase the University’s and OU-COM’s research
capabilities and broaden our capacity for accepting more
collaborative research proposals from other universities in the
United States and from around the globe.”
The facility soon
will have its own Web site, which will have information on its
advisory board, the application process to obtain samples for
research, a mission statement, a staff directory, links to
participating partners and a link to the International Society of
Biological and Environmental Repositories.
That Web site will be linked to from
ARHI’s Web site, says Ford.