A Johns Hopkins-led study
has found evidence that a genetic tendency toward
suicide has been linked to a particular area of the
genome on chromosome 2 that has been implicated in two
additional recent studies of attempted suicide.
“We’re hoping our findings
will eventually lead to tests that can identify those
at high risk for attempting suicide,” says Virginia
Willour, Ph.D., an assistant professor in the
Department of Psychiatry at the Johns Hopkins
University School of Medicine and lead author of the
study. An estimated 4.6 percent of Americans ages 15
to 54 have tried to take their lives, according to
Willour.
The investigators conducted
a family linkage study in which they searched for
commonalities in the genomes of family members with
bipolar disorder and a history of attempted suicide.
The same gene region on chromosome 2 that was
identified by this bipolar disorder and attempted
suicide study was recently identified by two
complementary family studies that looked at attempted
suicide in families with major depression and alcohol
dependence.
“Family linkage studies are
not always consistent, so the fact that all three
studies, including ours, point to the same region of
the genome is a good indication that we are on the
right track toward identifying a gene or genes that
play a role in why a person chooses to take his or her
own life,” says Willour.
In the multi-institutional
study, results of which appear in the March issue of
Biological Psychiatry, the researchers
examined data from 162 families with bipolar disorder.
They looked at attempted suicide in this sample
because it is an important clinical problem that tends
to occur more often in some of these families than in
others, suggesting a distinctive genetic basis,
according to senior author James B. Potash, M.D.,
M.P.H., of the Department of Psychiatry at Hopkins.
This technique, of looking at sub-types of illness, is
used by genetic researchers as a way to reduce genetic
complexity.
From the 162 families, the
researchers selected 417 subjects who were diagnosed
with schizoaffective/bipolar disorder, bipolar I
disorder or bipolar II disorder.
These subjects were asked
whether they had ever attempted suicide and the degree
of intent of the most serious attempt. One hundred
fifty-four subjects said they had attempted suicide,
and 122 stated that they had “definite” intent. For
the purpose of this study, the latter were considered
to have a history of attempted suicide.
Data for all 417 subjects
was entered into a computer program that looks for
genetic similarities between subjects with similar
psychological profiles. Results indicated that family
members with a history of attempted suicide and
bipolar disorder showed a high degree of genetic
similarity at a specific area -- DNA marker D2S1777 --
on a section of chromosome 2 referred to as 2p12. This
is the same marker implicated in a 2004 study from the
University of Pittsburgh School of Medicine that
looked at attempted suicide and major depression. And
it is close to another marker, D2S1790, located in the
2p11 region of chromosome 2, which was identified in a
2004 study from the University of Connecticut School
of Medicine that looked at alcoholism and attempted
suicide.
Willour says that although
the Hopkins-led study does not pinpoint a specific
gene responsible for attempted suicide, it does
suggest a “neighborhood” in which the gene might be
found. She adds that the next step is to further
narrow the search and find the “address.” “Once we
have located the specific gene,” she says, “we can
better identify people who might be at risk of suicide
and offer drug companies a target for possible
therapies.”
The data used by Willour
and her team -- DNA samples, medical histories and
psychiatric evaluations -- came from an independent
study, CHIP, conducted at the University of Chicago,
Johns Hopkins, and the National Institute of Mental
Health (NIMH) Intramural Program. The purpose of CHIP,
initiated in 1988 and funded through at least 2010, is
to find genes that predispose people to developing
bipolar disorder or particular subtypes of the
illness.
Other Johns Hopkins
researchers who contributed to this study are Peter P.
Zandi, Ph.D., from the Department of Mental Health in
the Bloomberg School of Public Health and J. Raymond
DePaulo Jr., M.D.; Dean F. MacKinnon, M.D.; and
Francis M. Mondimore, M.D., from the Department of
Psychiatry and Behavioral Sciences. Additional
researchers include Elliot S. Gershon, M.D., and
Judith A. Badner, M.D., Ph.D., from the Department of
Psychiatry at the University of Chicago; Francis J.
McMahon, M.D., from the NIMH Intramural Program; and
Melvin G. McInnis, M.D., from the Department of
Psychiatry at the University of Michigan, Ann Arbor.
Funding for this study came
from the National Institute of Mental Health.