![[ Back to EurekAlert! ]](http://www.eurekalert.org/images/back2e.gif){kind=small}
Public release date: 13-Nov-2012[ | E-mail |
Share ] Contact: Kory Zhao
kzhao2@partners.org
617-726-0274
Massachusetts General Hospital
New strategy for identifying risk-associated gene sets points to possible treatment target
Researchers using a new approach to identifying genes associated with depression have found that variants in a group of genes involved in transmission of signals by the neurotransmitter glutamate appear to increase the risk of depression. The report published in the journal Translational Psychiatry suggests that drugs targeting the glutamate system may help improve the limited success of treatment with current antidepressant drugs.
"Instead of looking at DNA variations one at a time, we looked at grouping of genes in the same biological pathways and found that a set of genes involved in glutamatergic transmisson was associated with the risk of depression," says Jordan Smoller, MD, ScD, director of the Psychiatric and Neurodevelopmental Genetics Unit in the Massachusetts General Hospital (MGH) Department of Psychiatry, senior author of the study. "Our findings are particularly interesting in light of recent studies showing that drugs affecting glutamate transmission can have rapid antidepressant effects."
While the risk of depression clearly runs in families, the genome-wide association studies typically used to identify gene variants that increase disease risk have been unable to find strongly associated genes. The research team which includes investigators from the Broad Institute of MIT and Harvard and other research centers in the U.S., Australia and the Netherlands adopted a strategy called gene set pathway analysis.
Starting with a set of genes that previous studies had implicated in depression, they used an analysis process called text mining to scan the medical literature for information on the biological function of these genes. Based on those findings, they identified 178 biological pathways that included these genes. Only one of those pathways the one involved in transmission of neural signals carried by glutamate was significantly associated with the risk for depression.
"Glutamate is the excitatory transmitter most widely used by the central nervous system, and several studies in animals and humans have suggested that it may play a role in depression," explains Smoller, an associate professor of Psychiatry at Harvard Medical School. "Most intriguingly, recent studies have found that ketamine a drug known to block one glutamate receptor appears to have antidepressant effects that are much faster than those of traditional antidepressants, which can take several weeks to become effective. Now additional research needs to confirm these findings and investigate exactly how variation in glutamate function affects brain systems involved in depression."
###
Phil Hyoun Lee, PhD, of the MGH Psychiatric and Neurodevelopmental Genetics Unit (PNGU) is lead author of the Translational Psychiatry report. Additional co-authors are Roy Perlis, MD, Richie Siburian, Stephen Haddad, MS, Catherine Mayerfeld, and Shaun Purcell, PhD, MGH PNGU; Erroll Rueckert, PhD, MGH Center for Human Genetic Research; Jae-Yoon Jung, PhD, Harvard Medical School; Enda Byrne, PhD, Naomi Wray, PhD, and Nicholas Martin, PhD, Queensland Institute of Medical Research, Australia; Andrew Heath, DPhil, Michele Pergadia, PhD, and Pamela Madden, PhD, Washington University, St. Louis; Dorret Boomsma, PhD, and B.W. Penninx, PhD, VU University, Amsterdam, The Netherlands; and Pamela Sklar, MD, PhD, Mount Sinai School of Medicine, New York. Lee, Perlis, Rueckert, Purcell and Smoller are also affiliated with the Broad Institute. The study was supported by grants from the National Institute of Mental Health.
Massachusetts General Hospital, founded in 1811, is the original and largest teaching hospital of Harvard Medical School. The MGH conducts the largest hospital-based research program in the United States, with an annual research budget of more than $750 million and major research centers in AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, human genetics, medical imaging, neurodegenerative disorders, regenerative medicine, reproductive biology, systems biology, transplantation biology and photomedicine. In July 2012, MGH moved into the number one spot on the 2012-13 U.S. News & World Report list of "America's Best Hospitals."
[ | E-mail | Share ] ?
AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.
Public release date: 13-Nov-2012[ | E-mail |
Share ] Contact: Kory Zhao
kzhao2@partners.org
617-726-0274
Massachusetts General Hospital
New strategy for identifying risk-associated gene sets points to possible treatment target
Researchers using a new approach to identifying genes associated with depression have found that variants in a group of genes involved in transmission of signals by the neurotransmitter glutamate appear to increase the risk of depression. The report published in the journal Translational Psychiatry suggests that drugs targeting the glutamate system may help improve the limited success of treatment with current antidepressant drugs.
"Instead of looking at DNA variations one at a time, we looked at grouping of genes in the same biological pathways and found that a set of genes involved in glutamatergic transmisson was associated with the risk of depression," says Jordan Smoller, MD, ScD, director of the Psychiatric and Neurodevelopmental Genetics Unit in the Massachusetts General Hospital (MGH) Department of Psychiatry, senior author of the study. "Our findings are particularly interesting in light of recent studies showing that drugs affecting glutamate transmission can have rapid antidepressant effects."
While the risk of depression clearly runs in families, the genome-wide association studies typically used to identify gene variants that increase disease risk have been unable to find strongly associated genes. The research team which includes investigators from the Broad Institute of MIT and Harvard and other research centers in the U.S., Australia and the Netherlands adopted a strategy called gene set pathway analysis.
Starting with a set of genes that previous studies had implicated in depression, they used an analysis process called text mining to scan the medical literature for information on the biological function of these genes. Based on those findings, they identified 178 biological pathways that included these genes. Only one of those pathways the one involved in transmission of neural signals carried by glutamate was significantly associated with the risk for depression.
"Glutamate is the excitatory transmitter most widely used by the central nervous system, and several studies in animals and humans have suggested that it may play a role in depression," explains Smoller, an associate professor of Psychiatry at Harvard Medical School. "Most intriguingly, recent studies have found that ketamine a drug known to block one glutamate receptor appears to have antidepressant effects that are much faster than those of traditional antidepressants, which can take several weeks to become effective. Now additional research needs to confirm these findings and investigate exactly how variation in glutamate function affects brain systems involved in depression."
###
Phil Hyoun Lee, PhD, of the MGH Psychiatric and Neurodevelopmental Genetics Unit (PNGU) is lead author of the Translational Psychiatry report. Additional co-authors are Roy Perlis, MD, Richie Siburian, Stephen Haddad, MS, Catherine Mayerfeld, and Shaun Purcell, PhD, MGH PNGU; Erroll Rueckert, PhD, MGH Center for Human Genetic Research; Jae-Yoon Jung, PhD, Harvard Medical School; Enda Byrne, PhD, Naomi Wray, PhD, and Nicholas Martin, PhD, Queensland Institute of Medical Research, Australia; Andrew Heath, DPhil, Michele Pergadia, PhD, and Pamela Madden, PhD, Washington University, St. Louis; Dorret Boomsma, PhD, and B.W. Penninx, PhD, VU University, Amsterdam, The Netherlands; and Pamela Sklar, MD, PhD, Mount Sinai School of Medicine, New York. Lee, Perlis, Rueckert, Purcell and Smoller are also affiliated with the Broad Institute. The study was supported by grants from the National Institute of Mental Health.
Massachusetts General Hospital, founded in 1811, is the original and largest teaching hospital of Harvard Medical School. The MGH conducts the largest hospital-based research program in the United States, with an annual research budget of more than $750 million and major research centers in AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, human genetics, medical imaging, neurodegenerative disorders, regenerative medicine, reproductive biology, systems biology, transplantation biology and photomedicine. In July 2012, MGH moved into the number one spot on the 2012-13 U.S. News & World Report list of "America's Best Hospitals."
[ | E-mail | Share ] ?
AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.
Source: http://www.eurekalert.org/pub_releases/2012-11/mgh-gns111312.php
sherry arnold snooty fox el debarge portland weather clintonville battlestar galactica blood and chrome my morning jacket
No comments:
Post a Comment