The Brain & Behavior Research Foundation Names Top 10 Advancements & Breakthroughs in 2016 by NARSAD Grantees
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The Brain & Behavior Research Foundation today announced the Top 10 Advancements & Breakthroughs of 2016 by researchers supported by its NARSAD Grants, which provide new insight into the mysteries of the brain and potential targets for understanding and treating psychiatric disorders that affect one in five people, including bipolar disorder, depression, multiple types of mental illness, schizophrenia, and post-traumatic stress disorder. Discoveries in basic research, new technology, next-generation treatments, early intervention and diagnostic tools, ranged from new experiments that reveal the brain circuitry behind the inability to experience pleasure, a milestone in the search for the cause of schizophrenia, and findings that explain how ketamine exerts its rapid antidepressant effects.
"The top 10 discoveries were selected because of their significant contributions to our understanding of brain and behavior disorders as well as potential new treatments," says Jeffrey Borenstein, M.D., president and CEO of the Brain & Behavior Research Foundation, the top non-governmental mental health research funder cited in published articles. "We are proud to be able to say that NARSAD Grants support a broad range of the best ideas in brain research and that our grantees have taken substantial steps forward on the path to developing new treatments and finding cures for mental illness."
Below are the Top 10 findings of 2016 by NARSAD Grantees:
Basic Research: Depression, Schizophrenia
1. New Experiments Reveal Brain Circuitry Behind Inability to Experience Pleasure
Anhedonia, or the inability to feel pleasure or enjoyment, is a key symptom in several mental illnesses including major depression and schizophrenia. This sense of pleasure is generated partly by the brain's neural pathways involved in seeking and experiencing reward. Using optogenetics to control the activity of dopamine neurons in a part of the brain called the medial prefrontal cortex, the team* was able to produce symptoms of anhedonia in rodents. Brain imaging helped reveal that this cortical reward circuitry can in turn suppress activity in other parts of the brain such as the striatum, that are involved in reward-seeking behavior. The findings were published in the Journal Science, January 1, 2016.
Conor Liston, M.D., Ph.D., Weill Cornell Medical College, 2016 Freedman Prizewinner Honorable Mention, 2013 NARSAD Young Investigator; Karl Deisseroth, M.D., Ph.D., Stanford University School of Medicine, Foundation Scientific Council Member, 2005 NARSAD Young Investigator Grant.
*The team also included 2012 Young Investigator Amit Etkin, M.D., Ph.D.; 2003 Young Investigator Brian Knutson, Ph.D.; and 2012 Young Investigator Melissa R. Warden, Ph.D.
Basic Research: Schizophrenia
2. A Milestone in the Search for Schizophrenia's Causes
Research by a large international team that included Drs. Sullivan and O'Donovan, who are leaders of the Psychiatric Genomics Consortium, points to one of the likely causes of schizophrenia in some people: overactive pruning of synapses - connections between nerve cells - in the brain's prefrontal cortex during the early years of life. The team focused on variation in genes giving rise to a vital group of proteins called the major histocompatibility complex (MHC). MHC proteins are part of the mechanism used by the immune system to fight off foreign invaders. The team found that variations in the expression of genes known as complement component 4 (C4) genes specifically impacted neuronal synapses, dendrites, axons, and cell bodies. In mice, C4 mediated synapse elimination during postnatal development. Excessive C4 activity may help explain the reduced numbers of synapses in the brains of individuals with schizophrenia. The findings were published in the Journal Nature January 27, 2016
Patrick F. Sullivan, M.D., FRANZCP, University of North Carolina at Chapel Hill, 2014 Lieber Prizewinner, 2010 NARSAD Distinguished Investigator Grant; Michael O'Donovan, M.D., Ph.D., Cardiff University, 2012 Lieber Prizewinner.
New Technology: Autism, Schizophrenia, Intellectual Disability
3. Genetic Anomalies Frequently Associated with Neurodevelopmental Disorders Can Now Be Efficiently Recreated in the Lab
A new method for recreating large-scale genetic anomalies known as copy number variations (CNVs) will make it easier for scientists to study the effects of those mutations, many of which have been linked to autism and other neurodevelopmental disorders. Drs. Gusella, Talkowski and colleagues have already used the approach, called SCORE, to create human cells that carry too many or too few copies of chromosomal regions known as 15q13.3 and 16p11.2 – CNVs associated with disorders such as autism, schizophrenia, and intellectual disability. The achievement paves the way for studying exactly what goes wrong in cells that carry such defects, and could help researchers find ways to correct those problems. SCORE is an important application of CRISPR, a research tool that is changing the way scientists "edit" genomes in the lab. The findings were published in the Journal Nature Neuroscience February 1, 2016.
James F. Gusella, Ph.D., Harvard University/Massachusetts General Hospital, 2007 NARSAD Distinguished Investigator Grant; Michael E. Talkowski, Ph.D., Harvard University/Massachusetts General Hospital, 2012 NARSAD Young Investigator Grant.
Next-Generation Treatments: Depression
4. Opioid Medication Combo Helps Patients Who Don't Respond to Antidepressants
Reviving an old treatment for mood problems, researchers find that adding certain opioid medications to depression treatment can help patients who don't respond well to conventional antidepressants. When Dr. Fava's team* gave a combination of opioid medication and antidepressants as an adjunct therapy to patients who had not responded to antidepressants alone, these patients saw greater improvements than their peers who received only antidepressants. The drug combination consisted of buprenorphine, an opioid medication, and samidorphan, an opioid antagonist included to block those effects of buprenorphine that are associated with its addictive potential. All patients continued on their current antidepressant therapy and on the same dosage throughout the course of the study. The findings were published in the American Journal of Psychiatry, February 12, 2016.
Maurizio Fava, M.D., Harvard University/Massachusetts General Hospital, 1994 NARSAD Young Investigator Grant.
*The team also included 2002 Independent Investigator and 1992 Young Investigator Madhukar H. Trivedi M.D.
Next-Generation Treatments: Suicide, Depression
5. Important Discovery by Foundation-Supported Researchers Explains How Ketamine Exerts its Rapid Antidepressant Effects
Ketamine, a drug approved long ago as an anesthetic but used recently on an experimental basis to treat resistant major depression, exerts rapid antidepressant effects in many patients, including those contemplating suicide. The new research suggests it may be possible to separate ketamine's benefits from its serious unwanted side effects. Inside the body, ketamine is broken down and forms several new compounds, called metabolites. The team discovered that one of these metabolites—a molecule called hydroxynorketamine (HNK)—can by itself generate the antidepressant effects seen in ketamine. Efforts are under way to develop and test an HNK-like drug in animals and then people. The findings appeared in the journal Nature, May 4, 2016.
Todd Denton Gould, M.D., National Institute of Mental Health (NIMH/NIH),2013 NARSAD Independent Investigator Grant, 2010 & 2004 NARSAD Young Investigator Grant; Carlos A. Zarate, M.D., National Institute of Mental Health (NIMH/NIH), 2011 Foundation Bipolar & Mood Disorder Research Prizewinner, 2005 NARSAD Independent Investigator Grant, 1996 NARSAD Young Investigator Grant.
Next-Generation Treatments: Multiple Illnesses
6. Treatment with Immune-Regulating Gut Bacteria May Boost Immune System Against Stress
Risk for psychiatric disorders ranging from depression to PTSD to schizophrenia is thought by some scientists to be linked to elevated levels of inflammation. By exposing mice to bacteria that help regulate the immune system, a team* led by Dr. Lowry was able to prevent stress from causing harmful inflammation, and in some cases, symptoms of illness. The researchers injected mice with a bacterium called M. vaccae, which is abundant in soil and has immune system-regulating effects. This prevented mice from getting colitis when put in highly stressful situations. In stressed mice, the treatment had anti-anxiety and fear-reducing effects. The findings, which were published in the Proceedings of the National Academy of Sciences, May 31, 2016, can help researchers develop microbiome- and immunoregulation-based strategies to prevent disorders related to stress.
Christopher A. Lowry, Ph.D., University of Colorado, Boulder, 2010 & 2007 NARSAD Young Investigator Grant.
*The team included: 2005 Independent Investigator Monika Fleshner, Ph.D. and 2013 NARSAD Independent Investigator Charles L. Raison, M.D.
Next-Generation Treatments: Depression
7. Brief Course of Psychotherapy Benefits Moms with Major Depression and Their Children
Children whose mothers have depression are more likely than others to develop childhood psychiatric illnesses. Dr. Swartz and colleagues* now show that these children do better when their mothers are treated for depression and their symptoms improve. Previously, such studies had involved women whose depression was treated with medication, not psychotherapy. 168 mothers participated in nine 45-minute psychotherapy sessions over three months. For one group, the therapy was specifically focused on the mother's relationship with her child; a second group of women had a more general form of therapy. Treatments helped all mothers, but those children whose mothers were in the former group had fewer mental health visits and were prescribed fewer antidepressant medications during the study than children whose mothers underwent the general therapy. The findings appeared in the Journal of the American Academy of Child & Adolescent Psychiatry, June 2016.
Holly A. Swartz, M.D., University of Pittsburgh, 2006 NARSAD Young Investigator Grant.
*The team included 2006 Ruane Prizewinner and 2001 Distinguished Investigator David A. Brent, M.D.; 1998 Distinguished Investigator Ellen Frank, Ph.D.; and 2002 Independent Investigator John C. Markowitz, M.D., Pharm.D.
Early Intervention/Diagnostic Tools: Psychosis
8. New Tool Calculates Patients' Personal Psychosis Risk
Most people who develop schizophrenia and other disorders involving psychosis (including some cases of bipolar disorder and depression) experience subtle changes in belief, thought, and perception that precede the onset of full psychosis. But fewer than 35 percent of people with these subtle changes actually develop full psychosis within three years of being identified as high-risk. Those who do become ill fare best when treated early. A team led by Dr. Cannon developed a new risk calculator to identify them, using data from 596 high-risk individuals. Dr. Carrión led another team that validated the risk calculator in a separate group of 210 high-risk individuals. The most important warning signs were: higher levels of unusual thought content and suspiciousness, as compared with others; lower verbal learning and memory capacity, slower cognitive processing, and greater decline in social functioning. Both papers appeared in the American Journal of Psychiatry, July 1, 2016.
Tyrone D. Cannon, Ph.D., Yale University, 2006 NARSAD Distinguished Investigator Grant 1997 NARSAD Independent Investigator Grant; Ricardo E. Carrión, Ph.D., Zucker Hillside Hospital Campus of the Feinstein Institute for Medical Research, 2012 NARSAD Young Investigator Grant. More than a dozen NARSAD grantees helped develop and validate the risk calculator.
Dr. Cannon's team included: 2005 & 2003 Young Investigator Carrie E. Bearden, Ph.D.; 1999 & 1992 Young Investigator Kristin Cadenhead, M.D.; 1990 Young Investigator Robert Heinssen, Ph.D.; Scientific Council Member, 2007 Independent Investigator & 2001 Young Investigator Daniel H. Mathalon, M.D., Ph.D.; 1997 Distinguished Investigator Thomas H. McGlashan, M.D.; 2004 & 1998 Independent Investigator Larry J. Seidman, Ph.D.; Scientific Council Member, 2010 Lieber Prizewinner and 1998 Distinguished Investigator Ming T. Tsuang,M.D., Ph.D., D.Sc.; 1989 Distinguished Investigator Elaine F. Walker, Ph.D.; and 2005 Distinguished Investigator and 1998 Independent Investigator Scott W. Woods, M.D.
Dr. Carrión's team included 2004 Young Investigator Andrea Auther, Ph.D.; Scientific Council Member, 2001 Klerman Prizewinner, 2007 Distinguished Investigator, 1997 & 1994 Young Investigator, Cameron S. Carter, M.D.; 2012 Young Investigator Tara A. Niendam, Ph.D.; and 1996 Young Investigator Stephan F. Taylor, M.D.
Next-Generation Treatments: Depression
9. Treating Metabolic Problems Improves Symptoms of Some Patients with Refractory Depression
Dr. Pan and colleagues* have discovered that some people who suffer from treatment-resistant depression may benefit from the diagnosis and treatment of metabolic deficiencies. In a study of patients with treatment-resistant depression, about two-thirds had metabolic deficiencies that affect the brain's ability to produce neurotransmitters. Patients' depression symptoms declined significantly when these metabolic problems were treated; some reached remission. The most common of the deficiencies observed in participants was in levels of cerebral folate, which is treatable with folinic acid. The findings appeared in the American Journal of Psychiatry, August 13, 2016.
Lisa A. Pan, M.D., University of Pittsburgh School of Medicine, 2012 NARSAD Young Investigator Grant.
* The team included: 2006 Ruane Prizewinner and 2001 Distinguished Investigator David A. Brent, M.D.
Basic Research: Schizophrenia
10. Researchers Catalog Subtle but Widespread Schizophrenia-Associated Differences in Gene Activity
Dr. Sklar led a large team* that identified nearly 700 genes whose activity levels differ in the brains of people with schizophrenia compared to those without it. Most of the differences were subtle, consistent with the idea that variations in many genes contribute to the risk of schizophrenia, each alone having a small effect. The team compared the activity of genes within the brain whose sequences had previously been shown to vary in small but significant numbers of patients. They manipulated the activity of five of the schizophrenia-linked genes in zebrafish (a "model organism" often used for genetics experiments), and found three genes whose alteration disrupted brain development. Other researchers can now extend the team's findings by further exploring genes on the list to begin teasing out the molecular basis of schizophrenia. The findings appeared in the Journal Nature Neuroscience, September 26, 2016.
Pamela B. Sklar, M.D., Ph.D., Icahn School of Medicine at Mount Sinai, Scientific Council Member 2016 Colvin Prizewinner, 2006 NARSAD Independent Investigator Grant 1998 & 1995 NARSAD Young Investigator Grant.
*The team included: 2016 Independent Investigator and 2012 Young Investigator Kristen Jennifer Brennand, Ph.D.; Foundation Scientific Council Member Joseph D. Buxbaum, Ph.D.; Foundation Scientific Council Member, 2009 Lieber Prizewinner and 1999 Distinguished Investigator, Raquel E. Gur, M.D., Ph.D.; 2010 Independent Investigator, 2002 and 2000 Young Investigator Chang-Gyu Hahn, M.D., Ph.D.; 1996 Distinguished Investigator Vahram Haroutunian, Ph.D.; 1997 Young Investigator Scott E. Hemby, Ph.D.; Foundation Scientific Council Member, 2005 Lieber Prizewinner and 2008 Distinguished Investigator David A. Lewis, M.D.; 1994 Young Investigator Barbara K. Lipska, Ph.D.; 2013 Young Investigator Edwin C. Oh, Ph.D.; 2006 Young Investigator Shaun Matthew Purcell, Ph.D.; 2013 Young Investigator Panagiotis Roussos, M.D., Ph.D.; 2015 Young Investigator Douglas Ruderfer, Ph.D.; 2013 Young Investigator Eli Ayumi Stahl, Ph.D.; and 2014 Lieber Prizewinner and 2010 Distinguished Investigator Patrick F. Sullivan, M.D., FRANZCP.
About the Brain & Behavior Research Foundation
For the past 30 years the Brain & Behavior Research Foundation has been committed to alleviating the suffering of mental illness by awarding grants that will lead to advances and breakthroughs in scientific research. The Foundation funds the most innovative ideas in neuroscience and psychiatry to better understand the causes and develop new ways to treat brain and behavior disorders. These disorders include depression, bipolar disorder, schizophrenia, autism, attention-deficit hyperactivity disorder, anxiety, borderline personality disorder, obsessive-compulsive disorder, and post-traumatic stress disorder. Since 1987, the Foundation has awarded more than $360 million to fund more than 5,000 grants to more than 4,000 leading scientists around the world. This has led to over $3.5 billion in additional funding for these scientists. The Foundation is also dedicated to educating the public about mental health and the importance of research, including the impact that new discoveries have on improving the lives of those with mental illness, which will ultimately enable people to live full, happy and productive lives. For more information, visit www.bbrfoundation.org.
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