After my brain injury

After my brain injury

Wednesday, November 18, 2015

On Brain Health | New Hope for the Damaged Brain

By Tori DeAngelis
May 2013, Vol 44, No. 5
American Psychological Association

Tori DeAngelis is a writer in Syracuse, N.Y.

Brain plasticity — the ability of the brain to renew itself — is a hot research topic for good reason: The Centers for Disease Control and Prevention predicts an epidemic of brain-related health problems as our society ages.

A major cause of such problems is stroke, the fourth leading cause of death in the United States and a major cause of long-term disability.

Elissa Newport, cognitive psychologist
Cognitive psychologist Elissa Newport is heading a new center at Georgetown University that promises to bring the best science to bear on the delicate task of stroke recovery.

In a groundbreaking effort to improve people's recovery after one of these devastating events, Georgetown University Medical Center has partnered with MedStar National Rehabilitation Hospital in Washington, D.C., to create the Center for Brain Plasticity and Recovery, which will apply new thinking and state-of-the-art research methods to improve recovery from stroke and, in the future, from other neurological disorders as well.

In July, Georgetown tapped cognitive psychologist Elissa Newport, PhD, of the University of Rochester's department of brain and cognitive sciences to head the new center, a post she assumed with Alexander Dromerick, MD, a Georgetown neurologist and stroke specialist, as its co-director.

"Elissa is an articulate spokesperson for the power of the interdisciplinary approach, and she lives and breathes science in a way that energizes [medical and psychology] students and fellows to pursue their work collaboratively and with great rigor," says Georgetown Medical Center's executive vice president, Howard Federoff, MD, PhD. "I'm confident that in future years, great young trainees will want to be part of the center because of her charisma and leadership."

At the center, scientists from a range of disciplines will study a variety of interventions that have the potential to enhance recovery after stroke, from cellular mechanisms that may facilitate healing to brain stimulation techniques that might optimize brain functioning.

The Monitor on Psychology (May 2013) spoke with Newport about the center's direction, the promise of plasticity research and the importance of interdisciplinary collaboration in addressing a public health problem that is bound to worsen as we face a "silver tsunami" of aging citizens.

How long has brain plasticity work been going on, and why is it vital to the new center's work
Scientists have been interested in brain plasticity since at least the 1930s. Early work suggested that there are critical periods for the development and reorganization of brain function, and showed that the brain's ability to change and learn declines with age. For example, when children experience damage to the left hemisphere, they reorganize language to the right hemisphere, but that no longer happens in adulthood. As a result, we used to think that extensive plasticity was not possible in the adult brain.

But in the last 10 or 15 years, researchers have begun to see evidence of residual plasticity in the adult brain, with a wave of research suggesting that the adult brain can still demonstrate plasticity in structure and function. So now, you see paper after paper in Nature and Science saying that taxi drivers in London have bigger hippocampi than those of other people, or that you can enlarge the areas of the brain dealing with sensory motor control by putting people in experiments where they learn to juggle.

These findings hint that there might be ways to harness such mechanisms after injury or disease — hints that we hope to exploit in our work at the center.

Why is interdisciplinary work so important when studying stroke recovery?
Stroke recovery is a complex process that involves the reduction of injury and the repair of damaged circuits, as well as the restoration or retraining of impaired physical, sensory and cognitive processes.

So it requires the input of many disciplines. One of these disciplines is represented by cellular-molecular people — scientists who study gene expression and cellular-molecular approaches to stimulating the formation of new synapses and circuits.

Then of course there are neurologists, who provide our clinical understanding of stroke and stroke recovery. This group includes pediatric and adult stroke neurologists, as well as neurologists who specialize in rehabilitation medicine and in clinical trials research.

A third group is cognitive neuroscientists, people like me who do basic research on learning, development and memory. We believe that rehabilitation involves many of the same mechanisms that underlie basic learning and memory, so if we understand how to control and enhance learning and memory, we'll also understand how to make rehabilitation work better at the times we need it.

What are some particularly promising directions the center will explore in studying stroke recovery and brain plasticity?
There are a few areas we're very interested in. One is something my colleague Alex Dromerick was already investigating at the National Rehabilitation Hospital that is related to my own interests in "critical periods" — windows of time where the brain shows more plasticity than others. In the case of stroke, the literature suggests there is a short period of time after the event where the brain tries to repair itself through processes such as sprouting new synaptic connections.

We don't know whether these processes are actually functional, but they happen pretty early on after a stroke, usually not at a time when people are well enough to undergo rehabilitation. So one promising direction is to test whether we can catch that very early period using appropriate rehabilitation methods, or, by manipulating the underlying molecular mechanisms, even push those processes to occur later, when patients are better able to work on rehabilitation training.

Several of our scientists, including Peter Turkeltaub, MD, PhD, and Michelle Harris-Love, PhD, are also using brain stimulation techniques to study whether stimulating or inhibiting specific parts of the brain can aid in recovery. In these techniques, you give participants magnetic resonance imaging that provides pictures of their brain and skull, then load the images into software that enables you to direct a stimulator on the skull to very precise areas of the brain.

Read the rest of this inspiring interview about combining stimulation techniques with behavioral training to enhance activity that is relevant to impaired cognitive functions.

Click here:
http://www.apa.org/monitor/2013/05/hope-brain.aspx

Wednesday, November 11, 2015

On Brain Health | Will the Brain Heal Itself after a Severe Brain Injury?





TED TALK |  After a traumatic brain injury, it sometimes happens that the brain can repair itself, building new brain cells to replace damaged ones.

But the repair doesn't happen quickly enough to allow recovery from degenerative conditions like motor neuron disease (also known as Lou Gehrig's disease or ALS).

Siddharthan Chandran, a regenative neurologist, walks through some new techniques using special stem cells that could allow the damaged brain to rebuild faster.  In a related topic, Siddharthan Chandran also explores how to heal damage from degenerative disorders such as MS and motor neuron disease (ALS).

In a TED Talk, Siddharthan Chandran states:

Well, you know what? I think there is hope. 
And there's hope in this next section, of this brain section of somebody else with M.S., because what it illustrates is, amazingly, the brain can repair itself. It just doesn't do it well enough. And so again, there are two things I want to show you. 
First of all is the damage of this patient with M.S. And again, it's another one of these white masses. But crucially, the area that's ringed red highlights an area that is pale blue. But that area that is pale blue was once white. So it was damaged. It's now repaired. 
Just to be clear: It's not because of doctors. It's in spite of doctors, not because of doctors. This is spontaneous repair. It's amazing and it's occurred because there are stem cells in the brain, even, which can enable new myelin, new insulation, to be laid down over the damaged nerves. And this observation is important for two reasons. 
The first is it challenges one of the orthodoxies that we learnt at medical school, or at least I did, admittedly last century, which is that the brain doesn't repair itself, unlike, say, the bone or the liver. But actually it does, but it just doesn't do it well enough. 
And the second thing it does, and it gives us a very clear direction of travel for new therapies -- I mean, you don't need to be a rocket scientist to know what to do here. You simply need to find ways of promoting the endogenous, spontaneous repair that occurs anyway."
See and hear Siddharthan Chandran's 2013 TED Talk by click here:
"Can the Damaged Brain Repair Itself?"




Wednesday, October 14, 2015

Business Wire | A New Development in Ground-Breaking Tools to Diagnose TBI

LEXINGTON, MA |   There is currently no way to identify individuals who are at the greatest risk for developing chronic symptoms related to the long-term effects of TBI.  That situation, however, may change.  How?

A new study identifies the correlation of tau accumulation in military personnel to those who experienced long-term neurological symptoms after a TBI. These findings will be used to identify patients who are most at risk.

National Institute of Nursing Research uses something called Quanterix’s Simoa Technology to identify the significance of key protein in long-term complications caused by Traumatic Brain Injury (TBI).

Quanterix headquarters, Lexington MA


To help identify biomarkers that could better pinpoint those at-risk, the researchers explored whether elevated levels of tau—a protein known to have a role in the development of Alzheimer’s disease and Parkinson’s disease—are related to chronic neurological symptoms in military personnel who had experienced TBI.

Quanterix Corporation, a leader in high definition diagnostics, announced on August 3 that JAMA Neurology has published a new study in which its Simoa (single molecule array) technology was used to identify a protein previously linked to acute symptoms following a traumatic brain injury (TBI). 

The study, led by the National Institute of Nursing Research (NINR), a component of the National Institutes of Health, was designed to determine whether levels of tau protein in the blood were correlated to long term effects of a TBI. 

The findings from the study will be used to provide a framework to identify patients who are most at risk for experiencing chronic symptoms related to a TBI.

As cited in the study, approximately one-third of all U.S. military personnel who serve in combat operations experience at least one TBI. Individuals with TBI are more likely to experience ongoing complications such as post-concussive disorder (PCD), post-traumatic stress disorder (PTSD) and depression.  They are also more likely to develop chronic traumatic encephalopathy (CTE)—progressive brain degeneration that leads to dementia following repetitive TBIs. 

Using Quanterix’s ultra-sensitive Simoa technology, researchers were able to accurately measure levels of tau in participants’ blood. Military participants who had elevated tau levels in their samples and had a history of TBI were compared with participants who had never suffered a TBI. Additionally, researchers found that participants with three or more deployment-related TBIs had significantly higher levels of tau compared with participants who had fewer TBIs. These results will be used in future studies to provide a therapeutic target for treating the causes of CTE and other neurodegenerative and psychological conditions that can result from these types of injury.

“When the brain experiences any kind of trauma, whether caused by a hit on the sidelines at a sporting event or someone impacted during combat while serving in the military, miniscule quantities of protein enter the blood stream. Our technology is the only one sensitive enough to measure these proteins in a way that no one thought possible,” said Kevin Hrusovsky, CEO and Executive Chairman, Quanterix. “This is one of the many studies in which Simoa is being used to further understand and quantify the long term effects of TBI and we are pleased to be working with NINR to continue our mission to understand what is going on in the human body and, in turn, improve the quality of care.”

The study sampled military personnel, with or without a history of TBI, who had been deployed for combat in Operation Enduring Freedom (Afghanistan) and/or Operation Iraqi Freedom within the previous 18 months. The researchers examined participant medical records as well as responses to the Warrior Administered Retrospective Casualty Assessment Tool to determine if participants had been diagnosed with or treated for a TBI. 

To read the full study published in the August 3 issue of JAMA Neurology, please visit: http://archneur.jamanetwork.com/journal.aspx.

About Quanterix
Quanterix is a developer of ground-breaking tools in high definition diagnostics. Its Simoa platform uses single molecule measurements to access previously undetectable proteins. With this unprecedented sensitivity and full automation, Simoa offers significant benefits to both research and clinical testing applications. Quanterix was established in 2007 and is located in Lexington, Massachusetts. 

To learn more about Quanterix and Simoa, please visit: www.quanterix.com.

View source version on businesswire.com: http://www.businesswire.com/news/home/20150803005072/en/

Wednesday, October 7, 2015

Join Brainline.org | 7 Things People with a Brain Injury Would Like to Hear...

NEW YORK CITY —   TBI as defined by the people who are living with it ...

Image result for Brain Injuries Do Not Discriminate
BrainLine asked its online community to share the things they would most like to hear from their friends and family, and the list below captures some of the many responses so generously provided by people with TBI.

Every individual’s experience with traumatic brain injury is unique, but there are many common symptoms and emotions. Anger, fear, sadness, and anxiety may be accompanied by difficulties with memory, pain, and the challenges of maintaining relationships.

We encourage you to add your own definitions in the comments section below, and to join the BrainLine community on Facebook, Twitter, YouTube, and Pinterest.

1. I'm sorry. How can I help?
– Alison

2. Please tell me what having a TBI is like. Can you tell me where I can read more about TBI?
– Melody

3. I don't know how you feel, but you are my friend and I will always be there for you.
– AmyRenee

4. I admire your willpower. You will get through this.
– Amina

5. I know I don't understand what it's like, but I will try my hardest to be patient and understanding.
– Christy

6. Take your time — we are not in a hurry.
– Lisa

7. I don't know what to say but I'm sorry it happened to you.
– Crystal

Please join the BrainLine community on FacebookTwitterYouTube, and Pinterest.

BrainLine - preventing, treating, and living with traumatic brain injury (TBI)