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High Rate of Head Injuries in Iraq Soldiers Portends Potential Wave of Epilepsy

September 14th, 2009

Tony Coelho is having déjà vu. The former congressman and author of the Americans with Disabilities Act recalls a commencement address he gave a quarter-century ago, in the wake of the Vietnam war, in which he warned of the potential for seizure disorders in returning troops who had suffered head injuries and called for more research on the link between traumatic brain injury (TBI) and epilepsy. Today, as he watches the storm build amid reports of alarmingly high TBI rates among soldiers returning from Iraq – and the military’s apparent inability to care for them properly – Coelho is struck by the parallels. “Here I am, 25 years later, talking about the same thing,” says Coelho, who has epilepsy as a result of a head injury and is the immediate past chair of the Epilepsy Foundation. “What have we learned?

Growing Chorus of Concern

Coelho is not alone in his concern for the long-term effects of the head injuries that have become the signature injury of the Iraq conflict. A chorus of concern is rising among veterans’ advocates and medical experts across the USA who understand the heightened risk America’s returning war heroes have for a range of posttraumatic europsychological problems. Epilepsy is prominent among them.

The risk is very real, even if the precise numbers are impossible to predict. Trauma to the brain, whether mild or severe, is a clearly defined risk factor for epilepsy. Studies suggest that about 20 to 25 percent of individuals with “closed-head” brain injuries will go on to develop what is termed post-traumatic epilepsy (PTE). PTE accounts for 5 percent of epilepsy overall. The only study that has investigated the prevalence of PTE in the military, reported in 1985, found that as many as 50 percent of Vietnam veterans who had suffered penetrating brain injuries during combat developed seizure disorders months or years later.

Penetrating injuries – when a foreign object or piece of fractured skull enters the brain – are the most severe form of TBI. They are relatively uncommon in civilians and are distinct from the types of head injuries most commonly seen in U.S. troops serving in Iraq. There, most head trauma seems to be a result of the “shock wave” of high pressure that reverberates out from the point of an explosion. Improvised Explosive Devices, or IED’s, have notoriously become the weapon of choice against U.S. troops; the Department of Veterans Affairs (VA) estimates that IED’s account for two-thirds of combat injuries. These “blast injuries” can – and apparently often do – cause brain trauma, even in the absence of obvious wounds.

There is little hard data on the incidence of blast-related head injuries among U.S. soldiers in Iraq, at least that is available to the public. 2003 data from the Walter Reed Army Medical Center found evidence of brain injury in 61 percent of returning soldiers who had been exposed to blasts, according to the Defense and Veterans Brain Injury Center, a partnership between the VA and the Department of Defense (DoD).

No one knows how many of those troops with brain injuries will eventually develop epilepsy.

But with an estimated 1.4 million troops who have served or are currently serving in Iraq, even the most conservative statistics portend a looming crisis of post-TBI neurologic problems that will haunt these soldier heroes, and society at large, for generations to come.

Preventing PTE: New Priority?

The specter of a coming wave of combat-related TBI has refocused attention on the critical need to better predict whom among the head-injured are likely to develop epilepsy, and how to prevent it. It also underscores how little we yet know about preventing epilepsy.

“For many years – even decades – epilepsy research has been focused primarily on the seizures themselves: what they are, how they are generated in the brain, how they spread and what drugs might control them,” says Marc Dichter, M.D., Ph.D., professor of neurology and pharmacology at the University of Pennsylvania. “Basically, we’ve been waiting for epilepsy to happen and then seeing if we can treat it.”

This approach is in stark contrast, Dichter says, to how we as a society deal with other public health problems, such as cancer or heart disease, where we identify risk factors and try to prevent disease from occurring.

“Why aren’t we paying attention to the development of epilepsy, as we do for every other medical disease?” he asks.

Dichter is leading a DoD-funded pilot study in civilians to determine if the anti-seizure drug topiramate (Topamax®)might decrease the risk of post-traumatic epilepsy if given within 12 hours or so of a head injury. Recruitment for the trial is just beginning.

Health and led by Pavel Klein, M.D., a neurologist with Washington Hospital Center in Washington D.C., is further along. The study is designed to evaluate the safety and tolerability of levetiracetam (Keppra®) in people who have suffered a head injury. (Keppra is approved as add-on therapy for partial seizures in adults.) Klein says about 50 adults and children with TBI had been enrolled as of late April, with an eventual goal of 90. If Keppra is found to be safe for use in this population – and so far Klein says it appears to be – the goal is to initiate a much larger study to investigate the drug’s efficacy in preventing PTE.

At least three well-designed clinical studies have previously investigated other anti-seizure medications for preventing injury-induced epilepsy. All have failed to show a benefit. The trials are exceedingly difficult to do, say Dichter and Klein, because they are labor intensive, costly, and take a long time to recruit enough subjects to have meaningful statistical power. Yet it’s critical that they be done. “If you don’t study the question, you’ll never get an answer,” says Dichter.

“Epilepsy is a chronic condition, and a proportion of people will develop refractory epilepsy, which requires life-long, extensive medical treatment and management,” says Klein. “It’s a complicated recovery, in many ways. Prevention is better than treatment.”

‘Strike While the Iron is Hot’

Coelho is particularly concerned that troops who develop seizures long after their active duty is finished may be denied disability benefits. “It has been a huge fight to get the VA and DoD to understand that epilepsy can be a delayed effect of war trauma,” he says.

Still, he points out, the current situation, dire though it is, presents an opportunity to act.

“Congress right now is very conscious of the need to take care of our military men and women,” Coelho says. “It is critically important that we take advantage of the heightened sensitivity to this situation to uncover the facts, identify the problems and go to Congress to get the appropriate funding to get the job done right. We need to strike while the iron is hot.”


Scientists find way to stop epilepsy in mice

August 19th, 2009

TUESDAY, Aug. 4 (HealthDay News) — Blocking a gene defect prevents epilepsy from being passed from adult mice to their offspring, a finding that may help in efforts to develop new treatments for people with epilepsy, British researchers say.

The study proves that a faulty version of a gene called ATP1A3 causes epileptic seizures in mice, said lead researcher Dr. Steve Clapcote, of the Faculty of Biological Sciences at University of Leeds, and colleagues.

“ATP1A3 makes an enzyme called a sodium-potassium pump that regulates levels of sodium and potassium in the brain’s nerve cells. An imbalance of sodium and potassium levels has long been suspected to lead to epileptic seizures, but our study is the first to show beyond any doubt that a defect in this gene is responsible,” Clapcote said in a university news release.

He and his team studied a special strain of mice with an inherited form of severe epilepsy and found that the mice had a defective ATP1A3 gene. When these mice were bred with mice that had an extra copy of the normal ATP1A3 gene, the additional normal gene counteracted the defective gene and the offspring didn’t have epilepsy.

“Our study has identified a new way in which epilepsy can be caused and prevented in mice, and therefore it may provide clues to potential causes, therapies and preventive measures in human epilepsy,” Clapcote said.

The study appears in this week’s online edition of the Proceedings of the National Academy of Sciences.

“Our results are very promising, but there’s a long way to go before this research could yield new antiepileptic therapies. However, the human ATP1A3 gene matches the mouse version of the gene by more than 99 percent, so we’ve already started to screen DNA samples from epilepsy patients to investigate whether ATP1A3 gene defects are involved in the human condition,” Clapcote said.

More information

The American Academy of Family Physicians has more about epilepsy.

 

– Robert Preidt

SOURCE: University of Leeds, news release, Aug. 3, 2009

Copyright © 2009 ScoutNews, LLC. All rights reserved.


Software tool helps web developers identify seizure causing content

July 22nd, 2009

July 22, 2009

by Sandra Knisely

In 1997, an episode of the popular Pokemon cartoon gained worldwide attention when more than 800 Japanese children with photosensitive seizure conditions were admitted to the hospital after viewing the cartoon or the subsequent news coverage of it.

Researchers from the UW-Madison Trace Center have released a software tool that could prevent similar incidences of media-triggered seizures in children who are browsing the Internet or using computer programs.

The software, called the Photosensitive Epilepsy Analysis Tool (PEAT), allows Web developers to evaluate their site content and determine whether the content presents a danger to people with photosensitive epilepsy.

PEAT is the first tool developed for evaluating Web-based content, and a beta version is available for free download from the Trace Center, a pioneer center that designs mainstream information technology accessible to people with disabilities.

Gregg Vanderheiden, a UW-Madison professor of industrial and systems engineering and biomedical engineering, directs the Trace Center.

“As Web content becomes more dynamic and Web pages begin to resemble television, it is important that we not start inadvertently triggering seizures in people with photosensitive seizure disorders,” he says. “PEAT can help prevent that.”

Approximately one in 4,000 people are diagnosed with photosensitive epilepsy and are subject to seizures triggered by certain types of flashing in Web, computer or television content. The condition usually begins before age 20 and is most common between ages 7 and 19. Seizures are most likely to occur when children or teenagers with the condition view content where large areas of a screen flash rapidly and flicker on and off repeatedly.

PEAT allows developers to capture on video a Web browser or application window and all of the actions that occur in the window. Developers then can analyze the video for seizure risk. Developers can also use PEAT to determine if Web content meets the new Web Content Accessibility Guidelines 2.0.

PEAT is the result of six years of collaboration between the Trace Center and professor Graham Harding from Cambridge Research Systems. The National Institute on Disability and Rehabilitation Research, which is part of the U.S. Department of Education, funded the development of PEAT.

source: University of Wisconsin http://www.news.wisc.edu/16917


Epilepsy Phenome/Genome Project

July 10th, 2009

The Epilepsy Phenome/Genome Project is a research study sponsored by the National Institute of Neurological Disorders and Stroke designed to answer the following questions: 

  • Why do some families have several people with epilepsy?
  • How can we predict the best anti-seizure drug to use?
  • What causes epilepsy? 

To learn more about this study, visit  www.epgp.org